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Number of items: 11.


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-+.


Wolking, Stefan, Moreau, Claudia, McCormack, Mark, Krause, Roland, Krenn, Martin, Berkovic, Samuel, Cavalleri, Gianpiero L, Delanty, Norman, Depondt, Chantal, Johnson, Michael R
et al (show 14 more authors) (2021) Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 8 (7). pp. 1376-1387.


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.


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-.


Heavin, Sinead B, McCormack, Mark, Wolking, Stefan, Slattery, Lisa, Walley, Nicole, Avbersek, Andreja, Novy, Jan, Sinha, Saurabh R, Radtke, Rod, Doherty, Colin
et al (show 21 more authors) (2019) Genomic and clinical predictors of lacosamide response in refractory epilepsies. EPILEPSIA OPEN, 4 (4). pp. 563-571.


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, Campbell, Ciaran, Stapleton, Caragh, McCormack, Mark, Delanty, Norman, Depondt, Chantal, Johnson, Michael R, Koeleman, Bobby PC, Krause, Roland, Kunz, Wolfram S
et al (show 8 more authors) (2021) Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. FRONTIERS IN PHARMACOLOGY, 12. 688386-.


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.


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) (2021) Using common genetic variants to find drugs for common epilepsies. Brain Communications, 3 (4). fcab287-.


Berghuis, Bianca, Stapleton, Caragh, Sonsma, Anja CM, Hulst, Janic, de Haan, Gerrit-Jan, Lindhout, Dick, Demurtas, Rita, EpiPGX Consortium, , Krause, Roland, Depondt, Chantal
et al (show 17 more authors) (2019) A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open, 4 (1). pp. 102-109.

This list was generated on Mon Jan 22 19:38:30 2024 GMT.