Publications

  1. McCormack, Mark, Hongsheng Gui, Andrés Ingason, Doug Speed, Galen E B Wright, Eunice J. Zhang, Rodrigo Secolin, et al. 2018. “Genetic Variation in CFH predicts Phenytoin-Induced Maculopapular Exanthema in European-Descent Patients.Neurology 90 (4): e332–41.
  2. Berghuis, Bianca, Job van der Palen, Gerrit Jan de Haan, Dick Lindhout, Bobby P.C. Koeleman, Josemir W. Sander, Rikke S. Møller, et al. 2017. “Carbamazepine- and Oxcarbazepine-Induced Hyponatremia in People with Epilepsy.Epilepsia 58 (7): 1227–33.
  3. Androsova, Ganna, Roland Krause, Mojgansadat Borghei, Merel Wassenaar, Pauls Auce, Andreja Avbersek, Felicitas Becker, et al. 2017. “Comparative Effectiveness of Antiepileptic Drugs in Patients with Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis.Epilepsia 58 (10): 1734–41.
  4. Djémié, Tania, Sarah Weckhuysen, Sarah von Spiczak, Gemma L. Carvill, Johanna Jaehn, Anna-Kaisa Anttonen, Eva Brilstra, et al. 2016. “Pitfalls in Genetic Testing: The Story of Missed SCN1A Mutations.Molecular Genetics & Genomic Medicine, 1–8.
  5. Leu, Costin, Simona Balestrini, Bridget Maher, Laura Hernández-Hernández, Padhraig Gormley, Eija Hämäläinen, Kristin Heggeli, et al. 2015. “Genome-Wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.EBioMedicine 2 (9). Elsevier B.V.: 1063–70.
  6. International League Against Epilepsy Consortium on Complex Epilepsies. “Genetic Determinants of Common Epilepsies: A Meta-Analysis of Genome-Wide Association Studies.The Lancet. Neurology 13 (9). International League Against Epilepsy Consortium on Complex Epilepsies.
  7. Kasperaviciute, Dalia, Claudia B Catarino, Mar Matarin, Costin Leu, Jan Novy, Anna Tostevin, Bárbara Leal, et al. 2013. “Epilepsy, Hippocampal Sclerosis and Febrile Seizures Linked by Common Genetic Variation around SCN1A.Brain : A Journal of Neurology, September, 1–11.