Browse by Current Cardiff authors

Saffie-Awad, Paula, Grant, Spencer M., Makarious, Mary B., Elsayed, Inas, Sanyaolu, Arinola O., Crea, Peter Wild, Schumacher Schuh, Artur F., Levine, Kristin S., Vitale, Dan, Koretsky, Mathew J., Kim, Jeffrey, Peixoto Leal, Thiago, Periñán, María Teresa, Dey, Sumit, Noyce, Alastair J., Reyes-Palomares, Armando, Rodriguez-Losada, Noela, Foo, Jia Nee, Mohamed, Wael, Heilbron, Karl, Norcliffe-Kaufmann, Lucy, undefined, undefined, 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., Rizig, Mie, Okubadejo, Njideka, Nalls, Mike A., Blauwendraat, Cornelis, Singleton, Andrew, Leonard, Hampton, undefined, undefined, 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, Rieder, Carlos, 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, Sergio, Gasser, Thomas, Fang, Zih-Hua, Akpalu, Albert, Xiromerisiou, Georgia, Hadjigeorgiou, Georgios, Dagklis, Ioannis, Tarnanas, Ioannis, Stefanis, Leonidas, Stamelou, Maria, Dardiotis, 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, Tay, Yi Wen, Martinez-Ramirez, Daniel, Rodriguez-Violante, Mayela, Reyes-Pérez, Paula, Tserensodnom, Bayasgalan, Ojha, Rajeev, Anderson, Tim J., Pitcher, Toni L., 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, Amod, Ferzana, Carr, Jonathan, Bardien, Soraya, Jeon, Beomseok, Kim, Yun Joong, Cubo, Esther, Alvarez, Ignacio, Hoenicka, Janet, Beyer, Katrin, Pastor, Pau, El-Sadig, Sarah, Zweier, Christiane, Krack, Paul, Lin, Chin-Hsien, Wu, Hsiu-Chuan, Kung, Pin-Jui, Wu, Ruey-Meei, Wu, Serena, Wu, Yih-Ru, Amouri, Rim, Ben Sassi, Samia, Başak, 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 Y., Wood, Nicholas, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Okunoye, Olaitan, Lewis, Patrick A., Kaiyrzhanov, Rauan, Weil, Rimona, Love, Seth, Stott, Simon, Jasaitye, Simona, 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, Shamim, Ejaz, Riley, Ekemini, Faghri, Faraz, Serrano, Geidy E., Iwaki, Hirotaka, Chen, Honglei, Sarmiento, Ignacio Juan Keller, Williamson, Jared, Jankovic, Joseph, Shulman, Joshua, Solle, Justin C., Murphy, Kaileigh, Nuytemans, Karen, Kieburtz, Karl, Markopoulou, Katerina, Marek, Kenneth, Chahine, Lana M., Screven, Laurel, Ruffrage, Lauren, Shulman, Lisa, Marsili, Luca, Kuhl, Maggie, Dean, Marissa, Inca-Martinez, Miguel, Louie, Naomi, Mencacci, Niccolò E., 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, Mata, Ignacio F. and Bandres-Ciga, Sara 2025. Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores. npj Parkinson's Disease 11 , 201. 10.1038/s41531-025-00967-4

Silva, Ana ORCID: https://orcid.org/0000-0002-1184-4909, Sønderby, Ida, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Abdellaoui, Abdel, Agartz, Ingrid, Ames, David, Armstrong, Nicola, Artiges, Eric, Banaschewski, Tobias, Basset, Anne, Bearden, Carrie, Blangero, John, Boen, Rune, Boomsma, Dorret, Bulow, Robin, Butcher, Nancy, Calhoun, Vince, Campbell, Linda, Chow, Eva, Ciufolini, Simone, Craig, Michael, Crespo-farrocco, Benedicto, Cunningham, Adam, Dalvie, Shareefa, Daly, Eileen, Dazzan, Paola, de Geus, Eco, Zubicaray, Greig, Doherty, Joanne, Donohoe, Gary, Drakesmith, Mark, Espeseth, Thomas, Frouin, Vincent, Garavan, Hugh, Glahn, David, Goodrich-Hunsaker, Naomi, Gowland, Penny, Grabe, Hans, Grigis, Antonie, Gudbrandsen, Maria, Gutman, Boris, Haavik, Jan, Haberg, Asta, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Heinz, Andreas, Hoh mann, Sarah, Hottenga, Jouke-Jan, Jacquemont, Sebastien, Jahanshad, Neda, Jones, Rachel, Jones, Derek ORCID: https://orcid.org/0000-0003-4409-8049, Jonsson, Erik, Koops, Sanne, Kumar, Kuldeep, Le Hellard, Stephanie, Lemaitre, Herve, Liu, Jingyu, Lundervold, Astri, Martinot, Jean-Luc, Mather, Karen, McDonald-McGinn, Donna, McMahon, Katie, McRae, Allan, Medland, Sarah, Moreau, Clara, Murphy, Kieran, Murphy, Declan, Murray, Robin, Nees, Frauke, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Papadopoulos Orfanos, Diimitri, Paus, Tomas, Poustka, Luise, Reis Marques, Tiago, Roalf, David, Sachdev, Perminder, Scheffler, Freda, Schmitt, Eric, Schumann, Gunter, Steen, Vidar, Stein, Dan, Strike, Lachlan, Teumer, Alexander, Thalamuthu, Anbupalam, Thomopoulos, Sophia, Tordesillas-Gutierrez, Diana, Trolbr, Julian, Uhlmann, Anne, Vajdi, Ariana, Van't Ent, Dennis, Van Amelsvoort, Therese, van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254, van der Meer, Dennis, Vazquez-Bourgon, Javier, Villalon-Reina, Julio, Volker, Uwe, Volzke, Henry, Vorstman, Jacob, Westlye, Lars, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Wittfeld, Katharina, Wright, Margaret, Thompson, Paul, Andreassen, Ole and Linden, David ORCID: https://orcid.org/0000-0002-5638-9292 2025. Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology. Biological Psychiatry 10.1016/j.bpsc.2025.05.010

Harvey, Joshua, Smith, Adam R., Weymouth, Luke S., Smith, Rebecca G., Castanho, Isabel, Hubbard, Leon, Creese, Byron, Bresner, Catherine ORCID: https://orcid.org/0000-0003-2673-9762, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Pishva, Ehsan and Lunnon, Katie 2025. Epigenetic insights into neuropsychiatric and cognitive symptoms in Parkinson's disease: A DNA co-methylation network analysis. npj Parkinson's Disease 11 (1) , p. 39. 10.1038/s41531-025-00877-5

Lange, Lara M., Levine, Kristin, Fox, Susan H., Marras, Connie, Ahmed, Nazish, Kuznetsov, Nicole, Vitale, Dan, Iwaki, Hirotaka, Lohmann, Katja, Marsili, Luca, Espay, Alberto J., Bauer, Peter, Beetz, Christian, Martin, Jessica, Factor, Stewart A., Higginbotham, Lenora A., Chen, Honglei, Leonard, Hampton, Nalls, Mike A., Mencacci, Niccolo E., Morris, Huw R., Singleton, Andrew B., Klein, Christine, Blauwendraat, Cornelis, Fang, Zih-Hua, 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, Olguin, Patricio, Miranda, Marcelo, Bustamante, Maria Leonor, 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, Vollstedt, Eva-Juliane, Madoev, Harutyun, Trinh, Joanne, Junker, Johanna, Illarionova, Anastasia, Mollenhauer, Brit, Hopfner, Franziska, Höglinger, Günter, Sharma, Manu, Gasser, Thomas, Groppa, Sergiu, Akpalu, Albert, Xiromerisiou, Georgia, Hadjigorgiou, Georgios, Dadiotis, Efthymios, Dagklis, Ioannis, Tarnanas, Ioannis, Stefanis, Leonidas, Stamelou, Maria, Medina, Alex, Chan, Germaine Hiu-Fai, Cheung, Nelson Yuk-Fai, Ip, Nancy, Chan, Phillip, Zhou, Xiaopu, Kishore, Asha, KP, Divya, Pal, Pramod, Kukkle, Prashanth Lingappa, Rajan, Roopa, Borgohain, Rupam, Salari, Mehri, Quattrone, Andrea, Gagliardi, Monica, Valente, Enza Maria, Avenali, Micol, Annesi, Grazia, Parnetti, Lucilla, Schirinzi, Tommaso, Funayama, Manabu, Hattori, Nobutaka, Shiraishi, Tomotaka, Karimova, Altynay, Kaishibayeva, Gulnaz, Shambetova, Cholpon, Krüger, Rejko, Tan, Ai Huey, Ahmad-Annuar, Azlina, Lim, Shen-Yang, Tay, Yi Wen, Norlinah, Mohamed Ibrahim, Murad, Nor Azian Abdul, Azmin, Shahrul, Mohamed, Wael, 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, Brolin, Kajsa, Zweier, Christiane, Krack, Paul, Tinkhauser, Gerd, Lin, Chin-Hsien, Kung, Pin-Jui, Wu, Hsiu-Chuan, Wu, Ruey-Meei, Wu, Yihru, Amouri, Rim, Ben Sassi, Samia, Ba?ak, A. Nazl?, Çakmak, Özgür Öztop, Ertan, Sibel, Genc, Gencer, Noyce, Alastair, Dey, Sumit, Martínez-Carrasco, Alejandro, Schrag, Anette, Schapira, Anthony, Stafford, Eleanor J., Houlden, Henry, Hardy, John, Mok, Kin Ying, Rizig, Mie, Wood, Nicholas, Okunoye, Olaitan, Kaiyrzhanov, Rauan, Weil, Rimona, Jasaityte, Simona, Obese, Vida, Carroll, Camille, Bale, Claire, Grosset, Donald, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Lewis, Patrick Alfryn, Love, Seth, Stott, Simon, Pantazis, Caroline B., Andersh, Kate, Screven, Laurel, Bandres-Ciga, Sara, Sarmiento, Ignacio Juan Keller, O?Grady, Alyssa, Siddiqi, Bernadette, Casey, Bradford, Fiske, Brian, Comart, Charisse, Solle, Justin C., Murphy, Kaileigh, Kuhl, Maggie, Louie, Naomi, Chowdhury, Sohini, Sherer, Todd, Sobering, Andrew K., Jonas, Cabell, Cruchaga, Carlos, Ibanez, Laura, Wegel, Claire, Foroud, Tatiana, Hall, Deborah, Hernandez, Dena, Kim, Jonggeol Jeff, Song, Yeajin, Shiamim, Ejaz, Riley, Ekemini, Serrano, Geidy E., Mata, Ignacio F., Inca-Martinez, Miguel, Williamson, Jared, Jankovic, Joseph, Shulman, Joshua, Galvelis, Kamalini Ghosh, Nuytemans, Karen, Kieburtz, Karl, Markopoulou, Katerina, Marek, Kenneth, Chahine, Lana M., Ruffrage, Lauren, Shulman, Lisa, Dean, Marissa, Farrer, Matthew, Puckelwartz, Megan J., Lubbe, Steven, Albin, Roger, Alcalay, Roy, Walker, Ruth, Dumanis, Sonya, Xie, Tao, Beach, Thomas, Faghri, Faraz, Makarious, Mary B., Koretsky, Mathew, Nguyen, Duan, Nguyen, Toan and Atadzhanov, Masharip 2025. The LRRK2 p.L1795F variant causes Parkinson's disease in the European population. npj Parkinson's Disease 11 (1) , 58. 10.1038/s41531-025-00896-2

Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura, Andlauer, Till, von Scheidt, Moritz, Schizophrenia Working Group of the Psychiatric Genomics Consorti, Budde, Monika, Heilbronner, Urs, Papiol, Sergei, Teumer, Alexander, Homouth, Georg, Falkai, Peter, Volzke, Henry, Dorr, Marcus, Schulze, Thomas, Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Kavanagh, David, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Legge, Sophie, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Richards, Alexander L., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412 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 ORCID: https://orcid.org/0000-0003-2673-9762, 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. ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0003-2673-9762, Blauwendraat, Cornelis, Singleton, Andrew B, Ryten, Mina, International Lewy Body Dementia Genomics Consortium, Scholz, Sonja W, Traynor, Bryan J, Williams, Nigel M ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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. 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Terwisscha van Scheltinga, Afke F., Bakker, Steven C., van Haren, Neeltje E.M., Derks, Eske M., Buizer-Voskamp, Jacobine E., Boos, Heleen B.M., Cahn, Wiepke, Hulshoff Pol, Hilleke E., Ripke, Stephan, Ophoff, Roel A., Kahn, René S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Dwyer, Sarah, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Georgieva, Lyudmila, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ruderfer, Doug, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2013. Genetic schizophrenia risk variants jointly modulate total brain and white matter volume. Biological Psychiatry 73 (6) , pp. 525-531. 10.1016/j.biopsych.2012.08.017

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Keller, Marguax F., Saad, Mohamad, Bras, Jose, Bettella, Francesco, Nicolaou, Nayia, Simon-Sanchez, Javier, Mittag, Florian, Buchel, Finja, Sharma, Manu, Gibbs, J. Raphael, Schulte, Claudia, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Durr, Alexandra, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kilarski, Laura, Guerreiro, Rita, Hernandez, Dena G., Brice, Alexis, Ylikotila, Pauli, Stefansson, Hreinn, Majamaa, Kari, Morris, Huw Rees, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Hardy, John, Martinez, Maria, Singleton, Andrew B. and Nalls, Michael A. 2012. Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics 21 (22) , pp. 4996-5009. 10.1093/hmg/dds335

Kilarski, Laura, Pearson, Justin Peter, Newsway, Victoria Elizabeth, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Knipe, M. Duleeka W., Misbahuddin, Anjum, Chinnery, Patrick F., Burn, David J., Clarke, Carl E., Marion, Marie-Helene, Lewthwaite, Alistair J., Nicholl, David J., Wood, Nicholas W., Morrison, Karen E., Williams-Gray, Caroline H., Evans, Jonathan R., Sawcer, Stephen J., Barker, Roger A., Wickremaratchi, Mirdhu M., Ben-Shlomo, Yoav, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw Rees 2012. Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1)andLRRK2in early-onset Parkinson's disease. Movement Disorders 27 (12) , pp. 1522-1529. 10.1002/mds.25132

Levinson, Douglas F., Shi, Jianxin, Wang, Kai, Oh, Sang, Riley, Brien, Pulver, Ann E., Wildenauer, Dieter B., Laurent, Claudine, Mowry, Bryan J., Gejman, Pablo V., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Kendler, Kenneth S., Nestadt, Gerald, Schwab, Sibylle G., Mallet, Jacques, Nertney, Deborah, Sanders, Alan R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Wormley, Brandon, Lasseter, Virginia K., Albus, Margot, Godard-Bauché, Stephanie, Alexander, Madeline, Duan, Jubao, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Walsh, Dermot, O'Neill, Anthony, Papadimitriou, George N., Dikeos, Dimitris, Maier, Wolfgang, Lerer, Bernard, Campion, Dominique, Cohen, David, Jay, Maurice, Fanous, Ayman, Eichhammer, Peter, Silverman, Jeremy M., Norton, Nadine, Zhang, Nancy, Hakonarson, Hakon, Gao, Cynthia, Citri, Ami, Hansen, Mark, Ripke, Stephan, Dudbridge, Frank and Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412 2012. Genome-wide association study of multiplex schizophrenia pedigrees. American Journal of Psychiatry 169 (9) , pp. 963-973. 10.1176/appi.ajp.2012.11091423

Mittag, Florian, Büchel, Finja, Saad, Mohamad, Jahn, Andreas, Schulte, Claudia, Bochdanovits, Zoltan, Simón-Sánchez, Javier, Nalls, Mike A., Keller, Margaux, Hernandez, Dena G., Gibbs, J. Raphael, Lesage, Suzanne, Brice, Alexis, Heutink, Peter, Martinez, Maria, Wood, Nicholas W, Hardy, John, Singleton, Andrew B., Zell, Andreas, Gasser, Thomas, Sharma, Manu, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw 2012. Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities. Human Mutation 33 (12) , pp. 1708-1718. 10.1002/humu.22161

Jia, Peilin, Wang, Lily, Fanous, Ayman H., Pato, Carlos N., Edwards, Todd L., Zhao, Zhongming, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2012. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS Computational Biology 8 (7) , e1002587. 10.1371/journal.pcbi.1002587

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Jia, P., Wang, L., Fanous, A. H., Chen, X., Kendler, K. S., Zhao, Z., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Georgieva, Lyudmila, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ruderfer, D.M., Williams, H. and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2012. A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics 49 (2) , pp. 96-103. 10.1136/jmedgenet-2011-100397

Stergiakouli, Evangelia, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2012. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry 169 (2) , pp. 186-194. 10.1176/appi.ajp.2011.11040551

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Mok, Kin, Traynor, Bryan J., Schymick, Jennifer, Tienari, Pentti J., Laaksovirta, Hannu, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Shatunov, Aleksey, Boeve, Bradley F., Boxer, Adam L., DeJesus-Hernandez, Mariely, Mackenzie, Ian R., Waite, Adrian James, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Simón-Sánchez, Javier, van Swieten, John C., Heutink, Peter, Restagno, Gabriella, Mora, Gabriele, Morrison, Karen E., Shaw, Pamela J., Rollinson, Pamela Sara, Al-Chalabi, Ammar, Rademakers, Rosa, Pickering-Brown, Stuart, Orrell, Richard W., Nalls, Michael A. and Hardy, John 2012. The chromosome 9 ALS and FTD locus is probably derived from a single founder. Neurobiology of Aging 33 (1) , 209.e3-209.e8. 10.1016/j.neurobiolaging.2011.08.005

Charlesworth, Gavin, Gandhi, Sonia, Bras, Jose M., Barker, Roger A., Burn, David J., Chinnery, Patrick F., Gentleman, Stephen M., Guerreiro, Rita, Hardy, John, Holton, Janice L., Lees, Andrew, Morrison, Karen, Sheerin, Una-Marie, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Morris, Huw Rees, Revesz, Tamas and Wood, Nicholas W. 2012. Tau acts as an independent genetic risk factor in pathologically proven PD. Neurobiology of Aging 33 (4) , 838.e7-838.e11. 10.1016/j.neurobiolaging.2011.11.001

Morris, Huw Rees, Waite, Adrian James, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Neal, James William and Blake, Derek J. ORCID: https://orcid.org/0000-0002-5005-4731 2012. Recent advances in the genetics of the ALS-FTLD complex. Current Neurology and Neuroscience Reports 12 (3) , pp. 243-250. 10.1007/s11910-012-0268-5

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Chen, J., Lee, G., Fanous, A. H., Zhao, Z., Jia, P., O'Neill, A., Walsh, D., Kendler, K. S., Chen, X., International Schizophrenia Consortium, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Georgieva, Lyudmila, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Ruderfer, Doug, Williams, Hywel and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 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.

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Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Dwyer, Sarah Lynne, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Nikolov, Ivan, Carroll, Liam, Georgieva, Lyudmila, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0002-3427-3950, Corvin, A., Holmans, Peter ALan ORCID: https://orcid.org/0000-0003-0870-9412, Rujescu, D., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Suren, S., Giegling, I., Wilkinson, Lawrence ORCID: https://orcid.org/0000-0002-9337-6124, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Rujescu, D., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Davies, William ORCID: https://orcid.org/0000-0002-7714-2440 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 ORCID: https://orcid.org/0000-0003-1177-6931, Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, 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 ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Toncheva, Draga, Milanova, Vihra and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 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 ORCID: https://orcid.org/0000-0002-8990-0958, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McGuffin, Peter, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240

Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 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 ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Russell, Elen, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Peirce, Timothy Rowan, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Greene, E., Farmer, A., McGuffin, P., Morris, D. W., Corvin, A., Gill, M., Rujescu, D., Sham, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Mantripragada, Kiran Kumar ORCID: https://orcid.org/0000-0003-2070-8105, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 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 ORCID: https://orcid.org/0000-0003-2800-1091, 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 ORCID: https://orcid.org/0000-0003-1177-6931 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 ORCID: https://orcid.org/0000-0001-7073-2379, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Georgieva, Lyudmila and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097

Newsway, Victoria Elizabeth, Fish, Mark, Rohrer, Jonathan D., Majounie, Elisa ORCID: https://orcid.org/0000-0003-2800-1091, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, 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

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Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Spurlock, Gillian, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Heyrman, Lien, Adolfsson, Rolf, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, 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 ORCID: https://orcid.org/0000-0003-1784-5483, Segurado, Ricardo, Nikolov, Ivan, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Ikeda, Masashi, Iwata, Nakao, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0001-7073-2379, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melvillle ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1784-5483, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Murphy, Kieran C., Williams, Hywel, Williams Melville, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-4357-574X, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, van Den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1784-5483, Peirce, Timothy Rowan, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Macgregor, Stuart, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Wilkinson, Jennifer Camilla, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Nikolov, Ivan, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Davis, Kenneth L., Haroutunian, Vahram, Buxbaum, Joseph D., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-3427-3950, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0003-1177-6931, Green, Elaine Karen, Dwyer, Sarah Lynne, Macgregor, Stuart, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Raybould, Rachel, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Lisa Anne, Cardno, Alastair George, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 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 ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Preece, Anna Charlotte, Haroutunian, Vahram, Buxbaum, Joseph D., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Preece, Anna, Haroutunian, V, Buxbaum, JD, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-3848-4288, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Morris, Derek W., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Preece, Anna Charlotte, Dwyer, Sarah, Wilkinson, Jennifer C., Spurlock, Gillian, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Buckland, Paul Robert, Waddington, John L., Gill, Michael, Corvin, Aiden P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael John ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, H., Cardno, Alastair G., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 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 ORCID: https://orcid.org/0000-0002-8990-0958, Bennett, Philip, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Segurado, Ricardo, Cardno, Alastair George, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Lambert, David, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Corvin, Aiden, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Gill, Michael, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 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 ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. 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 ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, MacGregor, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9) , pp. 1736-1738. 10.1176/appi.ajp.162.9.1736

Glaser, B1, Schumacher, J., Williams, H. J., Jamra, R. A., Ianakiev, N., Milev, R., Ohlraun, S., Schulze, T. G., Czerski, P. M., Hauser, J., Jonsson, E. G., Sedvall, G. C., Klopp, N., Illig, T., Becker, T., Propping, P., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cichon, S., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Rietschel, M., Murphy, K. C., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Nothen, M. M. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples. Biological psychiatry 58 (1) , pp. 78-80.

Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lisa Anne, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6) , pp. 642-648. 10.1001/archpsyc.62.6.642

Turic, D., Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Williams, H., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. A family based study 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 ORCID: https://orcid.org/0000-0001-6271-6301, Preece, Anna, Gerrish, Amy, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Yerassimou, P., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 , 23. 10.1186/1471-244X-5-23

Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Hollingworth, P., Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, 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 ORCID: https://orcid.org/0000-0003-1177-6931, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 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 ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna Charlotte, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics 14 (14) , pp. 1947-1954. 10.1093/hmg/ddi199

Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2005. 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 ORCID: https://orcid.org/0000-0003-1177-6931, Jones, Lisa, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 and Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Preece, Anna, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Norton, N, Wilkinson, J, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Allelic variation in the expression of neuropsychiatric candidate genes [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 25.

Peirce, T. R., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Haroutunian, V., Buxbaum, J., Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 81. 10.1002/ajmg.b.30101

Norton, N, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Morris, DW, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 18.

Mowry, B J, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Pulver, A E, Gejman, P V, Riley, B, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Laurent, C, Schwab, S G, Wildenauer, D B, Bauché, S, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wormley, B, Sanders, A R, Nestadt, G, Liang, K Y, Duan, J, Ribble, R, Norton, N, Soubigou, S, Maier, W, Ewen-White, K R, deMarchi, N, Carpenter, B, Walsh, D, Williams, H, Jay, M, Albus, M, Nertney, D A, Papadimitriou, G, O'Neill, A, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Deleuze, J-F, Lerer, F B, Dikeos, D, Kendler, K S, Mallet, J, Silverman, J M, Crowe, R R and Levinson, D F 2004. Multicenter linkage study of schizophrenia loci on chromosome 22q. Molecular Psychiatry 9 (8) , pp. 784-795. 10.1038/sj.mp.4001481

Morris, D.W., Ivanov, D. ORCID: https://orcid.org/0000-0001-6271-6301, Robinson, L., Williams, N. ORCID: https://orcid.org/0000-0003-1177-6931, Stevenson, J., Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862, Williams, J. and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 2004. Association analysis of two candidate phospholipase genes that map to the chromosome 15q15.1-15.3 region associated with reading disability. American Journal Of Medical Genetics Part A 129B (1) , pp. 97-103. 10.1002/ajmg.b.30033

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0002-3427-3950, Ivanov, Dobril ORCID: https://orcid.org/0000-0001-6271-6301, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biological psychiatry 55 (10) , pp. 971-975. 10.1016/j.biopsych.2004.01.025

Monslow, Jamie, Williams, John David, Guy, Carol, Price, Iain Kelsey, Craig, Kathrine Jane, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Martin, John, Coleman, Sharon Louise, Topley, Nicholas, Spicer, Andrew P., Buckland, Paul Robert, Davies, Malcolm and Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435 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 ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna, Mortis, DW, Spurlock, Gillian, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Stephens, M, Norton, N, Williams, H, Clement, M, Dwyer, S, Curran, C, Wilkinson, J, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Waddington, JL, Gill, M, Corvin, AP, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, McCreadie, Robin G, Buckland, Paul Robert, Sharkey, Val, Chowdari, Kodavali V., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Nimgaonkar, Vishwajit, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, Preece, Anna Charlotte, Morris, D. W., Spurlock, Gillian, Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Stephens, Mark Keith, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Clement, Mathew ORCID: https://orcid.org/0000-0002-9280-5281, Dwyer, Sarah Lynne, Curran, Catherine, Wilkinson, Jennifer Camilla, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Waddington, J. L., Gill, M., Corvin, A. P., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-4798-0862, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0002-2033-2657, Mills, S., Stephens, M., Lawson, D., Govan, Catherine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Kent, L., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 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 ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2004. 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 ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Ekholm, B., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0001-6271-6301, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Nikolov, Ivan, Tzwetkova, R., Stambolova, S. M., Murphy, Kieran Christopher, Toncheva, Draga, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2003. Recent advances in the genetics of schizophrenia. Human Molecular Genetics 12 (suppl) , R125-R133. 10.1093/hmg/ddg302

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Georgieva, Lyudmila, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Nikolov, Ivan, Norton, Nadine, Toncheva, Draga, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0002-3848-4288, Guy, Carol, Price, Iain Kelsey, Coleman, Sharon Louise, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Buckland, Paul Robert, Spicer, Andrew P., Topley, Nicholas, Davies, Malcolm and Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435 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 ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G., Jones, S., Owen, R., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2003. 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 ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Norton, N., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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. ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Norton, N., Ivanov, D. ORCID: https://orcid.org/0000-0001-6271-6301, McCreadie, R. G., Preece, A., Sharkey, V., Jones, S., Zammit, S. ORCID: https://orcid.org/0000-0002-2647-9211, Nikolov, I., Kehaiov, I., Thapar, A. ORCID: https://orcid.org/0000-0002-3689-737X, Murphy, K. C., Kirov, G. ORCID: https://orcid.org/0000-0002-3427-3950, Owen, M. J. ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, M. C. ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0003-3817-2142, 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0003-1177-6931, Preece, A, Spurlock, G, Norton, N, Williams, H J, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Gregory, John Welbourn ORCID: https://orcid.org/0000-0001-5189-3812, Evans, C., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0002-8990-0958, Milham, C, Hopkin, E, Pound, K, Fernando, S, Grierson, A, Easton, M, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, van den Bree, Marianne Bernadette ORCID: https://orcid.org/0000-0002-4426-3254, Chowdhury, R, Gruen, J, Stevenson, J, Krawczak, M, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 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 ORCID: https://orcid.org/0000-0003-3817-2142, Bell, C, Boltshauser, E, Donaghy, M, Harper, Peter, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0002-4357-574X, Buckland, Paul Robert, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-3817-2142, 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 ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, 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 ORCID: https://orcid.org/0000-0002-3427-3950, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, Gaynor, Jones, Susan, Owen, Richard, Krawczak, Michael, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel J., Spurlock, Gillian, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Morris, Derek W., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-0870-9412, Laurent, Claudine, Riley, Brien, Pulver, Ann E., Gejman, Pablo V., Schwab, Sibylle G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0001-7758-0312, 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 ORCID: https://orcid.org/0000-0001-7073-2379, 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 ORCID: https://orcid.org/0000-0003-0870-9412, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Giles, Peter ORCID: https://orcid.org/0000-0003-3143-6854, Tunstall, Nigel, Jones, Lesley ORCID: https://orcid.org/0000-0002-3007-4612, Lovestone, Simon, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, 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 ORCID: https://orcid.org/0000-0002-6083-407X, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, S., Jones, G., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Smith, K. J., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Krawczak, Michael, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Nikolov, Ivan, Georgieva, Lyudmila, Jones, S., Cardno, Alastair George, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Spurlock, Gillian, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2002. Genome scans and microarrays: converging on genes for schizophrenia? Genome Biology 3 (4) , Reviews1011-Reviews1011.5.

Bennett, P., Segurado, R., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Bort, S., McCandless, F., Lambert, D., Heron, J., Comerford, C., Middle, F., Corvin, A., Pelios, G., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Larsen, B., Mulcahy, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Connell, R., O'Mahony, E., Payne, A., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Gill, M. 2002. The Wellcome trust UK-Irish bipolar affective disorder sibling-pair genome screen: first stage report. Molecular Psychiatry 7 (2) , pp. 189-200. 10.1038/sj.mp.4000957

Sklar, P., Schwab, S. G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Daly, M., Schaffner, S., Maier, W., Albus, M., Trixler, M., Eichhammer, P., Lerer, B., Hallmayer, J., Norton, N., Williams, H., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, 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 ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Brzustowicz, L., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2001. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation [Letter]. Molecular Psychiatry 6 (3) , pp. 259-260. 10.1038/sj.mp.4000128

McEntagart, M., Norton, N., Williams, H., Teare, M. D., Dunstan, Melanie ORCID: https://orcid.org/0000-0003-3817-2142, Baker, P., Houlden, H., Reilly, M., Wood, N., Harper, P. S., Futreal, P. A., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 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 ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry 5 (5) , pp. 552-557. 10.1038/sj.mp.4000761

Levinson, D. F., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Straub, R. E., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Walters, S. E., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia. American Journal of Medical Genetics 96 (4) , p. 535.

Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics 10 (2) , pp. 83-86. 10.1097/00041444-200010020-00005

Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843

Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, McCandless, F., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Middle, F., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1) , pp. 51-54. 10.1097/00041444-200010010-00009

Austin, J., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693

Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Stephens, M., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. 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 ORCID: https://orcid.org/0000-0002-3427-3950, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Sham, P., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Rees, M. I., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs. Human Molecular Genetics 8 (9) , pp. 1729-1739. 10.1093/hmg/8.9.1729

Norton, N., Bray, Nicholas John ORCID: https://orcid.org/0000-0002-4357-574X, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42.

Rees, M. I., Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Cardno, Alastair G., Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, McGuffin, Peter, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12) , pp. 1592-1596. 10.1016/s0006-3223(99)00033-5

Fisher, P. J., Turic, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Asherson, P., Ball, D., Craig, I., Eley, T., Hill, L., Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics 8 (5) , pp. 915-922. 10.1093/hmg/8.5.915

Guy, Carol, Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, I. R., McCandless, F, McGuffin, P, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Goate, A., Hardy, J. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009

Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Oefner, P. J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Austin, J. and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 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 ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Hywel and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics 81 (6) , pp. 525-526.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Fenton, I. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6) , pp. 463-464.

Fisher, P. J., Turic, D., Asherson, P., Ball, D., Benbow, C., Chorney, M., Chorney, K., Craig, I., Eley, T., Hill, L., Lubinski, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6) , p. 469.

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 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 ORCID: https://orcid.org/0000-0003-1177-6931, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, McGuffin, P. and Plomin, R. 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6) , p. 486.

Wu, W. S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Hutton, M., Hardy, J., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619

Asherson, P., Mant, R., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A., Jones, L., Murphy, Kevin, Collier, D. A., Nanko, S., Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Morris, S., Muir, W., Blackwood, B., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry 3 (4) , pp. 310-320. 10.1038/sj.mp.4000399

Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816

Bowen, Timothy ORCID: https://orcid.org/0000-0001-6050-0435, Guy, Carol, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Cardno, A. G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400

Murphy, K. C., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X

Baboolal, K., Ravine, D., Daniels, J., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, 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 ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2) , pp. 83-85. 10.1097/00041444-199722000-00005

Daniels, J. K., Spurlock, G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Fenton, I., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1) , pp. 37-39. 10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S

Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Price, W., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94.

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Daniels, J., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairs. Molecular Psychiatry 1 (1) , pp. 59-64.

Daniels, J. K., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259, Jones, L. A., Cardno, A. G., Murphy, K. C., Spurlock, G., Riley, B., Scambler, P., Asherson, P., McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1996. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153 (2) , pp. 268-270. 10.1176/ajp.153.2.268

Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Gill, M. and Powell, J. F. 1996. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Cytogenetics and Cell Genetics 75 , pp. 2-3.

Lin, M. W., Curtis, D., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Gill, M. 1995. Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32. Psychiatric Genetics 5 (3) , pp. 117-126. 10.1097/00041444-199505030-00004

Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Roberts, Q., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, McGuffin, P. and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1995. Association study of bipolar disorder using a functional polymorphism (Ser311-->Cys) in the dopamine D2 receptor gene. Psychiatric Genetics 5 (2) , pp. 63-65.

Asherson, P, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Roberts, E, McGuffin, M and Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 1994. DRD2 Ser311/Cys311 polymorphism in schizophrenia. The Lancet 343 (8904) , p. 1045.