Author

Jong Hee Chae

Observed names: Chae, Jong Hee, Jong H. Chae

Institutions: Seoul National University, Seoul National University Hospital, Seoul National University Children's Hospital

Observed institutions: Seoul National University, Seoul National University Hospital, Seoul National University Children's Hospital

OpenAlex ID: A5113805248

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy

2026 · Adam Jackson, Alexander J. M. Blakes, et al. · Nature Genetics · 1

Case Report: Epileptic phenotype in a patient with a MARK2 variant: the first detailed description and review of the literature

2026 · Jin Sook Lee, You Min Kang, et al. · Frontiers in Pediatrics

Recurrent fever of unknown origin and unexplained bacteremia in a patient with a novel 4.5 Mb microdeletion in Xp11.23-p11.22

2024 · Cho-Rong Lee, Man Jin Kim, et al. · Scientific Reports

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

2019 · Lot Snijders Blok, Justine Rousseau, et al. · Newcastle University ePrints (Newcastle Univesity)

소아기 피부근염의 임상 양상과 치료 반응

2016 · 우혜원, 조재소, et al.

Works count: 11

Citation count: 2

H-index: 1

I10-index: