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홈 재단소개 전문의

전문의

GC Labs의 전문의를 소개합니다.

한성희 Sung Hee Han
이전
세포유전

이화여자대학교 의과대학원 의학박사 (2006)

이화여자대학교 의과대학원 의학석사 (2001)

이화여자대학교 의학사 (1998)

 

GC녹십자의료재단 진단검사의학본부 진검센터 센터장 (2023~)

GC녹십자의료재단 진단검사의학본부 전문의 (2023~)

임상유전학인증의 (2016~)

인바이츠바이오코아(주) 생명공학사업본부장 (2015~2023)

서울의과학연구소 인간유전, 세포유전 책임전문의 (2004~2015)

삼성서울병원 진단검사의학과 전임의 (2003~2004)

이화여자대학교 의료원 전공의 (1999~2002)

  • Mutation spectrum of NF1 gene in Korean unrelated patients with neurofibromatosis 1: Six novel pathogenic variants
    2024Journal of Genetic Medicine한성희
  • AI-assisted Karyotyping Improves Accuracy and Efficiency on a Large Scale in Cytogenetics Laboratories
    2023LMCE 2023 & KSLM 64th Annual Meeting한성희
  • 산전 CMA 검사 및 판독 시 고려해야 할 사항
    2022세포유전 미니워크숍한성희
  • Chromosomal abnormalities of 19,000 couples with recurrent spontaneous abortions: a multicenter study
    2022Fertility and Sterility한성희
  • Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study
    2021Neurogenetics한성희
  • Population-Based Analysis of BRCA1/2 Genes and Associated Breast and Ovarian Cancer Risk in Korean Patients: A Multicenter Cohort Study
    2021Cancers한성희
  • Investigation of Intestinal Microbiota and Fecal Calprotectin in NonToxigenic and Toxigenic Clostridioides difficile Colonization and Infection
    2020Microorganisms한성희
  • Mutation Spectrum and Genotype-Phenotype Correlations in 157 Korean Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Patients
    2020대한의학유전학회 제60차 추계학술대회한성희
  • First Korean case of factor V Leiden mutation in pregnant woman with a history of recurrent pregnancy loss
    2019J Genet Med한성희
  • First Korean case of factor V Leiden mutation in pregnant woman with a history of recurrent pregnancy loss
    2019대한의학유전학회 제59차 추계학술대회한성희
  • Composition of gut microbiota in patients with toxigenic Clostridioides (Clostridium) difficile: Comparison between subgroups according to clinical criteria and toxin gene load
    2019PLOS ONE한성희
  • Genetic Screening for Chromosomal Abnormalities and Y Chromosome Microdeletions in 846 Infertile Korean Men
    2018Lab Med Online한성희
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