Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya diseaseEunhee Kim, Han‐Wook Yoo, Mi‐Sun Yum et al.|Journal of neurosurgery|2015Cited by 116
PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype–phenotype correlation in Korean patients with Noonan syndromeJung Min Ko, Han‐Wook Yoo, Jae‐Min Kim et al.|Journal of Human Genetics|2008Cited by 108
Spectrum of Mutations in Noonan Syndrome and Their Correlation with PhenotypesBeom Hee Lee, Han‐Wook Yoo, Jae‐Min Kim et al.|The Journal of Pediatrics|2011Cited by 96
Diagnostic yield of targeted gene panel sequencing to identify the genetic etiology of disorders of sex developmentJa Hye Kim, Jin‐Ho Choi, Eungu Kang et al.|Molecular and Cellular Endocrinology|2017Cited by 78
A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutationYoo‐Mi Kim, Han‐Wook Yoo, Gu-Hwan Kim et al.|Metabolism|2013Cited by 76