Number of items: 2.
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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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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-.
This list was generated on Mon Jan 30 06:35:10 2023 GMT.