Apolipoprotein E genotype as a risk factor for susceptibility to and dementia in Parkinson’s Disease by Williams-Gray, C. H., Goris, A., Saiki, M., Foltynie, T., Compston, D. A. S., Sawcer, S. J., Barker, R. A.

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HLA-DR 15 is associated with female sex and younger age at diagnosis in multiple sclerosis by Hensiek, A E, Sawcer, S J, Feakes, R, Deans, J, Mander, A, Akesson, E, Roxburgh, R, Coraddu, F, Smith, S, Compston, D A S

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Autoimmune disease in first-degree relatives of patients with multiple sclerosis. A UK survey by Broadley, S A, Deans, J, Sawcer, S J, Clayton, D, Compston, D A

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Prevalence of the LRRK2 G2019S mutation in a UK community based idiopathic Parkinson’s disease cohort by Williams-Gray, C H, Goris, A, Foltynie, T, Brown, J, Maranian, M, Walton, A, Compston, D A S, Sawcer, S J, Barker, R A

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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease by GORIS, A, WILLIAMS-GRAY, C. H, FOLTYNIE, T, BROWN, J, MARANIAN, M, WALTON, A, COMPSTON, D. A. S, BARKER, R. A, SAWCER, S. J

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Searching for needles in haystacks—the genetics of multiple sclerosis and other common neurological diseases by Hensiek, Anke E., Sawcer, S.J., Compston, D.A.S.

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Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis by Hensiek, A.E., Roxburgh, R., Smilie, B., Coraddu, F., Åkesson, E., Holmans, P., Sawcer, S.J., Compston, D.A.S.

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GP.01 Childhood obesity and multiple sclerosis susceptibility: a Mendelian randomization study by Harroud, A, Mitchell, RE, Morris, JA, Forgetta, V, Sawcer, SJ, Smith, G Davey, Richards, B

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Osteopontin gene and clinical severity of multiple sclerosis by Hensiek, A E, Roxburgh, R, Meranian, M, Seaman, S, Yeo, T, Compston, D A S, Sawcer, S J

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No Evidence for Association with Parkinson Disease for 13 Single-Nucleotide Polymorphisms Identified by Whole-Genome Association Screening by Goris, A., Williams-Gray, C.H., Foltynie, T., Compston, D.A.S., Barker, R.A., Sawcer, S.J.

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No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by Broadley, S A, Sawcer, S J, Chataway, S J S, Coraddu, F, Coles, A, Gray, J, Roxburgh, R, Clayton, D, Compston, D A S

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A genome-wide screen for linkage disequilibrium in Australian HLA-DRB11501 positive multiple sclerosis patients by Ban, M., Sawcer, S.J., Heard, R.N.S., Bennetts, B.H., Adams, S., Booth, D., Perich, V., Setakis, E., Compston, A., Stewart, G.J.

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping by Sawcer, Stephen J, Maranian, Mel, Singlehurst, Sara, Yeo, TaiWai, Compston, Alastair, Daly, Mark J, De Jager, Philip L, Gabriel, Stacey, Hafler, David A, Ivinson, Adrian J, Lander, Eric S, Rioux, John D, Walsh, Emily, Gregory, Simon G, Schmidt, Silke, Pericak-Vance, Margaret A, Barcellos, Lisa, Hauser, Stephen L, Oksenberg, Jorge R, Kenealy, Shannon J, Haines, Jonathan L

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Multiple sclerosis and tonsillectomy: no evidence for an influence on the development of disease or clinical phenotype by Broadley, S A, Deans, J, Chataway, S JS, Sawcer, S J, Compston, D AS

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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility by Patsopoulos, Nikolaos A., Baranzini, Sergio E., Santaniello, Adam, Shoostari, Parisa, Cotsapas, Chris, Wong, Garrett, Beecham, Ashley H., James, Tojo, Replogle, Joseph, Vlachos, Ioannis S., McCabe, Cristin, Pers, Tune H., Brandes, Aaron, White, Charles, Keenan, Brendan, Cimpean, Maria, Winn, Phoebe, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F. M., Zarzycki, Onigiusz, Dubois, Bénédicte, Goris, An, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise Wegner, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Graetz, Christiane, Grummel, Verena, Hemmer, Bernhard, Hoshi, Muni, Knier, Benjamin, Korn, Thomas, Lill, Christina M., Luessi, Felix, Mühlau, Mark, Zipp, Frauke, Dardiotis, Efthimios, Agliardi, Cristina, Amoroso, Antonio, Barizzone, Nadia, Benedetti, Maria D., Bernardinelli, Luisa, Cavalla, Paola, Clarelli, Ferdinando, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Galimberti, Daniela, Guaschino, Clara, Leone, Maurizio A., Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Sorosina, Melissa, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Mancini, Nicasio, Zuccalà, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Bos, Steffan D., Celius, Elisabeth G., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Bomfim, Izaura L., Gomez-Cabrero, David, Hillert, Jan, Jagodic, Maja, Lindén, Magdalena, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Molyneux, Paul, Neville, Matthew

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Locus for severity implicates CNS resilience in progression of multiple sclerosis by Harroud, Adil, Stridh, Pernilla, McCauley, Jacob L., Saarela, Janna, van den Bosch, Aletta M. R., Engelenburg, Hendrik J., Beecham, Ashley H., Alfredsson, Lars, Alikhani, Katayoun, Amezcua, Lilyana, Andlauer, Till F. M., Ban, Maria, Barcellos, Lisa F., Barizzone, Nadia, Berge, Tone, Berthele, Achim, Bittner, Stefan, Bos, Steffan D., Briggs, Farren B. S., Caillier, Stacy J., Calabresi, Peter A., Caputo, Domenico, Carmona-Burgos, David X., Cavalla, Paola, Celius, Elisabeth G., Cerono, Gabriel, Chinea, Angel R., Chitnis, Tanuja, Clarelli, Ferdinando, Comabella, Manuel, Comi, Giancarlo, Cotsapas, Chris, Cree, Bruce C. A., D’Alfonso, Sandra, Dardiotis, Efthimios, De Jager, Philip L., Delgado, Silvia R., Dubois, Bénédicte, Engel, Sinah, Esposito, Federica, Fabis-Pedrini, Marzena J., Filippi, Massimo, Fitzgerald, Kathryn C., Gasperi, Christiane, Gomez, Lissette, Gomez, Refujia, Hadjigeorgiou, Georgios, Hamann, Jörg, Held, Friederike, Henry, Roland G., Hillert, Jan, Huang, Jesse, Huitinga, Inge, Islam, Talat, Isobe, Noriko, Jagodic, Maja, Kermode, Allan G., Khalil, Michael, Kilpatrick, Trevor J., Konidari, Ioanna, Kreft, Karim L., Lechner-Scott, Jeannette, Leone, Maurizio, Luessi, Felix, Malhotra, Sunny, Manouchehrinia, Ali, Manrique, Clara P., Martinelli-Boneschi, Filippo, Martinez, Andrea C., Martinez-Maldonado, Viviana, Mascia, Elisabetta, Metz, Luanne M., Midaglia, Luciana, Montalban, Xavier, Oksenberg, Jorge R., Olsson, Tomas, Oturai, Annette, Pääkkönen, Kimmo, Parnell, Grant P., Patsopoulos, Nikolaos A., Pericak-Vance, Margaret A., Piehl, Fredrik, Rubio, Justin P., Santaniello, Adam, Santoro, Silvia, Schaefer, Catherine, Sellebjerg, Finn, Shams, Hengameh, Shchetynsky, Klementy, Silva, Claudia, Siokas, Vasileios, Søndergaard, Helle B., Sorosina, Melissa, Taylor, Bruce, Vandebergh, Marijne, Vasileiou, Elena S., Vecchio, Domizia, Voortman, Margarete M., Weiner, Howard L., Wever, Dennis

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Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes by Ruderfer, Douglas M., Boocock, James, Stahl, Eli A., Charney, Alexander W., Ori, Anil P.S., Alliey-Rodriguez, Ney, Anjorin, Adebayo, Badner, Judith A., Band, Gavin, Bruggeman, Richard, Buccola, Nancy G., Bumpstead, Suzannah J., Casas, Juan P., Chan, Raymond C.K., Chen, Ronald Y.L., Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Curtis, David, Dannlowski, Udo, Davidson, Michael, Demontis, Ditte, Dronov, Serge, Elvsashagen, Torbjorn, Etain, Bruno, Fan, Chun Chieh, Forty, Liz, Fraser, Christine, Garnham, Julie, Gill, Michael, Gillman, Matthew, Gratten, Jacob, Gwilliam, Rhian, Hammer, Christian, Hansen, Thomas, Henskens, Frans A., Jamain, Stephane, Jankowski, Janusz, Joa, Inge, Julia, Antonio, Kandaswamy, Radhika, Kavanagh, David, Keller, Matthew C., Khrunin, Andrey, Lee, Phil H., Legge, Sophie E., Lencz, Todd, Levinson, Douglas F., Levy, Shawn E., Li, Tao, Lin, Kuang, Macek, Milan, McCarley, Robert W., McGuffin, Peter, McInnis, Melvin G., Meijer, Carin J., Melegh, Bela, Mesholam-Gately, Raquelle I., Myin-Germeys, Inez, Nicodemus, Kristin K., Nimgaonkar, Vishwajit, Nordin, Annelie, Nöthen, Markus M., Van Os, Jim, Owen, Michael J., Palmer, Colin N.A., Palotie, Aarno, Papadimitriou, George N., Pato, Michele T., Perlis, Roy H., Petryshen, Tracey L., Plomin, Robert, Potash, James B., Powell, John, Ramos-Quiroga, Josep Antoni, Rautanen, Anna, Reichenberg, Abraham, Ribases, Marta, Rice, John P., Richards, Alexander L., Ricketts, Michelle, Sanchez-Mora, Cristina, Sanders, Alan R., Schall, Ulrich, Serretti, Alessandro, Sham, Pak C., Straub, Richard E., Strauss, John S., Szatkiewicz, Jin P., Thompson, Robert C., Thorgeirsson, Thorgeir E., Treutlein, Jens, Vedder, Helmut, Wang, Qiang, Wu, Jing Qin, Sullivan, Patrick F., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S.

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Creutzfeldt-Jakob disease in an individual occupationally exposed to BSE by Sawcer, S.J., Yuill, G.M., Esmonde, T.F.G., Estibeiro, P., Ironside, J.W., Bell, J.E., Will, R.G.

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Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases by Rioux, John D, Goyette, Philippe, Vyse, Timothy J, Hammarström, Lennart, Fernando, Michelle M.A, Green, Todd, De Jager, Philip L, Foisy, Sylvain, Wang, Joanne, de Bakker, Paul I.W, Leslie, Stephen, McVean, Gilean, Padyukov, Leonid, Alfredsson, Lars, Annese, Vito, Hafler, David A, Pan-Hammarström, Qiang, Matell, Ritva, Sawcer, Stephen J, Compston, Alastair D, Cree, Bruce A.C, Mirel, Daniel B, Daly, Mark J, Behrens, Tim W, Klareskog, Lars, Gregersen, Peter K, Oksenberg, Jorge R, Hauser, Stephen L

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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data by Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre

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