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Mechelli, Rosella, Umeton, Renato, Policano, Claudia, Annibali, Viviana, Coarelli, Giulia, Ricigliano, Vito A. G., Vittori, Danila, Fornasiero, Arianna, Buscarinu, Maria Chiara, International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium,2, Romano, Silvia, Salvetti, Marco, Ristori, Giovanni and Brown, Matthew A. (2013) A "candidate-interactome" aggregate analysis of genome-wide association data in multiple sclerosis. PLoS One, 8 5: . doi:10.1371/journal.pone.0063300 57   3 Cited 4 times in Scopus4 10
Frayling, Timothy M., Timpson, Nicholas J., Weedon, Michael N., Zeggini, Eleftheria, Freathy, Rachel M., Lindgren, Cecilia M., Perry, John R. B., Elliott, Katherine S., Lango, Hana, Rayner, Nigel W., Shields, Beverley, Harries, Lorna W., Barrett, Jeffrey C., Ellard, Sian, Groves, Christopher J., Knight, Bridget, Patch, Ann-Marie, Ness, Andrew R., Ebrahim, Shah, Lawlor, Debbie A., Ring, Susan M., Ben-Shlomo, Yoav, Jarvelin, Marjo-Riitta, Sovio, Ulla, Bennett, Amanda J., Melzer, David, Ferrucci, Luigi, Loos, Ruth J. F., Barroso, Inês, Wareham, Nicholas J., Karpe, Fredrik, Owen, Katharine R., Cardon, Lon R., Walker, Mark, Hitman, Graham A., Palmer, Colin N. A., Doney, Alex S. F.Graham A., Morris, Andrew D., Smith, George Davey, Hattersley, Andrew T., McCarthy, Mark I. and Wellcome Trust Case Control (2007) A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science, 316 5826: 889-894. doi:10.1126/science.1141634 118   1689 Cited 1690 times in Scopus1690 102
Weedon, M. N., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2007) A common variant of HMGA2 is associated with adult and childhood height in the general population. Nature Genetics, 39 10: 1245-1250. doi:10.1038/ng2121 94   227 Cited 224 times in Scopus224 30
Psychosis Endophenotypes International Consortium, Wellcome Trust Case-Control Consortium and Brown, Matthew A. (2014) A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. Biological Psychiatry, 75 5: 386-397. doi:10.1016/j.biopsych.2013.03.033 37   3 Cited 1 times in Scopus1 1
Goode, Ellen L., Chenevix-Trench, Georgia, Song, Honglin, Ramus, Susan J., Notaridou, Maria, Lawrenson, Kate, Widschwendter, Martin, Vierkant, Robert A., Larson, Melissa C., Kjaer, Susanne K., Birrer, Michael J., Berchuck, Andrew, Schildkraut, Joellen, Tomlinson, Ian, Kiemeney, Lambertus A., Cook, Linda S., Gronwald, Jacek, Garcia-Closas, Montserrat, Gore, Martin E., Campbell, Ian, Whittemore, Alice S., Sutphen, Rebecca, Phelan, Catherine, Anton-Culver, Hoda, Pearce, Celeste Leigh, Lambrechts, Diether, Rossing, Mary Anne, Chang-Claude, Jenny, Moysich, Kirsten B., Goodman, Marc T., Dork, Thilo, Nevanlinna, Heli, Ness, Roberta B., Rafnar, Thorunn, Hogdall, Claus, Hogdall, Estrid, Fridley, Brooke L., Cunningham, Julie M., Sieh, Weiva, McGuire, Valerie, Godwin, Andrew K., Cramer, Daniel W., Hernandez, Dena, Levine, Douglas, Lu, Karen, Iversen, Edwin S., Palmieri, Rachel T., Houlston, Richard, van Altena, Anne M., Aben, Katja K. H., Massuger, Leon F. A. G., Brooks-Wilson, Angela, Kelemen, Linda E., Le, Nhu D., Jakubowska, Anna, Lubinski, Jan, Medrek, Krzysztof, Stafford, Anne, Easton, Douglas F., Tyrer, Jonathan, Bolton, Kelly L., Harrington, Patricia, Eccles, Diana, Chen, Ann, Molina, Ashley N., Davila, Barbara N., Arango, Hector, Tsai, Ya-Yu, Chen, Zhihua, Risch, Harvey A., McLaughlin, John, Narod, Steven A., Ziogas, Argyrios, Brewster, Wendy, Gentry-Maharaj, Aleksandra, Menon, Usha, Wu, Anna H., Stram, Daniel O., Pike, Malcolm C., The Wellcome Trust Case-Control Consortium, Beesley, Jonathan, Webb, Penelope M., The Australian Cancer Study (Ovarian Cancer), The Australian Ovarian Cancer Study Group, Chen, Xiaoqing, Ekici, Arif B., Thiel, Falk C., Beckmann, Matthias W., Yang, Hannah, Wentzensen, Nicolas, Lissowska, Jolanta, Fasching, Peter A., Despierre, Evelyn, Amant, Frederic, Vergote, Ignace, Doherty, Jennifer, Hein, Rebecca, Wang-Gohrke, Shan, Lurie, Galina, Carney, Michael E., Thompson, Pamela J., Runnebaum, Ingo, Hillemanns, Peter, Durst, Matthias, Antonenkova, Natalia, Bogdanova, Natalia, Leminen, Arto, Butzow, Ralf, Heikkinen, Tuomas, Stefansson, Kari, Sulem, Patrick, Besenbacher, Soren, Sellers, Thomas A., Gayther, Simon A., Pharoah, Paul D. P. and The Ovarian Cancer Association Consortium (OCAC) (2010) A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Nature Genetics, 42 10: 874-879. doi:10.1038/ng.668 263 2 85 Cited 118 times in Scopus118 17
Bellenguez, Celine, Strange, Amy, Freeman, Colin, Donnelly, Peter, Spencer, Chris C. A., Wellcome Trust Case Control Consortium and Brown, Matthew A. (2012) A robust clustering algorithm for identifying problematic samples in genome-wide association studies. Bioinformatics, 28 1: 134-135. doi:10.1093/bioinformatics/btr599 41   9 Cited 8 times in Scopus8 3
Dehghan, Abbas, Yang, Qiong, Peters, Annette, Basu, Saonli, Bis, Joshua, Rudnicka, Alicja, Kavousi, Maryam, Chen, Ming-Huei, Baumert, Jens, Lowe, Gordon, et al, Wellcome Trust Case Control Consortium, Brown, Matthew and Bradbury, Linda (2009) Association of novel genetic loci with circulating fibrinogen levels: A genome-wide association study in 6 population-based cohorts. Circulation: Cardiovascular Genetics, 2 2: 125-133. doi:10.1161/CIRCGENETICS.108.825224 81   44 Cited 48 times in Scopus48 0
Wellcome Trust Case control Consortium, The Australo-Anglo-American Spondylitis Consortium, Sims, A-M., Bradbury, L. A., Brown, M. A., Doan, T. and Dowling, A. (2007) Association scan of 14,000 nonsynonymous SNP's in four diseases identifies autoimmunity variants. Nature Genetics, 39 11: 1329-1337. doi:10.1038/ng.2007.17 175   656 Cited 675 times in Scopus675 3
Benyamin, B., St Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franic, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J., Harris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., de Geus, E. J. C., Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe, V. W. V., Starr, J. M., Verhulst, F. C., Pennell, C., Tiemeier, H., Iacono, W. G., Palmer, L. J., Montgomery, G. W., Martin, N. G., Boomsma, D. I., Posthuma, D., McGue, M., Wright, M. J., Davey Smith, G., Deary, I. J., Plomin, R. and Visscher, P. M. (2014) Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19 2: 253-258. doi:10.1038/mp.2012.184 162   20 Cited 20 times in Scopus20 98
Orozco, G., Hinks, A., Eyre, S., Ke, X. Y., Gibbons, L. J., Bowes, J., Flynn, E., Martin, P., Wellcome Trust Case Control Consortium, Brown, Matthew A., Linda Bradbury and et al (2009) Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.. Human Molecular Genetics, 18 14: 2693-2699. doi:10.1093/hmg/ddp193 57   51 Cited 53 times in Scopus53 7
van Koolwijk, Leonieke M. E., Ramdas, Wishal D., Ikram, M. Kamran, Jansonius, Nomdo M., Pasutto, Francesca, Hysi, Pirro G., Macgregor, Stuart, Janssen, Sarah F., Hewitt, Alex W., Viswanathan, Ananth C., ten Brink, Jacoline B., Hosseini, S. Mohsen, Amin, Najaf, Despriet, Dominiek D. G., Willemse-Assink, Jacqueline J. M., Kramer, Rogier, Rivadeneira, Fernando, Struchalin, Maksim, Aulchenko, Yurii S., Weisschuh, Nicole, Zenkel, Matthias, Mardin, Christian Y., Gramer, Eugen, Welge-Luessen, Ulrich, Montgomery, Grant W., Carbonaro, Francis, Young, Terri L., The DCCT/EDIC Research Group, Bellenguez, Celine, McGuffin, Peter, Foster, Paul J., Topouzis, Fotis, Mitchell, Paul, Wang, Jie Jin, Wong, Tien Y., Czudowska, Monika A., Hofman, Albert, Uitterlinden, Andre G., Wolfs, Roger C. W., de Jong, Paulus T. V. M., Oostra, Ben A., Paterson, Andrew D., Wellcome Trust Case Control Consortium 2, Mackey, David A., Bergen, Arthur A. B., Reis, Andre, Hammond, Christopher J., Vingerling, Johannes R., Lemij, Hans G., Klaver, Caroline C. W., van Duijn, Cornelia M. and Brown, Matthew A. (2012) Common genetic determinants of intraocular pressure and primary open-angle glaucoma. PLoS Genetics, 8 5: e1002611.1-e1002611.13. doi:10.1371/journal.pgen.1002611 55   36 Cited 34 times in Scopus34 2
Nolte, Ilja M., Wallace, Chris, Newhouse, Stephen J., Waggott, Daryl, Fu, Jingyuan, Soranzo, Nicole, Gwilliam, Rhian, Deloukas, Panos, Savelieva, Irina, Zheng, Dongling, Dalageorgou, Chrysoula, Farrall, Martin, Samani, Nilesh J., Connell, John, Brown, Morris, Dominiczak, Anna, Lathrop, Mark, Zeggini, Eleftheria, Wain, Louise V., The DCCT/EDIC Research Group, Newton-Cheh, Christopher, Eijgelsheim, Mark, Rice, Kenneth, de Bakke, Paul I. W., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Asselbergs, Folkert W., Spector, Tim D., Carter, Nicholas D., Jeffery, Steve, Tobin, Martin, Caulfield, Mark, Snieder, Harold, Paterson, Andrew D., Munroe, Patricia B., Jamshidi, Yalda, The Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda (2009) Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies. PLoS One, 4 7: e6138-1-e6138-10. doi:10.1371/journal.pone.0006138 108   30 Cited 32 times in Scopus32 0
Holliday, Elizabeth G., Maguire, Jane M., Evans, Tiffany-Jane, Koblar, Simon A., Jannes, Jim, Sturm, Jonathan W., Hankey, Graeme J., Baker, Ross, Golledge, Jonathan, Parsons, Mark W., Malik, Rainer, McEvoy, Mark, Biros, Erik, Lewis, Martin D., Lincz, Lisa F., Peel, Roseanne, Oldmeadow, Christopher, Smith, Wayne, Moscato, Pablo, Barlera, Simona, Bevan, Steve, Bis, Joshua C., Boerwinkle, Eric, Boncoraglio, Giorgio B., Brott, Thomas G., Brown, Robert D., Jr., Cheng, Yu-Ching, Cole, John W., Cotlarciuc, Ioana, Devan, William J., Fornage, Myriam, Furie, Karen L., Gretarsdottir, Solveig, Gschwendtner, Andreas, Ikram, M. Arfan, Longstreth, W. T., Jr., Meschia, James F., Mitchell, Braxton D., Mosley, Thomas H., Nalls, Michael A., Parati, Eugenio A., Psaty, Bruce M., Sharma, Pankaj, Stefansson, Kari, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Traylor, Matthew, Verhaaren, Benjamin F. J., Wiggins, Kerri L., Worrall, Bradford B., The Australian Stroke Genetics Collaborative, The International Stroke Genetics Consortium, The Wellcome Trust Case Control Consortium 2, Brown, Matthew A., Sudlow, Cathie, Rothwell, Peter M., Farrall, Martin, Dichgans, Martin, Rosand, Jonathan, Markus, Hugh S., Scott, Rodney J., Levi, Christopher and Attia, John (2012) Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Nature Genetics, 44 10: 1147-1151. doi:10.1038/ng.2397 75   36 Cited 35 times in Scopus35 2
Fakiola, Michaela, Strange, Amy, Cordell, Heather J., Miller, E. Nancy, Pirinen, Matti, Su, Zhan, Mishra, Anshuman, Mehrotra, Sanjana, Monteiro, Gloria R., Band, Gavin, Bellenguez, Celine, Dronov, Serge, Edkins, Sarah, Freeman, Colin, Giannoulatou, Eleni, Gray, Emma, Hunt, Sarah E., Lacerda, Henio G., Langford, Cordelia, Pearson, Richard, Pontes, Nubia N., Rai, Madhukar, Singh, Shri P., Smith, Linda, Sousa, Olivia, Vukcevic, Damjan, Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Wilson, Mary E., Deloukas, Panos, Peltonen, Leena, Christiansen, Frank, Witt, Campbell, Jeronimo, Selma M. B., Sundar, Shyam, Spencer, Chris C. A., Blackwell, Jenefer M., Donnelly, Peter, LeishGEN Consortium and Wellcome Trust Case Control Consortium 2 (2013) Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. Nature Genetics, 45 2: 208-213. doi:10.1038/ng.2518 65   17 Cited 16 times in Scopus16 12
Gharahkhani, Puya, Burdon, Kathryn P., Fogarty, Rhys, Sharma, Shiwani, Hewitt, Alex W., Martin, Sarah, Law, Matthew H., Cremin, Katie, Bailey, Jessica N. Cooke, Loomis, Stephanie J., Pasquale, Louis R., Haines, Jonathan L., Hauser, Michael A., Viswanathan, Ananth C., McGuffin, Peter, Topouzis, Fotis, Foster, Paul J., Graham, Stuart L., Casson, Robert J., Chehade, Mark, White, Andrew J., Zhou, Tiger, Souzeau, Emmanuelle, Landers, John, Fitzgerald, Jude T., Klebe, Sonja, Ruddle, Jonathan B., Goldberg, Ivan, Healey, Paul R., Wellcome Trust Case Control Consortium 2, NEIGHBORHOOD Consortium, Mills, Richard A., Wang, Jie Jin, Montgomery, Grant W., Martin, Nicholas G., Radford-Smith, Graham, Whiteman, David C., Brown, Matthew A., Wiggs, Janey L., Mackey, David A., Mitchell, Paul, MacGregor, Stuart and Craig, Jamie E. (2014) Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma. Nature Genetics, 46 10: 1120-1125. doi:10.1038/ng.3079 20 1 1 Cited 1 times in Scopus1 42
GoDARTS and UKPDS Diabetes Pharmacogenetics Study Group, Wellcome Trust Case Control Consortium 2, Zhou, Kaixin, Tavendale, Roger, Donnelly, Louise A., Schofield, Chris, Burch, Lindsay, Carr, Fiona, Colhoun, Helen, Morris, Andrew D., Sutherland, Calum, Palmer, Colin N. A., Pearson, Ewan, Bellenguez Celine, Spencer, Chris C. A., Strange, Amy, Freeman, Colin, Rautanen, Anna, McCarthy, Mark I., Donnelly, Peter, Bennett, Amanda J., Coleman, Ruth L., Groves, Christopher J., McCarthy, Mark I., Holman, Rury R., Hawley, Simon A., Hardie, Grahame, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Langford, Cordelia, Peltonen, Leena, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G, Trembath, Richard, Plomin, Robert, Sawcer, Stephen J., Samani, Nilesh J., Viswanathan, Aananth C., Wood, Nicholas W., Harries, Lorna W., Hattersley, Andrew T., Doney, Alex S. F., McCarthy, Mark I. and Donnelly, Peter (2011) Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. Nature Genetics, 43 2: 117-120. doi:10.1038/ng.735 144   108 Cited 140 times in Scopus140 2
Loos, Ruth J. F., Evans, David M., Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda A. (2008) Common variants near MC4R are associated with fat mass, weight and risk of obesity. Nature Genetics, 40 6: 768-775. doi:10.1038/ng.140 87   633 Cited 643 times in Scopus643 24
Codd, Veryan, Mangino, Massimo, van der Harst, Pim, Braund, Peter S., Kaiser, Michael, Beveridge, Alan J., Rafelt, Suzanne, Moore, Jasbir, Nelson, Chris, Soranzo, Nicole, Zhai, Guangju, Valdes, Ana M., Blackburn, Hannah, Mateo Leach, Irene, de Boer, Rudolf A., Kimura, Masayuki, Aviv, Abraham, Wellcome Trust Case Control Consortium, Goodall, Alison H., Ouwehand, Willem, van Veldhuisen, Dirk J., van Gilst, Wiek H., Navis, Gerjan, Burton, Paul R., Tobin, Martin D., Hall, Alistair S., Thompson, John R., Spector, Tim, Samani, Nilesh J., Brown, Matthew Arthur, Bradbury, Linda A. and Pointon, Jennifer J. (2010) Common variants near TERC are associated with mean telomere length. Nature Genetics, 42 3: 197-199. doi:10.1038/ng.532 222   103 Cited 108 times in Scopus108 15
Knight, Jo, Spain, Sarah L., Capon, Francesca, Hayday, Adrian, Nestle, Frank O., Clop, Alex, Wellcome Trust Case Control Consortium, Brown, Matthew A., Genetic Analysis of Psoriasis Consortium, Barker, Jonathan N., Weale, Michael E. and Trembath, Richard C. (2012) Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis. Human Molecular Genetics, 21 23: 5185-5192. doi:10.1093/hmg/dds344 42   11 Cited 12 times in Scopus12 1
Simon-Sanchez, Javier, Kilarski, Laura L., Nalls, Michael A., Martinez, Maria, Schulte, Claudia, Holmans, Peter, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium, Gasser, Thomas, Hardy, John, Singleton, Andrew B., Wood, Nicholas W., Brice, Alexis, Heutink, Peter, Williams, Nigel, Morris, Huw R. and Brown, Matthew (2012) Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's Disease. Plos One, 7 3: e28787.1-e28787.2. doi:10.1371/journal.pone.0028787 43   7 Cited 7 times in Scopus7 1
Newby, Paul R., Pickles, Oliver J., Mazumdar, Samaresh, Brand, Oliver J., Carr-Smith, Jaqueline D., Pearce, Simon H. S., Franklyn, Jayne A., Wellcome Trust Case Control Consortium, Evans, David M., Simmonds, Matthew J., Gough, Stephen C. L., Brown, Matthew A., Bradbury, Linda and Pointon, Jennifer (2010) Follow-up of potential novel Graves' disease susceptibility loci, identified in the UK WTCCC genome-wide nonsynonymous SNP study. European Journal of Human Genetics, 18 9: 1021-1026. doi:10.1038/ejhg.2010.55 95 5 8 Cited 9 times in Scopus9 3
Holmans, P., Green, E. K., Pahwa, J. S., Ferreira, M. A. R., Purcell, S. M., Sklar, P., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda, Owen, M. J., O'Donnovan, M. C. and Craddock, N. (2009) Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder. American Journal of Human Genetics, 85 1: 13-24. doi:10.1016/j.ajhg.2009.05.011 62   182 Cited 193 times in Scopus193 23
Fisher, Sheila A., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda A. and et al. (2008) Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease. Nature Genetics, 40 6: 710-712. doi:10.1038/ng.145 86   248 Cited 267 times in Scopus267 1
Sawcer, Stephen, Hellenthal, Garrett, Pirinen, Matti, Spencer, Chris C. A., Patsopoulos, Nikolaos A., Moutsianas, Loukas, Dilthey, Alexander, Su, Zhan, Freeman, Colin, Hunt, Sarah E., Edkins, Sarah, Gray, Emma, Booth, David R., Potter, Simon C., Goris, An, Band, Gavin, Oturai, Bang, Strange, Amy, Saarela, Janna, Bellenguez, Celine, Fontaine, Bertrand, Gillman, Matthew, Hemmer, Bernhard, Gwilliam, Rhian, Zipp, Frauke, Jayakumar, Alagurevathi, Martin, Roland, Leslie, Stephen, Hawkins, Stanley, Giannoulatou, Eleni, D'alfonso, Sandra, Blackburn, Hannah, Boneschi, Filippo Martinelli, Liddle, Jennifer, Harbo, Hanne F., Perez, Marc L., Spurkland, Anne, Waller, Matthew J., Mycko, Marcin P., Ricketts, Michelle, Comabella, Manuel, Hammond, Naomi, Kockum, Ingrid, McCann, Owen T., Ban, Maria, Whittaker, Pamela, Kemppinen, Anu, Weston, P, Hawkins, Clive, Widaa, Sara, Zajicek, John, Dronov, Serge, Robertson, Neil, Bumpstead, Suzannah J., Barcellos, Lisa F., Ravindrarajah, Rathi, Abraham, Roby, Alfredsson, Lars, Ardlie, Kristin, Aubin, Cristin, Baker, Amie, Baker, Katharine, Baranzini, Sergio E., Bergamaschi, Laura, Bergamaschi, Roberto, Bernstein, Allan, Berthele, Achim, Boggild, Mike, Bradfield, JP, Brassat, David, Broadley, Simon A., Buck, Dorothea, Butzkueven, Helmut, Capra, Ruggero, Carroll, William M., Cavalla, Paola, Celius, Elisabeth G., Cepok, Sabine, Chiavacci, Rosetta, Clerget-Darpoux, Francoise, Clysters, Katleen, Comi, Giancarlo, Cossburn, Mark, Cournu-Rebeix, Isabelle, Cox, Matthew B., Cozen, Wendy, Cree, Bruce A. C., Cross, Anne H., Cusi, Daniele, Daly, Mark J., Davis, Emma, de Bakker, Paul I. W., Debouverie, Marc, D'hooghe, Marie Beatrice, Dixon, Katherine, Dobosi, Rita, Dubois, Benedicte, Ellinghaus, David, Elovaara, Irina, Esposito, Federica, Fontenille, Claire, Foote, Simon, Franke, Andre, Galimberti, Daniela, Ghezzi, Angelo, Glessner, Joseph, Gomez, Refujia, Gout, Olivier, Graham, Colin, Grant, Struan F. A., Guerini, Franca Rosa, Hakonarson, Hakon, Hall, Per, Hamsten, Anders, Hartung, Hans-Peter, Heard, Rob N., Heath, Simon, Hobart, Jeremy, Hoshi, Muna, Infante-Duarte, Carmen, Ingram, Gillian, Ingram, Wendy, Islam, Talat, Jagodic, Maja, Kabesch, Michael, Kermode, Allan G., Kilpatrick, Trevor J., Kim, Cecilia, Klopp, Norman, Koivisto, Keijo, Larsson, Malin, Lathrop, Mark, Lechner-Scott, Jeannette S., Leone, Maurizio A., Leppa, Virpi, Liljedahl, Ulrika, Bomfim, Izaura Lima, Lincoln, Robin R., Link, Jenny, Liu, Jianjun, Lorentzen, Aslaug R., Lupoli, Sara, Macciardi, Fabio, Mack, Thomas, Marriott, Mark, Martinelli, Vittorio, Mason, Deborah, McCauley, Jacob L., Mentch, Frank, Mero, Inger-Lise, Mihalova, Tania, Montalban, Xavier, Mottershead, John, Myhr, Kjell-Morten, Naldi, Paola, Ollier, William, Page, Alison, Palotie, Aarno, Pelletier, Jean, Piccio, Laura, Pickersgill, Trevor, Piehl, Fredrik, Pobywajlo, Susan, Quach, Hong L., Ramsay, Patricia P., Reunanen, Mauri, Reynolds, Richard, Rioux, John D., Rodegher, Mariaemma, Roesner, Sabine, Rubio, Justin P., Ruckert, Ina-Maria, Salvetti, Marco, Salvi, Erika, Santaniello, Adam, Schaefer, Catherine A., Schreiber, Stefan, Schulze, Christian, Scott, Rodney J., Sellebjerg, Finn, Selmaj, Krzysztof W., Sexton, David, Shen, Ling, Simms-Acuna, Brigid, Skidmore, Sheila, Sleiman, Patrick M. A., Smestad, Cathrine, Sorensen, Per Soelberg, Sondergaard, Helle Bach, Stankovich, Jim, Strange, Richard C., Sulonen, Anna-Maija, Sundqvist, Emilie, Syvanen, Ann-Christine, Taddeo, Francesca, Taylor, Bruce, Blackwell, Jenefer M., Tienari, Pentti, Bramon, Elvira, Tourbah, Ayman, Brown, Matthew A., Tronczynska, Ewa, Casas, Juan P., Tubridy, Niall, Corvin, Aiden, Vickery, Jane, Jankowski, Janusz, Villoslada, Pablo, Markus, Hugh S., Wang, Kai, Mathew, Christopher G., Wason, James, Palmer, Colin N. A., Wichmann, H-Erich, Plomin, Robert, Willoughby, Ernest, Rautanen, Anna, Winkelmann, Juliane, Wittig, Michael, Trembath, Richard C., Yaouanq, Jacqueline, Viswanathan, Ananth C., Zhang, Haitao, Wood, Nicholas W., Zuvich, Rebecca, Deloukas, Panos, Langford, Cordelia, Duncanson, Audrey, Oksenberg, Jorge R., Pericak-Vance, Margaret A., Haines, Jonathan L., Olsson, Tomas, Hillert, Jan, Ivinson, Adrian J., De Jager, Philip L., Peltonen, Leena, Stewart, Graeme J., Hafler, David A., Hauser, Stephen L., McVean, Gil, Donnelly, Peter, Compston, Alstair, Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consor (2011) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature, 476 7359: 214-219. doi:10.1038/nature10251 701   578 Cited 644 times in Scopus644 72
Hamshere, M. L., Green, E. K., Jones, I. R., Moskvina, V., Kirov, G., Grozeva. D., Nikolov, I., Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, C., Russell, E., Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Wellcome Trust Case Control Consortium, Brown, M. A., Bradbury, L., Holmans P. A., Owen, M. J., O'Donovan, M. C. and Craddock, N. (2009) Genetic utility of broadly bipolar schizoaffective disorder as a diagnostic concept. British Journal of Psychiatry, 195 1: 23-29. doi:10.1192/bjp.bp.108.061424 91   39 Cited 44 times in Scopus44 7
Moskvina, V., Craddock, N., Holmans, P., Nikolov, I., Pahwa, J. S., Green, E., Wellcome Trust Case Control Consortium, Brown, Matthew A., Bradbury, Linda, Owen, M. J. and O'Donovan, M. C. (2009) Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.. Molecular Psychiatry, 14 3: 252-260. doi:10.1038/mp.2008.133 74   175 Cited 202 times in Scopus202 3
Jallow, M., Teo, Y. Y., Small, K. S., Rockett, K. A., Deloukas, P., Clark, T. G., Kivinen, K., Bojang, K. A., Conway, D. J., Pinder, M., et al, Wellcome Trust Case Control Consortium, Brown, Matthew A. and Bradbury, Linda (2009) Genome-wide and fine-resolution association analysis of malaria in West Africa. Nature Genetics, 41 6: 657-665. doi:10.1038/ng.388 52   150 Cited 165 times in Scopus165 17
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