Browse by Current Cardiff authors

, Georgieva, Lyudmila, Hamshere, Marian L.

, Kavanagh, David, Kirov, George

, Legge, Sophie, Owen, Michael J.

, Richards, Alexander L., Walters, James T. R.

and Holmans, Peter A.

2024. Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications 15 , 5534. 10.1038/s41467-024-49338-2

Tan, Manuela M. X., Lawton, Michael A., Pollard, Miriam I., Brown, Emmeline, Real, Raquel, Carrasco, Alejandro Martinez, Bekadar, Samir, Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine

, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Andreassen, Ole A., Toft, Mathias, Elbaz, Alexis, Artaud, Fanny, Brice, Alexis, Corvol, Jean-Christophe, Aasly, Jan, Farrer, Matthew J., Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M.

, Ben-Shlomo, Yoav, Hardy, John, Hu, Michele T. M., Grosset, Donald G., Shoai, Maryam, Pihlstrøm, Lasse and Morris, Huw R. 2024. Genome-wide determinants of mortality and motor progression in Parkinson’s disease. npj Parkinson's Disease 10 (1) , 113. 10.1038/s41531-024-00729-8

Wu, Lesley Yue, Real, Raquel, Martinez-Carrasco, Alejandro, Chia, Ruth, Lawton, Michael A, Shoai, Maryam, Bresner, Catherine

, Blauwendraat, Cornelis, Singleton, Andrew B, Ryten, Mina, International Lewy Body Dementia Genomics Consortium, Scholz, Sonja W, Traynor, Bryan J, Williams, Nigel M

, Hu, Michele T M, Ben-Shlomo, Yoav, Grosset, Donald G, Hardy, John and Morris, Huw R 2024. Investigation of the genetic aetiology of Lewy body diseases with and without dementia. Brain Communications 6 (4) , fcae190. 10.1093/braincomms/fcae190

Menon, Poornima Jayadev, Sambin, Sara, Criniere-Boizet, Baptiste, Courtin, Thomas, Tesson, Christelle, Casse, Fanny, Ferrien, Melanie, Mariani, Louise-Laure, Carvalho, Stephanie, Lejeune, Francois-Xavier, Rebbah, Sana, Martet, Gaspard, Houot, Marion, Lanore, Aymeric, Mangone, Graziella, Roze, Emmanuel, Vidailhet, Marie, Aasly, Jan, Gan Or, Ziv, Yu, Eric, Dauvilliers, Yves, Zimprich, Alexander, Tomantschger, Volker, Pirker, Walter, Álvarez, Ignacio, Pastor, Pau, Di Fonzo, Alessio, Bhatia, Kailash P., Magrinelli, Francesca, Houlden, Henry, Real, Raquel, Quattrone, Andrea, Limousin, Patricia, Korlipara, Prasad, Foltynie, Thomas, Grosset, Donald, Williams, Nigel

, Narendra, Derek, Lin, Hsin-Pin, Jovanovic, Carna, Svetel, Marina, Lynch, Timothy, Gallagher, Amy, Vandenberghe, Wim, Gasser, Thomas, Brockmann, Kathrin, Morris, Huw R., Borsche, Max, Klein, Christine, Corti, Olga, Brice, Alexis, Lesage, Suzanne and Corvol, Jean Christophe 2024. Genotype–phenotype correlation in PRKN- associated Parkinson’s disease. npj Parkinson's Disease 10 , 72. 10.1038/s41531-024-00677-3

Kim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cannon, Paul, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Kukar, Katelyn, Kwong, Alan, Lin, Keng-Han, Llamas, Bianca A., Lowe, Maya, McCreight, Jey C., McIntyre, Matthew H., Micheletti, Steven J., Moreno, Meghan E., Nandakumar, Priyanka, Nguyen, Dominique T., Noblin, Elizabeth S., O'Connell, Jared, Petrakovitz, Aaron A., Poznik, G. David, Reynoso, Alexandra, Schloetter, Madeleine, Schumacher, Morgan, Shastri, Anjali J., Shelton, Janie F., Shi, Jingchunzi, Shringarpure, Suyash, Su, Qiaojuan Jane, Tat, Susana A., Tchakouté, Christophe Toukam, Tran, Vinh, Tung, Joyce Y., Wang, Xin, Wang, Wei, Weldon, Catherine H., Wilton, Peter, Wong, Corinna D., Iwaki, Hirotaka, Lake, Julie, Solsberg, Caroline Warly, Leonard, Hampton, Makarious, Mary B., Tan, Eng-King, Singleton, Andrew B., Bandres-Ciga, Sara, Noyce, Alastair J., Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E., Koks, Sulev, Zimprich, Alexander, Schumacher-Schuh, Artur F., Rieder, Carlos, Awad, Paula Saffie, Tumas, Vitor, Camargos, Sarah, Fon, Edward A., Monchi, Oury, Fon, Ted, Galleguillos, Benjamin Pizarro, Miranda, Marcelo, Bustamante, Maria Leonor, Olguin, Patricio, Chana, Pedro, Tang, Beisha, Shang, Huifang, Guo, Jifeng, Chan, Piu, Luo, Wei, Arboleda, Gonzalo, Orozc, Jorge, del Rio, Marlene Jimenez, Hernandez, Alvaro, Salama, Mohamed, Kamel, Walaa A., Zewde, Yared Z., Brice, Alexis, Corvol, Jean-Christophe, Westenberger, Ana, Illarionova, Anastasia, Mollenhauer, Brit, Klein, Christine, Vollstedt, Eva-Juliane, Hopfner, Franziska, Höglinger, Günter, Madoev, Harutyun, Trinh, Joanne, Junker, Johanna, Lohmann, Katja, Lange, Lara M., Sharma, Manu, Groppa, Sergiu, Gasser, Thomas, Fang, Zih-Hua, Akpalu, Albert, Xiromerisiou, Georgia, Hadjigorgiou, Georgios, Dagklis, Ioannis, Tarnanas, Ioannis, Stefanis, Leonidas, Stamelou, Maria, Dadiotis, Efthymios, Medina, Alex, Chan, Germaine Hiu-Fai, Ip, Nancy, Cheung, Nelson Yuk-Fai, Chan, Phillip, Zhou, Xiaopu, Kishore, Asha, Divya, K. P., Pal, Pramod, Kukkle, Prashanth Lingappa, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Valente, Enza Maria, Parnetti, Lucilla, Avenali, Micol, Schirinzi, Tommaso, Funayama, Manabu, Hattori, Nobutaka, Shiraishi, Tomotaka, Karimova, Altynay, Kaishibayeva, Gulnaz, Shambetova, Cholpon, Krüger, Rejko, Tan, Ai Huey, Ahmad-Annuar, Azlina, Norlinah, Mohamed Ibrahim, Murad, Nor Azian Abdul, Azmin, Shahrul, Lim, Shen-Yang, Mohamed, Wael, Tay, Yi Wen, Martinez-Ramirez, Daniel, Rodriguez-Violante, Mayela, Reyes-Pérez, Paula, Tserensodnom, Bayasgalan, Ojha, Rajeev, Anderson, Tim J., Pitcher, Toni L., Sanyaolu, Arinola, Okubadejo, Njideka, Ojo, Oluwadamilola, Aasly, Jan O., Pihlstrøm, Lasse, Tan, Manuela, Ur-Rehman, Shoaib, Veliz-Otani, Diego, Cornejo-Olivas, Mario, Doquenia, Maria Leila, Rosales, Raymond, Vinuela, Angel, Iakovenko, Elena, Mubarak, Bashayer Al, Umair, Muhammad, Amod, Ferzana, Carr, Jonathan, Bardien, Soraya, Jeon, Beomseok, Kim, Yun Joong, Cubo, Esther, Alvarez, Ignacio, Hoenicka, Janet, Beyer, Katrin, Periñan, Maria Teresa, Pastor, Pau, El-Sadig, Sarah, Brolin, Kajsa, Zweier, Christiane, Tinkhauser, Gerd, Krack, Paul, Lin, Chin-Hsien, Wu, Hsiu-Chuan, Kung, Pin-Jui, Wu, Ruey-Meei, Wu, Yihru, Amouri, Rim, Sassi, Samia Ben, Baak, A. Nazl, Genc, Gencer, Çakmak, Özgür Öztop, Ertan, Sibel, Martínez-Carrasco, Alejandro, Schrag, Anette, Schapira, Anthony, Carroll, Camille, Bale, Claire, Grosset, Donald, Stafford, Eleanor J., Houlden, Henry, Morris, Huw R., Hardy, John, Mok, Kin Ying, Rizig, Mie, Wood, Nicholas, Williams, Nigel

, Okunoye, Olaitan, Lewis, Patrick Alfryn, Kaiyrzhanov, Rauan, Weil, Rimona, Love, Seth, Stott, Simon, Jasaityte, Simona, Dey, Sumit, Obese, Vida, Espay, Alberto, O'Grady, Alyssa, Sobering, Andrew K., Siddiqi, Bernadette, Casey, Bradford, Fiske, Brian, Jonas, Cabell, Cruchaga, Carlos, Pantazis, Caroline B., Comart, Charisse, Wegel, Claire, Hall, Deborah, Hernandez, Dena, Shiamim, Ejaz, Riley, Ekemini, Faghri, Faraz, Serrano, Geidy E., Chen, Honglei, Mata, Ignacio F., Sarmiento, Ignacio Juan Keller, Williamson, Jared, Jankovic, Joseph, Shulman, Joshua, Solle, Justin C., Murphy, Kaileigh, Nuytemans, Karen, Kieburtz, Karl, Markopoulou, Katerina, Marek, Kenneth, Levine, Kristin S., Chahine, Lana M., Ibanez, Laura, Screven, Laurel, Ruffrage, Lauren, Shulman, Lisa, Marsili, Luca, Kuhl, Maggie, Dean, Marissa, Koretsky, Mathew, Puckelwartz, Megan J., Inca-Martinez, Miguel, Louie, Naomi, Mencacci, Niccolò Emanuele, Albin, Roger, Alcalay, Roy, Walker, Ruth, Chowdhury, Sohini, Dumanis, Sonya, Lubbe, Steven, Xie, Tao, Foroud, Tatiana, Beach, Thomas, Sherer, Todd, Song, Yeajin, Nguyen, Duan, Nguyen, Toan, Atadzhanov, Masharip, Blauwendraat, Cornelis, Nalls, Mike A., Foo, Jia Nee and Mata, Ignacio 2024. Multi-ancestry genome-wide association meta-analysis of Parkinson?s disease. Nature Genetics 56 (1) , pp. 27-36. 10.1038/s41588-023-01584-8

Martínez Carrasco, Alejandro, Real, Raquel, Lawton, Michael, Hertfelder Reynolds, Regina, Tan, Manuela, Wu, Lesley, Williams, Nigel

, Carroll, Camille, Corvol, Jean-Christophe, Hu, Michele, Grosset, Donald, Hardy, John, Ryten, Mina, Ben-Shlomo, Yoav, Shoai, Maryam and Morris, Huw R. 2023. Genome-wide analysis of motor progression in parkinson disease. Neurology Genetics 9 (5) , e200092. 10.1212/NXG.0000000000200092

Hanna, Stephanie J., Thayer, Terri C., Robinson, Emma J. S., Vinh, Ngoc-Nga, Williams, Nigel

, Landry, Laurie G., Andrews, Robert, Siah, Qi Zhuang, Leete, Pia, Wyatt, Rebecca, McAteer, Martina A., Nakayama, Maki, Wong, F. Susan

, Yang, Jennie H. M., Tree, Timothy I. M., Ludvigsson, Johnny, Dayan, Colin M.

and Tatovic, Danijela

2023. Single-cell RNAseq identifies clonally expanded antigen-specific T-cells following intradermal injection of gold nanoparticles loaded with diabetes autoantigen in humans. Frontiers in Immunology 14 , 1276255. 10.3389/fimmu.2023.1276255

Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J., Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B., Casey, Bradford, Vitale, Dan, Levine, Kristin, Leonard, Hampton, Pantazis, Caroline B., Screven, Laurel A., Hernandez, Dena G., Wegel, Claire E., Solle, Justin, Nalls, Mike A., Blauwendraat, Cornelis, Singleton, Andrew B., Tan, Manuela M. X., Iwaki, Hirotaka, Morris, Huw R., Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E., Koks, Sulev, Zimprich, Alexander, Schumacher-Schuh, Artur F., Rieder, Carlos, Awad, Paula Saffie, Tumas, Vitor, Camargos, Sarah, Fon, Edward A., Monchi, Oury, Fon, Ted, Galleguillos, Benjamin Pizarro, Miranda, Marcelo, Bustamante, Maria Leonor, Olguin, Patricio, Chana, Pedro, Tang, Beisha, Shang, Huifang, Guo, Jifeng, Chan, Piu, Luo, Wei, Arboleda, Gonzalo, Orozco, Jorge, del Rio, Marlene Jimenez, Hernandez, Alvaro, Salama, Mohamed, Kamel, Walaa A., Zewde, Yared Z., Brice, Alexis, Corvol, Jean-Christophe, Westenberger, Ana, Illarionova, Anastasia, Mollenhauer, Brit, Klein, Christine, Vollstedt, Eva-Juliane, Hopfner, Franziska, Höglinger, Günter, Madoev, Harutyun, Trinh, Joanne, Junker, Johanna, Lohmann, Katja, Lange, Lara M., Sharma, Manu, Groppa, Sergiu, Gasser, Thomas, Fang, Zih-Hua, Akpalu, Albert, Xiromerisiou, Georgia, Hadjigorgiou, Georgios, Dagklis, Ioannis, Tarnanas, Ioannis, Stefanis, Leonidas, Stamelou, Maria, Dadiotis, Efthymios, Medina, Alex, Chan, Germaine Hiu-Fai, Ip, Nancy, Cheung, Nelson Yuk-Fai, Chan, Phillip, Zhou, Xiaopu, Kishore, Asha, KP, Divya, Pal, Pramod, Kukkle, Prashanth Lingappa, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Valente, Enza Maria, Parnetti, Lucilla, Avenali, Micol, Schirinzi, Tommaso, Funayama, Manabu, Hattori, Nobutaka, Shiraishi, Tomotaka, Karimova, Altynay, Kaishibayeva, Gulnaz, Shambetova, Cholpon, Krüger, Rejko, Tan, Ai Huey, Ahmad-Annuar, Azlina, Norlinah, Mohamed Ibrahim, Murad, Nor Azian Abdul, Azmin, Shahrul, Lim, Shen-Yang, Mohamed, Wael, Tay, Yi Wen, Martinez-Ramirez, Daniel, Rodriguez-Violante, Mayela, Reyes-Pérez, Paula, Tserensodnom, Bayasgalan, Ojha, Rajeev, Anderson, Tim J., Pitcher, Toni L., Sanyaolu, Arinola, Okubadejo, Njideka, Ojo, Oluwadamilola, Aasly, Jan O., Pihlstrøm, Lasse, Tan, Manuela, Ur-Rehman, Shoaib, Cornejo-Olivas, Mario, Doquenia, Maria Leila, Rosales, Raymond, Vinuela, Angel, Iakovenko, Elena, Mubarak, Bashayer Al, Umair, Muhammad, Tan, Eng-King, Foo, Jia Nee, Amod, Ferzana, Carr, Jonathan, Bardien, Soraya, Jeon, Beomseok, Kim, Yun Joong, Cubo, Esther, Alvarez, Ignacio, Hoenicka, Janet, Beyer, Katrin, Periñan, Maria Teresa, Pastor, Pau, El-Sadig, Sarah, Zweier, Christiane, Krack, Paul, Lin, Chin-Hsien, Wu, Hsiu-Chuan, Kung, Pin-Jui, Wu, Ruey-Meei, Wu, Yihru, Amouri, Rim, Sassi, Samia Ben, Baak, A. Nazl, Genc, Gencer, Çakmak, Özgür Öztop, Ertan, Sibel, Noyce, Alastair, Schrag, Anette, Schapira, Anthony, Carroll, Camille, Bale, Claire, Grosset, Donald, Houlden, Henry, Hardy, John, Mok, Kin Ying, Rizig, Mie, Wood, Nicholas, Williams, Nigel

, Okunoye, Olaitan, Lewis, Patrick Alfryn, Kaiyrzhanov, Rauan, Weil, Rimona, Love, Seth, Stott, Simon, Jasaitye, Simona, Dey, Sumit, Obese, Vida, Espay, Alberto, O'Grady, Alyssa, Sobering, Andrew K., Siddiqi, Bernadette, Fiske, Brian, Jonas, Cabell, Cruchaga, Carlos, Comart, Charisse, Wegel, Claire, Hall, Deborah, Hernandez, Dena, Shiamim, Ejaz, Riley, Ekemini, Faghri, Faraz, Serrano, Geidy E., Chen, Honglei, Mata, Ignacio F., Sarmiento, Ignacio Juan Keller, Williamson, Jared, Kim, Jonggeol Jeff, Jankovic, Joseph, Shulman, Joshua, Solle, Justin C., Murphy, Kaileigh, Nuytemans, Karen, Kieburtz, Karl, Markopoulou, Katerina, Marek, Kenneth, Levine, Kristin S., Chahine, Lana M., Ibanez, Laura, Screven, Laurel, Ruffrage, Lauren, Shulman, Lisa, Marsili, Luca, Kuhl, Maggie, Dean, Marissa, Koretsky, Mathew, Puckelwartz, Megan J., Inca-Martinez, Miguel, Louie, Naomi, Mencacci, Niccolò Emanuele, Albin, Roger, Alcalay, Roy, Walker, Ruth, Bandres-Ciga, Sara, Chowdhury, Sohini, Dumanis, Sonya, Lubbe, Steven, Xie, Tao, Foroud, Tatiana, Beach, Thomas, Sherer, Todd, Song, Yeajin, Nguyen, Duan, Nguyen, Toan and Atadzhanov, Masharip 2023. Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2). npj Parkinson's Disease 9 (1) , 131. 10.1038/s41531-023-00533-w

Martinez-Carrasco, Alejandro, Real, Raquel, Lawton, Michael, Iwaki, Hirotaka, Tan, Manuela M. X., Wu, Lesley, Williams, Nigel M.

, Carroll, Camille, Hu, Michele T. M., Grosset, Donald G., Hardy, John, Ryten, Mina, Foltynie, Tom, Ben-Shlomo, Yoav, Shoai, Maryam and Morris, Huw R. 2023. Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease. npj Parkinson's Disease 9 , 128. 10.1038/s41531-023-00573-2

Millrine, David, Cardus Figueras, Ana, Uceda Fernandez, Javier, Andrews, Robert, Szomolay, Barbara

, Cossins, Benjamin, Rice, Christopher M., Li, Jasmine, Tyrrell, Victoria, McLeod, Louise, Holmans, Peter

, O'Donnell, Valerie

, Taylor, Philip

, Turner, Stephen J., Jenkins, Brendan J., Jones, Gareth, Topley, Nicholas, Williams, Nigel

and Jones, Simon

2023. Th1 cells alter the inflammatory signature of IL-6 by channeling STAT transcription factors to Alu-like retroelements. The Journal of Immunology 211 (2) , pp. 274-286. 10.4049/jimmunol.2300114

Lin, Jhih-Rong, Zhao, Yingjie, Jabalameli, M Reza, Nguyen, Nha, Mitra, Joydeep, International 22q11.2DS Brain and Behavior Consortium*, Swillen, Ann, Vorstman, Jacob, Chow, Eva, van den Bree, Marianne

, Emanuel, Beverly, Vermeesch, Joris, Owen, Michael

, van den Bree, Marianne B. M.

, Bassett, Anne, McDonald-McGinn, Donna, Gur, Raquel, Bearden, Carrie, Morrow, Bernice, Lachman, Herbert and Zhang, Zhengdong 2023. Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular Psychiatry 28 , pp. 2071-2080. 10.1038/s41380-023-02009-y

Adams, Rachael L., Baird, Alister, Smith, Jacqueline, Williams, Nigel

, Linden, David E. J.

and Linden, Stefanie C.

2023. Psychopathology in adults with copy number variants. Psychological Medicine 53 (7) , pp. 3142-3149. 10.1017/S0033291721005201

Real, Raquel, Martinez-Carrasco, Alejandro, Reynolds, Regina, Lawton, Michael, Tan, Manuela, Shoai, Maryam, Corvol, Jean-Christophe, Ryten, Mina, Bresner, Catherine

, Hubbard, Leon, Brice, Alexis, Lesage, Suzanne, Faouzi, Johann, Elbaz, Alexis, Artaud, Fanny, Williams, Nigel

, Hu, Michele, Ben-Shlomo, Yoav, Grosset, Donald, Hardy, John and Morris, Huw 2023. Association between the LRP1B and APOE loci in the development of Parkinson’s disease dementia. Brain 146 (5) , pp. 1873-1887. 10.1093/brain/awac414

Chawner, Samuel J. R. A., Evans, Alexandra

, IMAGINE-ID consortium, Williams, Nigel

and van den Bree, Marianne B. M.

2023. Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational Psychiatry 13 , 7. 10.1038/s41398-022-02296-z

Winchester, Laura, Barber, Imelda, Lawton, Michael, Ash, Jessica, Liu, Benjamin, Evetts, Samuel, Hopkins-Jones, Lucinda, Lewis, Suppalak, Bresner, Catherine

, Malpartida, Ana Belen, Williams, Nigel

, Gentlemen, Steve, Wade-Martins, Richard, Ryan, Brent, Holgado-Nevado, Alejo, Hu, Michele, Ben-Schlomo, Yoav, Grosset, Donald and Lovestone, Simon 2023. Identification of a possible proteomic biomarker in Parkinson’s disease: discovery and replication in blood, brain and cerebrospinal fluid. Brain Communications 5 (1) , fcac343. 10.1093/braincomms/fcac343

Harvey, Joshua, Smith, Adam R., Weymouth, Luke Stephen, Smith, Rebecca G., Hubbard, Leon, Bresner, Kate, Pishva, Ehsan, Williams, Nigel

, Lunnon, Katie and Creese, Byron 2022. An epigenome wide association study of sub-phenotypes in Parkinson's disease. Alzheimer's & Dementia: The Journal of the Alzheimer's Association 18 (S4) , e069252. 10.1002/alz.069252

Sandor, Cynthia

, Millin, Stephanie, Dahl, Andrew, Schalkamp, Ann-Kathrin, Lawton, Michael, Hubbard, Leon, Rahman, Nabila, Williams, Nigel

, Ben-Shlomo, Yoav, Grosset, Donald G., Hu, Michele T., Marchini, Jonathan and Webber, Caleb

2022. Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine 14 , 129. 10.1186/s13073-022-01132-9

Lawton, Michael, Tan, Manuela M. X., Ben-Shlomo, Yoav, Baig, Fahd, Barber, Thomas, Klein, Johannes C., Evetts, Samuel G., Millin, Stephanie, Malek, Naveed, Grosset, Katherine, Barker, Roger A., Williams, Nigel

, Burn, David J., Foltynie, Thomas, Morris, Huw R., Wood, Nicholas, Grosset, Donald G. and Hu, Michele Tao-Ming 2022. Genetics of validated Parkinson’s disease subtypes in the Oxford Discovery and Tracking Parkinson’s cohorts. Journal of Neurology, Neurosurgery and Psychiatry 93 (9) , pp. 952-959. 10.1136/jnnp-2021-327376

Lobanov, Sergey

, McAllister, Branduff, McDade-Kumar, Mia, Landwehrmeyer, Bernhard, Orth, Michael, Rosser, Anne

, Paulsen, Jane, Lee, Jong-Min, MacDonald, Marcy, Gusella, James, Long, Jeffrey, Ryten, Mina, Williams, Nigel

, Holmans, Peter

, Massey, Thomas

and Jones, Lesley

2022. Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1. npj Genomic Medicine 7 , 53. 10.1038/s41525-022-00317-w

Vijiaratnam, Nirosen, Lawton, Michael, Heslegrave, Amanda J., Guo, Tong, Tan, Manuela, Jabbari, Edwin, Real, Raquel, Woodside, John, Grosset, Katherine, Chelban, Viorica, Athauda, Dilan, Girges, Christine, Barker, Roger A., Hardy, John, Wood, Nicholas, Houlden, Henry, Williams, Nigel

, Ben-Shlomo, Yoav, Zetterberg, Henrik, Grosset, Donald G., Foltynie, Thomas and Morris, Huw R. 2022. Combining biomarkers for prognostic modelling of Parkinson’s disease. Journal of Neurology, Neurosurgery and Psychiatry , jnnp-2021-328365. 10.1136/jnnp-2021-328365

McAllister, Branduff, Donaldson, Jasmine

, Binda, Caroline, Powell, Sophie, Chughtai, Uroosa, Edwards, Gareth, Stone, Joseph, Lobanov, Sergey

, Elliston, Linda, Schuhmacher, Laura, Rees, Elliott

, Menzies, Georgina

, Ciosi, Marc, Maxwell, Alastair, Chao, Michael, Eun Pyo, Hong, Lucente, Diane, Wheeler, Vanessa, Jong-Min, Lee, MacDonald, Marcy, Long, Jeffrey, Aylward, Elizabeth, Landwehrmeyer, G. Bernhard, Rosser, Anne

, REGISTRY Investigators of the European Huntington’s disease netw, Paulsen, Jane, PREDICT-HD Investigators of the Huntington Study Group, Williams, Nigel

, Gusella, James, Monckton, Darren, Allen, Nicholas, Holmans, Peter

, Jones, Lesley

and Massey, Thomas

2022. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset. Nature Neuroscience 25 , pp. 446-457. 10.1038/s41593-022-01033-5

Trubetskoy, Vassily, Pardinas, Antonio

, Qi, Ting, Panagiotaropoulou, Georgia, Awasthi, Swapnil, Bigdeli, Tim B., Bryois, Julien, Chen, Chia-Yen, Dennison, Charlotte A.

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, Hultman, C.M., Lichtenstein, P., Thelander, E.F., Sullivan, P., Morris, D.W., O'Dushlaine, C.T., Kenny, E., Quinn, E.M., Gill, M., Corvin, A., McQuillin, A., Choudhury, K., Datta, S., Pimm, J., Thirumalai, S., Puri, V., Krasucki, R., Lawrence, J., Quested, D., Bass, N., Gurling, H., Crombie, C., Fraser, G., Kuan, S.L., Walker, N., St Clair, D., Blackwood, D.H.R., Muir, W.J., McGhee, K.A., Pickard, B., Malloy, P., Maclean, A.W., Van Beck, M., Wray, N.R., Macgregor, S., Visscher, P.M., Pato, M.T., Medeiros, H., Middleton, F., Carvalho, C., Morley, C., Fanous, A., Conti, D., Knowles, J.A., Paz Ferreira, C., Macedo, A., Helena Azevedo, M., Pato, C.N., Stone, J.L., Ruderfer, D.M., Kirby, A.N., Ferreira, M.A.R., Daly, M.J., Purcell, S.M., Sklar, P., Stone, J.L., Chambert, K., Kuruvilla, F., Gabriel, S.B., Ardlie, K., Moran, J.L. and Scolnick, E.M. 2011. Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia Research 131 (1-3) , pp. 43-51. 10.1016/j.schres.2011.06.023

Williams, Hywel John

, Norton, Nadine

, Dwyer, Sarah Lynne, Escott-Price, Valentina

, Nikolov, Ivan, Carroll, Liam, Georgieva, Lyudmila, Williams, Nigel Melville

, Morris, D. W., Quinn, E. M., Giegling, I., Ikeda, Masashi, Wood, J., Lencz, T., Hultman, C., Lichtenstein, P., Thiselton, D., Maher, B. S., Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), SGENE-plus, GROUP, Malhotra, A. K., Riley, B., Kendler, K. S., Gill, M., Sullivan, P., Sklar, P., Purcell, S., Nimgaonkar, V. L., Kirov, George

, Corvin, A., Holmans, Peter ALan

, Rujescu, D., Craddock, Nicholas John

2011. Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry 16 (4) , pp. 429-441. 10.1038/mp.2010.36

Stergiakouli, Evangelia, Langley, Kate, Williams, Hywel, Walters, James Tynan Rhys

, Suren, S., Giegling, I., Wilkinson, Lawrence

, Rujescu, D., Thapar, Anita

and Davies, William

2011. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes Brain and Behavior 10 (3) , pp. 334-344. 10.1111/j.1601-183x.2010.00672.x

Pearson, Justin P., Williams, Nigel Melville

, Majounie, Elisa

, Waite, Adrian James, Stott, Jennifer, Newsway, Victoria, Murray, Alexandra, Hernandez, Dena, Guerreiro, Rita, Singleton, Andrew B., Neal, James William and Morris, Huw Rees 2011. Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. Journal of Neurology 258 (4) , pp. 647-655. 10.1007/s00415-010-5815-x

O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A, O'Donovan, Michael Conlon

, Georgieva, Lyudmila and Owen, Michael John

2011. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry 16 (3) , pp. 286-292. 10.1038/mp.2010.7

Nalls, M. A., Plagnol, V., Hernandez, D. G., Sharma, M., Sheerin, U. M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Stefansson, K., Martinez, M., Hardy, J., Heutink, P., Brice, A., Gasser, T., Singleton, A. B., Wood, N. M., Morris, Huw, Williams, Nigel Melville

and International Parkinson Disease Genomics Consortium 2011. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet 377 (9766) , pp. 641-649. 10.1016/S0140-6736(10)62345-8

Morris, Huw Rees, Pearson, Justin P., Williams, Nigel Melville

, Wickremaratchi, Mirdhu, International Parkinson's Disease Genomics Consortium (IPDGC) and Wellcome Trust Case Control Consortium (WTCCC) 2011. A two-stage meta-analysis identifies several new loci for Parkinson's Disease. PLoS Genetics 7 (6) , e1002142. 10.1371/journal.pgen.1002142

Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon

, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine

, Toncheva, Draga, Milanova, Vihra and Owen, Michael John

2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802

Williams, Nigel Melville

and Thapar, Anita

2011. Structural variations in attention-deficit hyperactivity disorder - Authors' reply [Letter]. The Lancet 377 (9763) , p. 378. 10.1016/S0140-6736(11)60121-9

Hamshere, Marian Lindsay

, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley

, Norton, Nadine

, McGuffin, Peter, O'Donovan, Michael Conlon

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

Langley, Kate

, Martin, Joanna

, Agha, Sharifah Shameem

, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan

and Thapar, Anita

2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403.

Carroll, Liam Stuart, Williams, Nigel Melville

, Russell, Elen, Norton, Nadine

, Peirce, Timothy Rowan, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Grozeva, Detelina

, Greene, E., Farmer, A., McGuffin, P., Morris, D. W., Corvin, A., Gill, M., Rujescu, D., Sham, P., Holmans, Peter Alan

, Jones, Ian Richard

2010. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry 15 (11) , pp. 1101-1111. 10.1038/mp.2009.96

Williams, Nigel Melville

, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate

, Mantripragada, Kiran Kumar

, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan

and Thapar, Anita

2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750) , pp. 1401-1408. 10.1016/S0140-6736(10)61109-9

Pearson, J. P., Kilarski, L. L., Newsway, V., Majounie, Elisa

, Perera, D., Misbahuddin, A., Chinnery, P. F., Burn, D. J., Lewthwaite, A. J., Clarke, C. E., Morrison, K. E., Evans, J. R., Sawcer, S. J., Barker, R. A., Wickremaratchi, M. M., Williams, Nigel Melville

and Morris, Huw 2010. Prevalence of mutations in Parkin, PINK1, and DJ-1 in early onset Parkinson's Disease - a community based and regional study [Conference Abstract]. Movement Disorders 25 (3) , S610-S610.

Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon

, Georgieva, Lyudmila and Owen, Michael John

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

Newsway, Victoria Elizabeth, Fish, Mark, Rohrer, Jonathan D., Majounie, Elisa

, Hack, Melissa Anne, Warren, Jason D. and Morris, Huw Rees 2010. Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure. Movement Disorders 25 (6) , pp. 767-770. 10.1002/mds.22950

Hinton, Elanor Clare, Isles, Anthony Roger

and Parkinson, John A. 2010. Excessive appetitive arousal in Prader–Willi syndrome. Appetite 54 (1) , pp. 225-228. 10.1016/j.appet.2009.12.002

Mantripragada, Kiran Kumar

, Carroll, Liam S. and Williams, Nigel Melville

2010. Experimental approaches for identifying schizophrenia risk genes. Current Topics in Behavioral Neuroscience 4 , pp. 587-610. 10.1007/7854_2010_58

Ikeda, Masashi, Williams, Nigel Melville

, Smith, Rhodri, Monks, Stephen, Owen, Michael John

, Murphy, Kieran C. and O'Donovan, Michael Conlon

2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 980-982. 10.1002/ajmg.b.31060

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan

, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard

, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, Roger, Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A, Brown, M. A., Burn, D., Casas, J.-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, Nicholas John

, Deloukas, P., Edkins, S., Evans, J., Freeman, C., Gray, E., Hardy, J., Hudson, G., Hunt, S., Jankowski, J., Langford, C., Lees, A. J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Morrison, K. E., Palmer, C. N. A., Pearson, J. P., Peltonen, L., Pirinen, M., Plomin, R., Potter, S., Rautanen, A., Sawcer, S. J., Su, Z., Trembath, R. C., Viswanathan, A. C., Williams, Nigel Melville

, Morris, Huw Rees, Donnelly, Peter and Wood, N. W. 2010. Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics 20 (2) , pp. 345-353. 10.1093/hmg/ddq469

Liu, Yang, Chen, Gang, Norton, Nadine, Liu, Wenmin, Zhu, Haining, Zhou, Peng, Luan, Meng, Yang, Shulin, Chen, Xing, Carroll, Liam, Williams, Nigel Melville

2009. Whole genome association study in a homogenous population in Shandong Peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Journal of Biomedicine and Biotechnology , 536918. 10.1155/2009/536918

Ng, M Y M, Levinson, D F, Faraone, S V, Suarez, B K, DeLisi, L E, Arinami, T, Riley, B, Paunio, T, Pulver, A E, Irmansyah, Holmans, Peter Alan

, Escamilla, M, Wildenauer, D B, Williams, Nigel Melville

, Laurent, C, Mowry, B J, Brzustowicz, L M, Maziade, M, Sklar, P, Garver, D L, Abecasis, G R, Lerer, B, Fallin, M D, Gurling, H M D, Gejman, P V, Lindholm, E, Moises, H W, Byerley, W, Wijsman, E M, Forabosco, P, Tsuang, M T, Hwu, H-G, Okazaki, Y, Kendler, K S, Wormley, B, Fanous, A, Walsh, D, O'Neill, F A, Peltonen, L, Nestadt, G, Lasseter, V K, Liang, K Y, Papadimitriou, G M, Dikeos, D G, Schwab, S G, Owen, Michael John

, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, V L, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, R R, Silverman, J M, Bassett, A S, Roy, M-A, Mérette, C, Pato, C N, Pato, M T, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, A R, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M and Lewis, C M 2009. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry 14 (8) , pp. 774-785. 10.1038/mp.2008.135

Holmans, Peter Alan

, Riley, B., Pulver, A. E., Owen, Michael John

, Wildenauer, D. B., Gejman, P. V., Mowry, B. J., Laurent, C., Kendler, K. S., Nestadt, G., Williams, Nigel Melville

, Schwab, S. G., Sanders, A. R., Nertney, D., Mallet, J., Wormley, B., Lasseter, V. K., O'Donovan, Michael Conlon

, Duan, J., Albus, M., Alexander, M., Godard, S., Ribble, R., Liang, K. Y., Norton, Nadine

, Maier, W., Papadimitriou, G., Walsh, D., Jay, M., O'Neill, A., Lerer, F. B., Dikeos, D., Crowe, R. R., Silverman, J. M. and Levinson, D. F. 2009. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry 14 (8) , pp. 786-795. 10.1038/mp.2009.11

O'Donovan, Michael Conlon

, Norton, Nadine

, Peirce, Timothy Rowan, Escott-Price, Valentina

, Nikolov, Ivan, Hamshere, Marian Lindsay

, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan

, Marchini, J. L., Spencer, C. C. A., Howie, B., Leung, H.T., Giegling, I., Hartmann, A. M., Möller, H.J., Morris, D. W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, Stanley

, Schumacher, J., Quinn, E. M., Schulze, T. G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A. R., Levinson, D. F., Adolfsson, R., Ösby, U., Terenius, L, Jönsson, E. G., Cichon, S., Nöthen, M. M., Gill, M., Corvin, A. P., Rujescu, D., Gejman, P. V., Kirov, George

2009. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry 14 (1) , pp. 30-36. 10.1038/mp.2008.108

Purcell, Shaun M., Wray, Naomi R., Stone, Jennifer L., Visscher, Peter M., O'Donovan, Michael Conlon

, Sullivan, Patrick F., Sklar, Pamela, Ruderfer, Douglas M., McQuillin, Andrew, Morris, Derek W., O'Dushlaine, Colm T., Corvin, Aiden, Holmans, Peter Alan

, Macgregor, Stuart, Gurling, Hugh, Blackwood, Douglas H. R., Craddock, Nicholas John

, Gill, Michael, Hultman, Christina M., Kirov, George

, Lichtenstein, Paul, Muir, Walter J., Owen, Michael John

, Pato, Carlos N., Scolnick, Edward M., St Clair, David, Williams, Nigel Melville

, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine

, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Quinn, Emma M., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Crombie, Caroline, Fraser, Gillian, Leh Kuan, Soh, Walker, Nicholas, McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Helena Azevedo, M., Kirby, Andrew N., Ferreira, Manuel A. R., Daly, Mark J., Chambert, Kimberly, Kuruvilla, Finny, Gabriel, Stacey B., Ardlie, Kristin, Moran, Jennifer L. and Daly, Mark J. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460 (7256) , pp. 748-752. 10.1038/nature08185

Wickremaratchi, Mindhu M., Majounie, Elisa

, Morris, Huw Rees, Williams, Nigel Melville

, Lewis, Helen, Gill, Steven S., Khan, Sadaquate, Heywood, Peter, Hardy, John, Wiles, Charles Mark, Singleton, Andrew B. and Quinn, Niall P. 2009. Parkin-related disease clinically diagnosed as a pallido-pyramidal syndrome [Letter]. Movement Disorders 24 (1) , pp. 138-140. 10.1002/mds.22181

Carroll, Liam Stuart, Kendall, Kimberley

2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7) , pp. 893-899. 10.1002/ajmg.b.30915

Dwyer, Sarah Lynne, Carroll, Liam Stuart, Mantripragada, Kiran Kumar

2009. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (3) , pp. 766-774. 10.1002/ajmg.b.31045

Wardle, Mark, Majounie, Elisa

, Muzaimi, Mustapha B., Williams, Nigel Melville

, Morris, Huw Rees and Robertson, Neil

2009. The genetic aetiology of late-onset chronic progressive cerebellar ataxia. Journal of Neurology 256 (3) , pp. 343-348. 10.1007/s00415-009-0015-2

Gerrish, Amy, Williams, Hywel John

2009. An examination of MUTED as a schizophrenia susceptibility gene [Letter]. Schizophrenia Research 107 (1) , pp. 110-111. 10.1016/j.schres.2008.08.011

Georgieva, Lyudmila, Dimitrova, Albena, Ivanov, Dobril

, Nikolov, Ivan, Williams, Nigel Melville

, Grozeva, Detelina

, Zaharieva, Irina Takova, Toncheva, Draga, Owen, Michael John

2008. Support for Neuregulin 1 as a susceptibility gene for Bipolar disorder and schizophrenia. Biological psychiatry 64 (5) , pp. 419-427. 10.1016/j.biopsych.2008.03.025

Sutrala, Smitha R., Norton, Nadine

and Buckland, Paul Robert 2008. Gene copy number variation in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (5) , pp. 606-611. 10.1002/ajmg.b.30645

Williams, Nigel Melville

, Glaser, Beate, Norton, Nadine

, Pierce, Timothy, Escott-Price, Valentina

, Monks, Stephen, Del Favero, Jurgen, Goossens, Dirk, Rujescu, Dan, Kirov, George

, Murphy, Kieran Christopher, O'Donovan, Michael Conlon

2008. Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics 17 (4) , pp. 555-566. 10.1093/hmg/ddm330

Williams, Nigel Melville

, Majounie, Elisa

, Norton, Nadine

, Glaser, Beate, Morris, Huw Rees, Owen, Michael John

2008. Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Research 36 (17) , e112-e112. 10.1093/nar/gkn495

Stone, Jennifer L., O'Donovan, Michael Conlon

, Gurling, Hugh, Kirov, George

, Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nicholas John

, Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael John

, St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M., Korn, Joshua, Macgregor, Stuart, Morris, Derek W., O'Dushlaine, Colm T., Daly, Mark J., Visscher, Peter M., Holmans, Peter Alan

, Scolnick, Edward M., Williams, Nigel Melville

, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine

, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Waddington, John L., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Curtis, David, Crombie, Caroline, Fraser, Gillian, Leh Kwan, Soh, Walker, Nicholas, Muir, Walter J., McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Azevedo, M. Helena, McCarroll, Steve A., Daly, Mark, Chambert, Kimberly, Gates, Casey, Gabriel, Stacey B., Mahon, Scott and Ardlie, Kristen 2008. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455 (7210) , pp. 237-241. 10.1038/nature07239

Wardle, M, Majounie, Elisa

, Rosser, Anne Elizabeth

, Morris, Huw Rees and Robertson, Neil

2008. Dentatorubral pallidoluysian atrophy in South Wales. Journal of Neurology, Neurosurgery and Psychiatry 79 (7) , pp. 804-807. 10.1136/jnnp.2007.128074

Bray, Nicholas John

, Jones, Lesley

, Elliston, Linda Anne, Hughes, Gareth, Richards, Alexander, Williams, Nigel Melville

2008. Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Human Molecular Genetics 17 (8) , pp. 1169-1174. 10.1093/hmg/ddn006

O'Donovan, Michael Conlon

, Norton, Nadine

, Peirce, Timothy Rowan, Escott-Price, Valentina

, Nikolov, Ivan, Hamshere, Marian Lindsay

, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan

, Marchini, Jonathan L, Spencer, Chris C A, Howie, Bryan, Leung, Hin-Tak, Hartmann, Annette M, Möller, Hans-Jürgen, Morris, Derek W, Shi, YongYong, Feng, GuoYin, Hoffmann, Per, Propping, Peter, Vasilescu, Catalina, Maier, Wolfgang, Rietschel, Marcella, Zammit, Stanley

, Schumacher, Johannes, Quinn, Emma M, Schulze, Thomas G, Williams, Nigel Melville

, Giegling, Ina, Iwata, Nakao, Ikeda, Masashi, Darvasi, Ariel, Shifman, Sagiv, He, Lin, Duan, Jubao, Sanders, Alan R, Levinson, Douglas F, Gejman, Pablo V, Gejman, Pablo V, Sanders, Alan R, Duan, Jubao, Levinson, Douglas F, Buccola, Nancy G, Mowry, Bryan J, Freedman, Robert, Amin, Farooq, Black, Donald W, Silverman, Jeremy M, Byerley, William F, Cloninger, C Robert, Cichon, Sven, Nöthen, Markus M, Gill, Michael, Corvin, Aiden, Rujescu, Dan, Kirov, George

, Craig, Kathrine Jane, Williams, John David, Williams, Nigel Melville

2008. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics 40 (9) , pp. 1053-1055. 10.1038/ng.201

Nair, S., Phillips, Aled Owain

, Norton, Nadine

, Spurlock, Gillian, Williams, Hywel John

and Bowen, Timothy

2008. Further evidence for the association of MMP9 with nephropathy in type 2 diabetes and application of DNA pooling technology to candidate gene screening. Journal of Nephology 21 (3) , pp. 400-405.

Williams, Hywel, Norton, Nadine, Peirce, Tim, Dwyer, Sarah, Williams, Nigel Melville

2007. Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia. Schizophrenia Research 97 (1-3) , pp. 271-276. 10.1016/j.schres.2007.09.004

Majounie, Elisa

, Wardle, Mark, Muzaimi, M., Cross, W. C., Robertson, Neil

and Morris, Huw Rees 2007. Case control analysis of repeat expansion size in ataxia. Neuroscience Letters 429 (1) , pp. 28-32. 10.1016/j.neulet.2007.09.055

Zammit, Stanley

, Spurlock, Gillian, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville

2007. Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. British Journal of Psychiatry 191 (5) , pp. 402-407. 10.1192/bjp.bp.107.036129

Sutrala, Smitha, Goossens, Dirk, Williams, Nigel Melville

, Heyrman, Lien, Adolfsson, Rolf, Norton, Nadine

, Buckland, Paul Robert and Del-Favero, Jurgen 2007. Gene copy number variation in schizophrenia. Schizophrenia Research 96 (1-3) , pp. 93-99. 10.1016/j.schres.2007.07.029

Norton, Nadine, Williams, Hywel J., Dwyer, Sarah, Carroll, Liam, Peirce, Tim, Escott-Price, Valentina

, Segurado, Ricardo, Nikolov, Ivan, Williams, Nigel Melville

, Ikeda, Masashi, Iwata, Nakao, Owen, Michael John

2007. Association analysis of AKT1 and schizophrenia in a UK case control sample. Schizophrenia Research 93 (1-3) , pp. 58-65. 10.1016/j.schres.2007.02.006

O'Donovan, Michael Conlon

, Williams, Nigel Melvillle

, Bray, Nicholas John

2007. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia [Conference Abstract]. Schizophrenia bulletin 33 (2) , pp. 311-312. 10.1093/schbul/sbm004

Glaser, Beate, Escott-Price, Valentina

, Murphy, Kieran C., Williams, Hywel, Williams Melville, Nigel

2006. Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility. Schizophrenia Research 87 (1-3) , p. 21. 10.1016/j.schres.2006.05.024

Bray, Nicholas John

, van Den Bree, Marianne Bernadette

, Jones, Lesley

2006. Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 723-724.

Georgieva, Lyudmila, Escott-Price, Valentina

, Peirce, Timothy Rowan, Norton, Nadine

, Bray, Nicholas John

, Jones, Lesley

, Macgregor, Stuart, Zammit, Stanley

, Wilkinson, Jennifer Camilla, Williams, Hywel John

, Nikolov, Ivan, Williams, Nigel Melville

, Ivanov, Dobril

, Davis, Kenneth L., Haroutunian, Vahram, Buxbaum, Joseph D., Craddock, Nicholas John

2006. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490 103 (33) , pp. 12469-12474. 10.1073/pnas.0603029103

Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George

, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael Conlon

, Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel Melville

, Wood, Joel, Zhang, Feng, Devlin, Bernie and Nimgaonkar, Vishwajit L. 2006. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological psychiatry 60 (2) , pp. 152-162. 10.1016/j.biopsych.2006.02.015

Paylor, R., Glaser, B., Mupo, A., Ataliotis, P., Spencer, C., Sobotka, A., Sparks, C., Choi, C.-H., Oghalai, J., Curran, S., Murphy, K. C., Monks, S., Williams, Nigel Melville

, Scambler, P. J. and Lindsay, E. 2006. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome. Proceedings of the National Academy of Sciences of the United States of America 103 (20) , pp. 7729-7734. 10.1073/pnas.0600206103

Williams, Nigel Melville

, Green, Elaine Karen, Dwyer, Sarah Lynne, Macgregor, Stuart, Norton, Nadine

, Raybould, Rachel, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay

, Jones, Lisa Anne, Cardno, Alastair George, Kirov, George

, Jones, Ian Richard

2006. Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry 63 (4) , pp. 366-373. 10.1001/archpsyc.63.4.366

Peirce, Timothy Rowan, Bray, Nicholas John

, Norton, Nadine

, Preece, Anna Charlotte, Haroutunian, Vahram, Buxbaum, Joseph D., Owen, Michael John

2006. Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of general psychiatry 63 (1) , pp. 18-24. 10.1001/archpsyc.63.1.18

Williams, Nigel Melville

2006. Chromosome 22 deletion syndrome and schizophrenia. International Review of Neurobiology 73 , pp. 1-27. 10.1016/S0074-7742(06)73001-X

Peirce, TR, Bray, Nicholas John

, Norton, N, Escott-Price, Valentina

, Preece, Anna, Haroutunian, V, Buxbaum, JD, Owen, Michael John

2006. Convergent evidence for 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of General Psychiatry 63 (1) , pp. 18-24.

Norton, Nadine

, Morris, Derek W., Bray, Nicholas John

, Preece, Anna Charlotte, Dwyer, Sarah, Wilkinson, Jennifer C., Spurlock, Gillian, Kirov, George

, Buckland, Paul Robert, Waddington, John L., Gill, Michael, Corvin, Aiden P., Owen, Michael John

and O'Donovan, Michael John

2006. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (1) , pp. 96-101. 10.1002/ajmg.b.30236

Hamshere, Marian Lindsay

, Norton, Nadine

, Williams, H., Cardno, Alastair G., Zammit, Stanley

, 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

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

Williams, Nigel Melville

2005. Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? Schizophrenia Bulletin 31 (4) , pp. 800-805. 10.1093/schbul/sbi061

Williams, H. J., Glaser, B., Williams, Nigel Melville

, Norton, N., Zammit, Stanley

, MacGregor, S., Kirov, George

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

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

, Cichon, S., Kirov, George

, Rietschel, M., Murphy, K. C., O'Donovan, Michael Conlon

, Nothen, M. M. and Owen, Michael John

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.

Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina

, Jones, Lisa Anne, Jones, Ian Richard

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

Turic, D., Langley, Kate

, Williams, H., Norton, N., Williams, Nigel Melville

2005. A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder. Biological psychiatry 57 (11) , pp. 1461-1466. 10.1016/j.biopsych.2005.03.025

Norton, Nadine, Williams, Hywel, Dwyer, Sarah, Ivanov, Dobril

, Preece, Anna, Gerrish, Amy, Williams, Nigel Melville

, Yerassimou, P., Zammit, Stanley

2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 , 23. 10.1186/1471-244X-5-23

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

and Williams, Julie

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

Bray, Nicholas John

, Preece, Anna Charlotte, Williams, Nigel Melville

, Buckland, Paul Robert, Owen, Michael John

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

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

Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel Melville

, Jones, Lisa, O'Donovan, Michael Conlon

, Jones, Ian Richard

2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018

Bray, Nicholas John

, Preece, Anna, Escott-Price, Valentina

, Williams, HJ, Norton, N, Wilkinson, J, Buckland, Paul Robert, Owen, Michael John

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

, Haroutunian, V., Buxbaum, J., Buckland, Paul Robert, Owen, Michael John

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

Norton, N, Escott-Price, Valentina

, Morris, DW, Bray, Nicholas John

, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George

, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John

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.

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

Morris, D.W., Ivanov, D.

, Robinson, L., Williams, N.

, Stevenson, J., Owen, M. J.

, Williams, J. and O'Donovan, M. C.

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

Williams, Nigel Melville

2004. Genetic abnormalities of chromosome 22 and the development of psychosis. Current Psychiatry Reports 6 (3) , pp. 176-182. 10.1007/s11920-004-0062-4

Kirov, George

, Ivanov, Dobril

, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon

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

Monslow, Jamie, Williams, John David, Guy, Carol, Price, Iain Kelsey, Craig, Kathrine Jane, Williams, Hywel John

, Martin, John, Coleman, Sharon Louise, Topley, Nicholas, Spicer, Andrew P., Buckland, Paul Robert, Davies, Malcolm and Bowen, Timothy

2004. Identification and analysis of the promoter region of the human hyaluronan synthase 2 gene. The Journal of Biological Chemistry 279 (20) , pp. 20576-20581. 10.1074/jbc.M312666200

Owen, Michael John

2004. Dysbindin-1 and schizophrenia: from genetics to neuropathology. The Journal of Clinical Investigation 113 (9) , pp. 1255-1257. 10.1172/JCI200421470

Williams, Nigel Melville

, Preece, Anna, Mortis, DW, Spurlock, Gillian, Bray, Nicholas John

, Stephens, M, Norton, N, Williams, H, Clement, M, Dwyer, S, Curran, C, Wilkinson, J, Escott-Price, Valentina

, Waddington, JL, Gill, M, Corvin, AP, Zammit, Stanley

2004. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Williams, Nigel Melville

, Preece, Anna Charlotte, Spurlock, Gillian, Norton, Nadine

, McCreadie, Robin G, Buckland, Paul Robert, Sharkey, Val, Chowdari, Kodavali V., Zammit, Stanley

, Nimgaonkar, Vishwajit, Kirov, George

2004. Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55 (2) , pp. 192-195. 10.1016/j.biopsych.2003.11.002

Williams, Nigel Melville

, Preece, Anna Charlotte, Morris, D. W., Spurlock, Gillian, Bray, Nicholas John

, Stephens, Mark Keith, Norton, Nadine

, Clement, Mathew

, Dwyer, Sarah Lynne, Curran, Catherine, Wilkinson, Jennifer Camilla, Escott-Price, Valentina

, Waddington, J. L., Gill, M., Corvin, A. P., Zammit, Stanley

2004. Identification in two independent samples of a novel schizophrenia risk haplotype of the dystobrevin binding protein gene (DTNBP1). Archives of general psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Owen, Michael John

2004. The molecular genetics of schizophrenia: new findings promise new insights. Molecular Psychiatry 9 (1) , pp. 14-27. 10.1038/sj.mp.4001444

Turic, Dragana, Langley, Kate

, Mills, S., Stephens, M., Lawson, D., Govan, Catherine, Williams, Nigel Melville

, Kent, L., Owen, Michael John

and Thapar, Anita

2004. Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Molecular Psychiatry 9 (2) , pp. 169-173. 10.1038/sj.mp.4001387

Norton, Nadine, Williams, Nigel Melville

2004. DNA pooling as a tool for large-scale association studies in complex traits. Annals of Medicine 36 (2) , pp. 146-152. 10.1080/07853890310021724

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

Ivanov, Dobril

, Norton, Nadine

, Nikolov, Ivan, Tzwetkova, R., Stambolova, S. M., Murphy, Kieran Christopher, Toncheva, Draga, Thapar, Anita

2003. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: Molecular genetic study. The British Journal of Psychiatry 183 (5) , pp. 409-413. 10.1192/bjp.183.5.409

O'Donovan, Michael Conlon

2003. Recent advances in the genetics of schizophrenia. Human Molecular Genetics 12 (suppl) , R125-R133. 10.1093/hmg/ddg302

Kirov, George

, Georgieva, Lyudmila, Williams, Nigel Melville

, Nikolov, Ivan, Norton, Nadine, Toncheva, Draga, O'Donovan, Michael Conlon

2003. Variation in the protocadherin - A gene cluster? Genomics 82 (4) , pp. 433-440. 10.1016/S0888-7543(03)00167-8

Monslow, Jamie, Williams, John David, Norton, Nadine

, Guy, Carol, Price, Iain Kelsey, Coleman, Sharon Louise, Williams, Nigel Melville

, Buckland, Paul Robert, Spicer, Andrew P., Topley, Nicholas, Davies, Malcolm and Bowen, Timothy

2003. The human hyaluronan synthase genes: genomic structures, proximal promoters and polymorphic microsatellite markers. The International Journal of Biochemistry & Cell Biology 35 (8) , pp. 1272-1283. 10.1016/S1357-2725(03)00048-7

Norton, N., Williams, H.J., Williams, Nigel Melville

, Spurlock, G., Zammit, Stanley

, Jones, G., Jones, S., Owen, R., O'Donovan, Michael Conlon

2003. Mutation screening of the Homer gene family and association analysis in schizophrenia. American Journal of Medical Genetics 120B (1) , pp. 18-21. 10.1002/ajmg.b.20032

Bray, Nicholas John

, Buckland, Paul Robert, Williams, Nigel Melville

, Norton, Nadine

2003. A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. The American Journal of Human Genetics 73 (1) , pp. 152-161. 10.1086/376578

Williams, H.J., Williams, Nigel Melville

, Spurlock, G., Norton, N., Zammit, Stanley

2003. Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia. American Journal of Medical Genetics 120B (1) , pp. 42-46. 10.1002/ajmg.b.20049

Williams, H. J., Williams, N.

, Spurlock, G., Norton, N., Ivanov, D.

, McCreadie, R. G., Preece, A., Sharkey, V., Jones, S., Zammit, S.

, Nikolov, I., Kehaiov, I., Thapar, A.

, Murphy, K. C., Kirov, G.

, Owen, M. J.

and O'Donovan, M. C.

2003. Association between PRODH and schizophrenia is not confirmed. Molecular Psychiatry 8 (7) , pp. 644-645. 10.1038/sj.mp.4001276

Lewis, Cathryn M., Levinson, Douglas F., Wise, Lesley H., DeLisi, Lynn E., Straub, Richard E., Hovatta, Iiris, Williams, Nigel Melville

, Schwab, Sibylle G., Pulver, Ann E., Faraone, Stephen V., Brzustowicz, Linda M., Kaufmann, Charles A., Garver, David L., Gurling, Hugh M.D., Lindholm, Eva, Coon, Hilary, Moises, Hans W., Byerley, William, Shaw, Sarah H., Mesen, Andrea, Sherrington, Robin, O'Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S., Ekelund, Jesper, Paunio, Tiina, Lönnqvist, Jouko, Peltonen, Leena, O'Donovan, Michael Conlon

, Wildenauer, Dieter B., Maier, Wolfgang, Nestadt, Gerald, Blouin, Jean-Louis, Antonarakis, Stylianos E., Mowry, Bryan J., Silverman, Jeremy M., Crowe, Raymond R., Cloninger, C. Robert, Tsuang, Ming T., Malaspina, Dolores, Harkavy-Friedman, Jill M., Svrakic, Dragan M., Bassett, Anne S., Holcomb, Jennifer, Kalsi, Gursharan, McQuillin, Andrew, Brynjolfson, Jon, Sigmundsson, Thordur, Petursson, Hannes, Jazin, Elena, Zoëga, Tomas and Helgason, Tomas 2003. Genome scan meta-analysis of schizophrenia and bipolar disorder, Part II: schizophrenia. American Journal of Human Genetics 73 (1) , pp. 34-48. 10.1086/376549

Rahman, Nazneen, Dunstan, Melanie

, Teare, M. Dawn, Hanks, Sandra, Douglas, Jenny, Coleman, Kim, Bottomly, William E., Campbell, Mary E., Berglund, Britta, Nordenskjöld, Magnus, Forssell, Bengt, Burrows, Nigel, Lunt, Peter, Young, Ian, Williams, Nigel Melville

, Bignell, Graham R., Futreal, P. Andrew and Pope, F. Michael 2003. Ehlers-Danlos sndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13. The American Journal of Human Genetics 73 (1) , pp. 198-204. 10.1086/376416

Williams, Nigel Melville

, Preece, A, Spurlock, G, Norton, N, Williams, H J, Zammit, Stanley

2003. Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia. Molecular Psychiatry 8 (5) , pp. 485-487. 10.1038/sj.mp.4001348

Jordan, Nicola, Williams, Nigel Melville

, Gregory, John Welbourn

, Evans, C., Owen, Michael John

and Ludgate, Marian Elizabeth 2003. The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population. Journal of Clinical Endocrinology & Metabolism 88 (3) , pp. 1002-5. 10.1210/jc.2002-021301

Turic, D, Robinson, L, Duke, M, Morris, D W, Webb, V, Hamshere, Marian Lindsay

, Milham, C, Hopkin, E, Pound, K, Fernando, S, Grierson, A, Easton, M, Williams, Nigel Melville

, Chowdhury, R, Gruen, J, Stevenson, J, Krawczak, M, Owen, Michael John

and Williams, Julie

2003. Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. Molecular Psychiatry 8 (2) , pp. 176-185. 10.1038/sj.mp.4001216

McEntagart, M, Dunstan, Melanie

, Bell, C, Boltshauser, E, Donaghy, M, Harper, Peter, Williams, Nigel Melville

, Teare, M. D. and Rahman, N 2002. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. Journal of Neurology, Neurosurgery & Psychiatry 73 (6) , p. 762. 10.1136/jnnp.73.6.762

Bray, Nicholas John

, Buckland, Paul Robert, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville

2002. Detection of cis-acting polymorphisms and epigenetic modification affecting gene expression [Conference Abstracts]. American Journal of Medical Genetics 114 (7) , p. 750. 10.1002/ajmg.10971

Rahman, Nazneen, Dunstan, Melanie

, Teare, M. Dawn, Hanks, Sandra, Edkins, Sarah J., Hughes, Jaime, Bignell, Graham R., Mancini, Grazia, Kleijer, Wim, Campbell, Mary, Keser, Gokhan, Black, Carol, Williams, Nigel Melville

, Arbour, Laura, Warman, Matthew, Superti-Furga, Andrea, Futreal, P. Andrew and Pope, F. Michael 2002. The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21. The American Journal of Human Genetics 71 (4) , pp. 975-980. 10.1086/342776

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

Norton, Nadine, Kirov, George

, Jones, Gaynor, Jones, Susan, Owen, Richard, Krawczak, Michael, Williams, Nigel Melville

2002. Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis. American Journal Of Medical Genetics Part A 114 (5) , pp. 491-496. 10.1002/ajmg.10517

Norton, Nadine, Williams, Nigel Melville

, Williams, Hywel J., Spurlock, Gillian, Kirov, George

, Morris, Derek W., Hoogendoorn, Bastiaan

2002. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Human Genetics 110 (5) , pp. 471-478. 10.1007/s00439-002-0706-6

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

Anney, Richard

, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville

, Norton, Nadine

, Cardno, Alastair George, Zammit, Stanley

, Jones, S., Jones, G., Hoogendoorn, Bastiaan

, Smith, K. J., Hamshere, Marian Lindsay

, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon

and Buckland, Paul Robert 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7 (5) , pp. 493-502. 10.1038/sj.mp.4001003

Williams, Nigel Melville

, Spurlock, Gillian, Norton, Nadine

, Krawczak, Michael, Kirov, George

, Nikolov, Ivan, Georgieva, Lyudmila, Jones, S., Cardno, Alastair George, O'Donovan, Michael Conlon

2002. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. Molecular Psychiatry 7 (10) , pp. 1092-1100. 10.1038/sj.mp.4001188

Williams, Nigel Melville

, Bowen, Timothy

, Spurlock, Gillian, Norton, Nadine

, Hoogendoorn, Bastiaan

2002. Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor. Molecular Psychiatry 7 (5) , pp. 508-514. 10.1038/sj.mp.4001030

Williams, Nigel Melville

2002. Genome scans and microarrays: converging on genes for schizophrenia? Genome Biology 3 (4) , Reviews1011-Reviews1011.5.

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

Sklar, P., Schwab, S. G., Williams, Nigel Melville

, Daly, M., Schaffner, S., Maier, W., Albus, M., Trixler, M., Eichhammer, P., Lerer, B., Hallmayer, J., Norton, N., Williams, H., Zammit, Stanley

, Cardno, A. G., Jones, S. and McCarthy, G. 2001. Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nature Genetics 28 (2) , pp. 126-128. 10.1038/88836

Bowen, Timothy

, Norton, Nadine

, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John

, Brzustowicz, L., Hoogendoorn, Bastiaan

, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John

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

McEntagart, M., Norton, N., Williams, H., Teare, M. D., Dunstan, Melanie

, Baker, P., Houlden, H., Reilly, M., Wood, N., Harper, P. S., Futreal, P. A., Williams, Nigel Melville

and Rahman, N. 2001. Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. American Journal of Human Genetics 68 (5) , pp. 1270-1276. 10.1086/320122

Austin, J., Buckland, Paul Robert, Cardno, Alastair G., Williams, Nigel Melville

, Spurlock, Gillian, Hoogendoorn, Bastiaan

, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John

, McGuffin, Peter, Owen, Michael John

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

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.

Walters, S. E., Williams, Nigel Melville

, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John

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.

Bray, Nicholas John

, Bowen, Timothy

, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon

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

Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay

, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John

, O'Donovan, Michael

and Williams, Julie

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

Austin, J., Hoogendoorn, Bastiaan

, Buckland, Paul Robert, Jones, Ian Richard

, McCandless, F., Williams, Nigel Melville

, Middle, F., Owen, Michael John

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

, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy

, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John

2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693

Kirov, George

, Stephens, M., Williams, Nigel Melville

2000. Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples. Balkan Journal of Medical Genetics 3 , pp. 23-28.

Kirov, George

, Sham, P., Craddock, Nicholas John

2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

Hoogendoorn, Bastiaan

, Norton, Nadine

, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John

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

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

Norton, N., Bray, Nicholas John

, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John

1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96.

Williams, Nigel Melville

, Bowen, Timothy

, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John

1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42.

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

Cardno, Alastair G., Bowen, Timothy

, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville

, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John

, McGuffin, Peter, Owen, Michael John

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

Fisher, P. J., Turic, D., Williams, Nigel Melville

, 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

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

Guy, Carol, Bowen, Timothy

, Jones, I. R., McCandless, F, McGuffin, P, Owen, Michael John

1999. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 57-60. 10.1002/(sici)1096-8628(19990205)88:1%3C57::aid-ajmg10%3E3.0.co;2-6

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

Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville

, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie

1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009

Hoogendoorn, Bastiaan

, Oefner, P. J., Williams, Nigel Melville

, Austin, J. and O'Donovan, Michael Conlon

1999. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Human Genetics 104 (1) , pp. 89-93. 10.1007/s004390050915

Spurlock, Gillian, Williams, Nigel Melville

, Williams, Hywel and Owen, Michael John

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.

Williams, Nigel Melville

, Fenton, I. and Owen, Michael John

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

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

1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6) , p. 469.

Williams, Nigel Melville

1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6) , p. 486.

Hill, L., Asherson, P., Ball, D., Craig, I., Daniels, J., Eley, T., Freeman, B., Ninomiya, T., Fisher, P., Turic, D., Williams, Nigel Melville

, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John

, 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.

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

Asherson, P., Mant, R., Williams, Nigel Melville

, Cardno, A., Jones, L., Murphy, Kevin, Collier, D. A., Nanko, S., Craddock, Nicholas John

, Morris, S., Muir, W., Blackwood, B., McGuffin, P. and Owen, Michael John

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

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

Bowen, Timothy

, Guy, Carol, Craddock, Nicholas John

, Cardno, A. G., Williams, Nigel Melville

, 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

, McGuffin, P., Owen, Michael John

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

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

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

Williams, Nigel Melville

, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John

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

Daniels, J. K., Spurlock, G., Williams, Nigel Melville

, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan

, Fenton, I., McGuffin, P. and Owen, Michael John

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, Nigel Melville

, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie

, McGuffin, P. and Owen, Michael John

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

Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville

, Price, W., Owen, Michael John

, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John

1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94.

Craddock, Nicholas John

, Daniels, J., Holmans, Peter Alan