Yushi Inoue

Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry

Torbjörn Tomson, Dina Battino, Erminio Bonizzoni et al. · The Lancet Neurology · 2018 · 521 citations · Full text

Urology, Pediatric Neurosurgery, Pediatrics +4

Mutations in EFHC1 cause juvenile myoclonic epilepsy

Toshimitsu Suzuki, Antonio V. Delgado‐Escueta, Kripamoy Aguan et al. · Nature Genetics · 2004 · 370 citations

Disease Gene Identification, Genetics, Neuroscience +1

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10

Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy

Takashi Sugawara, Emi Mazaki-Miyazaki, Katsuyuki Fukushima et al. · Neurology · 2002 · 236 citations

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

Itaru Kushima, Branko Aleksić, Masahiro Nakatochi et al. · Cell Reports · 2018 · 231 citations · Full text

Genetics, Genetic Epidemiology, Disease Gene Identification +16