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McCormack, M, Gui, Hongsheng, Ingason, Andrés, Speed, Doug, Wright, Galen EB, Zhang, Eunice J ORCID: 0000-0003-1813-2207, Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan et al (show 2 more authors) , Becker, Felicitas and Rau, Sarah (2017) Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology, 90 (4). E332-+.

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Kia, Demis A, Noyce, Alastair J ORCID: 0000-0003-3027-5497, White, Jon, Speed, Doug ORCID: 0000-0002-0096-9765, Nicolas, Aude, IPDGC collaborators, , Burgess, Stephen ORCID: 0000-0001-5365-8760, Lawlor, Debbie A ORCID: 0000-0002-6793-2262, Davey Smith, George ORCID: 0000-0002-1407-8314, Singleton, Andrew et al (show 3 more authors) , Nalls, Mike A, Sofat, Reecha ORCID: 0000-0002-0242-6115 and Wood, Nicholas W ORCID: 0000-0002-9500-3348 (2018) Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease. Annals of neurology, 84 (2). pp. 191-199.

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Mirza, Nasir, Stevelink, Remi, Taweel, Basel ORCID: 0000-0002-6157-2438, Koeleman, Bobby PC, Marson, Anthony G, Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J et al (show 151 more authors) , Bast, Thomas, Baum, Larry, Becker, Albert J, Berghuis, Felicitas Becker Bianca, Berkovic, Samuel F, Boysen, Katja E, Bradfield, Jonathan P, Brody, Lawrence C, Buono, Russell J, Campbell, Ellen, Cascino, Gregory D, Catarino, Claudia B, Cavalleri, Gianpiero L, Cherny, Stacey S, Chinthapalli, Krishna, Coffey, Alison J, Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J, de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien GF, Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J, Doherty, Colin P, Elger, Christian E, Eriksson, Johan G, Ferraro, Thomas N, Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A, Freytag, Saskia, Gaus, Verena, Geller, Eric B, Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B, Gui, Hongsheng, Guo, Youling, Haas, Kevin F, Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L, Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R, Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Trenite, Dorothee Kasteleijn-Nolst, Kirsch, Heidi E, Knowlton, Robert C, Koeleman, Bobby PC, Krause, Roland, Krenn, Martin, Kunz, Wolfram S, Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D, Lopes-Cendes, Iscia, Lowenstein, Daniel H, Malovini, Alberto, Marson, Anthony G ORCID: 0000-0002-6861-8806, Mayer, Thomas, McCormack, Mark, Mills, James L, Mirza, Nasir ORCID: 0000-0002-3538-0117, Moerzinger, Martina, Møller, Rikke S, Molloy, Anne M, Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M, Nürnberg, Peter, O’Brien, Terence J, Oliver, Karen L, Palotie, Aarno, Pangilinan, Faith, Peter, Sarah, Petrovski, Slavé, Poduri, Annapurna, Privitera, Michael, Radtke, Rodney, Rau, Sarah, Reif, Philipp S, Reinthaler, Eva M, Rosenow, Felix, Sander, Josemir W, Sander, Thomas, Scattergood, Theresa, Schachter, Steven C, Schankin, Christoph J, Scheffer, Ingrid E, Schmitz, Bettina, Schoch, Susanne, Sham, Pak C, Shih, Jerry J, Sills, Graeme J, Sisodiya, Sanjay M, Slattery, Lisa, Smith, Alexander, Smith, David F, Smith, Michael C, Smith, Philip E, Sonsma, Anja CM, Speed, Doug, Sperling, Michael R, Steinhoff, Bernhard J, Stephani, Ulrich, Stevelink, Remi, Strauch, Konstantin, Striano, Pasquale, Stroink, Hans, Surges, Rainer, Tan, K Meng, Thio, Liu Lin, Thomas, G Neil, Todaro, Marian, Tozzi, Rossana, Vari, Maria S, Vining, Eileen PG, Visscher, Frank, Spiczak, Sarah von, Walley, Nicole M, Weber, Yvonne G, Wei, Zhi, Weisenberg, Judith, Whelan, Christopher D, Widdess-Walsh, Peter, Wolff, Markus, Wolking, Stefan, Yang, Wanling, Zara, Federico and Zimprich, Fritz (2021) Using common genetic variants to find drugs for common epilepsies. Brain Communications, 3 (4). fcab287-.