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MEMBERS
Seung Woo Ryu, Ph.D.
INTERNSHIP
AFFILIATION
3billion Inc., Seoul, Republic of Korea
DEPARTMENT
Medical Genetics Division
EDUCATION
• 2015 - 2021 Ph.D., Biochemistry, University of Texas at Austin, Austin, TX, USA
• 2010 - 2014 B.S., Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL, USA
CONTACT
PUBLICATIONS
Selected
• 2025 Han HJ, et al. Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders. npj Genomic Medicine.
• 2025 Hwang SJ, et al. Clinical implementation of a multidisciplinary pipeline for genome sequencing in rare diseases: A prospective, multicenter, observational cohort study. Clinical and Translational Medicine.
• 2025 Khang R, et al. Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program. Human Mutation.
• 2024 Ryu SW, et al. Identification of recurrent MYH7 variant hypertrophic cardiomyopathy patients in Korea: a case series. Cardiovascular Diagnosis and Therapy.
• 2024 Ryu SW, et al. High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients. Frontiers in Cardiovascular Medicine.
• 2024 Ryu SW, et al. Identification of a complex intrachromosomal inverted insertion in chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular Genetics & Genomic Medicine.
• 2021 Lee JH, et al. Poly-ADP-ribosylation drives loss of protein homeostasis in ATM and Mre11 deficiency. Molecular Cell.
• 2020 Ryu SW, et al. Proteome-wide identification of HSP70/HSC70 chaperone clients in human cells. PLoS Biology.
Full Publication list
https://scholar.google.com/citations?user=CXgoHekAAAAJ&hl=ko&authuser=1
AWARDS
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PRESENTATIONS
Selected
• 2026 “Navigating Clinical Genomics Testing: When Panel Is Not Enough.” The Taiwan Human Genetics Society (THGS), Taiwan.
• 2025 “Genetic Diagnostics: Evaluation of Developmental Delay and Genetic Testing.” Rare Diseases — From Diagnosis to Family Planning, Chonnam National University Hwasun Hospital, Republic of Korea.
• 2024 “Genetic Testing in the Genomic Era: Experience from South Korea.” 49th Congreso Nacional de Genética Humana (CNGH) Asociación Mexicana de Genética Humana (AMGH), Mexico.
• 2024 “Rethinking Clinical Practice in Genomic Era.” 1st International Symposium and Workshop: [Medical Genetic Update: From Genomic to Clinic], Universitas YARSI, Indonesia.
• 2024 Poster. “High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients.” ASHG, United States.
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