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Number of items: 4.


Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K, Walters, Raymond K, Bras, Jose, Duncan, Laramie, Escott-Price, Valentina, Falcone, Guido J, Gormley, Padhraig, Malik, Rainer
et al (show 562 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313 - +.


Androsova, Ganna ORCID: 0000-0002-5417-4001, Krause, Roland ORCID: 0000-0001-9938-7126, Borghei, Mojgansadat, Wassenaar, Merel, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Berghuis, Bianca, Campbell, Ellen, Coppola, Antonietta
et al (show 16 more authors) (2017) Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. EPILEPSIA, 58 (10). 1734 - 1741.


McCormack, Mark, Gui, Hongsheng, Ingason, Andres, Speed, Doug, Wright, Galen EB, Zhang, Eunice J, Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan
et al (show 43 more authors) (2018) Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. NEUROLOGY, 90 (4). E332 - +.


May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline
et al (show 91 more authors) (2018) Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). 699 - 708.

This list was generated on Sat Dec 8 21:00:29 2018 GMT.