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Koko, Mahmoud ORCID: 0000-0001-9512-0184, Motelow, Joshua E ORCID: 0000-0002-4367-4182, Stanley, Kate E ORCID: 0000-0002-2861-9660, Bobbili, Dheeraj R ORCID: 0000-0002-1368-9623, Dhindsa, Ryan S ORCID: 0000-0002-8965-0813, May, Patrick ORCID: 0000-0001-8698-3770, Canadian Epilepsy Network, , Epi4K Consortium, , Epilepsy Phenome/Genome Project, , EpiPGX Consortium,
et al (show 1 more authors) (2022) Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia, 63 (3). pp. 723-735.


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.


Altmann, Andre ORCID: 0000-0002-9265-2393, Ryten, Mina, Di Nunzio, Martina, Ravizza, Teresa, Tolomeo, Daniele, Reynolds, Regina, Somani, Alyma, Bacigaluppi, Marco, Iori, Valentina, Micotti, Edoardo
et al (show 88 more authors) (2018) A systems-level analysis highlights microglial activation as a modifying factor in common forms of human epilepsy. Unknown. 470518-.

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