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Number of items: 213.

Greene, C, Kealy, J, Humphries, M M, Gong, Y, Hou, J, Hudson, N, Cassidy, L M, Martiniano, R, Shashi, V, Hooper, S R, Grant, G A, Kenna, P F, Norris, K, Callaghan, C K, Islam, M dN, O'Mara, S M, Najda, Z, Campbell, S G, Pachter, J S, Thomas, J, Williams, Nigel, Humphries, P, Murphy, K C and Campbell, M 2017. Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia. Molecular Psychiatry 10.1038/mp.2017.156
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Malek, Naveed, Lawton, Michael A., Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Ben-Shlomo, Yoav, Burn, David J., Foltynie, Tom, Hardy, John, Morris, Huw R., Williams, Nigel, Wood, Nicholas and Grosset, Donald G. 2017. Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases. Parkinsonism & Related Disorders 40 , pp. 40-46. 10.1016/j.parkreldis.2017.04.006

Marshall, Christian R., Howrigan, Daniel P., Merico, Daniele, Holmans, Peter Alan, Carrera, Noa, Craddock, Nicholas, Escott-Price, Valentina, Georgieva, Lyudmila, Kavanagh, David, Legge, Sophie, Pocklington, Andrew, Richards, Alexander, Ruderfer, Douglas M, Williams, Nigel, Kirov, George, Owen, Michael, Walters, James and O’Donovan, Michael Conlon 2017. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nature Genetics 49 (1) , pp. 27-35. 10.1038/ng.3725
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Lubbe, Steven J., Escott-Price, Valentina, Gibbs, J. Raphael, Nalls, Mike A., Bras, Jose, Price, T. Ryan, Nicolas, Aude, Jansen, Iris E., Mok, Kin Y., Pittman, Alan M., Tomkins, James E., Lewis, Patrick A., Noyce, Alastair J., Lesage, Suzanne, Sharma, Manu, Schiff, Elena R., Levine, Adam P., Brice, Alexis, Gasser, Thomas, Hardy, John, Heutink, Peter, Wood, Nicholas W., Singleton, Andrew B., Williams, Nigel and Morris, Huw R. 2016. Additional rare variant analysis in Parkinson?s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. Human Molecular Genetics 25 (24) , pp. 5483-5489. 10.1093/hmg/ddw348
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Lawton, Michael, Hu, Michele T.M., Baig, Fahd, Ruffmann, Claudio, Barron, Eilidh, Swallow, Diane M.A., Malek, Naveed, Grosset, Katherine A., Bajaj, Nin, Barker, Roger A., Williams, Nigel Melville, Burn, David J., Foltynie, Thomas, Morris, Huw R., Wood, Nicholas W., May, Margaret T., Grosset, Donald G. and Ben-Shlomo, Yoav 2016. Equating scores of the University of Pennsylvania smell identification test and sniffin' sticks test in patients with Parkinson's disease. Parkinsonism & Related Disorders 33 , pp. 96-101. 10.1016/j.parkreldis.2016.09.023
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Malek, Naveed, Lawton, Michael A., Swallow, Diane M. A., Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Hardy, John, Morris, Huw R., Williams, Nigel Melville, Wood, Nicholas, Ben-Shlomo, Yoav and Grosset, Donald G. 2016. Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease. Movement Disorders 31 (10) , pp. 1518-1526. 10.1002/mds.26698
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Swallow, Diane M. A., Lawton, Michael A., Grosset, Katherine A., Malek, Naveed, Klein, Johannes, Baig, Fahd, Ruffmann, Claudio, Bajaj, Nin P., Barker, Roger A., Ben-Shlomo, Yoav, Burn, David J., Foltynie, Thomas, Morris, Huw R., Williams, Nigel, Wood, Nicholas W., Hu, Michele T. M. and Grosset, Donald G. 2016. Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts. Journal of Neurology, Neurosurgery & Psychiatry 87 (11) , pp. 1183-1190. 10.1136/jnnp-2016-313642
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Mooney, Michael A., McWeeney, Shannon K., Faraone, Stephen, Hinney, Anke, Hebebrand, Johannes, Nigg, Joel T., Wilmot, Beth, Thapar, Anita, Martin, Joanna, O'Donovan, Michael Conlon, Owen, Michael John, Williams, Nigel Melville, Anney, Richard, Langley, Kate, Holmans, Peter Alan and German ADHD GWAS Group, 2016. Pathway analysis in attention deficit hyperactivity disorder: an ensemble approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (6) , pp. 815-826. 10.1002/ajmg.b.32446

Thapar, Anita, Martin, Joanna, Mick, E., Arias Vasquez, A., Langley, Kate, Scherer, S.W., Schacher, R., Crosbie, J., Williams, Nigel Melville, Franke, B., Elia, J., Glessner, J., Hakonarson, H., Owen, Michael John, Faraone, S.V., O'Donovan, Michael Conlon and Holmans, Peter Alan 2016. Psychiatric gene discoveries shape evidence on ADHD's biology. Molecular Psychiatry 21 (9) , pp. 1202-1207. 10.1038/mp.2015.163
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Swallow, Diane M.A., Lawton, Michael A., Grosset, Katherine A., Malek, Naveed, Smith, Callum R., Bajaj, Nin P., Barker, Roger A., Ben-Shlomo, Yoav, Burn, David J., Foltynie, Thomas, Hardy, John, Morris, Huw R., Williams, Nigel, Wood, Nicholas W. and Grosset, Donald G. 2016. Variation in recent onset Parkinson's disease: implications for prodromal detection. Journal of Parkinson's Disease 6 (2) , pp. 289-300. 10.3233/JPD-150741

Mok, Kin Y, Sheerin, Una, Simón-Sánchez, Javier, Salaka, Afnan, Chester, Lucy, Escott-Price, Valentina, Mantripragada, Kiran, Doherty, Karen M, Noyce, Alastair J, Mencacci, Niccolo E, Lubbe, Steven J, Williams-Gray, Caroline H, Barker, Roger A, van Dijk, Karin D, Berendse, Henk W, Heutink, Peter, Corvol, Jean-Christophe, Cormier, Florence, Lesage, Suzanne, Brice, Alexis, Brockmann, Kathrin, Schulte, Claudia, Gasser, Thomas, Foltynie, Thomas, Limousin, Patricia, Morrison, Karen E, Clarke, Carl E, Sawcer, Stephen, Warner, Tom T, Lees, Andrew J, Morris, Huw R, Nalls, Mike A, Singleton, Andrew B, Hardy, John, Abramov, Andrey Y, Plagnol, Vincent, Williams, Nigel Melville and Wood, Nicholas W 2016. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. The Lancet Neurology 15 (6) , pp. 585-596. 10.1016/S1474-4422(16)00071-5
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Franke, Barbara, Stein, Jason L, Ripke, Stephan, Anttila, Verneri, Hibar, Derrek P, van Hulzen, Kimm J E, Arias-Vasquez, Alejandro, Smoller, Jordan W, Nichols, Thomas E, Neale, Michael C, McIntosh, Andrew M, Lee, Phil, McMahon, Francis J, Meyer-Lindenberg, Andreas, Mattheisen, Manuel, Andreassen, Ole A, Gruber, Oliver, Sachdev, Perminder S, Roiz-Santiañez, Roberto, Saykin, Andrew J, Ehrlich, Stefan, Mather, Karen A, Turner, Jessica A, Schwarz, Emanuel, Thalamuthu, Anbupalam, Yao, Yin, Ho, Yvonne Y W, Martin, Nicholas G, Wright, Margaret J, Ripke, Stephan, Neale, Benjamin M, Corvin, Aiden, Walters, James Tynan Rhys, Farh, Kai-How, Holmans, Peter Alan, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A, Huang, Hailiang, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A, Begemann, Martin, Belliveau, Richard A, Bene, Judit, Bergen, Sarah E, Bevilacqua, Elizabeth, Bigdeli, Tim B, Black, Donald W, Bruggeman, Richard, Buccola, Nancy G, Buckner, Randy L, Byerley, William F, Cahn, Wiepke, Cai, Guiqing, Cairns, Murray J, Campion, Dominique, Cantor, Rita M, Carr, Vaughan J, Carrera, Noa, Catts, Stanley V, Chambert, Kimberley D, Chan, Raymond C K, Chen, Eric Y H, Chen, Ronald Y L, Cheng, Wei, Cheung, Eric F C, Chong, Siow Ann, Cloninger, C Robert, Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nicholas, Crespo-Facorro, Benedicto, Crowley, James J, Curtis, David, Davidson, Michael, Davis, Kenneth L, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H, Farrell, Martilias S, Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B, Friedman, Joseph I, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian Lindsay, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M, Henskens, Frans A, Herms, Stefan L, Hirschhorn, Joel N, Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V, Hougaard, David M, Ikeda, Masashi, Joa, Inge, Julià, Antonio, Kähler, Anna K, Kahn, René S, Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C, Kelly, Brian J, Kennedy, James L, Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A, Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S Hong, Keong, Jimmy Lee Chee, Legge, Sophie E., Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Lönnqvist, Jouko, Loughland, Carmel M, Lubinski, Jan, Macek, Milan, Magnusson, Patrik K E, Maher, Brion S, Maier, Wolfgang, Mallet, Jacques, Marsal, Sara, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W, McDonald, Colm, McIntosh, Andrew M, Meier, Sandra, Meijer, Carin J, Melegh, Bela, Melle, Ingrid, Mesholam-Gately, Raquelle I, Metspalu, Andres, Michie, Patricia T, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Morris, Derek W, Mors, Ole, Müller-Myhsok, Bertram, Murphy, Kieran C, Murray, Robin M, Myin-Germeys, Inez, Nelis, Mari, Nenadic, Igor, Nertney, Deborah A, Nestadt, Gerald, Nicodemus, Kristin K, Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, O'Callaghan, Eadbhard, O'Dushlaine, Colm, O'Neill, F Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Van Os, Jim, Pantelis, Christos, Papadimitriou, George N, Papiol, Sergi, Parkhomenko, Elena, Pato, Michele T, Paunio, Tiina, Perkins, Diana O, Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Reichenberg, Abraham, Reimers, Mark A, Richards, Alexander, Roffman, Joshua L, Roussos, Panos, Ruderfer, Douglas M., Salomaa, Veikko, Sanders, Alan R, Schall, Ulrich, Schubert, Christian R, Schulze, Thomas G, Schwab, Sibylle G, Scolnick, Edward M, Scott, Rodney J, Seidman, Larry J, Shi, Jianxin, Silverman, Jeremy M, Sim, Kang, Slominsky, Petr, Smoller, Jordan W, So, Hon-Cheong, Söderman, Erik, Spencer, Chris C A, Stahl, Eli A, Stogmann, Elisabeth, Straub, Richard E, Strengman, Eric, Strohmaier, Jana, Stroup, T Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Thirumalai, Srinivas, Toncheva, Draga, Tooney, Paul A, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T, Weiser, Mark, Wildenauer, Dieter B, Williams, Nigel Melville, Williams, Stephanie, Witt, Stephanie H, Wolen, Aaron R, Wong, Emily H M, Wormley, Brandon K, Wu, Jing Qin, Xi, Hualin Simon, Zai, Clement C, Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R, Visscher, Peter M, Adolfsson, Rolf, Andreassen, Ole A, Blackwood, Douglas H R, Børglum, Anders D, Bramon, Elvira, Buxbaum, Joseph D, Cichon, Sven, Darvasi, Ariel, Domenici, Enrico, Ehrenreich, Hannelore, Esko, Tõnu, Gejman, Pablo V, Gill, Michael, Gurling, Hugh, Hultman, Christina M, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kendler, Kenneth S, Kirov, George, Knight, Jo, Lencz, Todd, Levinson, Douglas F, Li, Qingqin S, Liu, Jianjun, Malhotra, Anil K, McCarroll, Steven A, McQuillin, Andrew, Moran, Jennifer L, Mortensen, Preben B, Mowry, Bryan J, Nöthen, Markus M, Ophoff, Roel A, Owen, Michael John, Palotie, Aarno, Pato, Carlos N, Petryshen, Tracey L, Posthuma, Danielle, Rietschel, Marcella, Riley, Brien P, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David, Weinberger, Daniel R, Wendland, Jens R, Werge, Thomas, Daly, Mark J, Sullivan, Patrick F, O'Donovan, Michael C, Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivières, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Chakravarty, M Mallar, Chen, Qiang, Ching, Christopher R K, Cuellar-Partida, Gabriel, den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J, Hoogman, Martine, Janowitz, Deborah, Jia, Tianye, Kim, Sungeun, Klein, Marieke, Kraemer, Bernd, Lee, Phil, Loohuis, Loes M Olde, Luciano, Michelle, Macare, Christine, Mather, Karen A, Mattheisen, Manuel, Milaneschi, Yuri, Nho, Kwangsik, Papmeyer, Martina, Ramasamy, Adaikalavan, Risacher, Shannon L, Roiz-Santiañez, Roberto, Rose, Emma J, Salami, Alireza, Sämann, Philipp G, Schmaal, Lianne, Schork, Andrew J, Shin, Jean, Strike, Lachlan T, Teumer, Alexander, van Donkelaar, Marjolein M J, van Eijk, Kristel R, Walters, Raymond K, Westlye, Lars T, Whelan, Christopher D, Winkler, Anderson M, Zwiers, Marcel P, Alhusaini, Saud, Athanasiu, Lavinia, Ehrlich, Stefan, Hakobjan, Marina M H, Hartberg, Cecilie B, Haukvik, Unn, Heister, Angelien J G A M, Höhn, David, Kasperaviciute, Dalia, Liewald, David C M, Lopez, Lorna M, Makkinje, Remco R R, Matarin, Mar, Naber, Marlies A M, McKay, David R, Needham, Margaret, Nugent, Allison C, Pütz, Benno, Royle, Natalie A, Shen, Li, Sprooten, Emma, Trabzuni, Daniah, van der Marel, Saskia S L, van Hulzen, Kimm J E, Walton, Esther, Wolf, Christiane, Almasy, Laura, Ames, David, Arepalli, Sampath, Assareh, Amelia A, Bastin, Mark E, Brodaty, Henry, Bulayeva, Kazima B, Carless, Melanie A, Cichon, Sven, Corvin, Aiden, Curran, Joanne E, Czisch, Michael, de Zubicaray, Greig I, Dillman, Allissa, Duggirala, Ravi, Dyer, Thomas D, Erk, Susanne, Fedko, Iryna O, Ferrucci, Luigi, Foroud, Tatiana M, Fox, Peter T, Fukunaga, Masaki, Gibbs, Raphael, Göring, Harald H H, Green, Robert C, Guelfi, Sebastian, Hansell, Narelle K, Hartman, Catharina A, Hegenscheid, Katrin, Heinz, Andreas, Hernandez, Dena G, Heslenfeld, Dirk J, Hoekstra, Pieter J, Holsboer, Florian, Homuth, Georg, Hottenga, Jouke-Jan, Ikeda, Masashi, Jack, Clifford R, Jenkinson, Mark, Johnson, Robert, Kanai, Ryota, Keil, Maria, Kent, Jack W, Kochunov, Peter, Kwok, John B, Lawrie, Stephen M, Liu, Xinmin, Longo, Dan L, McMahon, Katie L, Meisenzahl, Eva, Melle, Ingrid, Mohnke, Sebastian, Montgomery, Grant W, Mostert, Jeanette C, Mühleisen, Thomas W, Nalls, Michael A, Nichols, Thomas E, Nilsson, Lars G, Nöthen, Markus M, Ohi, Kazutaka, Olvera, Rene L, Perez-Iglesias, Rocio, Pike, G Bruce, Potkin, Steven G, Reinvang, Ivar, Reppermund, Simone, Rietschel, Marcella, Romanczuk-Seiferth, Nina, Rosen, Glenn D, Rujescu, Dan, Schnell, Knut, Schofield, Peter R, Smith, Colin, Steen, Vidar M, Sussmann, Jessika E, Thalamuthu, Anbupalam, Toga, Arthur W, Traynor, Bryan, Troncoso, Juan, Turner, Jessica A, Hernández, Maria C Valdés, Ent, Dennis van 't, van der Brug, Marcel, van der Wee, Nic J A, van Tol, Marie-Jose, Veltman, Dick J, Wassink, Thomas H, Westman, Eric, Zielke, Ronald H, Zonderman, Alan, Ashbrook, David G, Hager, Reinmar, Lu, Lu, McMahon, Francis J, Morris, Derek W, Williams, Robert W, Brunner, Han G, Buckner, Randy L, Buitelaar, Jan K, Cahn, Wiepke, Calhoun, Vince D, Cavalleri, Gianpiero L, Crespo-Facorro, Benedicto, Dale, Anders M, Davies, Gareth E, Delanty, Norman, Depondt, Chantal, Djurovic, Srdjan, Drevets, Wayne C, Espeseth, Thomas, Gollub, Randy L, Ho, Beng-Choon, Hoffmann, Wolfgang, Hosten, Norbert, Kahn, René S, LeHellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nauck, Matthias, Nyberg, Lars, Pandolfo, Massimo, Penninx, Brenda W J H, Roffman, Joshua L, Sisodiya, Sanjay M, Smoller, Jordan W, van Bokhoven, Hans, van Haren, Neeltje E M, Völzke, Henry, Walter, Henrik, Weiner, Michael W, Wen, Wei, White, Tonya, Agartz, Ingrid, Andreassen, Ole A, Blangero, John, Boomsma, Dorret I, Brouwer, Rachel M, Cannon, Dara M, Cookson, Mark R, de Geus, Eco J C, Deary, Ian J, Donohoe, Gary, Fernández, Guillén, Fisher, Simon E, Francks, Clyde, Glahn, David C, Grabe, Hans J, Gruber, Oliver, Hardy, John, Hashimoto, Ryota, Hulshoff Pol, Hilleke E, Jönsson, Erik G, Kloszewska, Iwona, Lovestone, Simon, Mattay, Venkata S, Mecocci, Patrizia, McDonald, Colm, McIntosh, Andrew M, Ophoff, Roel A, Paus, Tomas, Pausova, Zdenka, Ryten, Mina, Sachdev, Perminder S, Saykin, Andrew J, Simmons, Andy, Singleton, Andrew, Soininen, Hilkka, Wardlaw, Joanna M, Weale, Michael E, Weinberger, Daniel R, Adams, Hieab H H, Launer, Lenore J, Seiler, Stephan, Schmidt, Reinhold, Chauhan, Ganesh, Satizabal, Claudia L, Becker, James T, Yanek, Lisa, van der Lee, Sven J, Ebling, Maritza, Fischl, Bruce, Longstreth, W T, Greve, Douglas, Schmidt, Helena, Nyquist, Paul, Vinke, Louis N, van Duijn, Cornelia M, Luting, Xue, Mazoyer, Bernard, Bis, Joshua C, Gudnason, Vilmundur, Seshadri, Sudha, Ikram, M Arfan, Martin, Nicholas G, Wright, Margaret J, Schumann, Gunter, Franke, Barbara, Thompson, Paul M, Medland, Sarah E, O'Donovan, Michael Conlon, Thompson, Paul M, Neale, Benjamin M, Medland, Sarah E and Sullivan, Patrick F 2016. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept. Nature Neuroscience 19 (3) , pp. 420-431. 10.1038/nn.4228

Malek, N., Swallow, D. M. A., Grosset, K. A., Lawton, M. A., Smith, C. R., Bajaj, N. P., Barker, R. A., Ben-Shlomo, Y., Bresner, Catherine, Burn, D. J., Foltynie, T., Morris, H. R., Williams, Nigel, Wood, N. W. and Grosset, D. G. 2015. Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients. Acta Neurologica Scandinavica 134 (4) , pp. 271-276. 10.1111/ane.12538

Nalls, Mike A, McLean, Cory Y, Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J, Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel Melville, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T Ryan, Nicolas, Aude, Keller, Margaux F, Molony, Cliona, Gibbs, J Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S, Mapstone, Mark, Federoff, Howard J, Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M, Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G, Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie A M, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G, Stone, David J, Ioannidis, John P A and Singleton, Andrew B 2015. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. The Lancet Neurology 14 (10) , pp. 1002-1009. 10.1016/S1474-4422(15)00178-7

Nalls, Mike A., Escott-Price, Valentina, Williams, Nigel Melvillle, Lubbe, Steven, Keller, Margaux F., Morris, Huw R. and Singleton, Andrew B. 2015. Genetic risk and age in Parkinson's disease: Continuum not stratum. Movement Disorders 30 (6) , pp. 850-854. 10.1002/mds.26192

Escott-Price, Valentina, Nalls, Mike A., Morris, Huw R., Lubbe, Steven, Brice, Alexis, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Hardy, John, Singleton, Andrew B. and Williams, Nigel Melville 2015. Polygenic risk of Parkinson disease is correlated with disease age at onset. Annals of Neurology 77 (4) , pp. 582-91. 10.1002/ana.24335

Lubbe, Steven J, Escott-Price, Valentina, Brice, Alexis, Gasser, Thomas, Hardy, John, Heutink, Peter, Sharma, Manu, Wood, Nicholas W, Nalls, Mike, Singleton, Andrew B, Williams, Nigel Melville and Morris, Huw 2015. Is theMC1Rvariant p.R160W associated with Parkinson's? Annals of Neurology , n/a. 10.1002/ana.24527

Martin, Joanna, O'Donovan, Michael Conlon, Thapar, Anita, Langley, Kate and Williams, Nigel Melville 2015. The relative contribution of common and rare genetic variants to ADHD. Translational Psychiatry 5 (2) , e506. 10.1038/tp.2015.5
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Malek, Naveed, Swallow, Diane M.A., Grosset, Katherine A., Lawton, Michael A., Marrinan, Sarah L., Lehn, Alexander C., Bresner, Catherine, Bajaj, Nin, Barker, Roger A., Ben-Shlomo, Yoav, Burn, David J., Foltynie, Thomas, Hardy, John, Morris, Huw R., Williams, Nigel M., Wood, Nicholas and Grosset, Donald G. 2015. Tracking Parkinson's: study design and baseline patient data. Journal of Parkinson's Disease 5 (4) , pp. 947-959. 10.3233/JPD-150662
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Gusev, Alexander, Lee, S. Hong, Trynka, Gosia, Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli, Kähler, Anna K., Hultman, Christina M., Purcell, Shaun M., McCarroll, Steven A., Daly, Mark, Pasaniuc, Bogdan, Sullivan, Patrick F., Neale, Benjamin M., Wray, Naomi R., Raychaudhuri, Soumya, Price, Alkes L., Escott-Price, Valentina, Carrera, Noa, Hamshere, Marian Lindsay, Holmans, Peter ALan, Kirov, George, Legge, Sophie, Li, Meng, O'Donovan, Michael Conlon, Owen, Michael John, Pocklington, Andrew, Richards, Alexander, Walters, James Tynan Rhys and Williams, Nigel Melville 2014. Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. American Journal of Human Genetics 95 (5) , pp. 535-552. 10.1016/j.ajhg.2014.10.004

Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B, Williams, Nigel Melville and Morris, Huw 2014. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nature Genetics 46 (9) , pp. 989-993. 10.1038/ng.3043

Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James Tynan Rhys, Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau Jr, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard, Buccola, Nancy G., Buckner, Randy L., Byerley, William, Cahn, Wiepke, Cai, Guiqing, Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Catts, Stanley V., Chambert, Kimberly D., Chan, Raymond C. K., Chen, Ronald Y. L., Chen, Eric Y. H., Cheng, Wei, Cheung, Eric F. 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Ripke, Stephan, Sanders, Alan R., Kendler, Kenneth S., Levinson, Douglas F., Sklar, Pamela, Holmans, Peter Alan, Lin, Dan-Yu, Duan, Jubao, Ophoff, Roel A., Andreassen, Ole A., Scolnick, Edward, Cichon, Sven, St. Clair, David, Corvin, Aiden, Gurling, Hugh, Werge, Thomas, Rujescu, Dan, Blackwood, Douglas H. R., Pato, Carlos N., Malhotra, Anil K., Purcell, Shaun, Dudbridge, Frank, Neale, Benjamin M., Rossin, Lizzy, Visscher, Peter M., Posthuma, Danielle, Ruderfer, Douglas M., Fanous, Ayman, Stefansson, Hreinn, Steinberg, Stacy, Mowry, Bryan J., Golimbet, Vera, De Hert, Marc, Jönsson, Erik G., Bitter, István, Pietiläinen, Olli P. H., Collier, David A., Tosato, Sarah, Agartz, Ingrid, Albus, Margot, Alexander, Madeline, Amdur, Richard L., Amin, Farooq, Bass, Nicholas, Bergen, Sarah E., Black, Donald W., Børglum, Anders D., Brown, Matthew A., Bruggeman, Richard, Buccola, Nancy G., Byerley, William F., Cahn, Wiepke, Cantor, Rita M., Carr, Vaughan J., Catts, Stanley V., Choudhury, Khalid, Cloninger, C Robert, Cormican, Paul, Craddock, Nicholas John, Danoy, Patrick A., Datta, Susmita, de Haan, Lieuwe, Demontis, Ditte, Dikeos, Dimitris, Djurovic, Srdjan, Donnelly, Peter, Donohoe, Gary, Duong, Linh, Dwyer, Sarah Lynne, Fink-Jensen, Anders, Freedman, Robert, Freimer, Nelson B., Friedl, Marion, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Glenthøj, Birte, Godard, Stephanie, Hamshere, Marian Lindsay, Hansen, Mark, Hansen, Thomas, Hartmann, Annette M., Henskens, Frans A., Hougaard, David M., Hultman, Christina M., Ingason, Andrés, Jablensky, Assen V., Jakobsen, Klaus D., Jay, Maurice, Jürgens, Gesche, Kahn, René S., Keller, Matthew C., Kenis, Gunter, Kenny, Elaine, Kim, Yunjung, Kirov, George, Konnerth, Heike, Konte, Bettina, Krabbendam, Lydia, Krasucki, Robert, Lasseter, Virginia K., Laurent, Claudine, Lawrence, Jacob, Lencz, Todd, Lerer, F. Bernard, Liang, Kung-Yee, Lichtenstein, Paul, Lieberman, Jeffrey A., Linszen, Don H., Lönnqvist, Jouko, Loughland, Carmel M., Maclean, Alan W., Maher, Brion S., Maier, Wolfgang, Mallet, Jacques, Malloy, Pat, Mattheisen, Manuel, Mattingsdal, Morten, McGhee, Kevin A., McGrath, John J., McIntosh, Andrew, McLean, Duncan E., McQuillin, Andrew, Melle, Ingrid, Michie, Patricia T., Milanova, Vihra, Morris, Derek W., Mors, Ole, Mortensen, Preben B., Escott-Price, Valentina, Muglia, Pierandrea, Myin-Germeys, Inez, Nertney, Deborah A., Nestadt, Gerald, Nielsen, Jimmi, Nikolov, Ivan, Nordentoft, Merete, Norton, Nadine, Nöthen, Markus M., O'Dushlaine, Colm T., Olincy, Ann, Olsen, Line, O'Neill, F. Anthony, Ørntoft, Torben F., Owen, Michael John, Pantelis, Christos, Papadimitriou, George, Pato, Michele T., Peltonen, Leena, Petursson, Hannes, Pickard, Ben, Pimm, Jonathan, Pulver, Ann E., Puri, Vinay, Quested, Digby, Quinn, Emma M., Rasmussen, Henrik B., Réthelyi, János M., Ribble, Robert, Rietschel, Marcella, Riley, Brien P., Ruggeri, Mirella, Schall, Ulrich, Schulze, Thomas G., Schwab, Sibylle G., Scott, Rodney J., Shi, Jianxin, Sigurdsson, Engilbert, Silverman, Jeremy M., Spencer, Chris C. A., Stefansson, Kari, Strange, Amy, Strengman, Eric, Stroup, T. Scott, Suvisaari, Jaana, Terenius, Lars, Thirumalai, Srinivasa, Thygesen, Johan H., Timm, Sally, Toncheva, Draga, van den Oord, Edwin, van Os, Jim, van Winkel, Ruud, Veldink, Jan, Walsh, Dermot, Wang, August G., Wiersma, Durk, Wildenauer, Dieter B., Williams, Hywel John, Williams, Nigel Melville, Wormley, Brandon, Zammit, Stanley, Sullivan, Patrick F., O'Donovan, Michael Conlon, Daly, Mark J. and Gejman, Pablo V. 2011. Genome-wide association study identifies five new schizophrenia loci [Letter]. Nature Genetics 43 (10) , pp. 969-976. 10.1038/ng.940

Williams, Nigel Melville 2011. Molecular mechanisms in 22q11 deletion syndrome. Schizophrenia Bulletin 37 (5) , pp. 882-889. 10.1093/schbul/sbr095

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, Georgieva, Lyudmila, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, Doug, Williams, Hywel and Williams, Nigel Melville 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.

Williams, Hywel John, Norton, Nadine, Dwyer, Sarah Lynne, Escott-Price, Valentina, Nikolov, Ivan, Carroll, Liam, Georgieva, Lyudmila, Williams, Nigel Melville, Morris, D. W., Quinn, E. M., Giegling, I., Ikeda, Masashi, Wood, J., Lencz, T., Hultman, C., Lichtenstein, P., Thiselton, D., Maher, B. S., Molecular Genetics of Schizophrenia Collaboration (MGS), , International Schizophrenia Consortium (ISC), , SGENE-plus, , GROUP, , Malhotra, A. K., Riley, B., Kendler, K. S., Gill, M., Sullivan, P., Sklar, P., Purcell, S., Nimgaonkar, V. L., Kirov, George, Corvin, A., Holmans, Peter ALan, Rujescu, D., Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 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, Williams, Nigel Melville, Suren, S., Giegling, I., Wilkinson, Lawrence, Owen, Michael John, O'Donovan, Michael Conlon, Rujescu, D., Thapar, Anita and Davies, William 2011. Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder. Genes Brain and Behavior 10 (3) , pp. 334-344. 10.1111/j.1601-183x.2010.00672.x

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

O'Dushlaine, C, Kenny, E, Heron, E, Donohoe, G, Gill, M, Morris, D, Corvin, A, O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila and Owen, Michael John 2011. Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry 16 (3) , pp. 286-292. 10.1038/mp.2010.7

Nalls, M. A., Plagnol, V., Hernandez, D. G., Sharma, M., Sheerin, U. M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Stefansson, K., Martinez, M., Hardy, J., Heutink, P., Brice, A., Gasser, T., Singleton, A. B., Wood, N. M., Morris, Huw, Williams, Nigel Melville and International Parkinson Disease Genomics Consortium, 2011. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet 377 (9766) , pp. 641-649. 10.1016/S0140-6736(10)62345-8

Morris, Huw Rees, Pearson, Justin P., Williams, Nigel Melville, Wickremaratchi, Mirdhu, International Parkinson's Disease Genomics Consortium (IPDGC), and Wellcome Trust Case Control Consortium (WTCCC), 2011. A two-stage meta-analysis identifies several new loci for Parkinson's Disease. PLoS Genetics 7 (6) , e1002142. 10.1371/journal.pgen.1002142
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Bridges, Michael, Heron, Elizabeth A., O'Dushlaine, Colm, Segurado, Ricardo, Morris, Derek, Corvin, Aiden, Gill, Michael, Pinto, Carlos, O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra and Owen, Michael John 2011. Genetic classification of populations using supervised learning. PLoS ONE 6 (5) , e14802. 10.1371/journal.pone.0014802
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Williams, Nigel Melville, O'Donovan, Michael Conlon, Owen, Michael John and Thapar, Anita 2011. Structural variations in attention-deficit hyperactivity disorder - Authors' reply [Letter]. The Lancet 377 (9763) , p. 378. 10.1016/S0140-6736(11)60121-9

Hamshere, Marian Lindsay, Holmans, Peter Alan, McCarthy, Geraldine, Jones, Lisa, Murphy, Kieran C., Sanders, Robert D., Gray, Marion Y., Zammit, Stanley, Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, McGuffin, Peter, O'Donovan, Michael Conlon, Craddock, Nicholas John, Owen, Michael John and Cardno, Alastair G. 2011. Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (8) , pp. 929-940. 10.1002/ajmg.b.31240

Langley, Kate, Martin, Joanna, Agha, Sharifah Shameem, Davies, Charlotte, Stergiakouli, Evangelia, Holmans, Peter Alan, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2011. Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants. British Journal of Psychiatry 199 (5) , pp. 398-403. 10.1192/bjp.bp.111.092130

Carroll, Liam Stuart, Williams, Nigel Melville, Escott-Price, Valentina, Russell, Elen, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Grozeva, Detelina Valentinova, Greene, E., Farmer, A., McGuffin, P., Morris, D. W., Corvin, A., Gill, M., Rujescu, D., Sham, P., Holmans, Peter Alan, Jones, Ian Richard, Kirov, George, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 2010. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha. Molecular Psychiatry 15 (11) , pp. 1101-1111. 10.1038/mp.2009.96

Williams, Nigel Melville, Zaharieva, Irina, Martin, Andrew Kenneth, Langley, Kate, Mantripragada, Kiran Kumar, Fossdal, Ragnheidur, Stefansson, Hreinn, Stefansson, Kari, Magnusson, Pall, Gudmundsson, Olafur O., Gustafsson, Omar, Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2010. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis. The Lancet 376 (9750) , pp. 1401-1408. 10.1016/S0140-6736(10)61109-9

Pearson, J. P., Kilarski, L. L., Newsway, V., Majounie, Elisa, Perera, D., Misbahuddin, A., Chinnery, P. F., Burn, D. J., Lewthwaite, A. J., Clarke, C. E., Morrison, K. E., Evans, J. R., Sawcer, S. J., Barker, R. A., Wickremaratchi, M. M., Williams, Nigel Melville and Morris, Huw 2010. Prevalence of mutations in Parkin, PINK1, and DJ-1 in early onset Parkinson's Disease - a community based and regional study [Conference Abstract]. Movement Disorders 25 (3) , S610-S610.

Allison, David B., Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Daly, Mark J., O'Donovan, Michael Conlon, Kirov, George, Craddock, Nicholas John, Holmans, Peter Alan, Williams, Nigel Melville, Georgieva, Lyudmila and Owen, Michael John 2010. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics 6 (9) , e1001097. 10.1371/journal.pgen.1001097

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

Hinton, Elanor Clare, Isles, Anthony Roger, Williams, Nigel Melville and Parkinson, John A. 2010. Excessive appetitive arousal in Prader–Willi syndrome. Appetite 54 (1) , pp. 225-228. 10.1016/j.appet.2009.12.002

Mantripragada, Kiran Kumar, Carroll, Liam S. and Williams, Nigel Melville 2010. Experimental approaches for identifying schizophrenia risk genes. Current Topics in Behavioral Neuroscience 4 , pp. 587-610. 10.1007/7854_2010_58

Ikeda, Masashi, Williams, Nigel Melville, Williams, Hywel John, Smith, Rhodri, Monks, Stephen, Owen, Michael John, Murphy, Kieran C. and O'Donovan, Michael Conlon 2010. Failure to confirm association between PIK4CA and psychosis in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 980-982. 10.1002/ajmg.b.31060

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard, Langley, Kate, O'Donovan, Michael Conlon, Williams, Nigel Melville, Owen, Michael John, Thapar, Anita, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, Roger, Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A, Brown, M. A., Burn, D., Casas, J.-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, Nicholas John, Deloukas, P., Edkins, S., Evans, J., Freeman, C., Gray, E., Hardy, J., Hudson, G., Hunt, S., Jankowski, J., Langford, C., Lees, A. J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Morrison, K. E., Palmer, C. N. A., Pearson, J. P., Peltonen, L., Pirinen, M., Plomin, R., Potter, S., Rautanen, A., Sawcer, S. J., Su, Z., Trembath, R. C., Viswanathan, A. C., Williams, Nigel Melville, Morris, Huw Rees, Donnelly, Peter and Wood, N. W. 2010. Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics 20 (2) , pp. 345-353. 10.1093/hmg/ddq469

Liu, Yang, Chen, Gang, Norton, Nadine, Liu, Wenmin, Zhu, Haining, Zhou, Peng, Luan, Meng, Yang, Shulin, Chen, Xing, Carroll, Liam, Williams, Nigel Melville, O'Donovan, Michael Conlon, Kirov, George and Owen, Michael John 2009. Whole genome association study in a homogenous population in Shandong Peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Journal of Biomedicine and Biotechnology , 536918. 10.1155/2009/536918

Ng, M Y M, Levinson, D F, Faraone, S V, Suarez, B K, DeLisi, L E, Arinami, T, Riley, B, Paunio, T, Pulver, A E, Irmansyah, , Holmans, Peter Alan, Escamilla, M, Wildenauer, D B, Williams, Nigel Melville, Laurent, C, Mowry, B J, Brzustowicz, L M, Maziade, M, Sklar, P, Garver, D L, Abecasis, G R, Lerer, B, Fallin, M D, Gurling, H M D, Gejman, P V, Lindholm, E, Moises, H W, Byerley, W, Wijsman, E M, Forabosco, P, Tsuang, M T, Hwu, H-G, Okazaki, Y, Kendler, K S, Wormley, B, Fanous, A, Walsh, D, O'Neill, F A, Peltonen, L, Nestadt, G, Lasseter, V K, Liang, K Y, Papadimitriou, G M, Dikeos, D G, Schwab, S G, Owen, Michael John, O'Donovan, Michael Conlon, Norton, N, Hare, E, Raventos, H, Nicolini, H, Albus, M, Maier, W, Nimgaonkar, V L, Terenius, L, Mallet, J, Jay, M, Godard, S, Nertney, D, Alexander, M, Crowe, R R, Silverman, J M, Bassett, A S, Roy, M-A, Mérette, C, Pato, C N, Pato, M T, Roos, J Louw, Kohn, Y, Amann-Zalcenstein, D, Kalsi, G, McQuillin, A, Curtis, D, Brynjolfson, J, Sigmundsson, T, Petursson, H, Sanders, A R, Duan, J, Jazin, E, Myles-Worsley, M, Karayiorgou, M and Lewis, C M 2009. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Molecular Psychiatry 14 (8) , pp. 774-785. 10.1038/mp.2008.135

Holmans, Peter Alan, Riley, B., Pulver, A. E., Owen, Michael John, Wildenauer, D. B., Gejman, P. V., Mowry, B. J., Laurent, C., Kendler, K. S., Nestadt, G., Williams, Nigel Melville, Schwab, S. G., Sanders, A. R., Nertney, D., Mallet, J., Wormley, B., Lasseter, V. K., O'Donovan, Michael Conlon, Duan, J., Albus, M., Alexander, M., Godard, S., Ribble, R., Liang, K. Y., Norton, Nadine, Maier, W., Papadimitriou, G., Walsh, D., Jay, M., O'Neill, A., Lerer, F. B., Dikeos, D., Crowe, R. R., Silverman, J. M. and Levinson, D. F. 2009. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Molecular Psychiatry 14 (8) , pp. 786-795. 10.1038/mp.2009.11

O'Donovan, Michael Conlon, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan, Marchini, J. L., Spencer, C. C. A., Howie, B., Leung, H.T., Giegling, I., Hartmann, A. M., Möller, H.J., Morris, D. W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, Stanley, Schumacher, J., Quinn, E. M., Schulze, T. G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A. R., Levinson, D. F., Adolfsson, R., Ösby, U., Terenius, L, Jönsson, E. G., Cichon, S., Nöthen, M. M., Gill, M., Corvin, A. P., Rujescu, D., Gejman, P. V., Kirov, George, Craddock, Nicholas John, Williams, Nigel Melville and Owen, Michael John 2009. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Molecular Psychiatry 14 (1) , pp. 30-36. 10.1038/mp.2008.108

Purcell, Shaun M., Wray, Naomi R., Stone, Jennifer L., Visscher, Peter M., O'Donovan, Michael Conlon, Sullivan, Patrick F., Sklar, Pamela, Ruderfer, Douglas M., McQuillin, Andrew, Morris, Derek W., O'Dushlaine, Colm T., Corvin, Aiden, Holmans, Peter Alan, Macgregor, Stuart, Gurling, Hugh, Blackwood, Douglas H. R., Craddock, Nicholas John, Gill, Michael, Hultman, Christina M., Kirov, George, Lichtenstein, Paul, Muir, Walter J., Owen, Michael John, Pato, Carlos N., Scolnick, Edward M., St Clair, David, Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Quinn, Emma M., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Crombie, Caroline, Fraser, Gillian, Leh Kuan, Soh, Walker, Nicholas, McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Helena Azevedo, M., Kirby, Andrew N., Ferreira, Manuel A. R., Daly, Mark J., Chambert, Kimberly, Kuruvilla, Finny, Gabriel, Stacey B., Ardlie, Kristin, Moran, Jennifer L. and Daly, Mark J. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460 (7256) , pp. 748-752. 10.1038/nature08185

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

Carroll, Liam Stuart, Kendall, Kimberley, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Nigel Melville 2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7) , pp. 893-899. 10.1002/ajmg.b.30915

Dwyer, Sarah Lynne, Carroll, Liam Stuart, Mantripragada, Kiran Kumar, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Nigel Melville 2009. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (3) , pp. 766-774. 10.1002/ajmg.b.31045

Wardle, Mark, Majounie, Elisa, Muzaimi, Mustapha B., Williams, Nigel Melville, Morris, Huw Rees and Robertson, Neil 2009. The genetic aetiology of late-onset chronic progressive cerebellar ataxia. Journal of Neurology 256 (3) , pp. 343-348. 10.1007/s00415-009-0015-2

Gerrish, Amy, Williams, Hywel John, Escott-Price, Valentina, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Nigel Melville 2009. An examination of MUTED as a schizophrenia susceptibility gene [Letter]. Schizophrenia Research 107 (1) , pp. 110-111. 10.1016/j.schres.2008.08.011

Georgieva, Lyudmila, Dimitrova, Albena, Ivanov, Dobril Kirilov, Nikolov, Ivan, Williams, Nigel Melville, Grozeva, Detelina Valentinova, Zaharieva, Irina Takova, Toncheva, Draga, Owen, Michael John, Kirov, George and O'Donovan, Michael Conlon 2008. Support for Neuregulin 1 as a susceptibility gene for Bipolar disorder and schizophrenia. Biological psychiatry 64 (5) , pp. 419-427. 10.1016/j.biopsych.2008.03.025

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

Williams, Nigel Melville, Williams, Hywel John, Majounie, Elisa, Norton, Nadine, Glaser, Beate, Morris, Huw Rees, Owen, Michael John and O'Donovan, Michael Conlon 2008. Analysis of copy number variation using quantitative interspecies competitive PCR. Nucleic Acids Research 36 (17) , e112-e112. 10.1093/nar/gkn495

Stone, Jennifer L., O'Donovan, Michael Conlon, Gurling, Hugh, Kirov, George, Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nicholas John, Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael John, St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M., Korn, Joshua, Macgregor, Stuart, Morris, Derek W., O'Dushlaine, Colm T., Daly, Mark J., Visscher, Peter M., Holmans, Peter Alan, Scolnick, Edward M., Williams, Nigel Melville, Georgieva, Lyudmila, Nikolov, Ivan, Norton, Nadine, Williams, Hywel John, Toncheva, Draga, Milanova, Vihra, Thelander, Emma F., Kenny, Elaine, Waddington, John L., Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan, Thirumalai, Srinivasa, Puri, Vinay, Krasucki, Robert, Lawrence, Jacob, Quested, Digby, Bass, Nicholas, Curtis, David, Crombie, Caroline, Fraser, Gillian, Leh Kwan, Soh, Walker, Nicholas, Muir, Walter J., McGhee, Kevin A., Pickard, Ben, Malloy, Pat, Maclean, Alan W., Van Beck, Margaret, Pato, Michele T., Medeiros, Helena, Middleton, Frank, Carvalho, Celia, Morley, Christopher, Fanous, Ayman, Conti, David, Knowles, James A., Paz Ferreira, Carlos, Macedo, Antonio, Azevedo, M. Helena, McCarroll, Steve A., Daly, Mark, Chambert, Kimberly, Gates, Casey, Gabriel, Stacey B., Mahon, Scott and Ardlie, Kristen 2008. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455 (7210) , pp. 237-241. 10.1038/nature07239

Wardle, M, Majounie, Elisa, Williams, Nigel Melville, Rosser, Anne Elizabeth, Morris, Huw Rees and Robertson, Neil 2008. Dentatorubral pallidoluysian atrophy in South Wales. Journal of Neurology, Neurosurgery and Psychiatry 79 (7) , pp. 804-807. 10.1136/jnnp.2007.128074

O'Donovan, Michael Conlon, Craddock, Nicholas John, Norton, Nadine, Williams, Hywel John, Peirce, Timothy Rowan, Escott-Price, Valentina, Nikolov, Ivan, Hamshere, Marian Lindsay, Carroll, Liam Stuart, Georgieva, Lyudmila, Dwyer, Sarah Lynne, Holmans, Peter Alan, Marchini, Jonathan L, Spencer, Chris C A, Howie, Bryan, Leung, Hin-Tak, Hartmann, Annette M, Möller, Hans-Jürgen, Morris, Derek W, Shi, YongYong, Feng, GuoYin, Hoffmann, Per, Propping, Peter, Vasilescu, Catalina, Maier, Wolfgang, Rietschel, Marcella, Zammit, Stanley, Schumacher, Johannes, Quinn, Emma M, Schulze, Thomas G, Williams, Nigel Melville, Giegling, Ina, Iwata, Nakao, Ikeda, Masashi, Darvasi, Ariel, Shifman, Sagiv, He, Lin, Duan, Jubao, Sanders, Alan R, Levinson, Douglas F, Gejman, Pablo V, Gejman, Pablo V, Sanders, Alan R, Duan, Jubao, Levinson, Douglas F, Buccola, Nancy G, Mowry, Bryan J, Freedman, Robert, Amin, Farooq, Black, Donald W, Silverman, Jeremy M, Byerley, William F, Cloninger, C Robert, Cichon, Sven, Nöthen, Markus M, Gill, Michael, Corvin, Aiden, Rujescu, Dan, Kirov, George and Owen, Michael John 2008. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nature Genetics 40 (9) , pp. 1053-1055. 10.1038/ng.201

Bray, Nicholas John, Holmans, Peter Alan, van den Bree, Marianne Bernadette, Jones, Lesley, Elliston, Linda Anne, Hughes, Gareth, Richards, Alexander, Williams, Nigel Melville, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2008. Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Human Molecular Genetics 17 (8) , pp. 1169-1174. 10.1093/hmg/ddn006

Nair, S., Phillips, Aled Owain, Norton, Nadine, Spurlock, Gillian, Williams, Hywel John, Craig, Kathrine Jane, Williams, John David, Williams, Nigel Melville and Bowen, Timothy 2008. Further evidence for the association of MMP9 with nephropathy in type 2 diabetes and application of DNA pooling technology to candidate gene screening. Journal of Nephology 21 (3) , pp. 400-405.

Williams, Hywel, Norton, Nadine, Peirce, Tim, Dwyer, Sarah, Williams, Nigel Melville, Escott-Price, Valentina, Owen, Michael John and O'Donovan, Michael Conlon 2007. Association analysis of the glial cell line-derived neurotrophic factor (GDNF) gene in schizophrenia. Schizophrenia Research 97 (1-3) , pp. 271-276. 10.1016/j.schres.2007.09.004

Majounie, Elisa, Wardle, Mark, Muzaimi, M., Cross, W. C., Robertson, Neil, Williams, Nigel Melville and Morris, Huw Rees 2007. Case control analysis of repeat expansion size in ataxia. Neuroscience Letters 429 (1) , pp. 28-32. 10.1016/j.neulet.2007.09.055

Williams, Nigel Melville, Glaser, Beate, Norton, Nadine, Williams, Hywel John, Pierce, Timothy, Escott-Price, Valentina, Monks, Stephen, Del Favero, Jurgen, Goossens, Dirk, Rujescu, Dan, Kirov, George, Craddock, Nicholas John, Murphy, Kieran Christopher, O'Donovan, Michael Conlon and Owen, Michael John 2007. Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics 17 (4) , pp. 555-566. 10.1093/hmg/ddm330

Zammit, Stanley, Spurlock, Gillian, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2007. Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. British Journal of Psychiatry 191 (5) , pp. 402-407. 10.1192/bjp.bp.107.036129

Sutrala, Smitha, Goossens, Dirk, Williams, Nigel Melville, Heyrman, Lien, Adolfsson, Rolf, Norton, Nadine, Buckland, Paul Robert and Del-Favero, Jurgen 2007. Gene copy number variation in schizophrenia. Schizophrenia Research 96 (1-3) , pp. 93-99. 10.1016/j.schres.2007.07.029

Norton, Nadine, Williams, Hywel J., Dwyer, Sarah, Carroll, Liam, Peirce, Tim, Escott-Price, Valentina, Segurado, Ricardo, Nikolov, Ivan, Williams, Nigel Melville, Ikeda, Masashi, Iwata, Nakao, Owen, Michael John and O'Donovan, Michael Conlon 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, Holmans, Peter Alan, Zammit, Stanley, Williams, Nigel Melvillle, Escott-Price, Valentina, Kirov, George, Craddock, Nicholas John, Bray, Nicholas John and Owen, Michael John 2007. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia [Conference Abstract]. Schizophrenia bulletin 33 (2) , pp. 311-312. 10.1093/schbul/sbm004

Glaser, Beate, Escott-Price, Valentina, Kirov, George, Murphy, Kieran C., Williams, Hywel, Williams Melville, Nigel, Owen, Michael John and O'Donovan, Michael Conlon 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, Holmans, Peter Alan, van Den Bree, Marianne Bernadette, Williams, Nigel Melville, Jones, Lesley, Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 2006. Cis- and trans-acting loci influence expression of DTNBP1, a susceptibility gene for schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 723-724.

Georgieva, Lyudmila, Escott-Price, Valentina, Peirce, Timothy Rowan, Norton, Nadine, Bray, Nicholas John, Jones, Lesley, Holmans, Peter Alan, Macgregor, Stuart, Zammit, Stanley, Wilkinson, Jennifer Camilla, Williams, Hywel John, Nikolov, Ivan, Williams, Nigel Melville, Ivanov, Dobril Kirilov, Davis, Kenneth L., Haroutunian, Vahram, Buxbaum, Joseph D., Craddock, Nicholas John, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2006. Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America (PNAS) ISSN 1091-6490 103 (33) , pp. 12469-12474. 10.1073/pnas.0603029103

Talkowski, Michael E., Seltman, Howard, Bassett, Anne S., Brzustowicz, Linda M., Chen, Xiangning, Chowdari, Kodavali V., Collier, David A., Cordeiro, Quirino, Corvin, Aiden P., Deshpande, Smita N., Egan, Michael F., Gill, Michael, Kendler, Kenneth S., Kirov, George, Heston, Leonard L., Levitt, Pat, Lewis, David A., Li, Tao, Mirnics, Karoly, Morris, Derek W., Norton, Nadine, O'Donovan, Michael Conlon, Owen, Michael John, Richard, Christian, Semwal, Prachi, Sobell, Janet L., St Clair, David, Straub, Richard E., Thelma, B.K., Vallada, Homero, Weinberger, Daniel R., Williams, Nigel Melville, Wood, Joel, Zhang, Feng, Devlin, Bernie and Nimgaonkar, Vishwajit L. 2006. Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological psychiatry 60 (2) , pp. 152-162. 10.1016/j.biopsych.2006.02.015

Paylor, R., Glaser, B., Mupo, A., Ataliotis, P., Spencer, C., Sobotka, A., Sparks, C., Choi, C.-H., Oghalai, J., Curran, S., Murphy, K. C., Monks, S., Williams, Nigel Melville, O'Donovan, Michael Conlon, Owen, Michael John, Scambler, P. J. and Lindsay, E. 2006. Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome. Proceedings of the National Academy of Sciences of the United States of America 103 (20) , pp. 7729-7734. 10.1073/pnas.0600206103

Williams, Nigel Melville, Green, Elaine Karen, Dwyer, Sarah Lynne, Macgregor, Stuart, Norton, Nadine, Williams, Hywel John, Raybould, Rachel, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay, Zammit, Stanley, Jones, Lisa Anne, Cardno, Alastair George, Kirov, George, Jones, Ian Richard, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 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

Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2006. Chromosome 22 deletion syndrome and schizophrenia. International Review of Neurobiology 73 , pp. 1-27. 10.1016/S0074-7742(06)73001-X

Peirce, Timothy Rowan, Bray, Nicholas John, Williams, Nigel Melville, Norton, Nadine, Escott-Price, Valentina, Preece, Anna Charlotte, Haroutunian, Vahram, Buxbaum, Joseph D., Owen, Michael John and O'Donovan, Michael Conlon 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

Peirce, TR, Bray, Nicholas John, Williams, Nigel Melville, Norton, N, Escott-Price, Valentina, Preece, Anna, Haroutunian, V, Buxbaum, JD, Owen, Michael John and O'Donovan, Michael Conlon 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, Escott-Price, Valentina, Morris, Derek W., Bray, Nicholas John, Zammit, Stanley, Williams, Nigel Melville, Williams, Hywel John, Preece, Anna Charlotte, Dwyer, Sarah, Wilkinson, Jennifer C., Spurlock, Gillian, Kirov, George, Buckland, Paul Robert, Waddington, John L., Gill, Michael, Corvin, Aiden P., Owen, Michael John and O'Donovan, Michael John 2006. Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (1) , pp. 96-101. 10.1002/ajmg.b.30236

Hamshere, Marian Lindsay, Williams, Nigel Melville, Norton, Nadine, Williams, H., Cardno, Alastair G., Zammit, Stanley, Jones, L. A., Murphy, K. C., Sanders, Rebecca, McCarthy, G., Gray, M. Y., Jones, G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 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

Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2005. Is the dysbindin gene (DTNBP1) a susceptibility gene for schizophrenia? Schizophrenia Bulletin 31 (4) , pp. 800-805. 10.1093/schbul/sbi061

Hamshere, Marian Lindsay, Bennett, Philip, Williams, Nigel Melville, Segurado, Ricardo, Cardno, Alastair George, Norton, Nadine, Lambert, David, Williams, Hywel John, Kirov, George, Corvin, Aiden, Holmans, Peter Alan, Jones, Lisa Anne, Jones, Ian Richard, Gill, Michael, O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 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, H. J., Glaser, B., Williams, Nigel Melville, Norton, N., Zammit, Stanley, MacGregor, S., Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2005. No association between schizophrenia and polymorphisms in COMT in two large samples. American Journal of Psychiatry 162 (9) , pp. 1736-1738. 10.1176/appi.ajp.162.9.1736

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

Turic, D., Langley, Kate, Williams, H., Norton, N., Williams, Nigel Melville, Escott-Price, Valentina, van den Bree, Marianne Bernadette, Owen, Michael John, Thapar, Anita and O'Donovan, Michael Conlon 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

Green, Elaine Karen, Raybould, Rachel, Macgregor, Stuart, Gordon-Smith, Katherine Mary, Heron, Jess, Hyde, Sally, Grozeva, Detelina Valentinova, Hamshere, Marian Lindsay, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon, Jones, Lisa Anne, Jones, Ian Richard, Kirov, George and Craddock, Nicholas John 2005. Operation of the schizophrenia susceptibility gene, neuregulin 1, across traditional diagnostic boundaries to increase risk for bipolar disorder. Archives of general psychiatry 62 (6) , pp. 642-648. 10.1001/archpsyc.62.6.642

Norton, Nadine, Williams, Hywel, Dwyer, Sarah, Ivanov, D., Preece, Anna, Gerrish, Amy, Williams, Nigel Melville, Yerassimou, P., Zammit, Stanley, O'Donovan, Michael Conlon and Owen, Michael John 2005. No evidence for association between polymorphisms in GRM3 and schizophrenia. BMC Psychiatry 5 , p. 23. 10.1186/1471-244X-5-23

Holmans, Peter Alan, Hamshere, Marian Lindsay, Hollingworth, P., Rice, Frances, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon, Jones, Lesley, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John and Williams, Julie 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114

Bray, Nicholas John, Preece, Anna Charlotte, Williams, Nigel Melville, Escott-Price, Valentina, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2005. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Human Molecular Genetics 14 (14) , pp. 1947-1954. 10.1093/hmg/ddi199

Escott-Price, Valentina, Norton, Nadine, Williams, Nigel Melville, Holmans, Peter Alan, Owen, Michael John and O'Donovan, Michael Conlon 2005. Streamlined analysis of pooled genotype data in SNP-based association studies. Genetic Epidemiology 28 (3) , pp. 273-282. 10.1002/gepi.20062

Raybould, Rachel, Green, Elaine K., MacGregor, Stuart, Gordon-Smith, Katherine, Heron, Jess, Hyde, Sally, Caesar, Sian, Nikolov, Ivan, Williams, Nigel Melville, Jones, Lisa, O'Donovan, Michael Conlon, Owen, Michael John, Jones, Ian Richard, Kirov, George and Craddock, Nicholas John 2005. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biological psychiatry 57 (7) , pp. 696-701. 10.1016/j.biopsych.2005.01.018

Bray, Nicholas John, Preece, Anna, Escott-Price, Valentina, Williams, Nigel Melville, Williams, HJ, Norton, N, Wilkinson, J, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 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, Williams, Nigel Melville, Haroutunian, V., Buxbaum, J., Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2004. Convergent functional genomics, association and linkage analysis suggests 2 ',3 '-cyclic nucleotide 3 '-phosphodiesterase (CNP) as a potential susceptibility gene for schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 81. 10.1002/ajmg.b.30101

Norton, N, Escott-Price, Valentina, Morris, DW, Bray, Nicholas John, Zammit, Stanley, Williams, Nigel Melville, Williams, HJ, Preece, Anna, Dwyer, SL, Wilkinson, JC, Kirov, George, Buckland, Paul Robert, Waddington, JL, Gill, M, Corvin, AP, Owen, Michael John and O'Donovan, Michael Conlon 2004. Interaction between neuregulin 1 and its receptor ERBB4 increases susceptibility to schizophrenia [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 18.

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

Morris, D.W., Ivanov, D., Robinson, L., Williams, Nigel Melville, Stevenson, J., Owen, Michael John, Williams, J. and O'Donovan, Michael Conlon 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 129B (1) , pp. 97-103. 10.1002/ajmg.b.30033

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

Kirov, George, Ivanov, Dobril Kirilov, Williams, Nigel Melville, Preece, Anna Charlotte, Nikolov, Ivan, Milev, Radoi, Koleva, Svetlinka, Dimitrova, Albena, Toncheva, Draga, O'Donovan, Michael Conlon and Owen, Michael John 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, Williams, Nigel Melville, Martin, John, Coleman, Sharon Louise, Topley, Nicholas, Spicer, Andrew P., Buckland, Paul Robert, Davies, Malcolm and Bowen, Timothy 2004. Identification and analysis of the promoter region of the human hyaluronan synthase 2 gene. The Journal of Biological Chemistry 279 (20) , pp. 20576-20581. 10.1074/jbc.M312666200

Owen, Michael John, Williams, Nigel Melville and O'Donovan, Michael Conlon 2004. Dysbindin-1 and schizophrenia: from genetics to neuropathology. The Journal of Clinical Investigation 113 (9) , pp. 1255-1257. 10.1172/JCI200421470

Williams, Nigel Melville, Preece, Anna, Mortis, DW, Spurlock, Gillian, Bray, Nicholas John, Stephens, M, Norton, N, Williams, H, Clement, M, Dwyer, S, Curran, C, Wilkinson, J, Escott-Price, Valentina, Waddington, JL, Gill, M, Corvin, AP, Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2004. Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). Archives of General Psychiatry 61 (4) , pp. 336-344. 10.1001/archpsyc.61.4.336

Williams, Nigel Melville, Preece, Anna Charlotte, Spurlock, Gillian, Norton, Nadine, Williams, Hywel John, McCreadie, Robin G, Buckland, Paul Robert, Sharkey, Val, Chowdari, Kodavali V., Zammit, Stanley, Nimgaonkar, Vishwajit, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2004. Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55 (2) , pp. 192-195. 10.1016/j.biopsych.2003.11.002

Williams, Nigel Melville, Preece, Anna Charlotte, Morris, D. W., Spurlock, Gillian, Bray, Nicholas John, Stephens, Mark Keith, Norton, Nadine, Williams, Hywel John, Clement, Mathew, Dwyer, Sarah Lynne, Curran, Catherine, Wilkinson, Jennifer Camilla, Escott-Price, Valentina, Waddington, J. L., Gill, M., Corvin, A. P., Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 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, Williams, Nigel Melville and O'Donovan, Michael Conlon 2004. The molecular genetics of schizophrenia: new findings promise new insights. Molecular Psychiatry 9 (1) , pp. 14-27. 10.1038/sj.mp.4001444

Norton, Nadine, Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 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

Turic, Dragana, Langley, Kate, Mills, S., Stephens, M., Lawson, D., Govan, Catherine, Williams, Nigel Melville, van den Bree, Marianne Bernadette, Craddock, Nicholas John, Kent, L., Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2004. Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD. Molecular Psychiatry 9 (2) , pp. 169-173. 10.1038/sj.mp.4001387

Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, Ekholm, B., Hamshere, Marian Lindsay, Lindblom, Y., Chowdari, K. V., Cardno, Alastair George, Zammit, Stanley, Jones, Lisa Anne, Murphy, Kieran Christopher, Sanders, Robert David, McCarthy, Geraldine MaryTeresa, Gray, Marion Yvonne, Jones, G., Holmans, Peter Alan, Nimgaonkar, V., Adolfson, R., Osby, U., Terenius, L., Sedvall, G., O'Donovan, Michael Conlon and Owen, Michael John 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 Kirilov, Kirov, George, Norton, Nadine, Williams, Hywel John, Williams, Nigel Melville, Nikolov, Ivan, Tzwetkova, R., Stambolova, S. M., Murphy, Kieran Christopher, Toncheva, Draga, Thapar, Anita, O'Donovan, Michael Conlon and Owen, Michael John 2003. Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis. The British Journal of Psychiatry 183 (5) , pp. 409-413. 10.1192/bjp.183.5.409

O'Donovan, Michael Conlon, Williams, Nigel Melville and Owen, Michael John 2003. Recent advances in the genetics of schizophrenia. Human Molecular Genetics 12 (suppl) , R125-R133. 10.1093/hmg/ddg302

Kirov, George, Georgieva, Lyudmila, Williams, Nigel Melville, Nikolov, Ivan, Norton, Nadine, Toncheva, Draga, O'Donovan, Michael Conlon and Owen, Michael John 2003. Variation in the protocadherin - A gene cluster? Genomics 82 (4) , pp. 433-440. 10.1016/S0888-7543(03)00167-8

Monslow, Jamie, Williams, John David, Norton, Nadine, Guy, Carol, Price, Iain Kelsey, Coleman, Sharon Louise, Williams, Nigel Melville, Buckland, Paul Robert, Spicer, Andrew P., Topley, Nicholas, Davies, Malcolm and Bowen, Timothy 2003. The human hyaluronan synthase genes: genomic structures, proximal promoters and polymorphic microsatellite markers. The International Journal of Biochemistry & Cell Biology 35 (8) , pp. 1272-1283. 10.1016/S1357-2725(03)00048-7

Norton, N., Williams, H.J., Williams, Nigel Melville, Spurlock, G., Zammit, Stanley, Jones, G., Jones, S., Owen, R., O'Donovan, Michael Conlon and Owen, Michael John 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

Williams, H.J., Williams, Nigel Melville, Spurlock, G., Norton, N., Zammit, Stanley, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 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, Nigel Melville, Spurlock, G, Norton, N, Ivanov, D, McCreadie, R G, Preece, A, Sharkey, V, Jones, S, Zammit, Stanley, Nikolov, I, Kehaiov, I, Thapar, Anita, Murphy, K C, Kirov, George, Owen, Michael John and O'Donovan, Michael Conlon 2003. Association between PRODH and schizophrenia is not confirmed. Molecular Psychiatry 8 (7) , pp. 644-645. 10.1038/sj.mp.4001276

Lewis, Cathryn M., Levinson, Douglas F., Wise, Lesley H., DeLisi, Lynn E., Straub, Richard E., Hovatta, Iiris, Williams, Nigel Melville, Schwab, Sibylle G., Pulver, Ann E., Faraone, Stephen V., Brzustowicz, Linda M., Kaufmann, Charles A., Garver, David L., Gurling, Hugh M.D., Lindholm, Eva, Coon, Hilary, Moises, Hans W., Byerley, William, Shaw, Sarah H., Mesen, Andrea, Sherrington, Robin, O'Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S., Ekelund, Jesper, Paunio, Tiina, Lönnqvist, Jouko, Peltonen, Leena, O'Donovan, Michael Conlon, Owen, Michael John, Wildenauer, Dieter B., Maier, Wolfgang, Nestadt, Gerald, Blouin, Jean-Louis, Antonarakis, Stylianos E., Mowry, Bryan J., Silverman, Jeremy M., Crowe, Raymond R., Cloninger, C. Robert, Tsuang, Ming T., Malaspina, Dolores, Harkavy-Friedman, Jill M., Svrakic, Dragan M., Bassett, Anne S., Holcomb, Jennifer, Kalsi, Gursharan, McQuillin, Andrew, Brynjolfson, Jon, Sigmundsson, Thordur, Petursson, Hannes, Jazin, Elena, Zoëga, Tomas and Helgason, Tomas 2003. Genome scan meta-analysis of schizophrenia and bipolar disorder, Part II: schizophrenia. American Journal of Human Genetics 73 (1) , pp. 34-48. 10.1086/376549

Rahman, Nazneen, Dunstan, Melanie, Teare, M. Dawn, Hanks, Sandra, Douglas, Jenny, Coleman, Kim, Bottomly, William E., Campbell, Mary E., Berglund, Britta, Nordenskjöld, Magnus, Forssell, Bengt, Burrows, Nigel, Lunt, Peter, Young, Ian, Williams, Nigel Melville, Bignell, Graham R., Futreal, P. Andrew and Pope, F. Michael 2003. Ehlers-Danlos sndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13. The American Journal of Human Genetics 73 (1) , pp. 198-204. 10.1086/376416

Bray, Nicholas John, Buckland, Paul Robert, Williams, Nigel Melville, Williams, Hywel John, Norton, Nadine, Owen, Michael John and O'Donovan, Michael Conlon 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, Nigel Melville, Preece, A, Spurlock, G, Norton, N, Williams, H J, Zammit, Stanley, O'Donovan, Michael Conlon and Owen, Michael John 2003. Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia. Molecular Psychiatry 8 (5) , pp. 485-487. 10.1038/sj.mp.4001348

Jordan, Nicola, Williams, Nigel Melville, Gregory, John Welbourn, Evans, C., Owen, Michael John and Ludgate, Marian Elizabeth 2003. The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population. Journal of Clinical Endocrinology & Metabolism 88 (3) , pp. 1002-5. 10.1210/jc.2002-021301

Turic, D, Robinson, L, Duke, M, Morris, D W, Webb, V, Hamshere, Marian Lindsay, Milham, C, Hopkin, E, Pound, K, Fernando, S, Grierson, A, Easton, M, Williams, Nigel Melville, van den Bree, Marianne Bernadette, Chowdhury, R, Gruen, J, Stevenson, J, Krawczak, M, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Julie 2003. Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. Molecular Psychiatry 8 (2) , pp. 176-185. 10.1038/sj.mp.4001216

McEntagart, M, Dunstan, Melanie, Bell, C, Boltshauser, E, Donaghy, M, Harper, Peter, Williams, Nigel Melville, Teare, M. D. and Rahman, N 2002. Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. Journal of Neurology, Neurosurgery & Psychiatry 73 (6) , p. 762. 10.1136/jnnp.73.6.762

Bray, Nicholas John, Buckland, Paul Robert, Williams, Hywel, Norton, Nadine, Williams, Nigel Melville, Owen, Michael John and O'Donovan, Michael Conlon 2002. Detection of cis-acting polymorphisms and epigenetic modification affecting gene expression [Conference Abstracts]. American Journal of Medical Genetics 114 (7) , p. 750. 10.1002/ajmg.10971

Rahman, Nazneen, Dunstan, Melanie, Teare, M. Dawn, Hanks, Sandra, Edkins, Sarah J., Hughes, Jaime, Bignell, Graham R., Mancini, Grazia, Kleijer, Wim, Campbell, Mary, Keser, Gokhan, Black, Carol, Williams, Nigel Melville, Arbour, Laura, Warman, Matthew, Superti-Furga, Andrea, Futreal, P. Andrew and Pope, F. Michael 2002. The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21. The American Journal of Human Genetics 71 (4) , pp. 975-980. 10.1086/342776

Richards, A. J., Morgan, J., Bearcroft, P. W. P., Pickering, E., Owen, Michael John, Holmans, Peter Alan, Williams, Nigel Melville, 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, Zammit, Stanley, Jones, Gaynor, Jones, Susan, Owen, Richard, Krawczak, Michael, Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2002. Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis. American Journal of Medical Genetics 114 (5) , pp. 491-496. 10.1002/ajmg.10517

Norton, Nadine, Williams, Nigel Melville, Williams, Hywel J., Spurlock, Gillian, Kirov, George, Morris, Derek W., Hoogendoorn, Bastiaan, Owen, Michael John and O'Donovan, Michael Conlon 2002. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Human Genetics 110 (5) , pp. 471-478. 10.1007/s00439-002-0706-6

Levinson, Douglas. F., Holmans, Peter Alan, Laurent, Claudine, Riley, Brien, Pulver, Ann E., Gejman, Pablo V., Schwab, Sibylle G., Williams, Nigel Melville, Owen, Michael John, Wildenauer, Dieter B., Sanders, Alan R., Nestadt, Gerald, Mowry, Brian J., Wormley, Brandon, Bauche, Stephanie, Soubigou, Stephane, Ribble, Robert, Nertney, Deborah A., Liang, Kung Yee, Martinolich, Laura, Maier, Wolfgang, Norton, Nadine, Williams, Hywel John, Albus, Margot, Carpenter, Eric B., DeMarchi, Nicola, Ewen-White, Kelly R., Walsh, Dermot, Jay, Maurice, Deleuze, Jean-Francois, O'Neill, Anthony F., Papadimitriou, George, Weilbaecher, Ann, Lerer, Bernard, O'Donovan, Michael Conlon, Dikeos, Dimitris, Silverman, Jeremy M., Kendler, Kenneth S., Mallet, Jacques, Crowe, Raymond R. and Walters, Marilyn 2002. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 296 (5568) , pp. 739-741. 10.1126/science.1069914

Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan, Hamshere, Marian Lindsay, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances, Giles, Peter, Tunstall, Nigel, Jones, Lesley, Lovestone, Simon, Williams, Julie, Owen, Michael John, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal of Medical Genetics 114 (2) , pp. 235-244. 10.1002/ajmg.10183

Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2002. Genome scans and microarrays: converging on genes for schizophrenia? Genome Biology 3 (4) , Reviews1011-Reviews1011.5.

Anney, Richard, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, Cardno, Alastair George, Zammit, Stanley, Jones, S., Jones, G., Hoogendoorn, Bastiaan, Smith, K. J., Hamshere, Marian Lindsay, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon, Owen, Michael John and Buckland, Paul Robert 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7 (5) , pp. 493-502. 10.1038/sj.mp.4001003

Williams, Nigel Melville, Spurlock, Gillian, Norton, Nadine, Williams, Hywel John, Hamshere, Marian Lindsay, Krawczak, Michael, Kirov, George, Nikolov, Ivan, Georgieva, Lyudmila, Jones, S., Cardno, Alastair George, O'Donovan, Michael Conlon and Owen, Michael John 2002. Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach. Molecular Psychiatry 7 (10) , pp. 1092-1100. 10.1038/sj.mp.4001188

Williams, Nigel Melville, Bowen, Timothy, Spurlock, Gillian, Norton, Nadine, Williams, Hywel John, Hoogendoorn, Bastiaan, Owen, Michael John and O'Donovan, Michael Conlon 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

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

Sklar, P., Schwab, S. G., Williams, Nigel Melville, Daly, M., Schaffner, S., Maier, W., Albus, M., Trixler, M., Eichhammer, P., Lerer, B., Hallmayer, J., Norton, N., Williams, H., Zammit, Stanley, Cardno, A. G., Jones, S. and McCarthy, G. 2001. Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nature Genetics 28 (2) , pp. 126-128. 10.1038/88836

Bowen, Timothy, Williams, Nigel Melville, Norton, Nadine, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John, Brzustowicz, L., Hoogendoorn, Bastiaan, Zammit, Stanley, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John and O'Donovan, Michael Conlon 2001. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation [Letter]. Molecular Psychiatry 6 (3) , pp. 259-260. 10.1038/sj.mp.4000128

McEntagart, M., Norton, N., Williams, H., Teare, M. D., Dunstan, Melanie, Baker, P., Houlden, H., Reilly, M., Wood, N., Harper, P. S., Futreal, P. A., Williams, Nigel Melville and Rahman, N. 2001. Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. American Journal of Human Genetics 68 (5) , pp. 1270-1276. 10.1086/320122

Austin, J., Buckland, Paul Robert, Cardno, Alastair G., Williams, Nigel Melville, Spurlock, Gillian, Hoogendoorn, Bastiaan, Zammit, Stanley, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John, McGuffin, Peter, Owen, Michael John and O'Donovan, Michael Conlon 2000. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry 5 (5) , pp. 552-557. 10.1038/sj.mp.4000761

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

Murphy, K. C., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Holmans, Peter Alan, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Walters, S. E., Williams, Nigel Melville, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John 2000. Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia. American Journal of Medical Genetics 96 (4) , p. 535.

Bray, Nicholas John, Williams, Nigel Melville, Bowen, Timothy, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon and Owen, Michael John 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, Williams, Nigel Melville, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John, O'Donovan, Michael and Williams, Julie 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843

Austin, J., Hoogendoorn, Bastiaan, Buckland, Paul Robert, Jones, Ian Richard, McCandless, F., Williams, Nigel Melville, Middle, F., Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1) , pp. 51-54. 10.1097/00041444-200010010-00009

Austin, J., Hoogendoorn, Bastiaan, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy, Williams, Nigel Melville, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693

Kirov, George, Stephens, M., Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 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, Williams, Nigel Melville, Sham, P., Craddock, Nicholas John and Owen, Michael John 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

Hoogendoorn, Bastiaan, Norton, Nadine, Kirov, George, Williams, Nigel Melville, Hamshere, Marian Lindsay, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397

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

Norton, N., Bray, Nicholas John, Williams, Nigel Melville, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John 1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96.

Williams, Nigel Melville, Bowen, Timothy, Kirov, George, Williams, H., Hoogendorn, B., Asherson, P. and Owen, Michael John 1999. Polymorphism screening and association studies of the Wolfram syndrome gene in schizophrenia. Molecular Psychiatry 4 (supp1) , S42-S42.

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

Cardno, Alastair G., Bowen, Timothy, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John, McGuffin, Peter, Owen, Michael John and O'Donovan, Michael Conlon 1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12) , pp. 1592-1596. 10.1016/s0006-3223(99)00033-5

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

Guy, Carol, Bowen, Timothy, Williams, Nigel Melville, Jones, I. R., McCandless, F, McGuffin, P, Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 1999. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 57-60. 10.1002/(sici)1096-8628(19990205)88:1%3C57::aid-ajmg10%3E3.0.co;2-6

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan, Fenton, I., Williams, Nigel Melville, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie, Goate, A., Hardy, J. and Owen, Michael John 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie and Owen, Michael John 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, Owen, Michael John, Oefner, P. J., Williams, Nigel Melville, Austin, J. and O'Donovan, Michael Conlon 1999. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Human Genetics 104 (1) , pp. 89-93. 10.1007/s004390050915

Williams, Nigel Melville, Fenton, I. and Owen, Michael John 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6) , pp. 463-464.

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

Williams, Nigel Melville, Kirov, George, Craddock, Nicholas John and Owen, Michael John 1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6) , p. 486.

Hill, L., Asherson, P., Ball, D., Craig, I., Daniels, J., Eley, T., Freeman, B., Ninomiya, T., Fisher, P., Turic, D., Williams, Nigel Melville, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John, McGuffin, P. and Plomin, R. 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6) , p. 486.

Spurlock, Gillian, Williams, Nigel Melville, Williams, Hywel and Owen, Michael John 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics 81 (6) , pp. 525-526.

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

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

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

Bowen, Timothy, Guy, Carol, Craddock, Nicholas John, Cardno, A. G., Williams, Nigel Melville, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie, McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400

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

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

Williams, Nigel Melville, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2) , pp. 83-85. 10.1097/00041444-199722000-00005

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

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

Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville, Price, W., Owen, Michael John, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94.

Craddock, Nicholas John, Daniels, J., Holmans, Peter Alan, Williams, Nigel Melville and Owen, Michael John 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, Williams, Julie, Jones, L. A., Cardno, A. G., Murphy, K. C., Spurlock, G., Riley, B., Scambler, P., Asherson, P., McGuffin, P. and Owen, Michael John 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, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John, 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, Arranz, M., Nanko, S., Collier, D., McGuffin, P., Murray, R., Owen, Michael John 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, Roberts, Q., Williams, Nigel Melville, McGuffin, P. and Owen, Michael John 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, Roberts, E, McGuffin, M and Owen, Michael John 1994. DRD2 Ser311/Cys311 polymorphism in schizophrenia. The Lancet 343 (8904) , p. 1045.

This list was generated on Thu Dec 14 03:01:20 2017 GMT.