Dilşad Türkdoğan

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

A prevalence study of restless legs syndrome in Turkish children and adolescents

Dilşad Türkdoğan, Nural Bekiroğlu, Sennur Zaimoğlu · Sleep Medicine · 2011 · 118 citations

Turkish Children, Sleep, Sleep Disorder +7

PRRT2 Mutations are the major cause of benign familial infantile seizures

Julian Schubert, Roberta Paravidino, Felicitas Becker et al. · Human Mutation · 2012 · 104 citations

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa et al. · The American Journal of Human Genetics · 2021 · 58 citations · Full text

Mendelian Disorder, Female Infertility, Whole-exome Sequencing Study +9

Characteristic and Overlapping Features of Migraine and Tension‐Type Headache

Dilşad Türkdoğan, Didem Soylemez, Haydar Sur et al. · Headache The Journal of Head and Face Pain · 2006 · 53 citations