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Biorxiv : the Preprint Server for Biology|June 12, 2025
Integrated analysis of COVID-19 multi-omics data for eQTLs reveals genetic mechanisms underlying disease severityJeongha Lee, Eun Young Jeon, Liyang Yu, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 3, 2017
eIF2B-related multisystem disorder in two sisters with atypical presentationsJin Sook Lee, Sangmoon Lee, Murim Choi, et al.
Annals of Neurology|October 23, 2024
Polygenic Landscape of Cryptogenic New-Onset Refractory Status Epilepticus: A Comprehensive Whole-Genome Sequencing StudyYoonhyuk Jang, Sung Eun Hong, Soo Hyun Ahn, et al.
Brain & Development|July 3, 2017
Severe hypotonia and postnatal growth impairment in a girl with a missense mutation in COL1A1: Implication of expanded phenotypic spectrum of type I collagenopathyJin Sook Lee, Jieun Seo, Anna Cho, et al.
BMC Cancer|January 20, 2021
The mutation of BCOR is highly recurrent and oncogenic in mature T-cell lymphomaJin Hyun Kang, Seung Ho Lee, Jawon Lee, et al.
Nature Genetics|June 25, 2025
Single-cell eQTL analysis identifies genetic variation underlying metabolic dysfunction-associated steatohepatitisSung Eun Hong, Seon Ju Mun, Young Joo Lee, et al.
Gene Expression Patterns : GEP|August 26, 2010
Expression patterns of astrocyte elevated gene-1 (AEG-1) during development of the mouse embryoHyun Yong Jeon, Murim Choi, Eric L Howlett, et al.
Circulation Research|October 18, 2024
Latrophilin-2 Deletion in Cardiomyocyte Disrupts Cell Junction, Leading to D-CMPMinjun Kang, Choon-Soo Lee, HyunJu Son, et al.
Clinical Genetics|February 6, 2020
Genetic heterogeneity in Leigh syndrome: Highlighting treatable and novel genetic causesJin Sook Lee, Taekyeong Yoo, Moses Lee, et al.
Genes, Chromosomes & Cancer|June 27, 2012
Comprehensive DNA methylation analysis of benign and malignant adrenocortical tumorsAnnabelle L Fonseca, Johan Kugelberg, Lee F Starker, et al.
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