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BMC Musculoskeletal Disorders|September 14, 2023
Clinical, radiographic and molecular characterization of two unrelated families with multicentric osteolysis, nodulosis, and arthropathyTayyaba Ishaq, Petra Loid, Hafiza Abida Ishaq, et al.Annals of Pediatric Endocrinology & Metabolism|April 4, 2018
Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case reportDai Jung, Go Hun Seo, Yoon-Myung Kim, et al.Gene|July 1, 2023
Genomic analysis of multiplex consanguineous families reveals causes of neurodevelopmental disorders with epilepsyAnum Shafique, Tipu Sultan, Fatema Alzahrani, et al.Frontiers in Genetics|June 20, 2022
Phenotypic and Genetic Complexity in Pediatric Movement DisordersMin-Jee Kim, Mi-Sun Yum, Go Hun Seo, et al.Molecular Genetics & Genomic Medicine|March 4, 2024
A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE-1 insertion in LDLRYongjun Song, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, et al.Endocrine Journal|December 28, 2017
Broad clinical spectrum and diverse outcomes of prolactinoma with pediatric onset: medication-resistant and recurrent casesYoo-Mi Kim, Go Hun Seo, Yoon-Myung Kim, et al.Brain & Development|September 19, 2020
The first Korean cases of combined oxidative phosphorylation deficiency 35 with two novel TRIT1 mutations in two siblings confirmed by clinical and molecular investigationSukdong Yoo, Young A Kim, Ju Young Yoon, et al.Scientific Reports|February 19, 2026
Studies on intellectual disability identify variants in established genes as well as confirm candidature of new genesAmina Iftikhar Butt, Fariya Khan Bazai, Kaleemullah Kakar, et al.Journal of Human Genetics|December 14, 2017
Characteristic dysmorphic features in congenital disorders of glycosylation type IIbYoon-Myung Kim, Go Hun Seo, Euiseok Jung, et al.Journal of Korean Medical Science|May 11, 2021
Empty Sella Syndrome Associated with Growth Hormone Deficiency: the First Case Report of Weiss-Kruszka SyndromeJisun Park, Dong Jun Ha, Go Hun Seo, et al.Pageof 11