Betül Baykan

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens et al. · Nature Genetics · 2014 · 311 citations · Full text

Genetics, Neuroscience, Central Nervous System +3

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

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

Hsien-Yang Lee, Yong Huang, Nadine Bruneau et al. · Cell Reports · 2012 · 262 citations · Full text

One-year prevalence and the impact of migraine and tension-type headache in Turkey: a nationwide home-based study in adults

Mustafa Ertaş, Betül Baykan, Elif Kocasoy Orhan et al. · The Journal of Headache and Pain · 2012 · 195 citations · Full text

Consensus on diagnosis and management of JME: From founder's observations to current trends

Dorothée G.A. Kasteleijn- Nolst Trenité, Bettina Schmitz, Diéter Janz et al. · Epilepsy & Behavior · 2013 · 166 citations

Medicine, Disease Diagnosis, Diagnosis +1