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Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379
2024.
The genetics of cognition in schizophrenia.
Brain Medicine
Item availability restricted. |
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Kalman, Janos L., Olde Loohuis, Loes M., Vreeker, Annabel, McQuillin, Andrew, Stahl, Eli A., Ruderfer, Douglas, Grigoroiu-Serbanescu, Maria, Panagiotaropoulou, Georgia, Ripke, Stephan, Bigdeli, Tim B., Stein, Frederike, Meller, Tina, Meinert, Susanne, Pelin, Helena, Streit, Fabian, Papiol, Sergi, Adams, Mark J., Adolfsson, Rolf, Adorjan, Kristina, Agartz, Ingrid, Aminoff, Sofie R., Anderson-Schmidt, Heike, Andreassen, Ole A., Ardau, Raffaella, Aubry, Jean-Michel, Balaban, Ceylan, Bass, Nicholas, Baune, Bernhard T., Bellivier, Frank, Benabarre, Antoni, Bengesser, Susanne, Berrettini, Wade H, Boks, Marco P., Bromet, Evelyn J., Brosch, Katharina, Budde, Monika, Byerley, William, Cervantes, Pablo, Chillotti, Catina, Cichon, Sven, Clark, Scott R., Comes, Ashley L., Corvin, Aiden, Coryell, William, Craddock, Nick, Craig, David W., Croarkin, Paul E., Cruceanu, Cristiana, Czerski, Piotr M., Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Del Zompo, Maria, DePaulo, J. Raymond, Djurovic, Srdjan, Edenberg, Howard J., Eissa, Mariam Al, Elvsåshagen, Torbjørn, Etain, Bruno, Fanous, Ayman H., Fellendorf, Frederike, Fiorentino, Alessia, Forstner, Andreas J., Frye, Mark A., Fullerton, Janice M., Gade, Katrin, Garnham, Julie, Gershon, Elliot, Gill, Michael, Goes, Fernando S., Gordon-Smith, Katherine, Grof, Paul, Guzman-Parra, Jose, Hahn, Tim, Hasler, Roland, Heilbronner, Maria, Heilbronner, Urs, Jamain, Stephane, Jimenez, Esther, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa, Jonsson, Lina, Kahn, Rene S., Kelsoe, John R., Kennedy, James L., Kircher, Tilo, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kittel-Schneider, Sarah, Klöhn-Saghatolislam, Farah, Knowles, James A., Kranz, Thorsten M., Lagerberg, Trine Vik, Landen, Mikael, Lawson, William B., Leboyer, Marion, Li, Qingqin S., Maj, Mario, Malaspina, Dolores, Manchia, Mirko, Mayoral, Fermin, McElroy, Susan L., McInnis, Melvin G., McIntosh, Andrew M., Medeiros, Helena, Melle, Ingrid, Milanova, Vihra, Mitchell, Philip B., Monteleone, Palmiero, Monteleone, Alessio Maria, Nöthen, Markus M., Novak, Tomas, Nurnberger, John I., O'Brien, Niamh, O'Connell, Kevin S., O'Donovan, Claire, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Opel, Nils, Ortiz, Abigail, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pålsson, Erik, Pato, Carlos, Pato, Michele T., Pawlak, Joanna, Pfarr, Julia-Katharina, Pisanu, Claudia, Potash, James B., Rapaport, Mark H, Reich-Erkelenz, Daniela, Reif, Andreas, Reininghaus, Eva, Repple, Jonathan, Richard-Lepouriel, Hélène, Rietschel, Marcella, Ringwald, Kai, Roberts, Gloria, Rouleau, Guy, Schaupp, Sabrina, Scheftner, William A, Schmitt, Simon, Schofield, Peter R., Schubert, K. Oliver, Schulte, Eva C., Schweizer, Barbara, Senner, Fanny, Severino, Giovanni, Sharp, Sally, Slaney, Claire, Smeland, Olav B., Sobell, Janet L., Squassina, Alessio, Stopkova, Pavla, Strauss, John, Tortorella, Alfonso, Turecki, Gustavo, Twarowska-Hauser, Joanna, Veldic, Marin, Vieta, Eduard, Vincent, John B., Xu, Wei, Zai, Clement C., Zandi, Peter P., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Smoller, Jordan W., Biernacka, Joanna M., McMahon, Francis J., Alda, Martin, Müller-Myhsok, Bertram, Koutsouleris, Nikolaos, Falkai, Peter, Freimer, Nelson B., Andlauer, Till F.M., Schulze, Thomas G. and Ophoff, Roel A. 2021. Characterisation of age and polarity at onset in bipolar disorder. The British Journal of Psychiatry 219 (6) , pp. 659-669. 10.1192/bjp.2021.102 |
Jia, Xiaoming, Goes, Fernando S., Locke, Adam E., Palmer, Duncan, Wang, Weiqing, Cohen-Woods, Sarah, Genovese, Giulio, Jackson, Anne U., Jiang, Chen, Kvale, Mark, Mullins, Niamh, Nguyen, Hoang, Pirooznia, Mehdi, Rivera, Margarita, Ruderfer, Douglas M., Shen, Ling, Thai, Khanh, Zawistowski, Matthew, Zhuang, Yongwen, Abecasis, Gonçalo, Akil, Huda, Bergen, Sarah, Burmeister, Margit, Champion, Sinead, DelaBastide, Melissa, Juréus, Anders, Kang, Hyun Min, Kwok, Pui-Yan, Li, Jun Z., Levy, Shawn E., Monson, Eric T., Moran, Jennifer, Sobell, Janet, Watson, Stanley, Willour, Virginia, Zöllner, Sebastian, Adolfsson, Rolf, Blackwood, Douglas, Boehnke, Michael, Breen, Gerome, Corvin, Aiden, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Hultman, Christina M., Landen, Mikael, Lewis, Cathryn, McCarroll, Steven A., Richard McCombie, W., McGuffin, Peter, McIntosh, Andrew, McQuillin, Andrew, Morris, Derek, Myers, Richard M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Ophoff, Roel, Boks, Marco, Kahn, Rene, Ouwehand, Willem, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Pato, Carlos, Pato, Michele, Posthuma, Danielle, Potash, James B., Reif, Andreas, Sklar, Pamela, Smoller, Jordan, Sullivan, Patrick F., Vincent, John, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Neale, Benjamin, Purcell, Shaun, Risch, Neil, Schaefer, Catherine, Stahl, Eli A., Zandi, Peter P. and Scott, Laura J. 2021. Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder. Molecular Psychiatry 26 , pp. 5239-5250. 10.1038/s41380-020-01006-9 |
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Forsyth, Jennifer K., Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R. K., Villalon-Reina, Julio E., Thompson, Paul M., Bearden, Carrie E., Cunningham, Adam, Doherty, Joanne L., Linden, David E. ORCID: https://orcid.org/0000-0002-5638-9292, Moss, Hayley, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 2021. Prioritizing genetic contributors to cortical alterations in 22q11.2 deletion syndrome using imaging transcriptomics. Cerebral Cortex 31 (7) , pp. 3285-3298. 10.1093/cercor/bhab008 |
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Richards, Alexander, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Frizzati, Aura ORCID: https://orcid.org/0000-0002-7002-6180, Tansey, Katherine, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Legge, Sophie, Savage, Jeanna, Agartz, Ingrid, Andreassen, Ole, Blokland, Gabriella, Corvin, Aiden, Cosgrove, Donna, Degenhardt, Franzoska, Djurovic, Srdjan, Espeseth, Thomas, Ferraro, Laura, Gayer-Anderson, Charlotte, Giegking, Ina, van Haren, Neeltje, Hartmann, Annette, Hubert, John, Jonsson, Erik, Konte, Bettina, Lennertz, Leonhard, Olde Loohuis, Loes, Melle, Ingrid, Morgan, Craig, Morris, Derek, Murray, Robin, Nyman, Håkan, Ophoff, Roel, van Os, Jim, Petryshen, Tracey, Quattrone, Diego, Rietschel, Marcella, Rujescu, Dan, Ruttan, Bart, Streit, Fabin, Strohmaier, Janna, Sullivan, Patrick, Sundet, Kjetil, Wagner, MIchael, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Donohoe, Gary, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Schizophrenia Working Group of the Psychiatric Genomics Consorti and EUGEI WP Group 2020. The relationship between polygenic risk scores and cognition in schizophrenia. Schizophrenia Bulletin 46 (2) , -. 10.1093/schbul/sbz061 |
Sullivan, Patrick F. and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. Increasing the clinical psychiatric knowledge base about pathogenic copy number variation. American Journal of Psychiatry 177 (3) , pp. 204-209. 10.1176/appi.ajp.2019.19040335 |
Glanville, Kylie P., Coleman, Jonathan R.I., Hanscombe, Ken B., Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L., Breen, Gerome, Air, Tracy M., Andlauer, Till F.M., Baune, Bernhard T., Binder, Elisabeth B., Blackwood, Douglas H.R., Boomsma, Dorret I., Buttenschøn, Henriette N., Colodro-Conde, Lucía, Dannlowski, Udo, Direk, Nese, Dunn, Erin C., Forstner, Andreas J., de Geus, Eco J.C., Grabe, Hans J., Hamilton, Steven P., Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A., Knowles, James A., Kutalik, Zoltán, Levinson, Douglas F., Lewis, Glyn, Lind, Penelope A., Lucae, Susanne, Magnusson, Patrik K., McGuffin, Peter, McIntosh, Andrew M., Milaneschi, Yuri, Mors, Ole, Mostafavi, Sara, Müller-Myhsok, Bertram, Pedersen, Nancy L., Penninx, Brenda W.J.H., Potash, James B., Preisig, Martin, Ripke, Stephan, Shi, Jianxin, Shyn, Stanley I., Smoller, Jordan W., Streit, Fabian, Sullivan, Patrick F., Tiemeier, Henning, Uher, Rudolf, Van der Auwera, Sandra, Weissman, Myrna M., O'Reilly, Paul F., Lewis, Cathryn M., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan R.I., Colodro-Conde, Lucía, Couvy-Duchesne, Baptiste, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Crawford, Gregory E., Davies, Gail, Deary, Ian J., Degenhardt, Franziska, Derks, Eske M., Direk, Nese, Dolan, Conor V., Dunn, Erin C., Eley, Thalia C., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hassan Kiadeh, Farnush Farhadi, Finucane, Hilary K., Foo, Jerome C., Forstner, Andreas J., Frank, Josef, Gaspar, Héléna A., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Grove, Jakob, Hall, Lynsey, Hansen, Christine Søholm, Hansen, Thomas F., Herms, Stefan, Hickie, Ian B., Hoffmann, Per, Homuth, Georg, Horn, Carsten, Hottenga, Jouke-Jan, Hougaard, David M., Howard, David M., Ising, Marcus, Jansen, Rick, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A., Jorgenson, Eric, Knowles, James A., Kohane, Isaac S., Kraft, Julia, Kretzschmar, Warren W., Kutalik, Zoltán, Li, Yihan, Lind, Penelope A., MacIntyre, Donald J., MacKinnon, Dean F., Maier, Robert M., Maier, Wolfgang, Marchini, Jonathan, Mbarek, Hamdi, McGrath, Patrick, McGuffin, Peter, Medland, Sarah E., Mehta, Divya, Middeldorp, Christel M., Mihailov, Evelin, Milaneschi, Yuri, Milani, Lili, Mondimore, Francis M., Montgomery, Grant W., Mostafavi, Sara, Mullins, Niamh, Nauck, Matthias, Ng, Bernard, Nivard, Michel G., Nyholt, Dale R., O'Reilly, Paul F., Oskarsson, Hogni, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, Painter, Jodie N., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Peterson, Roseann E., Pettersson, Erik, Peyrot, Wouter J., Pistis, Giorgio, Posthuma, Danielle, Quiroz, Jorge A., Qvist, Per, Rice, John P., Riley, Brien P., Rivera, Margarita, Mirza, Saira Saeed, Schoevers, Robert, Schulte, Eva C., Shen, Ling, Shi, Jianxin, Shyn, Stanley I., Sigurdsson, Engilbert, Sinnamon, Grant C.B., Smit, Johannes H., Smith, Daniel J., Stefansson, Hreinn, Steinberg, Stacy, Streit, Fabian, Strohmaier, Jana, Tansey, Katherine E., Teismann, Henning, Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Traylor, Matthew, Treutlein, Jens, Trubetskoy, Vassily, Uitterlinden, Andrés G., Umbricht, Daniel, Van der Auwera, Sandra, van Hemert, Albert M., Viktorin, Alexander, Visscher, Peter M., Wang, Yunpeng, Webb, Bradley T., Weinsheimer, Shantel Marie, Wellmann, Jürgen, Willemsen, Gonneke, Witt, Stephanie H., Wu, Yang, Xi, Hualin S., Yang, Jian, Zhang, Futao, Arolt, Volker, Baune, Bernhard T., Berger, Klaus, Boomsma, Dorret I., Cichon, Sven, Dannlowski, Udo, de Geus, E.J.C., DePaulo, J. Raymond, Domenici, Enrico, Domschke, Katharina, Esko, Tõnu, Grabe, Hans J., Hamilton, Steven P., Hayward, Caroline, Heath, Andrew C., Kendler, Kenneth S., Kloiber, Stefan, Lewis, Glyn, Li, Qingqin S., Lucae, Susanne, Madden, Pamela AF., Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Metspalu, Andres, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Nordentoft, Merete, Nöthen, Markus M., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Paciga, Sara A., Pedersen, Nancy L., Penninx, Brenda W.J.H., Perlis, Roy H., Porteous, David J., Potash, James B., Preisig, Martin, Rietschel, Marcella, Schaefer, Catherine, Schulze, Thomas G., Smoller, Jordan W., Stefansson, Kari, Tiemeier, Henning, Uher, Rudolf, Völzke, Henry, Weissman, Myrna M., Werge, Thomas, Lewis, Cathryn, Levinson, Douglas F., Breen, Gerome, Børglum, Anders D., Sullivan, Patrick F. and Wray, Naomi 2020. Classical human leukocyte antigen alleles and C4 haplotypes are not significantly associated with depression. Biological Psychiatry 87 (5) , pp. 419-430. 10.1016/j.biopsych.2019.06.031 |
Morrison, Sinead, Chawner, Samuel J. R. A., van Amelsvoort, Therese A. M. J., Swillen, Ann, Vingerhoets, Claudia, Vergaelen, Elfi, Linden, David E. J. ORCID: https://orcid.org/0000-0002-5638-9292, Linden, Stefanie ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254 2020. Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology. Translational Psychiatry 10 , 53. 10.1038/s41398-020-0736-7 |
Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Moss, Hayley, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E., Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong and Zwick, Michael 2020. Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects. American Journal of Human Genetics 106 (1) , pp. 26-40. 10.1016/j.ajhg.2019.11.010 |
Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K. ORCID: https://orcid.org/0000-0002-6980-4053, Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kranzler, Henry R., Luykx, Jurjen J., Rohde, Luis A., Zai, Clement C., Agerbo, Esben, Arranz, M.J., Asherson, Philip, Bækvad-Hansen, Marie, Baldursson, Gísli, Bellgrove, Mark, Belliveau, Richard A., Buitelaar, Jan, Burton, Christie L., Bybjerg-Grauholm, Jonas, Casas, Miquel, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Cormand, Bru, Crosbie, Jennifer, Dalsgaard, Søren, Demontis, Ditte, Doyle, Alysa E., Dumont, Ashley, Elia, Josephine, Grove, Jakob, Gudmundsson, Olafur O., Haavik, Jan, Hakonarson, Hakon, Hansen, Christine S., Hartman, Catharina A., Hawi, Ziarih, Hervás, Amaia, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Kuntsi, Jonna, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Lesch, Klaus-Peter, Leung, Patrick W.L., Loo, Sandra K., Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, McGough, James J., Medland, Sarah E., Moran, Jennifer L., Mors, Ole, Mortensen, Preben B., Oades, Robert D., Palmer, Duncan S., Pedersen, Carsten B., Pedersen, Marianne G., Peters, Triinu, Poterba, Timothy, Poulsen, Jesper B., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Ribasés, Marta, Rothenberger, Aribert, Rovira, Paula, Sánchez-Mora, Cristina, Satterstrom, F. Kyle, Schachar, Russell, Artigas, Maria Soler, Steinberg, Stacy, Stefansson, Hreinn, Turley, Patrick, Walters, G. Bragi ORCID: https://orcid.org/0000-0002-6980-4053, Werge, Thomas, Zayats, Tetyana, Arking, Dan E., Bettella, Francesco, Buxbaum, Joseph D., Christensen, Jane H., Collins, Ryan L., Coon, Hilary, De Rubeis, Silvia, Delorme, Richard, Grice, Dorothy E., Hansen, Thomas F., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hope, Sigrun, Hultman, Christina M., Klei, Lambertus, Ladd-Acosta, Christine, Magnusson, Pall, Nærland, Terje, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Roeder, Kathryn, Rouleau, Guy A., Saemundsen, Evald, Sanders, Stephan J., Sandin, Sven, St Pourcain, Beate, Stefansson, Kari, Sutcliffe, James S., Talkowski, Michael E., Weiss, Lauren A., Willsey, A. Jeremy, Agartz, Ingrid, Akil, Huda, Albani, Diego, Alda, Martin, Als, Thomas D., Anjorin, Adebayo, Backlund, Lena, Bass, Nicholas, Bauer, Michael, Baune, Bernhard T., Bellivier, Frank, Bergen, Sarah E., Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H.R., Bøen, Erlend, Budde, Monika, Bunney, William, Burmeister, Margit, Byerley, William, Byrne, Enda M., Cichon, Sven, Clarke, Toni-Kim, Coleman, Jonathan R.I., Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Curtis, David, Czerski, Piotr M., Dale, Anders M., Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Elvsåshagen, Torbjørn, Etain, Bruno, Fischer, Sascha B., Forstner, Andreas J., Forty, Liz, Frank, Josef, Frye, Mark, Fullerton, Janice M., Gade, Katrin, Gaspar, Héléna A., Gershon, Elliot S., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Gordon-Smith, Katherine, Green, Melissa J., Greenwood, Tiffany A., Grigoroiu-Serbanescu, Maria, Guzman-Parra, José, Hauser, Joanna, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A. ORCID: https://orcid.org/0000-0001-5821-5889, Kandaswamy, Radhika, Kelsoe, John R., Kennedy, James L., Joachim, Oedegaard Ketil, Kittel-Schneider, Sarah, Kogevinas, Manolis, Koller, Anna C., Lavebratt, Catharina, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Loohuis, Loes M.O., Lucae, Susanne, Maaser, Anna, Malt, Ulrik F., Martin, Nicholas G. ORCID: https://orcid.org/0000-0002-8911-3479, Martinsson, Lina, McElroy, Susan L., McMahon, Francis J., McQuillin, Andrew, Melle, Ingrid, Metspalu, Andres, Millischer, Vincent, Mitchell, Philip B., Montgomery, Grant W., Morken, Gunnar, Morris, Derek W., Müller-Myhsok, Bertram, Mullins, Niamh, Myers, Richard M., Nievergelt, Caroline M., Nordentoft, Merete, Adolfsson, Annelie Nordin, Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paciga, Sara A., Pato, Carlos N., Pato, Michele T., Perlis, Roy H., Perry, Amy, Potash, James B., Reinbold, Céline S., Rietschel, Marcella, Rivera, Margarita, Roberson, Mary, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Serretti, Alessandro, Sigurdsson, Engilbert, Smeland, Olav B., Stordal, Eystein, Streit, Fabian, Strohmaier, Jana, Thorgeirsson, Thorgeir E., Treutlein, Jens, Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Wang, Yunpeng, Witt, Stephanie H., Zandi, Peter, Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Aschauer, Harald, Baker, Jessica H., Bencko, Vladimir, Bergen, Andrew W., Birgegård, Andreas, Perica, Vesna Boraska, Brandt, Harry, Burghardt, Roland, Carlberg, Laura, Cassina, Matteo, Clementi, Maurizio, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James J., Danner, Unna N., Davis, Oliver S.P., Degortes, Daniela, DeSocio, Janiece E., Dick, Danielle M., Dina, Christian, Docampo, Elisa, Egberts, Karin, Ehrlich, Stefan, Espeseth, Thomas, Fernández-Aranda, Fernando, Fichter, Manfred M., Foretova, Lenka, Forzan, Monica, Gambaro, Giovanni, Giegling, Ina, Gonidakis, Fragiskos, Gorwood, Philip, Mayora, Monica Gratacos, Guo, Yiran, Halmi, Katherine A., Hatzikotoulas, Konstantinos, Hebebrand, Johannes, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hinney, Anke, Imgart, Hartmut, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jennifer, Julià, Antonio, Kaminská, Deborah, Karhunen, Leila, Karwautz, Andreas, Kas, Martien J.H., Kaye, Walter H., Kennedy, Martin A., Kim, Youl-Ri, Klareskog, Lars, Klump, Kelly L., Knudsen, Gun Peggy S., Landén, Mikael, Le Hellard, Stephanie, Levitan, Robert D., Li, Dong, Lichtenstein, Paul, Maj, Mario, Marsal, Sara, McDevitt, Sara, Mitchell, James, Monteleone, Palmiero, Monteleone, Alessio Maria, Munn-Chernoff, Melissa A., Nacmias, Benedetta, Navratilova, Marie, O'Toole, Julie K., Padyukov, Leonid, Pantel, Jacques, Papezova, Hana, Rabionet, Raquel, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ricca, Valdo, Roberts, Marion, Rujescu, Dan, Rybakowski, Filip, Scherag, André, Schmidt, Ulrike, Seitz, Jochen, Slachtova, Lenka, Slof-Opt Landt, Margarita C.T., Slopien, Agnieszka, Sorbi, Sandro, Southam, Lorraine, Strober, Michael, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., Wade, Tracey D., Wagner, Gudrun, Walton, Esther, Watson, Hunna J., Wichmann, H-Erich, Woodside, D. Blake, Zeggini, Eleftheria, Zerwas, Stephanie, Zipfel, Stephan, Adams, Mark J., Andlauer, Till F.M., Berger, Klaus, Binder, Elisabeth B., Boomsma, Dorret I., Castelao, Enrique, Colodro-Conde, Lucía, Direk, Nese, Docherty, Anna R., Domenici, Enrico, Domschke, Katharina, Dunn, Erin C., Foo, Jerome C., de. Geus, E.J.C., Grabe, Hans J., Hamilton, Steven P., Horn, Carsten, Hottenga, Jouke-Jan, Howard, David, Ising, Marcus, Kloiber, Stefan, Levinson, Douglas F., Lewis, Glyn, Magnusson, Patrik K.E., Mbarek, Hamdi, Middeldorp, Christel M., Mostafavi, Sara, Nyholt, Dale R., Penninx, Brenda WJH., Peterson, Roseann E., Pistis, Giorgio, Porteous, David J., Preisig, Martin, Quiroz, Jorge A., Schaefer, Catherine, Schulte, Eva C., Shi, Jianxin, Smith, Daniel J., Thomson, Pippa A., Tiemeier, Henning, Uher, Rudolf, van der Auwera, Sandra, Weissman, Myrna M., Alexander, Madeline, Begemann, Martin, Bramon, Elvira, Buccola, Nancy G., Cairns, Murray J., Campion, Dominique, Carr, Vaughan J., Cloninger, C. Robert, Cohen, David, Collier, David A., Corvin, Aiden, DeLisi, Lynn E., Donohoe, Gary, Dudbridge, Frank, Duan, Jubao, Freedman, Robert, Gejman, Pablo V., Golimbet, Vera, Godard, Stephanie, Ehrenreich, Hannelore, Hartmann, Annette M., Henskens, Frans A., Ikeda, Masashi, Iwata, Nakao, Jablensky, Assen V., Joa, Inge, Jönsson, Erik G., Kelly, Brian J., Knight, Jo, Konte, Bettina, Laurent-Levinson, Claudine, Lee, Jimmy, Lencz, Todd, Lerer, Bernard, Loughland, Carmel M., Malhotra, Anil K., Mallet, Jacques, McDonald, Colm, Mitjans, Marina, Mowry, Bryan J., Murphy, Kieran C., Murray, Robin M., O'Neill, F. 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Green, Elaine K., Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Forty, Liz, Gordon-Smith, Katherine, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Fraser, Christine, Richards, Alexander L., Moran, Jennifer L., Purcell, Shaun, Sklar, Pamela, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nick ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa ORCID: https://orcid.org/0000-0001-5821-5889 and Jones, Ian R. ORCID: https://orcid.org/0000-0001-5821-5889 2017. Genome-wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (8) , pp. 767-771. 10.1002/ajmg.b.32572 |
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Bassett, Anne S., Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van Den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M., Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zackai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Clodagh, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J., Scherer, Stephen W., Emanuel, Beverly S., Guo, Tingwei, Morrow, Bernice E., Marshall, Christian R. and International 22q11.2DS Brain and Behavior Consortium 2017. Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome. American Journal of Psychiatry 174 (11) , pp. 1054-1063. 10.1176/appi.ajp.2017.16121417 |
Leonenko, Ganna ORCID: https://orcid.org/0000-0001-8025-661X, Richards, Alexander L., Walters, James T. ORCID: https://orcid.org/0000-0002-6980-4053, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Chambert, Kimberly, Al Eissa, Mariam M., Sharp, Sally I., O'Brien, Niamh L., Curtis, David, Bass, Nicholas J., McQuillin, Andrew, Hultman, Christina, Moran, Jennifer L., McCarroll, Steven A., Sklar, Pamela, Neale, Benjamin M., Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Sullivan, Patrick F. and O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 2017. Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 174 (7) , pp. 724-731. 10.1002/ajmg.b.32560 |
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Demaerel, Wolfram, Hestand, Matthew S., Vergaelen, Elfi, Swillen, Ann, López-Sánchez, Marcos, Pérez-Jurado, Luis A., McDonald-McGinn, Donna M., Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E., Breckpot, Jeroen, Devriendt, Koenraad, Vermeesch, Joris R., Antshel, Kevin, Arango, Celso, Armando, Marco, Bassett, Anne, Bearden, Carrie, Boot, Erik, Bravo-Sanchez, Marta, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Campbell, Linda, Carmel, Miri, Chow, Eva, Crowley, T. Blaine, Cubells, Joseph, Cutler, David, Demaerel, Wolfram, Digilio, Maria Cristina, Duijff, Sasja, Eliez, Stephan, Emanuel, Beverly, Epstein, Michael, Evers, Rens, Fernandez Garcia-Moya, Luis, Fiksinski, Ania, Fraguas, David, Fremont, Wanda, Fritsch, Rosemarie, Garcia-Minaur, Sixto, Golden, Aaron, Gothelf, Doron, Guo, Tingwei, Gur, Ruben, Gur, Raquel, Heine-Suner, Damian, Hestand, Matthew, Hooper, Stephen, Kates, Wendy, Kushan, Leila, Laorden-Nieto, Alejandra, Maeder, Johanna, Marino, Bruno, Marshall, Christian, McCabe, Kathryn, McDonald-McGinn, Donna, Michaelovosky, Elena, Morrow, Bernice, Moss, Edward, Mulle, Jennifer, Murphy, Declan, Murphy, Kieran, Murphy, Clodagh, Niarchou, Maria ORCID: https://orcid.org/0000-0002-8855-7393, Ornstein, Claudia, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Philip, Nicole, Repetto, Gabriela, Schneider, Maude, Shashi, Vandana, Simon, Tony, Swillen, Ann, Tassone, Flora, Unolt, Marta, van Amelsvoort, Therese, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, Van Duin, Esther, Vergaelen, Elfi, Vermeesch, Joris, Vicari, Stefano, Vingerhoets, Claudia, Vorstman, Jacob, Warren, Steve, Weinberger, Ronnie, Weisman, Omri, Weizman, Abraham, Zackai, Elaine, Zhang, Zhengdong and Zwick, Michael 2017. Nested inversion polymorphisms predispose chromosome 22q11.2 to meiotic rearrangements [RETRACTED]. American Journal of Human Genetics 101 (4) , pp. 616-622. 10.1016/j.ajhg.2017.09.002 |
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Reitz, Christine, Cheung, Rong, Rogaeva, Ekaterina, Lee, Joseph H., Tokuhiro, Shinya, Zou, Fanggeng, Bettens, Karolien, Sleegers, Kristel, Tan, Eng King, Kimura, Ryo, Shibata, Nobuto, Arai, Heii, Kamboh, Ilyas, Prince, Jonathan A., Maier, Wolfgang, Riemenschneider, Matthias, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Hollingworth, Paul, Cellini, Elena, Sorbi, Sandro, Nacmias, Benedetta, Takeda, Masatoshi, Pericak-Vance, Margaret A., Haines, Jonathan L., Younkin, Steven, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, van Broeckhoven, Christine, Farrer, Lindsay, St George-Hyslop, Peter and Mayeux, Richard 2011. Meta-analysis of the association between variants in SORL1 and Alzheimer Disease. Archives of Neurology 68 (1) , pp. 99-106. 10.1001/archneurol.2010.346 |
Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Raybould, Rachel, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, St. Clair, D., Young, A.H., Ferrier, I.N., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2011. DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (4) , pp. 490-492. 10.1002/ajmg.b.31187 |
Smith, Rhodri L., Knight, Deborah, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Dwyer, Sarah Lynne, Richards, Alexander, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (5) , pp. 532-535. 10.1002/ajmg.b.31191 |
Schosser, A., Gaysina, D., Cohen-Woods, S., Domenici, E., Perry, J., Tozzi, F., Korszun, A., Gunasinghe, C., Gray, J., Jones, L., Binder, E. B., Holsboer, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craig, I. W., Farmer, A. E., Muglia, P. and McGuffin, P. 2011. A follow-up case-control association study of tractable (druggable) genes in recurrent major depression. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (6) , pp. 640-650. 10.1002/ajmg.b.31204 |
Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Dwyer, Sarah Lynne, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Pahwa, Jaspreet Singh, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216 |
Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Smith, Rhodri L., Dwyer, Sarah Lynne, Russo, Giancarlo, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2011. Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 781-784. 10.1002/ajmg.b.31219 |
Carroll, Liam Stuart, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 844-849. 10.1002/ajmg.b.31231 |
Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McGuffin, Peter, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240 |
Peall, Kathryn J. ORCID: https://orcid.org/0000-0003-4749-4944, Waite, Adrian James, Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Morris, Huw Rees 2011. Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic review. Movement Disorders 26 (10) , pp. 1939-1942. 10.1002/mds.23791 |
Boot, Erik, Booij, Jan, Zinkstok, Janneke R., Baas, Frank, Swillen, Ann, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, Declan G., Murphy, Kieran C., Linszen, Don H. and Van Amelsvoort, Thérèse A. 2011. COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome. Synapse 65 (9) , pp. 967-970. 10.1002/syn.20932 |
Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Mattheisen, Manuel, Miró, Xavier, Strohmaier, Jana, Steffens, Michael, Meesters, Christian, Herms, Stefan, Weingarten, Moritz, Priebe, Lutz, Haenisch, Britta, Alexander, Michael, Vollmer, Jennifer, Breuer, René, Schmäl, Christine, Tessmann, Peter, Moebus, Susanne, Wichmann, H.-Erich, Schreiber, Stefan, Müller-Myhsok, Bertram, Lucae, Susanne, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Henry, Chantal, Kahn, Jean-Pierre, Heath, Simon, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Reif, Andreas, Sasse, Johanna, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Mitchell, Philip B., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Gustafsson, Omar, Andreassen, Ole, Djurovic, Srdjan, Sigurdsson, Engilbert, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Kapur-Pojskic, Lejla, Oruc, Liliana, Rivas, Fabio, Mayoral, Fermín, Chuchalin, Alexander, Babadjanova, Gulja, Tiganov, Alexander S., Pantelejeva, Galina, Abramova, Lilia I., Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C., Czerski, Piotr M., Hauser, Joanna, Zimmer, Andreas, Lathrop, Mark, Schulze, Thomas G., Wienker, Thomas F., Schumacher, Johannes, Maier, Wolfgang, Propping, Peter, Rietschel, Marcella and Nöthen, Markus M. 2011. Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. American Journal of Human Genetics 88 (3) , pp. 372-381. 10.1016/j.ajhg.2011.01.017 |
Hansen, Thomas, Ingason, Andrés, Djurovic, Srdjan, Melle, Ingrid, Fenger, Mogens, Gustafsson, Omar, Jakobsen, Klaus D., Rasmussen, Henrik B., Tosato, Sarah, Rietschel, Marcella, Frank, Josef, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Bonetto, Chiara, Suvisaari, Jaana, Thygesen, Johan Hilge, Pétursson, Hannes, Lönnqvist, Jouko, Sigurdsson, Engilbert, Giegling, Ina, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ruggeri, Mirella, Cichon, Sven, Ophoff, Roel A., Pietiläinen, Olli, Peltonen, Leena, Nöthen, Markus M., Rujescu, Dan, St. Clair, David, Collier, David A., Andreassen, Ole A. and Werge, Thomas 2011. At-risk variant in TCF7L2 for type II diabetes increases risk of schizophrenia. Biological Psychiatry 70 (1) , pp. 59-63. 10.1016/j.biopsych.2011.01.031 |
Donohoe, Gary, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053, Morris, Derek W., Da Costa, Andreia, Rose, Emma, Hargreaves, April, Maher, Katie, Hayes, Eimear, Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Muglia, Pierandrea, Moskvina, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Gill, Michael, Corvin, Aiden and Rujescu, Dan 2011. A neuropsychological investigation of the genome wide associated schizophrenia risk variant NRGN rs12807809 [Letter]. Schizophrenia Research 125 (2-3) , pp. 304-306. 10.1016/j.schres.2010.10.019 |
Proitsi, P., Hamilton, G., Tsolaki, M., Lupton, M., Daniilidou, M., Hollingworth, Paul, Archer, N., Foy, C., Stylios, F., McGuinness, B., Todd, S., Lawlor, B., Gill, M., Brayne, C., Rubinsztein, D.C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, John David, Craig, D., Passmore, P., Lovestone, S. and Powell, J. F. 2011. A Multiple Indicators Multiple Causes (MIMIC) model of Behavioural and Psychological Symptoms in Dementia (BPSD). Neurobiology of Aging 32 (3) , pp. 434-442. 10.1016/j.neurobiolaging.2009.03.005 |
Steinberg, S., de Jong, S., Andreassen, O. A., Werge, T., Borglum, A. D., Mors, O., Mortensen, P. B., Gustafsson, O., Costas, J., Pietilainen, O. P. H., Demontis, D., Papiol, S., Huttenlocher, J., Mattheisen, M., Breuer, R., Vassos, E., Giegling, I., Fraser, G., Walker, N., Tuulio-Henriksson, A., Suvisaari, J., Lonnqvist, J., Paunio, T., Agartz, I., Melle, I., Djurovic, S., Strengman, E., Jurgens, G., Glenthoj, B., Terenius, L., Hougaard, D, Orntoft, T., Wiuf, C., Didriksen, M., Hollegaard, M. V., Nordentoft, M., van Winkel, R., Kenis, G., Abramova, L., Kaleda, V., Arrojo, M., Sanjuan, J., Arango, C., Sperling, S., Rossner, M., Ribolsi, M., Magni, V., Siracusano, A., Christiansen, C., Kiemeney, L. A., Veldink, J., van den Berg, L., Ingason, A., Muglia, P., Murray, R., Nothen, M. M., Sigurdsson, E., Petursson, H., Thorsteinsdottir, U., Kong, A., Rubino, I. A., De Hert, M., Rethelyi, J. M., Bitter, I., Jonsson, E. G., Golimbet, V., Carracedo, A., Ehrenreich, H., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Ruggeri, M., Tosato, S., Peltonen, L., Ophoff, R. A., Collier, D. A., St Clair, D., Rietschel, M., Cichon, S., Stefansson, H., Rujescu, D. and Stefansson, K. 2011. Common variants at VRK2 and TCF4 conferring risk of schizophrenia. Human Molecular Genetics 20 (20) , pp. 4076-4081. 10.1093/hmg/ddr325 |
Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Kamatani, Y., Kamatani, N., Stoianov, D., Vazharova, R., Karachanak, S., Zaharieva, I., Dimova, I., Hadjidekova, S., Milanova, V., Madjirova, N., Gerdjikov, I., Tolev, T., Poryazova, N., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Toncheva, D. and Nakamura, Y. 2011. Genome-wide association study on bipolar disorder in the Bulgarian population. Genes, Brain and Behavior 10 (7) , pp. 789-797. 10.1111/j.1601-183X.2011.00721.x |
Samaan, Zainab, Gaysina, Daria, Cohen-Woods, Sarah, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Jones, Lisa, Korszun, Ania, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mente, Andrew, McGuffin, Peter and Farmer, Anne 2011. Methylenetetrahydrofolate reductase gene variant (MTHFR C677T) and migraine: a case control study and meta-analysis. BMC Neurology 11 , pp. 66-74. 10.1186/1471-2377-11-66 |
Breen, Gerome, Webb, Bradley Todd, Butler, Amy W., van den Oord, Edwin J. C. G., Tozzi, Federica, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos, Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Cohen-Woods, Sarah, Perry, Julia, Galwey, Nicholas W., Upmanyu, Ruchi, Craig, Ian, Lewis, Cathryn M., Ng, Mandy, Brewster, Shyama, Preisig, Martin, Rietschel, Marcella, Jones, Lisa, Knight, Jo, Rice, John, Muglia, Pierandrea, Farmer, Anne E. and McGuffin, Peter 2011. A genome-wide significant linkage for severe depression on chromosome 3: the depression network study. American Journal of Psychiatry 168 (8) , pp. 840-847. 10.1176/appi.ajp.2011.10091342 |
Schosser, Alexandra, Butler, Amy W., Ising, Marcus, Perroud, Nader, Uher, Rudolf, Ng, Mandy Y., Cohen-Woods, Sarah, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Korszun, Ania, Jones, Lisa, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Gill, Michael, Rice, John P., Maier, Wolfgang, Mors, Ole, Rietschel, Marcella, Lucae, Susanne, Binder, Elisabeth B., Preisig, Martin, Perry, Julia, Tozzi, Federica, Muglia, Pierandrea, Aitchison, Katherine J., Breen, Gerome, Craig, Ian W., Farmer, Anne E., Müller-Myhsok, Bertram, McGuffin, Peter and Lewis, Cathryn M. 2011. Genomewide association scan of suicidal thoughts and behaviour in major depression. PLoS ONE 6 (7) , e20690. 10.1371/journal.pone.0020690 |
Ruderfer, D. M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Chambert, K., Moran, J. L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Sklar, P. and Purcell, S. M. 2011. A family-based study of common polygenic variation and risk of schizophrenia [Letter]. Molecular Psychiatry 16 (9) , pp. 887-888. 10.1038/mp.2011.34 |
Rivera, M., Cohen-Woods, S., Kapur, K., Breen, G., Ng, M. Y., Butler, A. W., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, M., Korszun, A., Maier, W., Mors, O., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Preisig, M., Bergmann, S., Tozzi, F., Rice, J., Rietschel, M., Rucker, J., Schosser, A., Aitchison, K. J., Uher, R., Craig, I. W., Lewis, C. M., Farmer, A. E. and McGuffin, P. 2011. Depressive disorder moderates the effect of the FTO gene on body mass index. Molecular Psychiatry 17 (6) , pp. 604-611. 10.1038/mp.2011.45 |
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Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Moskvina, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca ORCID: https://orcid.org/0000-0002-3885-1199, Gerrish, Amy, Pahwa, Jaspreet Singh, Jones, Nicola, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, Heun, Reinhard, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Peters, Oliver, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Mayo, Kevin, Morris, John C., Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panos, Al-Chalabi, Ammar, Shaw, Christopher E., Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H.-Erich, Rüther, Eckhard, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Hardy, John, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS ONE 5 (11) , e13950. 10.1371/journal.pone.0013950 |
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Nishikawa, Keizo, Nakashima, Tomoki, Takeda, Shu, Isogai, Masashi, Hamada, Michito, Kimura, Ayako, Kodama, Tatsuhiko, Yamaguchi, Akira, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Takahashi, Satoru and Takayanagi, Hiroshi 2010. Maf promotes osteoblast differentiation in mice by mediating the age-related switch in mesenchymal cell differentiation. The Journal of Clinical Investigation 120 (10) , pp. 3455-3465. 10.1172/JCI42528 |
Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097 |
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Green, Elaine Karen, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa, Forty, Elizabeth, Caesar, Sian, Gordon-Smith, Katherine, Fraser, Christine, Russell, Elen, St Clair, David, Young, Allan H., Ferrier, Nicol, Farmer, Anne, McGuffin, Peter, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2010. Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (7) , pp. 1347-1349. 10.1002/ajmg.b.31108 |
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Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Turic, D., Peirce, T. R., Mills, S., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2005. No support for association between the dopamine transporter (DAT1) gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 139B (1) , pp. 7-10. 10.1002/ajmg.b.30206 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Kraepelinian dichotomy - Author's reply. British Journal of Psychiatry 187 , pp. 485-486. |
Li, Y., Rowland, C., Tacey, K., Catanese, J., Sninsky, J., Hardy, J., Powell, J., Lovestone, S., Morris, J. C., Thal, L., Goate, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Grupe, A. 2005. The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Molecular Psychiatry 10 (9) , pp. 809-810. 10.1038/sj.mp.4001702 |
Williams, H. J., Glaser, B., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, MacGregor, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9) , pp. 1736-1738. 10.1176/appi.ajp.162.9.1736 |
Ahuja, Alka, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Genetics of mental retardation. Indian Journal of Medical Sciences 59 (9) , pp. 407-417. 10.4103/0019-5359.16820 |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Tredget, John, John, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lazarus, J. H. 2005. A cross-sectional and a prospective study of thyroid disorders in lithium-treated patients. Journal of affective disorders 87 (2-3) , pp. 313-317. 10.1016/j.jad.2005.03.010 |
Glaser, B1, Schumacher, J., Williams, H. J., Jamra, R. A., Ianakiev, N., Milev, R., Ohlraun, S., Schulze, T. G., Czerski, P. M., Hauser, J., Jonsson, E. G., Sedvall, G. C., Klopp, N., Illig, T., Becker, T., Propping, P., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cichon, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rietschel, M., Murphy, K. C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Nothen, M. M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 58 (1) , pp. 78-80. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Finding schizophrenia genes. The Journal of Clinical Investigation 115 (6) , pp. 1440-1448. 10.1172/JCI24759 |
Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6) , pp. 642-648. 10.1001/archpsyc.62.6.642 |
Norton, Nadine, Williams, Hywel, Dwyer, Sarah, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Preece, Anna, Gerrish, Amy, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Yerassimou, P., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 , 23. 10.1186/1471-244X-5-23 |
Lambert, D., Middle, F., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Segurado, Ricardo, Raybould, Rachel, Corvin, A., Green, Elaine Karen, O'Mahony, E., Nikolov, Ivan, Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lendon, C., Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Gill, M. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22. Molecular psychiatry 10 (9) , pp. 831-841. 10.1038/sj.mp.4001684 |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna Charlotte, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics 14 (14) , pp. 1947-1954. 10.1093/hmg/ddi199 |
Cope, Natalie Alexandra, Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Hill, Gary Trevor, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Stevenson, Jim, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O’Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 76 (4) , pp. 581-591. 10.1086/429131 |
Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Tacey, K., Doil, L., van Luchene, R., Garcia, V., Rowland, V., Lau, K., Cantanese, J., Sninsky, J., Hardy, J., Thal, L., Morris, J. C., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Grupe, A. 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3) , pp. 270-277. 10.1002/humu.20138 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Linkage studies in schizophrenia: New findings promise new insights. European Psychiatry 20 (1) , S36-S36. |
Cope, N. A., Hill, G., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Harold, D., Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Green, E. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Molecular Psychiatry 10 (3) , pp. 237-238. 10.1038/sj.mp.4001596 |
Turic, D., Williams, Hywel, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. A family based study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD). American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 133B (1) , pp. 64-67. 10.1002/ajmg.b.30123 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Harrison, P. J. 2005. Schizophrenia: a genetic disorder of the synapse? British Medical Journal (BMJ) 330 (7484) , pp. 158-159. 10.1136/bmj.330.7484.158 |
Glaser, B., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Green, E., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 132B (1) , pp. 38-45. 10.1002/ajmg.b.30081 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. Genomic approaches to schizophrenia. Clinical Therapeutics 27 (A) , S2-S7. |
Dimitrova, A., Milanova, V., Krastev, S., Nikolov, I., Toncheva, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2005. Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment. The Pharmacogenomics Journal 5 (1) , pp. 35-41. 10.1038/sj.tpj.6500273 |
Norton, N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. HTR2A: association and expression studies in neuropsychiatric genetics. Annals of Medicine 37 (2) , pp. 121-129. |
McGuffin, Peter, Knight, Jo, Breen, Gerome, Brewster, Shyama, Boyd, Peter R., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, Mike, Korszun, Ania, Maier, Wolfgang, Middleton, Lefkos, Mors, Ole, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Perry, Julia, Preisig, Martin, Reich, Theodore, Rice, John, Rietschel, Marcella, Jones, Lisa, Sham, Pak and Farmer, Anne E. 2005. Whole genome linkage scan of recurrent depressive disorder from the depression network study. Human Molecular Genetics 14 (22) , pp. 3337-3345. 10.1093/hmg/ddi363 |
Kent, L., Green, Elaine, Hawi, Z., Kirley, A., Dudbridge, F., Lowe, N., Raybould, Rachel, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Fitzgerald, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Gill, M., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry 10 (10) , pp. 939-943. 10.1038/sj.mp.4001696 |
Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, Lisa, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018 |
Farmer, A., Breen, G., Brewster, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Perry, J., Preisig, M., Rietschel, M., Reich, T., Jones, L. ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889 and McGuffin, P. 2004. The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study. BMC Psychiatry 4 , 42. 10.1186/1471-244X-4-42 |
Jones, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Genetics: The implications for forensic psychiatry. Journal of Forensic Psychiatry & Psychology 15 (4) , pp. 696-704. 10.1080/14789940410001729509 |
Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Smemo, Scott, Kauwe, John S. K., Hinrichs, Anthony L., Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Gogic, Goran, Chan, Joanne, Cravchik, Anibal, Ross, David, Lau, Kit, Kwok, Shirley, Chang, Sheng-Yung, Catanese, Joseph, Sninsky, John, White, Thomas J., Hardy, John, Powell, John, Lovestone, Simon, Morris, John C., Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, Alison and Grupe, Andrew 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44) , pp. 15688-15693. 10.1073/pnas.0403535101 |
van Amelsvoort, T., Daly, E., Henry, J., Robertson, D., Ng, V., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. 2004. Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia: preliminary results of a structural magnetic resonance imaging study. Archives of General Psychiatry 61 (11) , pp. 1085-1096. 10.1001/archpsyc.61.11.1085 |
van Amelsvoort, T, Henry, J, Morris, R, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Linszen, D, Murphy, K and Murphy, D 2004. Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome. Schizophrenia Research 70 (2-3) , pp. 223-232. 10.1016/j.schres.2003.10.004 |
Fowler, T. A., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Turic, Dragana, Whittinger, N., van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Aggleton, John Patrick ORCID: https://orcid.org/0000-0002-5573-1308, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Early onset antisocial behaviour in children with ADHD is associated with a functional variant in the catechol-O-methyltransferase (COMT) gene [Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 98. 10.1002/ajmg.b.30101 |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Norton, N, Wilkinson, J, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic variation in the expression of neuropsychiatric candidate genes [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 25. |
Peirce, T. R., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Haroutunian, V., Buxbaum, J., Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 81. 10.1002/ajmg.b.30101 |
Farbrother, Jane Elizabeth, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Guggenheim, Jeremy Andrew ORCID: https://orcid.org/0000-0001-5164-340X 2004. Family aggregation of high myopia: estimation of the sibling recurrence risk ratio. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2873-2878. 10.1167/iovs.03-1155 |
Farbrother, Jane Elizabeth, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pong-Wong, Ricardo, Haley, Chris S. and Guggenheim, Jeremy Andrew ORCID: https://orcid.org/0000-0001-5164-340X 2004. Linkage analysis of the genetic loci for high myopia on chromosomes 18p, 12q and 17q in 51 UK families. Investigative Ophthalmology and Visual Science 45 (9) , pp. 2879-2885. 10.1167/iovs.03-1156 |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jehu, Luke, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic expression of APOE in brain [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 61. |
Norton, N, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Morris, DW, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 18. |
Li, Yonghong, Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Lau, Kit, Catanese, Joe, Sninsky, John, Nowotny, Petra, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hardy, John, Powell, John, Lovestone, Simon, Thal, Leon, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie, Goate, Alison and Grupe, Andrew 2004. Association of ABCA1 with late-onset Alzheimer?s disease is not observed in a case-control study. Neuroscience Letters 366 (3) , pp. 268-271. 10.1016/j.neulet.2004.05.047 |
Mowry, B J, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R and Levinson, D F 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8) , pp. 784-795. 10.1038/sj.mp.4001481 |
Morris, D.W., Ivanov, D. ORCID: https://orcid.org/0000-0001-6271-6301, Robinson, L., Williams, N. ORCID: https://orcid.org/0000-0003-1177-6931, Stevenson, J., Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J. and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 2004. Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability. American Journal Of Medical Genetics Part A 129B (1) , pp. 97-103. 10.1002/ajmg.b.30033 |
Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Gaynor, Jones, Susan J., Norton, Nadine, Sanders, Robert D., Milham, Charis, McCarthy, Geraldine M., Jones, Lisa A., Cardno, Alastair G., Gray, Marion, Murphy, Kieran C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Polymorphisms in the MAOA, MAOB, and COMT genes and aggressive behavior in schizophrenia. American Journal of Medical Genetics 128B (1) , pp. 19-20. 10.1002/ajmg.b.30021 |
Harvey, Kirsten, Duguid, Ian C, Alldred, Melissa J., Beatty, Sarah E., Ward, Hamish, Keep, Nicholas H., Lingenfelter, Sue E., Pearce, Brian R., Lundgren, Johan, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Smart, Trevor G., Lüscher, Bernhard, Rees, Mark I. and Harvey, Robert J. 2004. The GDP-GTP exchange factor collybistin: an essential determinant of neuronal gephyrin clustering. Journal of neuroscience 24 (25) , pp. 5816-5826. 10.1523/JNEUROSCI.1184-04.2004 |
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Plomin, R, Turic, D M, Hill, L, Turic, D E, Stephens, M, Williams, J, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability. Molecular Psychiatry 9 (6) , pp. 582-586. 10.1038/sj.mp.4001441 |
Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Allebeck, P, Dalman, C, Lundberg, I, Hemmingson, T, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lewis, G 2004. Parental age difference and schizophrenia - Reply. British Journal of Psychiatry 184 , pp. 540-541. |
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Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biological psychiatry 55 (10) , pp. 971-975. 10.1016/j.biopsych.2004.01.025 |
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Fekadu, Abebaw, Shibre, Teshome, Alem, Atalay, Kebede, Derge, Kebreab, Samuel, Negash, Alemayehu and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Bipolar disorder among an isolated island community in Ethiopia. Journal of affective disorders 80 (1) , pp. 1-10. 10.1016/S0165-0327(02)00345-2 |
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Rees, Mark I., Harvey, Kirsten, Ward, Hamish, White, Julia H., Evans, Luc, Duguid, Ian C., Hsu, Cynthia C.-H., Coleman, Sharon Louise, Miller, Jan, Baer, Kristin, Waldvogel, Henry J., Gibbon, Francis, Smart, Trevor G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Harvey, Robert J. and Snell, Russell G. 2003. Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia. Journal of Biological Chemistry 278 (27) , pp. 24688-24696. 10.1074/jbc.M301070200 |
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Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. Schizophrenia and genetics. Plomin, R., DeFries, J. C., Craig, I. C. and McGuffin, P., eds. Behavioral Genetics in the Postgenomic Era, Washington, DC: APA Books, pp. 463-480. (10.1037/10480-023) |
Green, Elaine K., Elvidge, Gareth P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2003. Mutational analysis of two positional candidate susceptibility genes for bipolar disorder on chromosome 12q23-q24: phenylalanine hydroxylase and human LIM-homeobox LHX5. Psychiatric Genetics 13 (2) , pp. 97-101. 10.1097/01.ypg.0000057882.80011.9e |
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Dimitrova, Albena, Georgieva, Lyudmila, Nikolov, Ivan, Poriazova, Nadejda, Krastev, Stefan, Toncheva, Draga, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2002. Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies. Psychiatric Genetics 12 (3) , pp. 137-141. 10.1097/00041444-200209000-00004 |
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Wickham, Harvey, Walsh, Cathy, Asherson, Philip, Gill, Mike, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter, Murray, Robin and Sham, Pak 2002. Familiality of clinical characteristics in schizophrenia. Journal of Psychiatric Research 36 (5) , pp. 325-329. 10.1016/S0022-3956(02)00008-0 |
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Vrieze, F. W. D., Hardy, J., Rudrasingham, V., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lahiri, D. 2002. APP promotor variability as a risk factor for AD. Neurobiology of Aging 23 (1) , S299-S299. |
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Sedvall, O., Adolfsson, R., Agartz, I., Arnborg, S., Ekholm, B., Hall, H., Jonsson, E., McNeil, T.F., Okugawa, G., Osby, U., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Terenius, L. 2002. The Swedish HUBIN Project on Schizophrenia. European Psychiatry 17 (1) , 4S-5S. 10.1016/S0924-9338(02)80018-9 |
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Scourfield, Jane and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Genetic counselling. McGuffin, P., Owen, M. J. and Gottesman, I. I., eds. Psychiatric Genetics and Genomics, Oxford Medical Publications, Oxford: Oxford University Press, pp. 415-424. |
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Tsuang, M. T. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Molecular and population genetics of schizophrenia. Davis, K. L., Charney, D., Coyle, J. T. and Nemeroff, C., eds. Neuropsychopharmacology - 5th Generation of Progress, Philadelphia, PA: Lippincott, Williams and Wilkins, pp. 671-687. |
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Bennett, P., Segurado, R., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Larsen, B., Mulcahy, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 2002. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry 7 (2) , pp. 189-200. 10.1038/sj.mp.4000957 |
Holmes, Jane, Payton, Antony, Barrett, Jennifer, Harrington, Richard, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, William, Worthington, Jane, Gill, Michael, Kirley, Aiveen, Hawi, Ziarih, Fitzgerald, Michael, Asherson, Philip, Curran, Sarah, Mill, John, Gould, Alison, Taylor, Eric, Kent, Lyndsey, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2002. Association of DRD4 in children with ADHD and comorbid conduct problems. American Journal of Medical Genetics 114 (2) , pp. 150-153. 10.1002/ajmg.10149 |
Hawi, Z, Dring, M, Kirley, A, Foley, D, Kent, L, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Asherson, P, Curran, S, Gould, A, Richards, S, Lawson, D, Pay, H, Turic, D, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Fitzgerald, M and Gill, M 2002. Serotonergic system and attention deficit hyperactivity disorder (ADHD): a potential susceptibility locus at the 5-HT(1B) receptor gene in 273 nuclear families from a multi-centre sample. Molecular Psychiatry 7 (7) , pp. 718-725. 10.1038/sj.mp.4001048 |
Payton, A., Holmes, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2001. Susceptibility genes for a trait measure of attention deficit hyperactivity disorder: a pilot study in a non-clinical sample of twins. Psychiatry Research 105 (3) , 273 -278. 10.1016/S0165-1781(01)00342-0 |
Jurewicz, I, Owen, R.J, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Searching for susceptibility genes in schizophrenia. European Neuropsychopharmacology 11 (6) , pp. 395-398. 10.1016/S0924-977X(01)00116-X |
Abraham, Richard, Myers, Amanda, Wavrant-DeVrieze, Fabienne, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Thomas, Hollie Victoria, Marshall, Helen, Compton, Danielle, Spurlock, Gillian, Turic, Dragana, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Kwon, Jennifer M., Petersen, Ronald C., Tangalos, Eric, Norton, Joanne, Morris, John C., Bullock, Roger, Liolitsa, Danae, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 2001. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics 109 (6) , pp. 646-652. 10.1007/s00439-001-0614-1 |
Plomin, R., Hill, L., Craig, I. W., McGuffin, P., Purcell, S., Sham, P., Lubinski, D., Thompson, L. A., Fisher, P. J., Turic, D. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behaviour Genetics 31 (6) , pp. 497-509. 10.1023/A:1013385125887 |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. British Journal of Psychiatry 179 (5) , pp. 397-402. 10.1192/bjp.179.5.397 |
Jones, R. G., Morley-Canellas, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murphy, K. C. 2001. Chromosome 22q11 deletions and severe learning disability [comment]. The British Journal of Psychiatry 179 (5) , pp. 466-467. 10.1192/bjp.179.5.466-a |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lowry, C. A., Stephens, M., Oldfield, S., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Lightman, S. L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder. Molecular Psychiatry 6 (6) , pp. 671-677. 10.1038/sj.mp.4000899 |
Stephens, M, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. ADARB1, a brain specific member of the RNA-specific adenosine deaminase family and bipolar affective disorder. American Journal of Medical Genetics 105 (7) , p. 622. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stehens, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening of three candidate genes in the bipolar candidate region on chromosome 21q22.3. American Journal of Medical Genetics 105 (7) , p. 612. |
Green, Elaine Karen, Elvidge, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Mutational analysis of 2 positional candidate susceptibility genes for bipolar disorder: PAH and LHX5. American Journal of Medical Genetics 105 (7) , pp. 610-611. |
Williams, H., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Meyer, J., Lesch, K. P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Further analysis of KIAA0027 in schizophrenic patients. American Journal of Medical Genetics 105 (7) , p. 561. |
Reid, S. J., Rees, M. I., van Roon-Mom, W. M. C., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, McDonald, M. E., Sutherland, G. T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Dragunow, M. and Snell, R. G. 2001. Expression and population studies of the TATA-box binding protein polyglutamine region at normal and expanded lengths. American Journal of Human Genetics 69 (4) , p. 424. |
Hamshere, Marian Linsday ORCID: https://orcid.org/0000-0002-8990-0958, Giles, Peter ORCID: https://orcid.org/0000-0003-3143-6854, Krawczak, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Statistical analysis of genotypic association data with HAPMAXII. AMERICAN JOURNAL OF HUMAN GENETICS 69 (4) , p. 390. |
Rees, M. I., Baer, K., Ward, H., Coleman, Sharon Louise, Evans, I. L., Miller, J., Waldvogel, H., Faull, R. L. M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Snell, R. G. 2001. A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. American Journal of Human Genetics 69 (4) , p. 627. |
Jones, Gaynor, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Jones, S. J., Milham, C., Sanders, R. D., McCarthy, G. M., Jones, L. A., Cardno, Alastair G., Gray, M., Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype. British Journal of Psychiatry 179 (4) , pp. 351-355. 10.1192/bjp.179.4.351 |
Rees, M. I., Lewis, T. M., Vafa, B., Ferrie, C., Corry, P., Muntoni, F, Jungbluth, H., Stephenson, J. B., Kerr, Michael Patrick, Snell, R. G., Schofield, P.R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Hum Genet 109 (3) , pp. 267-270. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Simple and complex genetics of Alzheimer's disease. Journal of Medical Genetics 38 , S29-S29. |
2001. Evidence of association between DRD4 and ADHD with conduct disturbance. Presented at: Behavior Genetics Association Meeting, Cambridge, 11 July 2001. Published in: Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Holmes, J., Payton, A., Barrett, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Gill, M., Kirley, A., Hawi, Z., Fitzgerald, M., Asherson, P., Curran, S., Mill, J., Gould, A., Taylor, E., Kent, L., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Worthingon, J. eds. Behavior Genetics. Behavior Genetics Association Meeting Abstracts , vol.31 (5) Springer Verlag, pp. 470-471. |
Campbell, L. E., Stevens, A. F., Morris, R., Karmiloff-Smith, A., Siminoff, E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, D. G. M. and Murphy, K. C. 2001. Neuropsychological profile of children with Velo-cardio-facial syndrome (VCFS). Journal of Medical Genetics 38 , S39-S39. |
Liddell, M., Lovestone, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Advising relatives of risk of Alzheimer's disease - Authors' reply. British Journal of Psychiatry 179 (1) , pp. 73-74. 10.1192/bjp.179.1.73 |
Payton, A., Holmes, J., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2001. Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. Neuroscience Letters 105 (5) , pp. 464-470. 10.1002/ajmg.1407 |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Brzustowicz, L., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2001. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation [Letter]. Molecular Psychiatry 6 (3) , pp. 259-260. 10.1038/sj.mp.4000128 |
van Amelsvoort, T., Daly, E., Robertson, D., Suckling, J., Ng, V., Critchley, H., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Henry, J., Murphy, K. C. and Murphy, D. G. 2001. Structural brain abnormalities associated with deletion at chromosome 22q11. British Journal of Psychiatry (178) , pp. 412-419. 10.1192/bjp.178.5.412 |
Wang, Edward Chung Yern ORCID: https://orcid.org/0000-0002-2243-4964, Thern, Anette, Denzel, Angela, Kitson, Jeremy, Farrow, Stuart N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. DR3 regulates negative selection during thymocyte development. Molecular and cellular biology 21 (10) , pp. 3451-61. 10.1128/MCB.21.10.3451-3461.2001 |
Williams, H. J., Murphy, K. C., Spurlock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. No association between a promoter polymorphism of the UFD1L gene and schizophrenia in individuals with or without velo-cardio-facial syndrome (VCFS). Schizophrenia Research 49 , p. 81. |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Searching for schizophrenia genes. Trends in Molecular Medicine 7 (4) , pp. 169-174. |
Jones, L. A., Cardno, A. G., Sanders, R. D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2001. Sustained and selective attention as measures of genetic liability to schizophrenia. Schizophrenia Research 48 (2-3) , pp. 263-267. |
Wickham, H., Walsh, C., Asherson, P., Taylor, C., Sigmundson, T., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P., Murray, R. and Sham, P. 2001. Familiality of symptom dimensions in schizophrenia. Schizophrenia Research 47 (2-3) , pp. 223-232. 10.1016/S0920-9964(00)00098-0 |
Turic, D., Fisher, P. J., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. No association between apolipoprotein E polymorphisms and general cognitive ability in children. Neuroscience Letters 299 (1-2) , pp. 97-100. 10.1016/S0304-3940(00)01789-4 |
Wang, Edward Chung Yern ORCID: https://orcid.org/0000-0002-2243-4964, Kitson, Jeremy, Thern, Anette, Williamson, Jill, Farrow, Stuart N. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Genomic structure, expression, and chromosome mapping of the mouse homologue for the WSL-1 (DR3, Apo3, TRAMP, LARD, TR3, TNFRSF12) gene. Immunogenetics 53 (1) , pp. 59-63. 10.1007/s002510000290 |
Liddell, M. B., Lovestone, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. Genetic risk of Alzheimer's disease: advising relatives. British Journal of Psychiatry 178 (1) , pp. 7-11. 10.1192/bjp.178.1.7 |
Jacobsen, Nick J. O., Elvidge, Gareth, Franks, Emily K. E., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2001. CUX2, a potential regulator of NCAM expression: Genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 105 (3) , pp. 295-300. 10.1002/ajmg.1325 |
Elvidge, Gareth, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, Fiona, Asherson, Phil, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Allelic variation of aBalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis. American Journal of Medical Genetics 105 (4) , pp. 307-311. 10.1002/ajmg.1353 |
Jacobsen, N. J. O., Franks, E. K. E., Elvidge, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2001. Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular Psychiatry 6 (1) , pp. 92-97. 10.1038/sj.mp.4000774 |
Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Davis, K.L., Buxbaum, J.D., Haroutunian, V., Saunders, R., Cardno, A.G., McCarthy, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2001. Screening of candidate genes related to myelination for mutations associated with schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 105 (7) , p. 589. |
Myers, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Abraham, R., Tunstall, N., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, S., Perez-Tur, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304 |
Vincent, John B., Qiu-Ping, Yuan, Schalling, Martin, Adolfsson, R., Azevedo, M. Helena, Macedo, Antonio, Bauer, Amy, Dalla Torre, Camille, Medeiros, Helena M., Pato, Carlos N., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Paterson, Andrew D., Petronis, Arturas and Kennedy, James L. 2000. Long repeat tracts at SCA8 in major psychosis. American Journal of Medical Genetics 96 (6) , pp. 873-876. 10.1002/1096-8628(20001204)96:6<873::AID-AJMG37>3.0.CO;2-9 |
Sham, P. C., Sterne, A., Purcell, S., Cherny, S., Webster, M., Rijsdijk, F., Asherson, P., Ball, D., Craig, I., Eley, T., Goldberg, D., Gray, J., Mann, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 2000. GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Research 3 (4) , pp. 316-322. 10.1375/136905200320565292 |
Deb, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Apolipoprotein E, Alzheimer's disease and Down's syndrome - Reply. British Journal of Psychiatry 177 , pp. 469-470. |
Jones, L. A., Cardno, A. G., Murphy, K. C., Sanders, R. D., Gray, M. Y., McCarthy, G., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2000. The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability. Schizophrenia Research 45 (3) , pp. 213-221. 10.1016/S0920-9964(99)00183-8 |
Snell, R. G., Miller, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Rees, M. I. 2000. Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes. American Journal of Human Genetics 67 (4) , p. 385. |
Rees, M. I., Lewis, T. M., Mortier, G., Snell, R. G., Schofield, P. R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). American Journal of Human Genetics 67 (4) , p. 391. |
Austin, J., Buckland, Paul Robert, Cardno, Alastair G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry 5 (5) , pp. 552-557. 10.1038/sj.mp.4000761 |
Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58. |
van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, J. C., Suckling, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implications for psychosis. Journal of Medical Genetics 37 , S26-S26. |
Holmes, J., Payton, A., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2000. A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder. Molecular Psychiatry 5 (5) , pp. 523-530. 10.1038/sj.mp.4000751 |
Levinson, D. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Straub, R. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041 |
Williams, H.J. ORCID: https://orcid.org/0000-0001-7758-0312, Murphy, K.C., Spurlock, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2000. No association of the -277A variant allele of the UFD1L promoter polymorphism and schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , pp. 533-534. |
Van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, D., Suckling, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implicatons for psychosis. American Journal of Medical Genetics 96 (4) , p. 551. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stephens, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Examining the 4p16 region for association with bipolar disorder using DNA pooling. American Journal of Medical Genetics 96 (4) , p. 548. |
Walters, S. E., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia. American Journal of Medical Genetics 96 (4) , p. 535. |
Payton, A., Holmes, J., Barrett, J., Hever, T., Fitzpatrick, H., Trumper, A., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ollier, W., Worthington, J. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2000. A family based candidate gene association study of Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics 96 (4) , p. 489. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Evidence for association between polymorphisms of the catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. American Journal of Medical Genetics 96 (4) , p. 476. |
Henry, J. C., van Amelsvoort, T., Morris, R. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murphy, K. C. and Murphy, D. G. M. 2000. The neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS). American Journal of Medical Genetics 96 (4) , p. 474. |
McCarthy, G. M., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Investigating familiality of subtypes in schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 473-474. |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jacobsen, N., Spurlock, Gillian, Austin, Jehanine, Williams, Hywel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. A functional and positional candidate gene for schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 461-462. |
Elvidge, G. P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2000. Mutational analysis of purinergic receptor, P2X4: A positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 96 (4) , p. 493. |
Jacobsen, N. J., Franks, E. K., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Genomic characterisation and mutational analysis of CUX2, a potential regulator of NCAM expression, mapping to chromosome 12q23-q24.1. American Journal of Medical Genetics 96 (4) , pp. 493-494. |
Fitzpatrick, E., Spurlock, G., Coleman, Sharon Louise, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Buckland, Paul Robert 2000. Association studies of polymorphisms in the promoter region of the dopamine D4 receptor and the D2 receptor [Abstract]. American Journal of Medical Genetics 96 (4) , p. 530. 10.1002/1096-8628(20000807)96:4<515::AID-AJMG6>3.0.CO;2-U |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics 10 (2) , pp. 83-86. 10.1097/00041444-200010020-00005 |
Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 2000. A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers. Journal of Psychiatric Research 34 (3) , pp. 239-244. 10.1016/S0022-3956(00)00013-3 |
Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome. British Journal of Psychiatry 176 , pp. 468-472. 10.1192/bjp.176.5.468 |
Middle, F., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Barrett, T., Khanim, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lendon, C. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2000. Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. American Journal of Medical Genetics 96 (2) , pp. 154-157. 10.1002/(sici)1096-8628(20000403)96:2%3C154::aid-ajmg5%3E3.0.co;2-f |
Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Molecular genetic studies of schizophrenia. Brain research. Brain research reviews 31 (2-3) , pp. 179-186. 10.1016/S0165-0173(99)00035-1 |
Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Middle, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1) , pp. 51-54. 10.1097/00041444-200010010-00009 |
Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693 |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Cardno, A. G., Vincent, J. B., Kennedy, J. L., Jones, L. A., Gray, M, Sanders, Rhys, McCarthy, G, Murphy, K. C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics 10 (1) , pp. 33-37. 10.1097/00041444-200010010-00006 |
Farmer, A. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 2000. Bioethics and genetic research in psychiatry. British Journal of Psychiatry 176 , pp. 105-108. 10.1192/bjp.176.2.105 |
Rees, M. I., Watts, P., Fenton, I., Clarke, A., Snell, R. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gray, J. 2000. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). Human Genetics 106 (2) , pp. 206-209. 10.1007/s004390051029 |
Tunstall, N., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Carty, S., Lillystone, S., Fraser, L., Kehoe, P., Neill, D., Rudrasingham, V., Sham, P. and Lovestone, S. 2000. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. British Journal of Psychiatry 176 , pp. 156-159. 10.1192/bjp.176.2.156 |
Buckland, J., Pennington, D. J., Bruno, L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Co-ordination of the expression of the protein tyrosine kinase p56(lck) with the pre-T cell receptor during thymocyte development. European Journal of Immunology 30 (1) , pp. 8-18. 10.1002/1521-4141(200001)30:1<8::AID-IMMU8>3.0.CO;2-8 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Cardno, A. G. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Psychiatric genetics: back to the future. Molecular Psychiatry 5 (1) , pp. 22-31. 10.1038/sj.mp.4000702 |
Cardno, A. G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Genetic risk factors for schizophrenia. International Journal of Mental Health 29 (3) , pp. 13-38. |
Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome. Journal of Intellectual Disability Research 44 , p. 259. |
Murphy, K.C., Jones, L.A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS). Schizophrenia Research 41 (1) , p. 29. 10.1016/S0920-9964(00)90364-5 |
Speight, G., Turic, Dragana, Austin, Jehannine, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Cardno, Alistair, Jones, L., Murphy, K. C., Sanders, R., McCarthy, G., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Buckland, Paul Robert and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder. Molecular Psychiatry 5 (3) , pp. 327-331. 10.1038/sj.mp.4000717 |
Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397 |
Watts, Patrick, Rees, Mark I., Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286, Beck, Lyn, Lane, Carol M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gray, Jonathon 2000. Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13. Eye 14 (2) , pp. 172-175. 10.1038/eye.2000.48 |
Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Bowen, T. ORCID: https://orcid.org/0000-0001-6050-0435, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Austin, J., Walters, A., Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 2000. Identification and characterisation of SNPs in candidate genes for schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , p. 462. |
Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Spurlock, G., Williams, H. ORCID: https://orcid.org/0000-0001-7758-0312, Norton, N., Walters, A., Saunders, R., Cardno, A.G., McCarthy, G., O'Donovan, M.C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 2000. Linkage disequilibrium mapping and candidate gene screening of the VCFS deleted region for mutations associated with schizophrenia. American Journal of Medical Genetics - Neuropsychiatric Genetics 96 (4) , p. 475. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Norton, N., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. International Journal of Neuropsychopharmacology 2 (4) , pp. 293-298. 10.1017/s1461145799001601 |
Willliams, Hywel, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Murphy, K. C., Cardno, A. G., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No evidence for allelic association between schizophrenia and a functional variant of the human dopamine beta-hydroxylase gene (DBH). American Journal Of Medical Genetics Part A 88 (5) , pp. 557-559. 10.1002/(SICI)1096-8628(19991015)88:5<557::AID-AJMG22>3.0.CO;2-F |
Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Archives of General Psychiatry 56 (10) , pp. 940-945. 10.1001/archpsyc.56.10.940 |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Identification of new microsatellite markers on chromosome 4p16. American Journal of Human Genetics 65 (4) , A257-A257. |
Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. High rates of schizophrenia in velo-cardio-facial syndrome. American Journal of Human Genetics 65 (4) , A336-A336. |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Gill, M., Spurlock, Gillian, Vallada, H. P., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Medical Genetics 15 (88) , pp. 503-509. 10.1002/(SICI)1096-8628(19991015)88:5<503::AID-AJMG13>3.0.CO;2-U |
McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Intra-pair correlations of symptom dimensions in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S26-S27. |
Fisher, P. J., Hill, L., Turic, D., Asherson, P., Benbow, C., Chorney, K., Chorney, M., Craig, I., Lubinski, D., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 1999. A high resolution genome scan made possible with DNA pooling. Molecular Psychiatry 4 (1) , S10-S10. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Evidence of novel loci in late onset Alzheimer's disease. Molecular Psychiatry 4 (1) , S9-S9. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No association between polymorphisms of catechol-O-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Journal of Medical Genetics 36 , S78-S78. |
Murphy, K., Thompson, P. W., Davies, S. J., Groves, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Stuart, G. 1999. The prevalence of chromosome 22q11 deletions in an adult congenital heart disease population. Journal of Medical Genetics 36 , S59-S59. |
Jones, L. A., Sanders, R. D., Cardno, A. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 1999. Sustained and selective attention as quantitative measures of schizophrenia liability. Molecular Psychiatry 4 , S117-S117. |
Emilien, Gérard, Maloteaux, Jean-Marie, Geurts, Muriel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Dopamine receptors and schizophrenia: contribution of molecular genetics and clinical neuropsychology. The International Journal of Neuropsychopharmacology 2 (3) , p. 197. 10.1017/S1461145799001479 |
Williams, H. J., McCarthy, G. M., Saunders, R. D., Cardno, A. G., Gray, M. Y., Murphy, K. C., Jones, L. A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Characterization, mutational analysis, and association of the human proline oxidase gene: A candidate gene for schizophrenia. Molecular Psychiatry 4 , S115-S115. |
Sanders, R. D., Norton, Nadine, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Pre-pulse inhibition in the functional psychoses. Molecular Psychiatry 4 , S121-S121. |
Hill, L., Chorney, M. J., Chorney, K., Craig, I., Fisher, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1999. IGF2R and cognitive ability. Molecular Psychiatry 4 , S108-S108. |
Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 1999. Monoamine oxidase a promoter polymorphism and relationships to monoamine metabolite concentrations in CSF. Molecular Psychiatry 4 , S97-S98. |
Norton, N., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96. |
Middle, F. A., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, MacCandless, F., Khanim, F., Barrett, T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lendon, C. L. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Association studies between bipolar disorder and a polymorphism in the Wolfram gene. Molecular Psychiatry 4 , S76-S76. |
Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Payton, T., Holmes, J., Harrington, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Poulton, K., Barrett, I., Ollier, W. and Worthington, J. 1999. A quantitative trait loci study of attention deficit hyperactivity disorder. Molecular Psychiatry 4 , S52-S53. |
McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Familial aggregation of clinical variables in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S121-S121. |
Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Rees, M. I., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9) , pp. 1729-1739. 10.1093/hmg/8.9.1729 |
O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Candidate-gene association studies of schizophrenia. American Journal of Human Genetics 65 (3) , pp. 587-592. 10.1086/302560 |
Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Cardno, A. G., Fitzpatrick, E. R., Buckland, Paul Robert and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Embryonic NCAM and schizophrenia: Genetic analysis of regulatory enzymes. Molecular Psychiatry 4 , S32-S32. |
Jacobsen, N. J., Lyons, I., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Burge, S., Kwok, P. Y., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes. Human Molecular Genetics 8 (9) , pp. 1631-1636. 10.1093/hmg/8.9.1631 |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rees, M., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Bipolar disorder and the serotonin transporter gene: a family-based association study. Psychological Medicine -London- 29 (5) , pp. 1249-1254. 10.1017/s003329179900882x |
Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42. |
Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kehoe, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Roehl, K., Laliiri, D. K., Shears, S., Booth, J., Wu, W., Goate, A., Chartier-Harlin, M. C., Hardy, J. and Perez-Tur, J. 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2) , pp. 67-70. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, A. G. 1999. Psychiatric genetics: progress, problems, and potential. The Lancet 354 (1) , SI11-SI14. 10.1016/S0140-6736(99)90242-8 |
Rees, M. I., Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521 |
Cardno, Alastair G., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12) , pp. 1592-1596. 10.1016/s0006-3223(99)00033-5 |
Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Kehoe, P. G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Case-control study of presenelin-1 intronic polymorphism. Journal of Neurology, Neurosurgery & Psychiatry 66 (6) , p. 702. 10.1136/jnnp.66.6.702 |
Fisher, P. J., Turic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Asherson, P., Ball, D., Craig, I., Eley, T., Hill, L., Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics 8 (5) , pp. 915-922. 10.1093/hmg/8.5.915 |
Jacobsen, N. J., Franks, E. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder. Molecular Psychiatry 4 (3) , pp. 274-279. 10.1038/sj.mp.4000476 |
Amelsvoort, T. V., Daly, E., Critchley, H., Robertson, D., Murphy, K., Simmons, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Henry, J. and Murphy, D. G. M. 1999. An MRI and fMRI study on the effect of deletions on chromosome 22 on brain. Biological psychiatry 45 (8) , 110S-111S. |
Hill, L., Craig, I. W., Asherson, P., Ball, D., Eley, T., Ninomiya, T., Fisher, P. J., Turic, D., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Thompson, L. A. and Plomin, R. 1999. DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. NeuroReport 10 (4) , pp. 843-848. 10.1097/00001756-199903170-00032 |
Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Perez-Tur, J., Frigard, B., Morric, J. C., Carty, S., Cottel, D., Tunstall, N., Lovestone, S., Petersen, R. C., Chartier-Harlin, M. C., Goate, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Hardy, J. 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2) , pp. 137-139. 10.1016/S0304-3940(99)00035-X |
Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C. S., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kucherlapati, R., Rees, J. L., Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Lathrop, G. M., Monaco, A. P., Strachan, T. and Hovnanian, A. 1999. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics 21 (3) , pp. 271-277. |
Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, A., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237 |
Kehoe, P., Krawczak, M., Harper, P. S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612 1999. Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length. Journal of Medical Genetics 36 (2) , pp. 108-111. 10.1136/jmg.36.2.108 |
Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009 |
Kerwin, R and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Genetics of novel therapeutic targets in schizophrenia. The British journal of psychiatry. Supplement. 38 , pp. 1-4. |
Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1999. Dimensions of psychosis in affected sibling pairs. Schizophrenia Bulletin 25 (4) , pp. 841-850. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, I., McCandless, F. and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1999. Tryptophan hydroxylase gene and manic-depressive illness [letter]. Archives of General Psychiatry 56 (1) , pp. 98-99. 10.1001/archpsyc.56.1.98 |
Kehoe, P. G., Williams, H., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12) , pp. 1034-1035. 10.1136/jmg.35.12.1034 |
Spurlock, Gillian, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics 81 (6) , pp. 525-526. |
Poulton, K., Holmes, J., Hever, T., Trumper, A., Fitzpatrick, H., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Worthington, J., Ollier, W., Harrington, R. and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 1998. A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorder. American Journal of Medical Genetics 81 (6) , p. 458. |
Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Fenton, I. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6) , pp. 463-464. |
Fisher, P. J., Turic, D., Asherson, P., Ball, D., Benbow, C., Chorney, M., Chorney, K., Craig, I., Eley, T., Hill, L., Lubinski, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6) , p. 469. |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Family-based association studies of candidate genes in bipolar disorder. American Journal of Medical Genetics 81 (6) , pp. 476-477. |
Bennett, P., Mulcahy, T., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 1998. The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21. American Journal of Medical Genetics 81 (6) , p. 541. |
Hill, L., Asherson, P., Ball, D., Craig, I., Daniels, J., Eley, T., Freeman, B., Ninomiya, T., Fisher, P., Turic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6) , p. 486. |
Spurlock, G., Williams, N.M. ORCID: https://orcid.org/0000-0001-7758-0312, Williams, H.J. ORCID: https://orcid.org/0000-0001-7758-0312 and Owen, M.J. ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polymorphism screening of the human type 1 Sigma (σ) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics - Neuropsychiatric Genetics 81 (6) , pp. 525-526. |
Deb, S., Braganza, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kehoe, P., Williams, H. and Norton, N. 1998. No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome. Alzheimers Reports 1 (6) , pp. 365-368. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22qII deletions and aggressive behaviour. British Journal of Psychiatry 173 , pp. 353-354. 10.1192/bjp.173.4.353b |
Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Hutton, M., Hardy, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619 |
Straub, R. E., Vallada, H., Curtis, D., Sham, P., Kunugi, H., Zhao, J. H., Murray, R., McGuffin, P., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Collier, D. A., Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E., Goldin, L., Freedman, R., Laurent, C., Bodeau-Pean, S., d'Amato, T., Jay, M., Campion, D., Mallet, J., Wildenauer, D. B., Lerer, B., Albus, M., Ackenheil, M., Ebstein, R. P., Hallmayer, J., Maier, W., Gurling, H., Curtis, D., Kalsi, G., Brynjolfsson, J., Sigmundson, T., Petursson, H., Blackwood, D., Muri, W., StClair, D., He, L., Maguire, S., Moises, H. W., Hwu, H. G., Yang, L., Wiese, C., Kristbjarnarson, H., Levinson, D. F., Mowry, B. J., Donis-Keller, H., Hayward, N. K., Crowe, R. R., Silverman, J. M., Nancarrow, D. J. and Read, C. M. 1998. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22. Schizophrenia Research 32 (2) , pp. 115-121. 10.1016/S0920-9964(98)00048-6 |
Wright, P., Dawson, E., Donaldson, P. T., Underhill, J. A., Sham, P. C., Zhao, J., Gill, M., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Murray, R. M. 1998. A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research 32 (2) , pp. 75-80. 10.1016/S0920-9964(98)00050-4 |
Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1998. Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables. Psychological Medicine 28 (4) , pp. 815-823. 10.1017/S0033291798006783 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1998. Chromosome 11 workshop. Psychiatric Genetics 8 (2) , pp. 89-92. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1998. The programmed alliance of two disciplines. La Recherche 311 , pp. 38-39. |
Asherson, P., Mant, R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A., Jones, L., Murphy, Kevin, Collier, D. A., Nanko, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Morris, S., Muir, W., Blackwood, B., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry 3 (4) , pp. 310-320. 10.1038/sj.mp.4000399 |
Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Murphy, K. C., Arranz, M. J., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1998. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3 (4) , pp. 342-345. 10.1038/sj.mp.4000385 |
Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816 |
Chorney, M.J., Chorney, K., Seese, N., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Daniels, J., McGuffin, P., Thompson, L.A., Detterman, D.K., Benbow, C., Lubinski, D., Eley, T. and Plomin, R. 1998. A Quantitative Trait Locus Associated With Cognitive Ability in Children. Psychological Science 9 (3) , pp. 159-166. 10.1111/1467-9280.00032 |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Cardno, A. G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400 |
Daniels, J., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Plomin, R. 1998. Molecular genetic studies of cognitive ability. Human Biology 70 (2) , pp. 281-296. |
Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Spurlock, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149. |
Spurlock, G., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Aschauer, H. N., Lenzinger, E., Fuchs, K., Sieghart, W. C., Meszaros, K., Fathi, N., Laurent, C., Mallet, J., Macciardi, F., Pedrini, S., Gill, M., Hawi, Z., Gibson, S., Jazin, E. E., Yang, H. T., Adolfsson, R., Pato, C. N., Dourado, A. M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics 81 (1) , pp. 24-28. 10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N |
Cardno, A. G., Murphy, K. C., Jones, L. A., Cobb, A. M., Gray, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polydactyly and psychosis. Five cases of co-occurrence. British Journal of Psychiatry 172 , pp. 184-185. 10.1192/bjp.172.2.184 |
Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. British Journal of Psychiatry 172 , pp. 180-183. 10.1192/bjp.172.2.180 |
Ball, D., Hill, L., Eley, T. C., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1998. Dopamine markers and general cognitive ability. NeuroReport 9 (2) , pp. 347-349. 10.1097/00001756-199801260-00031 |
Arranz, M. J., Munro, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Spurlock, G., Sham, P. C., Zhao, J., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Collier, D. A. and Kerwin, R. W. 1998. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry 3 (1) , pp. 61-66. 10.1038/sj.mp.4000348 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Psychiatric disorders in Wolfram syndrome heterozygotes. Molecular Psychiatry 3 (1) , pp. 12-13. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. The behavioural phenotype in velo-cardio-facial syndrome. Schizophrenia Research 29 (1-2) , p. 132. |
Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X |
Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Chromosome 22q11 deletions - An under-recognized cause of idiopathic learning disability? Schizophrenia Research 29 (1-2) , p. 132. 10.1016/S0920-9964(97)88634-3 |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Norton, N, Jacobsen, N. J., Guy, Carol, Daniels, J. K., Sanders, Rebecca, Cardno, A. G., Jones, L. A., Murphy, Kevin, McGuffin, P, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry 3 (1) , pp. 67-71. 10.1038/sj.mp.4000293 |
Spurlock, G., Heils, A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, J., D'Souza, U. M., Cardno, A., Murphy, K. C., Jones, L., Buckland, Paul Robert, McGuffin, P., Lesch, K. .P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1) , pp. 42-49. 10.1038/sj.mp.4000342 |
Cardno, A. G., McCandless, F., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Jones, L. A., Murphy, Kevin, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1998. Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification [comparative study]. Psychiatric Genetics 8 (1) , pp. 29-32. 10.1097/00041444-199800810-00005 |
Vallada, H. P., Vasques, L., Curtis, D, Zatz, M., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lauriano, V., Gentil, V., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Collier, D. A. 1998. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics 8 (3) , pp. 183-186. 10.1097/00041444-199800830-00008 |
Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Middle, F., Guy, Carol, Spurlock, G., Cairns, N. J., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia. Molecular Psychiatry 2 (6) , pp. 478-482. 10.1038/sj.mp.4000297 |
Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Nothen, . and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. A meta analysis of association between the 5-HT2a receptor, T102C polymorphism and schizophrenia. American Journal of Medical Genetics 74 (6) , p. 612. |
Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Chromosome 22q11 deletions: An underrecognized cause of idiopathic learning disability? American Journal of Medical Genetics 74 (6) , p. 567. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. The behavioral phenotype in velo-cardio-facial syndrome. American Journal of Medical Genetics 74 (6) , p. 660. |
Vallada, H. P., Vasques, L., Curtis, D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Gentil, V., Zatz, M., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Collier, D. A. 1997. Linkage studies in bipolar affective disorder with markers on chromosome Xq25-27. American Journal of Medical Genetics 74 (6) , pp. 679-680. |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McKeon, P., Moorhead, S., Guy, Carol, Harrison, D., Mynett-Johnson, L., Claffey, E., Feldman, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity. Biological psychiatry 42 (10) , pp. 876-881. 10.1016/s0006-3223(96)00516-1 |
Kunugi, H., Vallada, H. P., Sham, P. C., Hoda, F., Arranz, M. J., Li, T., Nanko, S., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. A. 1997. Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatric Genetics 7 (3) , pp. 97-101. 10.1097/00041444-199723000-00001 |
Davies, S. J., Norton, N., Daniels, J. K. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Parietal foramina and multiple exostoses - familial inheritance of a molecular deletion. American Journal of Human Genetics 61 (4) , A95-A95. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1997. Genetics and psychiatry. British Journal of Psychiatry 171 , pp. 201-202. 10.1192/bjp.171.3.201 |
Rees, M., Norton, N., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Scourfield, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Moorhead, S., Feldman, E., Sadler, S., Cole, T., Redman, K., Farmer, A., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5) , pp. 398-402. 10.1038/sj.mp.4000256 |
Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Daniels, J. K., Speight, G., McKeon, P., Mynett-Johnson, L., Claffey, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. American Journal of Psychiatry 154 (8) , pp. 1146-1147. |
Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2) , pp. 83-85. 10.1097/00041444-199722000-00005 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4) , pp. 270-273. 10.1038/sj.mp.4000292 |
Daniels, J. K., Spurlock, G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R |
Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, Peter, Nothen, Markus and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia. The Lancet 349 (9060) , p. 1221. 10.1016/S0140-6736(05)62413-0 |
Speight, G., Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Asherson, P., McGuffin, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1997. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. American Journal of Medical Genetics 74 (2) , pp. 204-206. 10.1002/(SICI)1096-8628(19970418)74:2<204::AID-AJMG19>3.0.CO;2-M |
Spurlock, Gillian, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, Peter, Mallet, Jacques, Nöthen, Markus, Gill, Michael, Aschauer, Harald, Adlfsson, Rolf, Macciardi, Fabio and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene. Schizophrenia Research 24 (1-2) , p. 91. 10.1016/S0920-9964(97)82247-5 |
Arranz, M.J., Munro, J., Sham, P., Zhao, J., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Sodhi, M., Spurlock, G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Collier, D.A. and Kerwin, R. 1997. Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82243-8 |
Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1) , pp. 37-39. 10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S |
Andrew, M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Hyperekplexia: abnormal startle response due to glycine receptor mutations. British Journal of Psychiatry 170 , pp. 106-108. 10.1192/bjp.170.2.106 |
Petrill, S. A., Plomin, R., McClearn, G. E., Smith, D. L., Vignetti, S., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1997. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behavior Genetics 27 (1) , pp. 29-31. 10.1023/A:1025659124405 |
Jonsson, E. G., Goldman, D., Spurlock, G., Gustavsson, J. P., Nielsen, D. A., Linnoila, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Sedvall, G. C. 1997. Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience 247 (6) , pp. 297-230. 10.1007/BF02922258 |
Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Price, W., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94. |
Petrill, Stephen A., Ball, David, Eley, Thalia, Hill, Linzy, Plomin, Robert, Mcclearn, Gerald E., Smith, Deborah L., Chorney, Karen, Chorney, Michael, Hershz, Milton S., Detterman, Douglas K., Thompson, Lee A., Benbow, Camilla, Lubinski, David, Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1997. Failure to replicate a QTL association between a DNA marker identified by EST00083 and IQ. Intelligence 25 (3) , pp. 179-184. 10.1016/S0160-2896(97)90041-6 |
Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Scott, L. C., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1996. Factor analysis of schizophrenic symptoms using the OPCRIT checklist. Schizophrenia Research 22 (3) , pp. 233-239. 10.1016/S0920-9964(96)00060-6 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Candidate gene association studies in psychiatric genetics: a SERTain future? Molecular Psychiatry 1 (6) , pp. 434-436. |
Cardno, A. G., Murphy, K. C., Jones, L. A., Guy, C. A., Asherson, P., De Azevedo, M. H., Coelho, I. M., de Macedo e Santos, A. J., Pato, C. N., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1996. Expanded CAG/CTG repeats in schizophrenia. A study of clinical correlates. British Journal of Psychiatry 169 (6) , pp. 766-771. 10.1192/bjp.169.6.766 |
Vallada, H., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Vasques, L., Curtis, D., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Lauriano, V., Gentil, V., Passos-Beuno, R., Murray, R. M., Zatz, M., McGuffin, P., Powell, J. F., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. A. 1996. Linkage studies in bipolar affective disorder with markers on chromosome 21. Journal of affective disorders 41 (3) , pp. 217-221. 10.1016/s0165-0327(96)00055-9 |
O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, McKeon, P., Macedo, A., Maier, W., Wildenauer, D., Aschauer, H. N., Sorbi, S., Feldman, E., Mynett-Johnson, L., Claffey, E., Nacmias, B., Valente, J., Dourado, A., Grassi, E., Lenzinger, E., Heiden, A. M., Moorhead, S., Harrison, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder. Psychological Medicine -London- 26 (6) , pp. 1145-1153. 10.1017/s0033291700035868 |
Levinson, D. F., Wildenauer, D. B., Schwab, S. G., Albus, M., Hallmayer, J., Lerer, B., Maier, W., Blackwood, D., Muir, W., StClair, D., Morris, S., Moises, H. W., Yang, L., Kristbjarnarson, H., Helgason, T., Wiese, C., Collier, D. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Daniels, J., Rees, M., Asherson, P., Roberts, Q., Cardno, A., Arranz, M. J., Vallada, H., McGuffin, D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pulver, A. E., Antonarakis, S. E., Babb, R., Blouin, J. L., DeMarchi, N., Dombroski, B., Housman, D., Karayiorgou, M., Ott, J., Kasch, L., Kazazian, H., Lasseter, V. K., Loetscher, E., Luebbert, H., Nestadt, G., Ton, C., Wolyniec, P. S., Laurent, C., deChaldee, M., Thibaut, F., Jay, M., Samolyk, D., Petit, M., Campion, D., Mallet, J., Straub, R. E., MacLean, C. J., Easter, S. M., ONeill, F. A., Walsh, D., Kendler, K. S., Gejman, P. V., Cao, Q. H., Gershon, E., Badner, J., Beshah, E., Zhang, J., Riley, B. P., Rajagopalan, S., MogudiCarter, M., Jenkins, T., Williamson, R., DeLisi, L. E., Garner, C., Kelly, M., LeDuc, C., Cardon, L., Lichter, J., Harris, T., Loftus, J., Shields, G., Comasi, M., Vita, A., Smith, A., Dann, J., Joslyn, G., Gurling, H., Kalsi, G., Brynjolfsson, J., Curtis, D., Sigmundsson, T., Butler, R., Read, T., Murphy, P., Chen, A. C. H., Petursson, H., Byerley, B., Hoff, M., Holik, J., Nancarrow, D. J., Crowe, R. R., Andreasen, N., Silverman, J. M., Mohs, R. C., Siever, L. J., Endicott, J., Sharpe, L., Walters, M. K., Lennon, D. P., Hayward, N. K., Sandkuijl, L. A., Mowry, B. J., Aschauer, H. N., Meszaros, K., Lenzinger, E., Fuchs, K., Heiden, A. M., Kruglyak, L., Daly, M. J. and Matise, T. C. 1996. Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8. American Journal of Medical Genetics 67 (6) , pp. 580-594. 10.1002/(SICI)1096-8628(19961122)67:6<580::AID-AJMG11>3.0.CO;2-P |
Petrill, Stephen A., Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Thompson, Lee A., Detterman, Douglas K., Benbow, Camilla, Lubinski, David, Daniels, Joanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1996. DNA markers associated with general and specific cognitive abilities. Intelligence 23 (3) , p. 191. 10.1016/S0160-2896(96)90003-3 |
Kunugi, H., Curtis, D., Vallada, H. P., Nanko, S., Powell, J. F., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. A. 1996. A linkage study of schizophrenia with DNA markers from chromosome 8p21-p22 in 25 multiplex families. Schizophrenia Research 22 (1) , pp. 61-68. 10.1016/0920-9964(96)00048-5 |
Daniels, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Molecular genetic research on IQ: can it be done? Should it be done? Journal of Biosocial Science 28 (4) , pp. 491-507. 10.1017/S0021932000022550 |
Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Speight, G., Jones, L., Cardno, A., Murphy, Kevin, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1996. Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. American Journal of Human Genetics 59 (4) , pp. 912-917. |
Kehoe, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Liddell, M., Lovestone, S., Holmes, C., Powell, J., Neal, J., Wilcock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13) , pp. 2155-2158. 10.1097/00001756-199609020-00019 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kehoe, P. and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 1996. Presenilin-1 polymorphism and Alzheimer's disease. The Lancet 348 (9024) , p. 414. 10.1016/S0140-6736(05)65041-6 |
Farmer, A. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Genomics: the next psychiatric revolution? British Journal of Psychiatry 169 (2) , pp. 135-138. 10.1192/bjp.169.2.135 |
Ashworth, A., Abusaad, I., Walsh, C., Nanko, S., Murray, R. M., Asherson, P., McGuffin, P., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. A. 1996. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat. Psychiatric Genetics 6 (2) , pp. 81-86. 10.1097/00041444-199622000-00008 |
Parfitt, E., Asherson, P., Roberts, E., Mant, R., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. No evidence for linkage between schizophrenia and eight microsatellite markers on chromosome 19. Human Heredity 46 (4) , pp. 191-196. 10.1159/000154352 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J., McGuffin, P. and Farmer, A. E. 1996. Concurrent validity of the OPCRIT diagnostic system. Comparison of OPCRIT diagnoses with consensus best-estimate lifetime diagnoses. British Journal of Psychiatry 169 (1) , pp. 58-63. 10.1192/bjp.169.1.58 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Modern molecular genetic approaches to psychiatric disease. British Medical Bulletin 52 (3) , pp. 434-452. 10.1093/oxfordjournals.bmb.a011558 |
Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Spurlock, G., McGuffin, P., Mallet, J., Nothen, M. M., Gill, M., Aschauer, H., Nylander, P. O., Macciardi, F. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. The Lancet 347 (9011) , pp. 1294-1296. 10.1016/S0140-6736(96)90939-3 |
Asherson, P., Mant, R., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Cardno, A., Murphy, K., Jones, L., Collier, D., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2) , pp. 125-132. |
Kehoe, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Lovestone, S., Wilcock, G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Presenilin-1 polymorphism and Alzheimer's disease. The UK Alzheimer's Disease Collaborative Group. The Lancet 347 (9009) , p. 1185. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Schizophrenia, CATCH 22 and FISH. British Journal of Psychiatry 168 (4) , pp. 397-398. |
Lim, Lionel C. C., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Sham, Pak, Nothen, Markus M., Korner, Judith, Rietschel, Marcella, Fimmer, Rolf, Propping, Peter, McGuffin, Peter, Murray, Robin and Gill, Michael 1996. Assessing the statistical power to detect linkage in a sample of 51 bipolar affective disorder pedigrees. Behavior Genetics 26 (2) , pp. 113-122. 10.1007/bf02359889 |
Gill, M., Vallada, H., Collier, D., Sham, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Murray, R., McGuffin, P., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., Straub, R. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E. and Read, C. M. 1996. A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22). American Journal of Medical Genetics 67 (1) , pp. 40-45. 10.1002/(SICI)1096-8628(19960216)67:1<40::AID-AJMG6>3.0.CO;2-W |
Cardno, Alastair, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Harvey, I., Williams, M. B., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1996. Factor-derived subsyndromes of schizophrenia and familial morbid risks. Schizophrenia Research 18 (2-3) , IVA2-IVA2. |
Murphy, K. C. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Minor physical anomalies and their relationship to the aetiology of schizophrenia. British Journal of Psychiatry 168 (2) , pp. 139-142. 10.1192/bjp.168.2.139 |
Daniels, J. K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Jones, L. A., Cardno, A. G., Murphy, K. C., Spurlock, G., Riley, B., Scambler, P., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153 (2) , pp. 268-270. 10.1176/ajp.153.2.268 |
O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Dynamic mutations and psychiatric genetics. Psychological Medicine 26 (1) , pp. 1-6. 10.1017/S0033291700033663 |
Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Powell, J. F. 1996. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Cytogenetics and Cell Genetics 75 , pp. 2-3. |
Jacobsen, N., Daniels, J., Moorhead, S., Harrison, D., Feldman, E., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1996. Association study of bipolar disorder at the phospholipase A2 gene (PLA2A) in the Darier's disease (DAR) region of chromosome 12q23-q24.1. Psychiatric Genetics 6 (4) , pp. 195-199. 10.1097/00041444-199624000-00005 |
Roberts, A. G., Whatley, S. D., Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thompson, P., Long, C. and Elder, G. H. 1995. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23. Human Molecular Genetics 4 (12) , pp. 2387-2390. 10.1093/hmg/4.12.2387 |
Arranz, M., Sharma, T., Sham, P., Kerwin, R., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Collier, D. 1995. Schizophrenia and the androgen receptor gene: report of a sibship showing co-segregation with Reifenstein syndrome but no evidence for linkage in 23 multiply affected families. American Journal of Medical Genetics 60 (5) , pp. 377-381. 10.1002/ajmg.1320600506 |
Dawson, E., Powell, J. F., Sham, P., Shaikh, S., Taylor, C., Clements, A., Asherson, P., Sargeant, M., Collier, D., Nanko, S., Whatley, S., Murray, R., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1995. Systematic search for major genes in schizophrenia: methodological issues and results from chromosome 12. American Journal of Medical Genetics 60 (5) , pp. 424-433. 10.1002/ajmg.1320600513 |
Okoro, C., Bell, R., Sham, P., Nanko, S., Asherson, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M., McGuffin, P., Murray, R. M. and Collier, D. 1995. No evidence for linkage between the X-chromosome marker DXS7 and schizophrenia. American Journal of Medical Genetics 60 (5) , pp. 461-464. 10.1002/ajmg.1320600520 |
Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1995. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics 5 (3) , pp. 117-126. 10.1097/00041444-199505030-00004 |
Vallada, H., Curtis, D., Sham, P. C., Murray, R. M., McGuffin, P., Nanko, S., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. 1995. Chromosome 22 markers demonstrate transmission disequilibrium with schizophrenia. Psychiatric Genetics 5 (3) , pp. 127-130. 10.1097/00041444-199505030-00005 |
McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Farmer, A. E. 1995. Genetic basis of schizophrenia. The Lancet 346 (8976) , pp. 678-682. 10.1016/S0140-6736(95)92285-7 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Roberts, E., Rees, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No evidence for allelic association between bipolar disorder and monoamine oxidase A gene polymorphisms. American Journal of Medical Genetics 60 (4) , pp. 322-324. 10.1002/ajmg.1320600412 |
O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Murphy, Kevin, Cardno, Alastair G., Jones, L. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1995. Expanded CAG repeats in schizophrenia and bipolar disorder [letter]. Nature Genetics 10 (4) , pp. 380-381. 10.1038/ng0895-380 |
Skuder, Patricia, Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Petrill, Stephen A., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1995. A polymorphism in mitochondrial DNA associated with IQ? Intelligence 21 (1) , pp. 1-11. 10.1016/0160-2896(95)90035-7 |
Liddell, M. B., Bayer, Antony James ORCID: https://orcid.org/0000-0002-7514-248X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease. Human Molecular Genetics 4 (5) , pp. 853-858. 10.1093/hmg/4.5.853 |
Vallada, H. P., Gill, M., Sham, P., Lim, L. C., Nanko, S., Asherson, P., Murray, R. M., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Collier, D. 1995. Linkage studies on chromosome 22 in familial schizophrenia. American Journal of Medical Genetics 60 (2) , pp. 139-146. 10.1002/ajmg.1320600210 |
Dawson, E., Parfitt, E., Roberts, Q., Daniels, J., Lim, L., Sham, P., Nothen, M., Propping, P., Lanczik, M., Maier, W., Reuner, U., Weissenbach, J., Gill, M., Powell, J., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 1995. Linkage studies of bipolar disorder in the region of the Darier's disease gene on chromosome 12q23-24.1. American Journal of Medical Genetics 60 (2) , pp. 94-102. 10.1002/ajmg.1320600203 |
Mullan, M., Bennett, C., Figueredo, C., Hughes, D., Mant, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Warren, A., McInnis, M., Marshall, A., Lantos, P., Collinge, J., Goate, A. M., Houlden, H. and Crawford, F. 1995. Clinical features of early onset, familial Alzheimer's disease linked to chromosome 14. American Journal of Medical Genetics 60 (1) , pp. 44-52. 10.1002/ajmg.1320600109 |
Daniels, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. No association between schizophrenia and polymorphisms within the genes for debrisoquine 4-hydroxylase (CYP2D6) and the dopamine transporter (DAT). American Journal of Medical Genetics 60 (1) , pp. 85-87. 10.1002/ajmg.1320600115 |
Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Skuder, Patricia, Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Petrill, Stephen A., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1995. Allelic associations between 100 DNA markers and high versus low IQ. Intelligence 21 (1) , p. 31. 10.1016/0160-2896(95)90037-3 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Roberts, Q., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. Association study of bipolar disorder using a functional polymorphism (Ser311-->Cys) in the dopamine D2 receptor gene. Psychiatric Genetics 5 (2) , pp. 63-65. |
Rees, M. I., Andrew, M., Jawad, S. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Human Molecular Genetics 3 (12) , pp. 2175-2179. 10.1093/hmg/3.12.2175 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Is there an inverse relationship between Down's syndrome and bipolar affective disorder? literature review and genetic implications [Review]. Journal of Intellectual Disability Research 38 (6) , pp. 613-620. 10.1111/j.1365-2788.1994.tb00462.x |
McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Asherson, P. and Farmer, A. E. 1994. Genetics, chance and dysmorphogenesis in schizophrenia. British Journal of Psychiatry 165 , pp. 694-695. 10.1192/bjp.165.5.693b |
Daniels, J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Mant, R., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Repeat length variation in the dopamine D4 receptor gene shows no evidence of association with schizophrenia. American Journal of Medical Genetics 54 (3) , pp. 256-258. 10.1002/ajmg.1320540313 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Darier's disease cosegregating with affective disorder [letter]. British Journal of Psychiatry 165 (2) , p. 272. 10.1192/bjp.165.2.272a |
Plomin, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1994. The genetic basis of complex human behaviors. Science 264 (5166) , pp. 1733-1739. 10.1126/science.8209254 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, Jo, McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Variation at the fragile X locus does not influence susceptibility to bipolar disorder. American Journal of Medical Genetics 54 (2) , pp. 141-143. 10.1002/ajmg.1320540209 |
Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Gottesman, I. I., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and McGuffin, P. 1994. The genetics of mental retardation. The British Journal of Psychiatry 164 (6) , p. 747. 10.1192/bjp.164.6.747 |
James, C. M., Daniels, J., Wiles, Charles Mark and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Debrisoquine hydroxylase gene polymorphism in motor-neuron disease. Neurodegeneration 3 (2) , pp. 149-152. |
McGuffin, P, Asherson, P, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Farmer, A 1994. The strength of the genetic effect. Is there room for an environmental influence in the aetiology of schizophrenia? British Journal of Psychiatry 164 (5) , pp. 593-599. 10.1192/bjp.164.5.593 |
Asherson, P., Walsh, C., Williams, J., Sargeant, M., Taylor, C., Clements, A., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1994. Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia? The British Journal of Psychiatry 164 (5) , pp. 619-624. 10.1192/bjp.164.5.619 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Chromosomal aberrations and bipolar affective disorder [review]. British Journal of Psychiatry 164 (4) , pp. 507-512. 10.1192/bjp.164.4.507 |
Asherson, P, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Roberts, E, McGuffin, M and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. DRD2 Ser311/Cys311 polymorphism in schizophrenia. The Lancet 343 (8904) , p. 1045. |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Brockington, I., Mant, R., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Bipolar affective puerperal psychosis associated with consanguinity. British Journal of Psychiatry 164 (3) , pp. 359-364. 10.1192/bjp.164.3.359 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Burge, S., Kurian, B., Thomas, P. and McGuffin, P. 1994. Familial cosegregation of major affective disorder and Darier's disease (keratosis follicularis). British Journal of Psychiatry 164 (3) , pp. 355-358. 10.1192/bjp.164.3.355 |
Pulver, Ann E., Karayiorgou, Maria, Lasseter, Virginia K., Wolyniec, Paula, Kasch, Laura, Antonarakis, Stylianos, Housman, David, Kazazian, Haig H., Meyers, Deborah, Nestadt, Gerald, Ott, Jurg, Liang, Kung-Yee, Lamacz, Malgorzata, Thomas, Marion, Childs, Barton, Diehl, Scott R., Wang, Shengbiao, Murphy, Bernadette, Sun, Cui-E, O'Neill, F. Anthony, Nie, Li, Sham, Pak, Burke, John, Duke, Betty W., Duke, Fiona, Kipps, Barbara R., Bray, Joseph, Hunt, Wanda, Shinkwin, Rosmarie, Nuallain, Maurin Ni, Su, Ying, Maclean, Charles J., Walsh, Dermot, Kendler, Kenneth S., Gill, Michael, Vallada, Homero, Mant, Rebecca, Asherson, Philip, Collier, David, Parfitt, Elizabeth, Roberts, Enriquetta, Nanko, Shin, Walsh, Cathy, Daniels, Johanna, Murray, Robin, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Laurent, Claudine, Dumas, Jean-Baptiste, d'Amato, Thierry, Jay, Maurice, Martinez, Maria, Campion, Dominique and Mallet, Jacques 1994. Follow-up of a report of a potential linkage for schizophrenia on chromosome 22q12-q13.1: Part 2. American Journal of Medical Genetics 54 (1) , pp. 44-50. 10.1002/ajmg.1320540109 |
Shaikh, S., Gill, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Asherson, P., McGuffin, P., Nanko, S., Murray, R. M. and Collier, D. A. 1994. Failure to find linkage between a functional polymorphism in the dopamine D4 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1) , pp. 8-11. 10.1002/ajmg.1320540104 |
Mant, R., Williams, J., Asherson, P., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. American Journal of Medical Genetics 54 (1) , pp. 21-26. 10.1002/ajmg.1320540106 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Liddell, M and McGuffin, P 1994. Alzheimer's disease. British Medical Journal (BMJ) 308 (6930) , pp. 672-673. 10.1136/bmj.308.6930.672 |
Plomin, Robert, McClearn, Gerald E., Smith, Deborah L., Vignetti, Sylvia, Chorney, Michael J., Chorney, Karen, Venditti, Charles P., Kasarda, Steven, Thompson, Lee A., Detterman, Douglas K., Daniels, Johanna, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, Peter 1994. DNA markers associated with high versus low IQ: The IQ quantitative trait loci (QTL) project. Behavior Genetics 24 (2) , pp. 107-118. 10.1007/BF01067815 |
Liddell, Malcolm Brandon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Bayer, Antony James ORCID: https://orcid.org/0000-0002-7514-248X, Kaiser, F. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease. Journal of Medical Genetics 31 (3) , pp. 197-200. 10.1136/jmg.31.3.197 |
Asherson, P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. Anticipation in mental illness. The American Journal of Human Genetics 54 (2) , pp. 386-387. |
Parfitt, E., Burge, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Roberts, E., McLean, W. H., Weissenbach, J., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. The gene for Darier's disease maps between D12S78 and D12S79. Human Molecular Genetics 3 (1) , pp. 35-38. 10.1093/hmg/3.1.35 |
Vallada, H, Gill, M, Nanko, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Murray, R.M and Collier, C 1994. Is there a major gene for schizophrenia on chromosome-22. Schizophrenia Research 11 (2) , p. 147. |
Korner, J., Rietschel, M., Hunt, N., Castle, D., Gill, M., Nothen, M. M., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Fimmers, R., Fritze, J., Moller, H. -J. and Propping, P. 1994. Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls. Psychiatric Genetics 4 (3) , pp. 167-175. 10.1097/00041444-199400430-00007 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. The molecular genetics of Alzheimer's disease. Molecular and Cell Biology of Human Diseases Series 1994 (4) , pp. 92-109. |
McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlan ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Gottesman, Irving I. 1994. Seminars in psychiatric genetics. Gaskell, Royal College of Psychiatrists. |
Daniels, J.K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter, Thompson, Lee, Detterman, Douglas K., Chorney, Michael, Chorney, Karen, Smith, Deborah, Skuder, Patricia, Vignetti, Sylvia, McClearn, Gerald E. and Plomin, Robert 1994. IQ and variation in the number of fragile X CGG repeats: No association in a normal sample. Intelligence 19 (1) , pp. 45-50. 10.1016/0160-2896(94)90052-3 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dawson, Elisabeth, Burge, Susan, Parfitt, Liz, Mant, Becky, Roberts, Queta, Daniels, Jo, Gill, Mike, McGuffin, Peter, Powell, John and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. The gene for Darier's disease maps to chromosome 12q23-q24.1. Human Molecular Genetics 2 (11) , pp. 1941-1943. 10.1093/hmg/2.11.1941 |
McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Molecular-genetics and schizophrenia - the current picture. Behavior Genetics 23 (6) , p. 558. |
Saudino, K. J., Chorney, M., McClern, G. E., McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Smith, D., Detterman, D., Thompson, L. and Plomin, R. 1993. Applying a QTL association approach to temperament. Behavior Genetics 23 (6) , p. 564. |
Asherson, P., Mant, R., Taylor, C., Sargeant, M., Collier, D., Clements, A., Nanko, S., Whatley, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Failure to find linkage between schizophrenia and genetic markers on chromosome 21. American Journal of Medical Genetics 48 (3) , pp. 161-165. 10.1002/ajmg.1320480310 |
Mant, R., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P., Parfitt, E., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Susceptibility to schizophrenia and the dopamine d3 receptor gene. American Journal of Human Genetics 53 (3) , p. 1654. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P 1993. Association and linkage: complementary strategies for complex disorders. Journal of Medical Genetics 30 (8) , pp. 638-639. 10.1136/jmg.30.8.638 |
Shaikh, S., Ball, D., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Castle, D., Hunt, N., Mant, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Collier, D. and Gill, M. 1993. The dopamine D3 receptor gene: no association with bipolar affective disorder. Journal of Medical Genetics 30 (4) , pp. 308-309. 10.1136/jmg.30.4.308 |
Gill, M., McGuffin, P., Parfitt, E., Mant, R., Asherson, P., Vallada, H., Collier, D., Powell, J., Taylor, C., Sargeant, M., Clements, A., Nanko, S., Whatley, S., Murray, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. A linkage study of schizophrenia with DNA markers from the long arm of chromosome 11. Psychological Medicine 23 (1) , pp. 27-44. 10.1017/S0033291700038824 |
Jones, P. B., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, S. W. and Murray, R. M. 1993. A case-control study of family history and cerebral cortical abnormalities in schizophrenia. Acta Psychiatrica Scandinavica 87 (1) , pp. 6-12. 10.1111/j.1600-0447.1993.tb03322.x |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Burge, S., Parfitt, L. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1993. Linkage is excluded between Darier's disease and the Duffy blood group locus in five British families. Annales de Genetique 36 (4) , pp. 211-213. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Liddell, M 1992. Role of amyloid beta-protein in Alzheimer's disease. The Lancet 340 (8823) , p. 851. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1992. The molecular genetics of schizophrenia. British Medical Journal (BMJ) 305 (6855) , pp. 664-665. 10.1136/bmj.305.6855.664 |
Mant, R., Asherson, P., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. Schizophrenia scepticism. Nature Genetics 2 (1) , p. 12. 10.1038/ng0992-12 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mant, R., Parfitt, E., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Asherson, P., O'Mahoney, G., Van Os, J., Llewellyn, D., Collier, D., Gill, M. and McGuffin, P. 1992. No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia. Human Genetics 90 (1-2) , pp. 131-132. 10.1007/BF00210756 |
Vallada, Homero, Collier, David, Dawson, Elisabeth, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Nanko, Shin, Murray, Robin and Gill, Mike 1992. Debrisoquine 4-hydroxylase (CYP2D) locus and possible susceptibility to schizophrenia. The Lancet 340 (8812) , pp. 181-182. 10.1016/0140-6736(92)93266-P |
Asherson, Philip, Parfitt, E., Sargeant, M., Tidmarsh, Simon, Buckland, Paul Robert, Taylor, C., Clements, A., Gill, M., McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. No evidence for a pseudoautosomal locus for schizophrenia. Linkage analysis of multiply affected families. British Journal of Psychiatry 161 (1) , pp. 63-68. 10.1192/bjp.161.1.63 |
Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1992. Christmas disease and major affective disorder [letter]. British Journal of Psychiatry 160 , p. 715. 10.1192/bjp.160.5.715a |
Nanko, Shinichiro, Gill, Michael, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Takazawa, Noboru, Moridaira, Junko and Kazamatsuri, Hajime 1992. Linkage Study of Schizophrenia with Markers on Chromosome 11 in Two Japanese Pedigrees. Psychiatry and Clinical Neurosciences 46 (1) , pp. 155-159. 10.1111/j.1440-1819.1992.tb00828.x |
Shaikh, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1992. DRD2 (TGn) repeat polymorphism in a large family data set. Schizophrenia Research 6 (2) , p. 91. 10.1016/0920-9964(92)90088-M |
Dawson, E., Shaikh, S., Vallada, H., Powell, J., Collier, D., Nanko, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1992. Genetic linkage analysis of schizophrenia using microsatellite repeat polymorphisms on chromosome 12. Schizophrenia Research 6 (2) , p. 90. 10.1016/0920-9964(92)90086-K |
Collier, DavidA., Gill, Michael, Nanko, Shen, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Vallada, Homero 1992. Linkage analysis of schizophrenia on chromosome 22. Schizophrenia Research 6 (2) , pp. 89-90. 10.1016/0920-9964(92)90085-J |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and GILL, M. 1992. Looking for genes in schizophrenia. Clinical Neuropharmacology 15 (Suppl1) , 222A-223A. 10.1097/00002826-199201001-00116 |
Upadhyaya, M, Lunt, P W, Sarfarazi, M, Broadhead, W, Daniels, J, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Harper, P S 1991. A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. Journal of Medical Genetics 28 (10) , pp. 665-671. 10.1136/jmg.28.10.665 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Parfitt, E., Sargeant, M., Asherson, P., McGuffin, P., Taylor, C., Collier, D., Powell, J., Murray, R. and Gill, M. 1991. Linkage studies of schizophrenia with markers of chromosome-11q. American Journal of Human Genetics 49 (4) , p. 354. |
Mant, R., Parfitt, E., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. Mononucleotide repeat polymorphism in the APP gene. Nucleic Acids Research 19 (16) , p. 4572. 10.1093/nar/19.16.4572-a |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Goate, A.M. and Hardy, J.A. 1991. A polymorphic microsatellite repeat sequence on chromosome 21 (D21S80). Nucleic Acids Research 19 (16) , pp. 4574-4571. 10.1093/nar/19.16.4574 |
Foerster, A., Lewis, S. W., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R. M. 1991. Low birth weight and a family history of schizophrenia predict poor premorbid functioning in psychosis. Schizophrenia Research 5 (1) , pp. 13-20. 10.1016/0920-9964(91)90049-W |
Goate, Alison, Chartier-Harlin, Marie-Christine, Mullan, Mike, Brown, Jeremy, Crawford, Fiona, Fidani, Liana, Giuffra, Luis, Haynes, Andrew, Irving, Nick, James, Louise, Mant, Rebecca, Newton, Phillippa, Rooke, Karen, Roques, Penelope, Talbot, Chris, Pericak-Vance, Margaret, Roses, Alien, Williamson, Robert, Rossor, Martin, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Hardy, John 1991. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature 349 (6311) , pp. 704-706. 10.1038/349704a0 |
Foerster, A., Lewis, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R. 1991. Pre-morbid adjustment and personality in psychosis. Effects of sex and diagnosis. British Journal of Psychiatry 158 (2) , pp. 171-176. 10.1192/bjp.158.2.171 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and McGuffin, P. 1991. DNA-and classical genetic markers in schizophrenia. European Archives of Psychiatry and Clinical Neuroscience 240 (3) , pp. 197-203. 10.1007/BF02190764 |
McGuffin, Peter and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. The molecular genetics of schizophrenia: An overview and forward view. European Archives of Psychiatry and Clinical Neuroscience 240 (3) , pp. 169-173. 10.1007/BF02190759 |
Mant, R, Asherson, P, Sargeant, M, Hicks, A, Darlison, M, Johnstone, K, Sander, T, Taylor, C, Murray, R, Whatley, S, Gill, M, McGuffin, P and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1991. Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker. Cytogenetics and Cell Genetics 58 (3-4) , pp. 1900-1991. |
Upadhyaya, M., Lunt, P.W., Sarfarazi, M., Broadhead, W., Daniels, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Harper, P.S. 1990. DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease. The Lancet 336 (8726) , pp. 1320-1321. 10.1016/0140-6736(90)93005-A |
St George-Hyslop, P. H., Haines, J. L., Farrer, L. A., Polinsky, R., Broeckhoven, C. Van, Goate, A., McLachlan, D. R. Crapper, Orr, H., Bruni, A. C., Sorbi, S., Rainero, I., Foncin, J.-F., Pollen, D., Cantu, J-M., Tupler, R., Voskresenskaya, N., Mayeux, R., Growdon, J., Fried, V. A., Myers, R. H., Nee, L., Backhovens, H., Martin, J-J., Rossor, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mullan, M., Percy, M. E., Karlinsky, H., Rich, S., Heston, L., Montesi, M., Mortilla, M., Nacmias, N., Gusella, J. F. and Hardy, J. A. 1990. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature 347 (6289) , pp. 194-197. 10.1038/347194a0 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, Peter and Andrews, R.C.Richardson 1990. Obstetric complications and schizophrenia. The Lancet 336 (8707) , p. 122. 10.1016/0140-6736(90)91643-O |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craufurd, D. and St Clair, D. 1990. Localisation of a susceptibility locus for schizophrenia on chromosome 5. British Journal of Psychiatry 157 (1) , pp. 123-127. 10.1192/bjp.157.1.123 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, James, L.A., Hardy, J.A., Williamson, R and Goate, A.M. 1990. Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21. American Journal of Human Genetics 46 (2) , pp. 316-322. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Mullan, Michael J. 1990. Molecular genetic studies of manic-depression and schizophrenia. Trends in Neurosciences 13 (1) , pp. 29-31. 10.1016/0166-2236(90)90059-J |
Goate, A.M., Hardy, J.A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Haynes, A., James, L., Farrell, M., Mullan, M.J., Roques, P. and Rossor, M.N. 1990. Genetics of Alzheimer's disease. Advances in Neurology -New York- Raven Press- 51 , pp. 197-198. |
Hardy, John, Goate, Alison, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Rossor, Martin 1989. Presenile dementia associated with mosaic trisomy 21 in a patient with a down syndrome child. The Lancet 334 (8665) , p. 743. 10.1016/S0140-6736(89)90805-2 |
Hardy, J.A., Goate, A.M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Mullan, M.J., Rossor, M.N. and Pearson, R.C.A. 1989. Modelling the occurrence and pathology of Alzheimer's disease. Neurobiology of Aging 10 (5) , pp. 429-431. 10.1016/0197-4580(89)90084-5 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, S. W. and Murray, R. M. 1989. Family history and cerebral ventricular enlargement in schizophrenia. A case control study. British Journal of Psychiatry 154 (5) , pp. 629-634. 10.1192/bjp.154.5.629 |
Goate, AlisonM., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, James, LouiseA., Mullan, MichaelJ., Rossor, MartinN., Haynes, AndrewR., Farrall, Martin, Lai, LawrenceY.C., Roques, Penelope, Williamson, Robert and Hardy, JohnA. 1989. Predisposing locus for Alzheimer's disease on chromosome 21. The Lancet 333 (8634) , pp. 352-355. 10.1016/S0140-6736(89)91725-X |
HARDY, J. A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, GOATE, A. M., JAMES, L. A., HAYNES, A. R., ROSSOR, M. N., ROQUES, P. and MULLAN, M. J. 1989. Molecular genetics of Alzheimer's disease. Biochemical Society Transactions 17 (1) , pp. 75-76. 10.1042/bst0170075 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Murray, R.M. 1988. Blue genes. British Medical Journal (BMJ) 297 (6653) , pp. 871-872. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lewis, S. W. 1988. Risk factors in schizophrenia. British Journal of Psychiatry 153 (3) , p. 407. 10.1192/bjp.153.3.407a |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Whatley, S.A. 1988. Polymorphic DNA markers and mental disease. Psychological Medicine 18 (3) , pp. 529-533. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Lewis, Shôn W. and Murray, Robin M. 1988. Obstetric complications and schizophrenia: a computed tomographic study. Psychological Medicine 18 (02) , pp. 331-339. 10.1017/S003329170000787X |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Nimgaonkar, V.L. 1987. The continuum of psychosis and the gene. British Journal of Psychiatry 150 , pp. 566-567. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Lweis, S.W. 1986. Lateral ventricular size in schizophrenia. The Lancet 2 (8500) , pp. 223-224. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1984. Does amnesia after transection of the fornix in monkeys reflect abnormal sensitivity to proactive interference? Behavioural Brain Research 14 (3) , pp. 183-192. |
Gaffan, D, Saunders, RC, Gaffan, EA, Harrison, S, Shields, C and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1984. Effects of fornix transection upon associative memory in monkeys: role of the hippocampus in learned action. Quarterly Journal of Experimental Psychology 36 (3) , pp. 173-221. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1981. Amnesia after transection of the fornix in monkeys: Long-term memory impaired, short-term memory intact. Behavioural Brain Research 3 (1) , pp. 115-123. 10.1016/0166-4328(81)90032-2 |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1980. Effects of fornix lesions on recognition memory in the monkey. Journal of Anatomy 131 (DEC) , p. 771. |
Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Butler, S.R. 1980. The effects of fornix lesions on latent learning in the rat. Physiology & Behavior 24 (5) , pp. 817-822. 10.1016/0031-9384(80)90133-X |