Browse by Current Cardiff authors

, O’Donovan, Michael C.

2025. Effects of shared and nonshared schizophrenia and bipolar disorder alleles on cognition and educational attainment in the UK Biobank. Biological Society: Global Open Science 5 (6) , 100601. 10.1016/j.bpsgos.2025.100601

Smart, Sophie E.

, Legge, Sophie E., Fenner, Eilidh, Pardiñas, Antonio F.

, Woolway, Grace, Lynham, Amy J.

, Escott‐Price, Valentina

, Wilkinson, Lawrence

and Walters, James T.R.

2025. The role of SLC39A8.p.( Ala391Thr ) in schizophrenia symptom severity and cognitive ability: cross‐sectional studies of schizophrenia and the general UK population. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 198 (7) , pp. 135-146. 10.1002/ajmg.b.33037

Barnett, Eric, Hess, Jonathan, Hou, Jiahui, Escott-Price, Valentina

, Fennema-Notestine, Christine, Kremen, William, Lin, Shu-Ju, Zhang, Chunling, Gaiteri, Chris, Elman, Jeremy, Holmans, Peter

, Faraone, Stephen and Glatt, Stephen 2025. A novel method to disentangle tightly linked risk and resilience genes for brain disorders: application to Alzheimer's disease. [Online]. medRxiz: openRxiv. Available at: https://doi.org/10.1101/2025.02.26.25322962

Chick, Sophie L., Holmans, Peter

, Cameron, Darren, Grozeva, Detelina

, O’Donovan, Michael C.

and Rees, Elliott

2025. Whole-exome sequencing analysis identifies risk genes for schizophrenia. Nature Communications 16 (1) , 7102. 10.1038/s41467-025-62429-y

Nicolas, Aude, Sherva, Richard, Grenier-Boley, Benjamin, Kim, Yoontae, Kikuchi, Masataka, Timsina, Jigyasha, de Rojas, Itziar, Dalmasso, María Carolina, Zhou, Xiaopu, Le Guen, Yann, Arboleda-Bustos, Carlos E., Camargos Bicalho, Maria Aparecida, Guerchet, Maëlenn, van der Lee, Sven, Goss, Monica, Castillo, Atahualpa, Bellenguez, Céline, Küçükali, Fahri, Satizabal, Claudia L., Fongang, Bernard, Yang, Qiong, Peters, Oliver, Schneider, Anja, Dichgans, Martin, Rujescu, Dan, Scherbaum, Norbert, Deckert, Jürgen, Riedel-Heller, Steffi, Hausner, Lucrezia, Molina-Porcel, Laura, Düzel, Emrah, Grimmer, Timo, Wiltfang, Jens, Heilmann-Heimbach, Stefanie, Moebus, Susanne, Tegos, Thomas, Scarmeas, Nikolaos, Dols-Icardo, Oriol, Moreno, Fermin, Pérez-Tur, Jordi, Bullido, María J., Pastor, Pau, Sánchez-Valle, Raquel, Álvarez, Victoria, Cao, Han, Ip, Nancy Y., Fu, Amy K. Y., Ip, Fanny C. F., Olivar, Natividad, Muchnik, Carolina, Cuesta, Carolina, Campanelli, Lorenzo, Solis, Patricia, Politis, Daniel Gustavo, Kochen, Silvia, Brusco, Luis Ignacio, Boada, Mercè, García-González, Pablo, Puerta, Raquel, Mir, Pablo, Real, Luis M., Piñol-Ripoll, Gerard, García-Alberca, Jose María, Royo, Jose Luís, Rodriguez-Rodriguez, Eloy, Soininen, Hilkka, Heikkinen, Sami, de Mendonça, Alexandre, Mehrabian, Shima, Traykov, Latchezar, Hort, Jakub, Vyhnalek, Martin, Rasmussen, Katrine Laura, Thomassen, Jesper Qvist, Pijnenburg, Yolande A. L., Holstege, Henne, van Swieten, John C., Seelaar, Harro, Claassen, Jurgen A. H. R., Jansen, Willemijn J., Ramakers, Inez, Verhey, Frans, van der Lugt, Aad, Scheltens, Philip, Ortega-Rojas, Jenny, Concha Mera, Ana Gabriela, Mahecha, Maria F., Pardo, Rodrigo, Arboleda, Gonzalo, Bahrami, Shahram, Fominykh, Vera, Selbæk, Geir, Graff, Caroline, Papenberg, Goran, Giedraitis, Vilmantas, Boland, Anne, Deleuze, Jean-François, de Marco, Luiz Armando, de Moraes, Edgar Nunes, de Mattos Viana, Bernardo, Túlio Gualberto Cintra, Marco, Juarez-Cedillo, Teresa, Griswold, Anthony J., Forund, Tatiana, Haines, Jonathan, Farrer, Lindsay, DeStefano, Anita, Wijsman, Ellen, Mayeux, Richard, Pericak-Vance, Margaret, Kunkle, Brian, Goate, Alison, Schellenberg, Gerard D., Vardarajan, Badri, Wang, Li-San, Leung, Yuk Yee, Dalgard, Clifton L., Nicolas, Gael, Wallon, David, Dufouil, Carole, Pasquier, Florence, Hanon, Olivier, Debette, Stéphanie, Grünblatt, Edna, Popp, Julius, Angel, Bárbara, Gloger, Sergio, Chacon, Maria Victoria, Aranguiz, Rafael, Orellana, Paulina, Slachevsky, Andrea, Gonzalez-Billault, Christian, Albala, Cecilia, Fuentes, Patricio, Sachdev, Perminder, Mather, Karen A., Hauger, Richard L., Merritt, Victoria, Panizzon, Matthew, Zhang, Rui, Gaziano, J. Michael, Ghidoni, Roberta, Galimberti, Daniela, Arosio, Beatrice, Mecocci, Patrizia, Solfrizzi, Vincenzo, Parnetti, Lucilla, Squassina, Alessio, Tremolizzo, Lucio, Borroni, Barbara, Nacmias, Benedetta, Caffarra, Paolo, Seripa, Davide, Rainero, Innocenzo, Daniele, Antonio, Piras, Fabrizio, Moreno-Grau, Sonia, Amin, Najaf, Holmans, Peter A.

, Kleineidam, Luca, Aarsland, Dag, Garcia-Gonzalez, Pablo, Abdelnour, Carla, Alarcón-Martín, Emilio, Alcolea, Daniel, Alegret, Montserrat, Alvarez, Ignacio, Armstrong, Nicola J., Anthoula, Tsolaki, Appollonio, Ildebrando, Arcaro, Marina, Archetti, Silvana, Arias Pastor, Alfonso, Athanasiu, Lavinia, Bailly, Henri, Banaj, Nerisa, Baquero, Miquel, Pastor, Ana Belén, Bellini, Sonia, Berr, Claudine, Besse, Céline, Bessi, Valentina, Binetti, Giuliano, Bizarro, Alessandra, Blesa, Rafael, Boschi, Silvia, Bossù, Paola, Bråthen, Geir, Bresner, Catherine

, Brodaty, Henry, Brookes, Keeley J., Buiza-Rueda, Dolores, Bûrger, Katharina, Burholt, Vanessa, Calero, Miguel, Chene, Geneviève, Carracedo, Ángel, Cecchetti, Roberta, Cervera-Carles, Laura, Charbonnier, Camille, Chillotti, Caterina, Ciccone, Simona, Clarimon, Jordi, Clark, Christopher, Conti, Elisa, Corma-Gómez, Anaïs, Giuffrè, Guido Maria, Custodero, Carlo, Daian, Delphine, Dardiotis, Efthimios, de Deyn, Peter Paul, del Ser, Teodoro, Denning, Nicola, Diehl-Schmid, Janine, Diez-Fairen, Mónica, Rossi, Paolo Dionigi, Djurovic, Srdjan, Duron, Emmanuelle, Engelborghs, Sebastiaan, Espinosa, Ana, Ewers, Michael, Fabrizio, Tagliavini, Nielsen, Sune Fallgaard, Farotti, Lucia, Fenoglio, Chiara, Fernández-Fuertes, Marta, Ferreira, Catarina B., Ferri, Evelyn, Fin, Bertrand, Fischer, Peter, Fladby, Tormod, Fließbach, Klaus, Fortea, Juan, Foroud, Tatiana M., Fostinelli, Silvia, Fox, Nick C., Franco-Macías, Emlio, Frank-García, Ana, Froelich, Lutz, García-Alberca, Jose Maria, Garcia-Madrona, Sebastian, Garcia-Ribas, Guillermo, Giegling, Ina, Giorgio, Giaccone, Goldhardt, Oliver, González-Pérez, Antonio, Grande, Giulia, Green, Emma, Guetta-Baranes, Tamar, Haapasalo, Annakaisa, Hadjigeorgiou, Georgios, Hampel, Harald, Hardy, John, Hartmann, Annette M., Harwood, Janet, Helisalmi, Seppo, Heneka, Michael T., Hernández, Isabel, Herrmann, Martin J., Hoffmann, Per, Holmes, Clive, Huerto Vilas, Raquel, Hulsman, Marc, Biessels, Geert Jan, Johansson, Charlotte, Kilander, Lena, Ståhlbom, Anne Kinhult, Kivipelto, Miia, Koivisto, Anne, Kornhuber, Johannes, Kosmidis, Mary H., Lage, Carmen, Laukka, Erika J., Lauria, Alessandra, Lehtisalo, Jenni, Lerch, Ondrej, Lleó, Alberto, López-de Munain, Adolfo, Love, Seth, Löwemark, Malin, Luckcuck, Lauren, Macías, Juan, MacLeod, Catherine A., Maier, Wolfgang, Mangialasche, Francesca, Spallazzi, Marco, Marquié, Marta, Marshall, Rachel, Montes, Angel Martín, Martínez Rodríguez, Carmen, Mead, Simon, Medina, Miguel, Meggy, Alun, Mendoza, Silvia, Menéndez-González, Manuel, Mol, Merel, Montrreal, Laura, Morgan, Kevin, Möthen, Markus M., Ngandu, Tiia, Nordestgaard, Børge G., Olaso, Robert, Orellana, Adelina, Orsini, Michela, Ortega, Gemma, Padovani, Alessandro, Pérez-Cordón, Alba, Pericard, Pierre, Pineda, Juan A., Pisanu, Claudia, Polak, Thomas, Posthuma, Danielle, Priller, Josef, Quenez, Olivier, Quintela, Inés, Rábano, Alberto, Reinders, Marcel J. T., Riederer, Peter, Roberto, Natalia, Rongve, Arvid, Allende, Irene Rosas, Rosende-Roca, Maitée, Royo, Jose Luis, Rubino, Elisa, Sáez, María Eugenia, Sakka, Paraskevi, Saltvedt, Ingvild, Sanabria, Ángela, Bernal Sánchez-Arjona, María, Sanchez-Garcia, Florentino, Sánchez-Juan, Pascual, Sando, Sigrid B., Scamosci, Michela, Scarpini, Elio, Scherer, Martin, Schmid, Matthias, Schott, Jonathan M., Shadrin, Alexey A., Skrobot, Olivia, Solomon, Alina, Sorbi, Sandro, Sotolongo-Grau, Oscar, Spottke, Annika, Stordal, Eystein, Tartan, Juan Pablo, Tárraga, Lluís, Tesí, Niccolo, Thalamuthu, Anbupalam, Thomas, Tegos, Tybjærg-Hansen, Anne, Uitterlinden, Andre, Ullgren, Abbe, Ulstein, Ingun, Valero, Sergi, Van Broeckhoven, Christine, Van Dongen, Jasper, Vandenberghe, Rik, Vidal, Jean-Sébastien, Vogelgsang, Jonathan, Wagner, Michael, Weinhold, Leonie, Windle, Gill, Woods, Bob, Yannakoulia, Mary, Zulaica, Miren, Leonard, Hampton L., Yokoyama, Jenifer S., Nalls, Mike A., Miyashita, Akinori, Hara, Norikazu, Ozaki, Kouichi, Niida, Shumpei, Williams, Julie

, Masullo, Carlo, Amouyel, Philippe, Preux, Pierre-Marie, Mbelesso, Pascal, Bandzouzi, Bébène, Saykin, Andy, Jessen, Frank, Kehoe, Patrick G., Van Duijn, Cornelia, Ben Salem, Nesrine, Frikke-Schmidt, Ruth, Cherni, Lotfi, Greicius, Michael D., Tsolaki, Magda, Sánchez-Juan, Pascual, Romano Silva, Marco Aurélio, Porter, Tenielle, Laws, Simon M., Sleegers, Kristel, Ingelsson, Martin, Dartigues, Jean-François, Seshadri, Sudha, Rossi, Giacomina, Morelli, Laura, Hiltunen, Mikko, Sims, Rebecca

, van der Flier, Wiesje, Andreassen, Ole A., Arboleda, Humberto, Cruchaga, Carlos, Escott-Price, Valentina

, Ruiz, Agustín, Lee, Kun Ho, Ikeuchi, Takeshi, Ramirez, Alfredo, Gim, Jungsoo, Logue, Mark and Lambert, Jean-Charles 2025. Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations. Nature Genetics 57 , pp. 1598-1610. 10.1038/s41588-025-02227-w

Bracher-Smith, Matthew, Melograna, Federico, Ulm, Brittany, Bellenguez, Céline, Grenier-Boley, Benjamin, Duroux, Diane, Nevado, Alejo J., Holmans, Peter

, Tijms, Betty M., Hulsman, Marc, de Rojas, Itziar, Campos-Martin, Rafael, der Lee, Sven van, Castillo, Atahualpa, Küçükali, Fahri, Peters, Oliver, Schneider, Anja, Dichgans, Martin, Rujescu, Dan, Scherbaum, Norbert, Deckert, Jürgen, Riedel-Heller, Steffi, Hausner, Lucrezia, Molina-Porcel, Laura, Düzel, Emrah, Grimmer, Timo, Wiltfang, Jens, Heilmann-Heimbach, Stefanie, Moebus, Susanne, Tegos, Thomas, Scarmeas, Nikolaos, Dols-Icardo, Oriol, Moreno, Fermin, Pérez-Tur, Jordi, Bullido, María J., Pastor, Pau, Sánchez-Valle, Raquel, Álvarez, Victoria, Boada, Mercè, García-González, Pablo, Puerta, Raquel, Mir, Pablo, Real, Luis M., Piñol-Ripoll, Gerard, García-Alberca, Jose María, Rodriguez-Rodriguez, Eloy, Soininen, Hilkka, Heikkinen, Sami, de Mendonça, Alexandre, Mehrabian, Shima, Traykov, Latchezar, Hort, Jakub, Vyhnalek, Martin, Sandau, Nicolai, Thomassen, Jesper Qvist, Pijnenburg, Yolande A. L., Holstege, Henne, van Swieten, John, Ramakers, Inez, Verhey, Frans, Scheltens, Philip, Graff, Caroline, Papenberg, Goran, Giedraitis, Vilmantas, Williams, Julie

, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Nicolas, Gael, Dufouil, Carole, Pasquier, Florence, Hanon, Olivier, Debette, Stéphanie, Grünblatt, Edna, Popp, Julius, Ghidoni, Roberta, Galimberti, Daniela, Arosio, Beatrice, Mecocci, Patrizia, Solfrizzi, Vincenzo, Parnetti, Lucilla, Squassina, Alessio, Tremolizzo, Lucio, Borroni, Barbara, Wagner, Michael, Nacmias, Benedetta, Spallazzi, Marco, Seripa, Davide, Rainero, Innocenzo, Daniele, Antonio, Piras, Fabrizio, Masullo, Carlo, Rossi, Giacomina, Jessen, Frank, Kehoe, Patrick, Magda, Tsolaki, Sánchez-Juan, Pascual, Sleegers, Kristel, Ingelsson, Martin, Hiltunen, Mikko, Sims, Rebecca

, van der Flier, Wiesje, Andreassen, Ole A., Ruiz, Agustín, Ramirez, Alfredo, Frikke-Schmidt, Ruth, Amin, Najaf, Roshchupkin, Gennady, Lambert, Jean-Charles, Van Steen, Kristel, van Duijn, Cornelia and Escott-Price, Valentina

2025. Machine learning in Alzheimer’s disease genetics. Nature Communications 16 (1) , 6726. 10.1038/s41467-025-61650-z

Hou, Jiahui, Hess, Jonathan L., Zhang, Chunling, van Rooij, Jeroen G. J., Hearn, Gentry C., Fan, Chun Chieh, Faraone, Stephen V., Fennema‐Notestine, Christine, Lin, Shu‐Ju, Escott‐Price, Valentina

, Seshadri, Sudha, Holmans, Peter

, Tsuang, Ming T., Kremen, William S., Gaiteri, Chris and Glatt, Stephen J. 2025. Meta‐analysis of transcriptomic studies of blood and six brain regions identifies a consensus of 15 cross‐tissue mechanisms in Alzheimer's disease and suggests an origin of cross‐study heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 198 (4) , e33019. 10.1002/ajmg.b.33019
Item availability restricted.

Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium, Wills, Christopher, Massey, Thomas H.

2025. Genetic modifiers of somatic expansion and clinical phenotypes in Huntington’s disease highlight shared and tissue-specific effects. Nature Genetics 57 , pp. 1426-1436. 10.1038/s41588-025-02191-5
Item availability restricted.

Katzourou, Ioanna, Barroso, Ines, Benger, Lauren, Ingason, Andres, Stow, Daniel, Tsang, Ruby, Wood, Megan, Kirov, George

, Van den Bree, Marianne B.M

and Consortium, LINC 2025. Contributions of common and rare genetic variation to different measures of mood and anxiety disorder in UK Biobank. BJPsych Open 11 (3) , e97. 10.1192/bjo.2025.43

Thomassen, Jesper, Hampton, Leonard, Ulms, Brittany, Grenier-Boley, Benjamin, Heikkinen, Sami, Garcia, Pablo, Castillo-Morales, Atahualapa, Kikuchi, Masataka, Gim, Jungsoo, Cao, Han, Küçükali, Fahri, Amin, Najaf, Yoon, Dabin, de Rojas, Itziar, Alvarez Jerez, Pilar, Alvarez, Victoria, Arosio, Beatrice, Bellenguez, Céline, Bergh, Sverre, Billingsley, Kimberly, Blauwendraat, Cornelis, Boada, Merce, Borroni, Barbara, Bossù, Paola, Bullido, María, Daniele, Antonio, Carracedo, Ángel, de Mendonça, Alexandre, Cookson, Mark, Deckert, Jürgen, Dichgans, Martin, Djurovic, Srdjan, Dols-Icardo, Oriol, Dufouil, Carole, Düzel, Emrah, Escott-Price, Valentina

, Fladby, Tormod, Fratiglioni, Laura, K.Y. Fu, Amy, Galimberti, Daniela, Maria Garcia-Alberca, Jose, Giedraitis, Vilmantas, Garcia-Ribas, Guillermo, Graff, Caroline, Grimmer, Timo, Grünblatt, Edna, Hanon, Olivier, Hausner, Lucrezia, Heilmann-Hemibach, Stefanie, Hort, Jakub, Jessen, Frank, Jensen, Kendall, Jonson, Caroline, Kim, Yoontae, Kuznetsov, Nicole, Leinonen, Ville, Lipponen, Anssi, Luo, Jiao, Makarious, Mary, Martiskainen, Henna, Masullo, Carlo, Mecocci, Patrizia, Mehrabian, Shima, Mir, Pablo, Miyashita, Akinori, Moebus, Susanne, Mok, Kin, Molina Porcel, Laura, Moreno, Fermin, Nacmias, Benedetta, Parnetti, Lucilla, Pastor, Pau, Pérez-Tur, Jordi, Peters, Oliver, Pijnenburg, Yolande, Piñol-Ripoll, Gerard, Popp, Julius, Rainero, Innocenzo, Real, Luis, Riedel-Heller, Steffi, Rodriguez-Rodriguez, Eloy, Rongve, Arvid, Rossi, Giacomina, Luis Royo, Jose, Rujescu, Dan, Saltvedt, Ingvild, Eugenia Sáez, María, Sánchez-Valle, Raquel, Sanchez-Garcia, Florentino, Sandau, Nicolai, Scarmeas, Nikolaos, Scheffler, Katja, Scherbaum, Norbert, Schneider, Anja, Selbæk, Geir, Seripa, Davide, Solfrizzi, Vincenzo, Spallazzi, Marco, Squassina, Alessio, Stordal, Eystein, Tesi, Niccoló, Tremolizzo, Lucio, Tripathi, Kumar, van der Flier, Wiesje, Williams, Julie

, Wiltfang, Jens, Aarsland, Dag, Singleton, Andrew, Amouyel, Philippe, Debette, Stéphanie, Nicolas, Gael, van der Lee, Sven, Holstege, Henne, Victoria Fernandez, Maria, Gavin Kehoe, Patrick, Sleegers, Kristel, Ingelsson, Martin, Ghidoni, Roberta, Andreassen, Ole, Holmans, Peter

, Sánchez-Juan, Pascual, Sims, Rebecca

, Ip, Nancy, Ho Lee, Kun, Ikeuchi, Takeshi, Ramirez, Alfredo, Ruiz, Agustin, Hiltunen, Mikko, Lambert, Jean-Charles, van Duijn, Cornelia, Nalls, Mike and Frikke-Schmidt, Ruth 2025. APOE stratified genome-wide association studies provide novel insights into the genetic etiology of Alzheimers's disease. [Online]. medRxiv: openRxiv. Available at: https://doi.org/10.1101/2025.05.07.25327065

O'Connell, Kevin S., Koromina, Maria, van der Veen, Tracey, Boltz, Toni, David, Friederike S., Yang, Jessica Mei Kay, Lin, Keng-Han, Wang, Xin, Coleman, Jonathan R. I., Mitchell, Brittany L., McGrouther, Caroline C., Rangan, Aaditya V., Lind, Penelope A., Koch, Elise, Harder, Arvid, Parker, Nadine, Bendl, Jaroslav, Adorjan, Kristina, Agerbo, Esben, Albani, Diego, Alemany, Silvia, Alliey-Rodriguez, Ney, Als, Thomas D., Andlauer, Till F. M., Antoniou, Anastasia, Ask, Helga, Bass, Nicholas, Bauer, Michael, Beins, Eva C., Bigdeli, Tim B., Pedersen, Carsten Bøcker, Boks, Marco P., Børte, Sigrid, Bosch, Rosa, Brum, Murielle, Brumpton, Ben M., Brunkhorst-Kanaan, Nathalie, Budde, Monika, Bybjerg-Grauholm, Jonas, Byerley, William, Cabana-Domínguez, Judit, Cairns, Murray J., Carpiniello, Bernardo, Casas, Miquel, Cervantes, Pablo, Chatzinakos, Chris, Chen, Hsi-Chung, Clarence, Tereza, Clarke, Toni-Kim, Claus, Isabelle, Coombes, Brandon, Corfield, Elizabeth C., Cruceanu, Cristiana, Cuellar-Barboza, Alfredo, Czerski, Piotr M., Dafnas, Konstantinos, Dale, Anders M., Dalkner, Nina, Degenhardt, Franziska, DePaulo, J. Raymond, Djurovic, Srdjan, Drange, Ole Kristian, Escott-Price, Valentina

, Fanous, Ayman H., Fellendorf, Frederike T., Ferrier, I. Nicol, Forty, Elizabeth, Frank, Josef, Frei, Oleksandr, Freimer, Nelson B., Fullard, John F., Garnham, Julie, Gizer, Ian R., Gordon, Scott D., Gordon-Smith, Katherine, Greenwood, Tiffany A., Grove, Jakob, Guzman-Parra, José, Ha, Tae Hyon, Hahn, Tim, Haraldsson, Magnus, Hautzinger, Martin, Havdahl, Alexandra, Heilbronner, Urs, Hellgren, Dennis, Herms, Stefan, Hickie, Ian B., Hoffmann, Per, Holmans, Peter A.

, Huang, Ming-Chyi, Ikeda, Masashi, Jamain, Stéphane, Johnson, Jessica S., Jonsson, Lina, Kalman, Janos L., Kamatani, Yoichiro, Kennedy, James L., Kim, Euitae, Kim, Jaeyoung, Kittel-Schneider, Sarah, Knowles, James A., Kogevinas, Manolis, Kranz, Thorsten M., Krebs, Kristi, Kushner, Steven A., Lavebratt, Catharina, Lawrence, Jacob, Leber, Markus, Lee, Heon-Jeong, Liao, Calwing, Lucae, Susanne, Lundberg, Martin, MacIntyre, Donald J., Maier, Wolfgang, Maihofer, Adam X., Malaspina, Dolores, Manchia, Mirko, Maratou, Eirini, Martinsson, Lina, Mattheisen, Manuel, McGregor, Nathaniel W., McInnis, Melvin G., McKay, James D., Medeiros, Helena, Meyer-Lindenberg, Andreas, Millischer, Vincent, Morris, Derek W., Moutsatsou, Paraskevi, Mühleisen, Thomas W., O'Donovan, Claire, Olsen, Catherine M., Panagiotaropoulou, Georgia, Papiol, Sergi, Pardinas, Antonio F.

, Park, Hye Youn, Perry, Amy, Pfennig, Andrea, Pisanu, Claudia, Potash, James B., Quested, Digby, Rapaport, Mark H., Regeer, Eline J., Rice, John P., Rivera, Margarita, Schulte, Eva C., Senner, Fanny, Shadrin, Alexey, Shilling, Paul D., Sigurdsson, Engilbert, Sindermann, Lisa, Sirignano, Lea, Siskind, Dan, Slaney, Claire, Sloofman, Laura G., Smeland, Olav B., Smith, Daniel J., Sobell, Janet L., Soler Artigas, Maria, Stein, Dan J., Stein, Frederike, Su, Mei-Hsin, Sung, Heejong, Swiatkowska, Beata, Terao, Chikashi, Tesfaye, Markos, Tesli, Martin, Thorgeirsson, Thorgeir E., Thorp, Jackson G., Toma, Claudio, Tondo, Leonardo, Tooney, Paul A., Tsai, Shih-Jen, Tsermpini, Evangelia Eirini, Vawter, Marquis P., Vedder, Helmut, Vreeker, Annabel, Walters, James T. R., Winsvold, Bendik S., Witt, Stephanie H., Won, Hong-Hee, Ye, Robert, Young, Allan H., Zandi, Peter P., Zillich, Lea, Lee, Byung-Chul, Kim, Ji-Woong, Lee, Young Kee, Kang, Joon Ho, Cheon, Myeong Jae, Kim, Dong Jun, Aslan, Mihaela, Harvey, Philip D., Huang, Grant D., Adolfsson, Rolf, Alda, Martin, Alfredsson, Lars, Backlund, Lena, Baune, Bernhard T., Bellivier, Frank, Bengesser, Susanne, Berrettini, Wade H., Biernacka, Joanna M., Boehnke, Michael, Børglum, Anders D., Breen, Gerome, Carr, Vaughan J., Catts, Stanley, Cichon, Sven, Corvin, Aiden, Craddock, Nicholas, Dannlowski, Udo, Dikeos, Dimitris, Etain, Bruno, Ferentinos, Panagiotis, Frye, Mark, Fullerton, Janice M., Gawlik, Micha, Gershon, Elliot S., Goes, Fernando S., Green, Melissa J., Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Henskens, Frans A., Hjerling-Leffler, Jens, Hougaard, David M., Hveem, Kristian, Iwata, Nakao, Jones, Ian, Jones, Lisa A., Kahn, René S., Kelsoe, John R., Kircher, Tilo, Kirov, George, Kuo, Po-Hsiu, Landén, Mikael, Leboyer, Marion, Li, Qingqin S., Lissowska, Jolanta, Lochner, Christine, Loughland, Carmel, Luykx, Jurjen J., Martin, Nicholas G., Mathews, Carol A., Mayoral, Fermin, McElroy, Susan L., McIntosh, Andrew M., McMahon, Francis J., Medland, Sarah E., Melle, Ingrid, Milani, Lili, Mitchell, Philip B., Morken, Gunnar, Mors, Ole, Mortensen, Preben Bo, Müller-Myhsok, Bertram, Myers, Richard M., Myung, Woojae, Neale, Benjamin M., Nievergelt, Caroline M., Nordentoft, Merete, Nöthen, Markus M., Nurnberger, John I., O'Donovan, Michael C.

, Oedegaard, Ketil J., Olsson, Tomas, Owen, Michael J., Paciga, Sara A., Pantelis, Christos, Pato, Carlos N., Pato, Michele T., Patrinos, George P., Pawlak, Joanna M., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Reininghaus, Eva Z., Ribasés, Marta, Rietschel, Marcella, Ripke, Stephan, Rouleau, Guy A., Roussos, Panos, Saito, Takeo, Schall, Ulrich, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Scott, Rodney J., Serretti, Alessandro, Smoller, Jordan W., Squassina, Alessio, Stahl, Eli A., Stefansson, Hreinn, Stefansson, Kari, Stordal, Eystein, Streit, Fabian, Sullivan, Patrick F., Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Waldman, Irwin D., Weickert, Cynthia S., Weickert, Thomas W., Werge, Thomas, Whiteman, David C., Zwart, John-Anker, Edenberg, Howard J., McQuillin, Andrew, Forstner, Andreas J., Mullins, Niamh, Di Florio, Arianna

, Ophoff, Roel A., Andreassen, Ole A., van der Veen, Tracey and Siskind, Dan 2025. Genomics yields biological and phenotypic insights into bipolar disorder. Nature 639 , pp. 968-975. 10.1038/s41586-024-08468-9
Item availability restricted.

Cardno, Alastair G., Allardyce, Judith

, Bakker, Steven C., Toulopoulou, Timothea, Kravariti, Eugenia, Picchioni, Marco M., Kane, Fergus, Rijsdijk, Frühling V., Mahmood, Tariq, Nasser El Din, Soumaya, du Toit, Deline, Jones, Lisa A., Quattrone, Diego, Walters, James T. R.

, Legge, Sophie E., Holmans, Peter A.

, Murray, Robin M. and Vassos, Evangelos 2025. Associations of psychotic symptom dimensions with clinical and developmental variables in twin and general clinical samples. The British Journal of Psychiatry 226 (1) , pp. 16-23. 10.1192/bjp.2024.129

Harrison, Judith R.

, Foley, Sonya F.

, Simmonds, Emily, Bracher-Smith, Matthew, Holmans, Peter

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, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan

2006. Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. Journal of Medical Genetics 43 (7) , pp. 563-567. 10.1136/jmg.2005.035345

Macgregor, Stuart, Craddock, Nicholas John

2006. Use of phenotypic covariates in association analysis by sequential addition of cases. European Journal of Human Genetics 14 (5) , pp. 529-534. 10.1038/sj.ejhg.5201604

Hamshere, Marian Lindsay

, MacGregor, S., Escott-Price, Valentina

, Nikolov, I. N. and Holmans, Peter Alan

2005. Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction. BMC Genetics 6 (1) , S45. 10.1186/1471-2156-6-S1-S45

Levinson, D. F. and Holmans, Peter Alan

2005. The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees. BMC Genetics 6 (1) , S6-S6. 10.1186/1471-2156-6-S1-S6

Hamshere, Marian Lindsay

, Bennett, Philip, Williams, Nigel Melville

, Segurado, Ricardo, Cardno, Alastair George, Norton, Nadine

, Lambert, David, Williams, Hywel John

, Corvin, Aiden, Holmans, Peter Alan

, Jones, Lisa Anne, Jones, Ian Richard

, Gill, Michael, O'Donovan, Michael Conlon

2005. Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of general psychiatry 62 (10) , pp. 1081-1088. 10.1001/archpsyc.62.10.1081

Hodges, A., Strand, A. D., Aragaki, A. K., Sengstag, T., Hughes, G., Elliston, Linda Anne, Hartog, C., Goldstein, D. R., Thu, D., Hollingsworth, Z. R., Collin, F., Synek, B., Holmans, Peter Alan

, Young, A. B., Wexler, N. S., Delorenzi, M., Kooperberg, C., Augood, S. J., Faull, R. L. M., Olson, J. M., Luthi-Carter, R. and Jones, Lesley

2005. Regional specificity of transcriptional changes in early grade Huntington's disease brain. Journal of Neurology, Neurosurgery and Psychiatry 76 , A16-A16.

Hughes, G. P., Brooks, Simon P.

, Hodges, A. H., Holmans, Peter Alan

, Thomas, J. M., Goldstein, D., Dunnett, Stephen Bruce

and Jones, Lesley

2005. Integrating behaviour and brain gene expression in Huntington's disease transgenic mouse models. Journal of Neurology, Neurosurgery and Psychiatry 76 , A41-A41.

Nowotny, P., Hinrichs, A. L., Smemo, S., Kauwe, J. S., Maxwell, T., Holmans, Peter Alan

, Turic, D., Jehu, L., Hollingworth, P., Moore, P., Bryden, L., Myers, A., Doil, L. M., Tacey, K. M., Gibson, A. M., McKeith, I. G., Perry, R. H., Morris, C. M., Thal, L., Morris, J. C., O'Donovan, Michael Conlon

, Lovestone, S. and Grupe, A. 2005. Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 136B (1) , pp. 62-68. 10.1002/ajmg.b.30186

Holmans, Peter Alan

, Hollingworth, P., Rice, Frances

, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville

, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon

, Jones, Lesley

, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John

2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114

Lambert, D., Middle, F., Hamshere, Marian Lindsay

, Segurado, Ricardo, Raybould, Rachel, Corvin, A., Green, Elaine Karen, O'Mahony, E., Nikolov, Ivan, Mulcahy, T., Haque, S., Bort, S., Bennett, P., Norton, Nadine

, Lendon, C., Jones, Lisa Anne, Jones, Ian Richard

, Gill, M. and Craddock, Nicholas John

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

Cope, Natalie Alexandra, Harold, Denise

, Hill, Gary Trevor, Escott-Price, Valentina

, Stevenson, Jim, Holmans, Peter Alan

, O’Donovan, Michael Conlon

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

Escott-Price, Valentina

, Norton, Nadine

2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3) , pp. 273-282. 10.1002/gepi.20062

Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan

, 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

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

Escott-Price, Valentina

, Schmidt, Karl Michael

2005. Design of Case-controls Studies with Unscreened Controls. Annals of Human Genetics 69 (5) , pp. 566-576. 10.1111/j.1529-8817.2005.00175.x

Seaman, S. R. and Holmans, Peter Alan

2005. Effect of genotyping error on type-I error rate of affected sib pair studies with genotyped parents. Human Heredity 59 (3) , pp. 157-164. 10.1159/000085939

Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan

, 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

, 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

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

, Hardy, John, Powell, John, Lovestone, Simon, Thal, Leon, Owen, Michael John

, 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

, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville

, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John

, 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

, 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

Holmans, Peter Alan

, Zubenko, George S., Crowe, Raymond R., DePaulo, J. Raymond Jr., Scheftner, William A., Weissman, Myrna M., Zubenko, Wendy N., Boutelle, Sandra, Murphy-Eberenz, Kathleen, MacKinnon, Dean, McInnis, Melvin G., Marta, Diana H., Adams, Philip, Knowles, James A., Gladis, Madeline, Thomas, Jo, Chellis, Jennifer, Miller, Erin and Levinson, Douglas F. 2004. Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. The American Journal of Human Genetics 74 (6) , pp. 1154-1167. 10.1086/421333

Bernardinelli, L., Berzuini, C., Seaman, S. and Holmans, Peter Alan

2004. Bayesian trio models for association in the presence of genotyping errors. Genetic Epidemiology 26 (1) , pp. 70-80. 10.1002/gepi.10291

Myers, Amanda J., Marshall, Helen, Holmans, Peter Alan

, Compton, Danielle, Crook, Richard J.P., Mander, Adrian P., Nowotny, Petra, Smemo, Scott, Dunstan, Melanie

, Jehu, Luke, Wang, Jen C., Hamshere, Marian Lindsay

, Morris, John C., Norton, Joanne, Chakraventy, Sumi, Tunstall, Nigel, Lovestone, Simon, Petersen, Ronald, O'Donovan, Michael Conlon

, Jones, Lesley

, Hardy, John and Goate, Alison 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1) , pp. 29-37. 10.1002/ajmg.b.20036

Busby, Victoria, Goossens, Steven, Nowotny, Petra, Hamilton, Gillian, Smemo, Scott, Harold, Denise, Turic, Dragana, Jehu, Luke, Myers, Amanda, Womick, Meredith, Woo, Daniel, Compton, Danielle, Doil, Lisa M., Tacey, Kristina M., Lau, Kit F., Al-Saraj, Safa, Killick, Richard, Pickering-Brown, Stuart, Moore, Pamela, Hollingworth, Paul, Archer, Nicola, Foy, Catherine, Walter, Sarah, Lovestone, Simon, O'Donovan, Michael Conlon

, Jones, Lesley

2004. Alpha-T-Catenin Is Expressed in Human Brain and Interacts With the Wnt Signaling Pathway But Is Not Responsible for Linkage to Chromosome 10 in Alzheimer's Disease. Neuromolecular Medicine 5 (2) , pp. 133-146. 10.1385/NMM:5:2:133

Williams, Nigel Melville

, Norton, Nadine

, Ekholm, B., Hamshere, Marian Lindsay

, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley

, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan

, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon

2003. A systematic genomewide linkage study in 353 sib pairs with schizophrenia. The American journal of human genetics 73 (6) , pp. 1355-1367. 10.1086/380206

Hensiek, A.E., Roxburgh, R., Smilie, B., Coraddu, F., Åkesson, E., Holmans, Peter Alan

, Sawcer, S.J. and Compston, D.A.S. 2003. Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis. Journal of Neuroimmunology 143 (1-2) , pp. 25-30. 10.1016/j.jneuroim.2003.08.007

Levinson, Douglas F., Zubenko, George S., Crowe, Raymond R., DePaulo, Raymond J., Scheftner, William S., Weissman, Myrna M., Holmans, Peter Alan

, Zubenko, Wendy N., Boutelle, Sandra, Murphy-Eberenz, Kathleen, MacKinnon, Dean, McInnis, Melvin G., Marta, Diana H., Adams, Philip, Sassoon, Stephanie, Knowles, James A., Thomas, Jo and Chellis, Jennifer 2003. Genetics of recurrent early-onset depression (GenRED): Design and preliminary clinical characteristics of a repository sample for genetic linkage studies. American Journal of Medical Genetics 119B (1) , pp. 118-130. 10.1002/ajmg.b.20009

Rice, K. M. and Holmans, Peter Alan

2003. Allowing for Genotyping Error in Analysis of Unmatched Case-Control Studies. Annals of Human Genetics 67 (2) , pp. 165-174. 10.1046/j.1469-1809.2003.00020.x

McInnis, M G, Lan, T-H, Willour, V L, McMahon, F J, Simpson, S G, Addington, A M, MacKinnon, D F, Potash, J B, Mahoney, A T, Chellis, J, Huo, Y, Swift-Scanlan, T, Chen, H, Koskela, R, Colin Stine, O, Jamison, K R, Holmans, Peter Alan

, Folstein, S E, Ranade, K, Friddle, C, Botstein, D, Marr, T, Beaty, T H, Zandi, P and Raymond DePaulo, J 2003. Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12. Molecular Psychiatry 8 (3) , pp. 288-298. 10.1038/sj.mp.4001277

Levinson, D.F., Holmans, Peter Alan

, Laurent, C., Mallet, J., Riley, B., Kendler, K.S., Pulver, A.E., Gejman, P.V., Sanders, A.R., Schwab, S.G., Wildenauer, D.B., Owen, Michael John

and Mowry, B.J. 2002. Is schizophrenia linked to chromosome 1q? Response. Science 298 (5602) , pp. 2277-2279.

Richards, A. J., Morgan, J., Bearcroft, P. W. P., Pickering, E., Owen, Michael John

, Tysoe, C., Pope, F. M., Snaed, M. P. and Hughes, H. 2002. Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. Journal of Medical Genetics 39 (9) , pp. 661-665. 10.1136/jmg.39.9.661

Akesson, E, Oturai, A, Berg, J, Fredrikson, S, Andersen, O, Harbo, H F, Laaksonen, M, Myhr, K M, Nyland, H I, Ryder, L P, Sandberg-Wollheim, M, Sorensen, P S, Spurkland, A, Svejgaard, A, Holmans, Peter

, Compston, A, Hillert, J and Sawcer, S 2002. A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis. Genes and Immunity 3 (5) , pp. 279-285. 10.1038/sj.gene.6363866

Levinson, Douglas. F., Holmans, Peter Alan

, Laurent, Claudine, Riley, Brien, Pulver, Ann E., Gejman, Pablo V., Schwab, Sibylle G., Williams, Nigel Melville

, Wildenauer, Dieter B., Sanders, Alan R., Nestadt, Gerald, Mowry, Brian J., Wormley, Brandon, Bauche, Stephanie, Soubigou, Stephane, Ribble, Robert, Nertney, Deborah A., Liang, Kung Yee, Martinolich, Laura, Maier, Wolfgang, Norton, Nadine, Williams, Hywel John

, Albus, Margot, Carpenter, Eric B., DeMarchi, Nicola, Ewen-White, Kelly R., Walsh, Dermot, Jay, Maurice, Deleuze, Jean-Francois, O'Neill, Anthony F., Papadimitriou, George, Weilbaecher, Ann, Lerer, Bernard, O'Donovan, Michael Conlon

, Dikeos, Dimitris, Silverman, Jeremy M., Kendler, Kenneth S., Mallet, Jacques, Crowe, Raymond R. and Walters, Marilyn 2002. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 296 (5568) , pp. 739-741. 10.1126/science.1069914

Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan

, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville

, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances

, Giles, Peter

, Tunstall, Nigel, Jones, Lesley

, Lovestone, Simon, Williams, Julie

, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal Of Medical Genetics Part A 114 (2) , pp. 235-244. 10.1002/ajmg.10183

Holmans, Peter Alan

2002. Detecting gene-gene interactions using affected sib pair analysis with covariates. Human Heredity 53 (2) , pp. 92-102. 10.1159/000057987

Bennett, P., Segurado, R., Jones, Ian Richard

, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George

, Larsen, B., Mulcahy, T., Williams, Nigel Melville

, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John

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

Holmans, Peter Alan

2001. Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: issues of power and type I error rate. Genetic Epidemiology 20 (1) , pp. 44-56. 10.1002/1098-2272(200101)

Myers, A., Holmans, Peter Alan

, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay

, Abraham, R., Tunstall, N., Rice, Frances

, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley

, Lovestone, S., Perez-Tur, J., Williams, Julie

, 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

Levinson, D. F., Holmans, Peter Alan

, Straub, R. E., Owen, Michael John

, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville

, 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

Murphy, K. C., Williams, Nigel Melville

, Cardno, A. G., Jones, L. A., Holmans, Peter Alan

, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John

2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Bandmann, O., Vaughan, J. R., Holmans, Peter Alan

, Marsden, C. D. and Wood, N. W. 2000. Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. Movement Disorders 15 (1) , pp. 30-35. 10.1002/1531-8257(200001)15:13.0.CO;2-V

Neuman, R. J., Saccone, N. L., Holmans, Peter Alan

, Rice, J. P. and Sun, L. 2000. Clustering methods applied to allele sharing data. Genetic Epidemiology 19 (1) , pp. 57-63. 10.1002/1098-2272(2000)19:1+<::AID-GEPI9>3.0.CO;2-D

Williams, Nigel Melville

, Rees, M. I., Holmans, Peter Alan

, 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

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

Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan

, Kehoe, P., Owen, Michael John

, 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.

Hateboer, N., Lazarou, L. P., Williams, A. J., Holmans, Peter Alan

and Ravine, D. 1999. Familial phenotype differences in PKD11. Kidney International 56 (1) , pp. 34-40. 10.1046/j.1523-1755.1999.00541.x

Rees, M. I., Fenton, I., Williams, Nigel Melville

, 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

1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan

, Rice, Frances

, 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

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

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan

, Fenton, I., Williams, Nigel Melville

, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie

, Goate, A., Hardy, J. and Owen, Michael John

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

Bandmann, O., Vaughan, J., Holmans, Peter Alan

, Marsden, C. D. and Wood, N. W. 1999. Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2. Advances in Neurology -New York- Raven Press- 80 , pp. 199-204.

Holmans, Peter Alan

1998. Affected sib-pair methods for detecting linkage to dichotomous traits: review of the methodology. Human biology 70 (6) , pp. 1025-1040.

Kehoe, P. G., Williams, H., Holmans, Peter Alan

, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John

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

Bandmann, O., Valente, E. M., Holmans, Peter Alan

, Surtees, R. A., Walters, J. H., Wevers, R. A., Marsden, C. D. and Wood, N. W. 1998. Dopa-responsive dystonia: a clinical and molecular genetic study. Annals of Neurology 44 (4) , pp. 649-656. 10.1002/ana.410440411

Wu, W. S., Holmans, Peter Alan

, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville

, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie

, Hutton, M., Hardy, J., Owen, Michael John

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

Daniels, J., Holmans, Peter Alan

, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John

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

Williams, Julie

, Spurlock, G., Holmans, Peter Alan

, 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

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.

Holmans, Peter Alan

1998. Efficient strategies for genome scanning with affected sib pairs - Reply. American Journal of Human Genetics 62 (1) , pp. 205-207. 10.1086/301683

Hateboer, N., Lazarou, L., Holmans, Peter Alan

, Williams, A. J. and Ravine, D. 1998. Inter-family variability of phenotype in autosomal dominant polycystic kidney disease type 1. European Journal of Human Genetics 6 (1) , p. 71.

Murphy, K. C., Williams, Nigel Melville

, Cardno, A. G., Jones, L. A., Holmans, Peter Alan

, McGuffin, P. and Owen, Michael John

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

Spurlock, G., Heils, A., Holmans, Peter Alan

, 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

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

Bandmann, O., Vaughan, J., Holmans, Peter Alan

, Marsden, C. D. and Wood, N. W. 1997. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. The Lancet 350 (9085) , pp. 1136-1139. 10.1016/S0140-6736(97)03495-8

Hateboer, N., Torra, R., Estivill, E., Bogdanova, N., Davies, F., Lazarou, L., vonDijk, M., Breuning, M., SaggarMalik, A., Jeffery, S., SanMillan, J. L., Martinez, I., Walker, R., Holmans, Peter Alan

and Ravine, D. 1997. PKD2: The phenotype defined. Kidney International 52 (4) , p. 1122.

Baboolal, K., Ravine, D., Daniels, J., Williams, Nigel Melville

, Coles, G. A. and Williams, J. D. 1997. Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease. Kidney International 52 (3) , pp. 607-613. 10.1038/ki.1997.373

Hateboer, N., Dijk, M., Torra, R., Bogdanova, N., Davies, F., Lazarou, L., Breuning, M., SaggarMalik, A. K., Jeffery, S., Millan, J. L. S., Martinez, I., Walker, R., Holmans, Peter Alan

, Ravine, D. and Coles, G. A. 1997. Phenotype PKD2 vs. PKD1; results from the European concerted action. Journal of the American Society of Nephrology 8 , A1722-A1722.

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