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Number of items: 7.


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 561 more authors) (2018) Analysis of shared heritability in common disorders of the brain. SCIENCE, 360 (6395). 1313-+.


Silvennoinen, Katri, de Lange, Nikola, Zagaglia, Sara, Balestrini, Simona, Androsova, Ganna, Wassenaar, Merel, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Berghuis, Bianca
et al (show 21 more authors) (2019) Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy. EPILEPSIA OPEN, 4 (3). pp. 420-430.


Androsova, Ganna, Krause, Roland, Borghei, Mojgansadat, Wassenaar, Merel, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Berghuis, Bianca, Campbell, Ellen, Coppola, Antonietta
et al (show 15 more authors) (2017) Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis. EPILEPSIA, 58 (10). pp. 1734-1741.


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) (2017) Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Neurology, 90 (4). E332-+.


Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L, Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Bruenger, Tobias, Thomas, Rhys H
et al (show 313 more authors) (2023) Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals. NATURE COMMUNICATIONS, 14 (1). 4392-.


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 88 more authors) (2018) Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). pp. 699-708.


Wolking, Stefan, Moreau, Claudia, Nies, Anne T, Schaeffeler, Elke, McCormack, Mark, Auce, Pauls, Avbersek, Andreja, Becker, Felicitas, Krenn, Martin, Moller, Rikke S
et al (show 21 more authors) (2020) Testing association of rare genetic variants with resistance to three common antiseizure medications. EPILEPSIA, 61 (4). pp. 657-666.

This list was generated on Mon Apr 15 10:37:21 2024 BST.