The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression

by Dempster, Emma L, Mill, Jonathan, Craig, Ian W, Collier, David A
Published 2006

Random or Stochastic Monoallelic Expressed Genes Are Enriched for Neurodevelopmental Disorder Candidate Genes

by Jeffries, Aaron R., Collier, David A., Vassos, Evangelos, Curran, Sarah, Ogilvie, Caroline M., Price, Jack
Published 2013

Identification and Potential Regulatory Properties of Evolutionary Conserved Regions (ECRs) at the Schizophrenia-Associated MIR137 Locus

by Gianfrancesco, Olympia, Griffiths, Daniel, Myers, Paul, Collier, David A., Bubb, Vivien J., Quinn, John P.
Published 2016

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders

by Curran, Sarah, Ahn, Joo Wook, Grayton, Hannah, Collier, David A, Ogilvie, Caroline Mackie
Published 2013

Sensorimotor Gating Depends on Polymorphisms of the Serotonin-2A Receptor and Catechol-O-Methyltransferase, but Not on Neuregulin-1 Arg38Gln Genotype: A Replication Study

by Quednow, Boris B., Schmechtig, Anne, Ettinger, Ulrich, Petrovsky, Nadine, Collier, David A., Vollenweider, Franz X., Wagner, Michael, Kumari, Veena
Published 2009

BBGRE: brain and body genetic resource exchange

by Ahn, Joo Wook, Dixit, Abhishek, Johnston, Caroline, Ogilvie, Caroline M., Collier, David A., Curran, Sarah, Dobson, Richard J. B.
Published 2013

Advanced paternal age increases the risk of schizophrenia and obsessive–compulsive disorder in a Chinese Han population

by Wu, Yuejing, Liu, Xiang, Luo, Hongrong, Deng, Wei, Zhao, Gaofeng, Wang, Qiang, Zhang, Lan, Ma, Xiaohong, Liu, Xiehe, Murray, Robin A., Collier, David A., Li, Tao
Published 2012

StemBANCC: Governing Access to Material and Data in a Large Stem Cell Research Consortium

by Morrison, Michael, Klein, Christine, Clemann, Nicole, Collier, David A., Hardy, John, Heiβerer, Barbara, Cader, M. Zameel, Graf, Martin, Kaye, Jane
Published 2015

Genetic targeting of NRXN2 in mice unveils role in excitatory cortical synapse function and social behaviors

by Born, Gesche, Grayton, Hannah M., Langhorst, Hanna, Dudanova, Irina, Rohlmann, Astrid, Woodward, Benjamin W., Collier, David A., Fernandes, Cathy, Missler, Markus
Published 2015

Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women

by Shifman, Sagiv, Johannesson, Martina, Bronstein, Michal, Chen, Sam X, Collier, David A, Craddock, Nicholas J, Kendler, Kenneth S, Li, Tao, O'Donovan, Michael, O'Neill, F. Anthony, Owen, Michael J, Walsh, Dermot, Weinberger, Daniel R, Sun, Cuie, Flint, Jonathan, Darvasi, Ariel
Published 2008

Therapygenetics: The 5HTTLPR and response to psychological therapy

by Eley, Thalia C, Hudson, Jennifer L, Creswell, Cathy, Tropeano, Maria, Lester, Kathryn J, Cooper, Peter, Farmer, Anne, Lewis, Cathryn M., Lyneham, Heidi J, Rapee, Ronald M, Uher, Rudolf, Zavos, Helena MS, Collier, David A
Published 2011

Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders

by Tropeano, Maria, Ahn, Joo Wook, Dobson, Richard J. B., Breen, Gerome, Rucker, James, Dixit, Abhishek, Pal, Deb K., McGuffin, Peter, Farmer, Anne, White, Peter S., Andrieux, Joris, Vassos, Evangelos, Ogilvie, Caroline Mackie, Curran, Sarah, Collier, David A
Published 2013

Genome-Wide Association of Heroin Dependence in Han Chinese

by Kalsi, Gursharan, Euesden, Jack, Coleman, Jonathan R. I., Ducci, Francesca, Aliev, Fazil, Newhouse, Stephen J., Liu, Xiehe, Ma, Xiaohong, Wang, Yingcheng, Collier, David A., Asherson, Philip, Li, Tao, Breen, Gerome
Published 2016

Using ancestry-informative markers to identify fine structure across 15 populations of European origin

by Huckins, Laura M, Boraska, Vesna, Franklin, Christopher S, Floyd, James A B, Southam, Lorraine, Sullivan, Patrick F, Bulik, Cynthia M, Collier, David A, Tyler-Smith, Chris, Zeggini, Eleftheria, Tachmazidou, Ioanna
Published 2014

Genome-Wide Association Analysis of Eating Disorder-Related Symptoms, Behaviors, and Personality Traits

by Boraska, Vesna, Davis, Oliver SP, Cherkas, Lynn F, Helder, Sietske G, Harris, Juliette, Krug, Isabel, Pei-Chi Liao, Thomas, Treasure, Janet, Ntalla, Ioanna, Karhunen, Leila, Keski-Rahkonen, Anna, Christakopoulou, Danai, Raevuori, Anu, Shin, So-Youn, Dedoussis, George V, Kaprio, Jaakko, Soranzo, Nicole, Spector, Tim D, Collier, David A, Zeggini, Eleftheria
Published 2012

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

by Davies, Matthew N, Krause, Lutz, Bell, Jordana T, Gao, Fei, Ward, Kirsten J, Wu, Honglong, Lu, Hanlin, Liu, Yuan, Tsai, Pei-Chein, Collier, David A, Murphy, Therese, Dempster, Emma, Mill, Jonathan, Battle, Alexis, Mostafavi, Sara, Zhu, Xiaowei, Henders, Anjali, Byrne, Enda, Wray, Naomi R, Martin, Nicholas G, Spector, Tim D, Wang, Jun
Published 2014

An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylation

by Hannon, Eilis, Dempster, Emma, Viana, Joana, Burrage, Joe, Smith, Adam R., Macdonald, Ruby, St Clair, David, Mustard, Colette, Breen, Gerome, Therman, Sebastian, Kaprio, Jaakko, Toulopoulou, Timothea, Pol, Hilleke E. Hulshoff, Bohlken, Marc M., Kahn, Rene S., Nenadic, Igor, Hultman, Christina M., Murray, Robin M., Collier, David A., Bass, Nick, Gurling, Hugh, McQuillin, Andrew, Schalkwyk, Leonard, Mill, Jonathan
Published 2016

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

by Leblond, Claire S., Heinrich, Jutta, Delorme, Richard, Proepper, Christian, Betancur, Catalina, Huguet, Guillaume, Konyukh, Marina, Chaste, Pauline, Ey, Elodie, Rastam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Gillberg, I. Carina, Melke, Jonas, Toro, Roberto, Regnault, Beatrice, Fauchereau, Fabien, Mercati, Oriane, Lemière, Nathalie, Skuse, David, Poot, Martin, Holt, Richard, Monaco, Anthony P., Järvelä, Irma, Kantojärvi, Katri, Vanhala, Raija, Curran, Sarah, Collier, David A., Bolton, Patrick, Chiocchetti, Andreas, Klauck, Sabine M., Poustka, Fritz, Freitag, Christine M., Waltes, Regina, Kopp, Marnie, Duketis, Eftichia, Bacchelli, Elena, Minopoli, Fiorella, Ruta, Liliana, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Sequeira, Ana F., Oliveira, Barbara, Vicente, Astrid, Oliveira, Guiomar, Pinto, Dalila, Scherer, Stephen W., Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Bonneau, Dominique, Guinchat, Vincent, Devillard, Françoise, Assouline, Brigitte, Mouren, Marie-Christine, Leboyer, Marion, Gillberg, Christopher, Boeckers, Tobias M., Bourgeron, Thomas
Published 2012

Biological Insights From 108 Schizophrenia-Associated Genetic Loci

by Ripke, Stephan, Neale, Benjamin M, Corvin, Aiden, Walters, James TR, 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, 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, Kimberley D, Chan, Raymond CK, Chan, Ronald YL, Chen, Eric YH, Cheng, Wei, Cheung, Eric FC, Chong, Siow Ann, Cloninger, C Robert, Cohen, David, Cohen, Nadine, Cormican, Paul, Craddock, Nick, Crowley, James J, Curtis, David, Davidson, Michael, Davis, Kenneth L, Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Essioux, Laurent, Fanous, Ayman H, Farrell, Martilias S, Frank, Josef, Franke, Lude, Freedman, Robert, Freimer, Nelson B, Friedl, Marion, Friedman, Joseph I, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Giusti-Rodríguez, Paola, Godard, Stephanie, Goldstein, Jacqueline I, Golimbet, Vera, Gopal, Srihari, Gratten, Jacob, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L, Hansen, Mark, Hansen, Thomas, Haroutunian, Vahram, Hartmann, Annette M, Henskens, Frans A, Herms, Stefan, Hirschhorn, Joel N, Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V, Hougaard, David M, Ikeda, Masashi, Joa, Inge, Julià, Antonio, Kahn, René S, Kalaydjieva, Luba, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C, Kennedy, James L, Khrunin, Andrey, Kim, Yunjung, Klovins, Janis, Knowles, James A, Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Kähler, Anna K, Laurent, Claudine, Lee, Jimmy, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Li, Miaoxin, Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M, Lubinski, Jan, Lönnqvist, Jouko, Macek, Milan, Magnusson, Patrik KE, 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, Murphy, Kieran C, Murray, Robin M, Myin-Germeys, Inez, Müller-Myhsok, Bertram, 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, Pejovic-Milovancevic, Milica, Perkins, Diana O, Pietiläinen, Olli, Pimm, Jonathan, Pocklington, Andrew J, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Reichenberg, Abraham, Reimers, Mark A, Richards, Alexander L, 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, Sigurdsson, Engilbert, Silagadze, Teimuraz, Silverman, Jeremy M, Sim, Kang, Slominsky, Petr, Smoller, Jordan W, So, Hon-Cheong, Spencer, Chris C A, Stahl, Eli A, Stefansson, Hreinn, Steinberg, Stacy, Stogmann, Elisabeth, Straub, Richard E, Strengman, Eric, Strohmaier, Jana, Stroup, T Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Söderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Waddington, John, Walsh, Dermot, Wang, Dai, Wang, Qiang, Webb, Bradley T, Weiser, Mark, Wildenauer, Dieter B, Williams, Nigel M, Williams, Stephanie, Witt, Stephanie H, Wolen, Aaron R, Wong, Emily HM, Wormley, Brandon K, Xi, Hualin Simon, Zai, Clement C, Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R, Stefansson, Kari, Visscher, Peter M, Adolfsson, Rolf, Andreassen, Ole A, Blackwood, Douglas HR, Bramon, Elvira, Buxbaum, Joseph D, Børglum, Anders 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 J, 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
Published 2014