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성문우 교수

Moon-Woo Seong

서울대학교 검사의학교실 · 의학

연구실 소개

성문우 교수의 연구실은 유전질환과 감염병의 분자 기반 메커니즘을 밝히는 데 초점을 맞추고 있습니다. 특히 림프구성형 근이영양증(LGMD), 난시성 망막병증(LCA), 유방암 관련 BRCA1/BRCA2 유전자 변이 등 희귀유전질환의 정밀 유전체 분석을 통해 진단 및 예후 생물학적 마커를 규명하고 있습니다. 또한 코로나19와 MERS 등 감염병의 단백질 동역학과 바이러스 유전체 변화를 종단적 분석함으로써 질병 진행 예측 및 유전적 이질성에 대한 통찰을 제공합니다.

유전체 분석희귀유전질환감염병 생물학예후 마커단백질 동역학

연구 현황

논문 수
370
총 인용 수
5,766
최근 5년 논문
82
주요 분야
의학

연구 성과 추이

표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.

5개년 연도별 논문 게재 수
82총합
2022
2023
2024
2025
2026
5개년 연도별 피인용 수
351총합
20222023202420252026

주요 논문

15
1
논문|인용수 81·2020
Evidence of Severe Acute Respiratory Syndrome Coronavirus 2 Reinfection After Recovery from Mild Coronavirus Disease 2019
Jee‐Soo Lee, So Yeon Kim, Taek Soo Kim, Ki Ho Hong, Nam Hee Ryoo, Jaehyeon Lee, Jae Hyeon Park, Sung Im Cho, Man Jin Kim, Young-Gon Kim, Boram Kim, Ho Seob Shin
SJR Q1FWCI 2.0Clinical Infectious DiseasesOA

Reinfection with a genetically distinct SARS-CoV-2 strain may occur in an immunocompetent patient shortly after recovery from mild COVID-19. SARS-CoV-2 infection may not confer immunity against a different SARS-CoV-2 strain.

Infectious DiseasesMedicine
2
논문|인용수 50·2015
Clinical applications of next‐generation sequencing‐based gene panel in patients with muscular dystrophy: Korean experience
Moon‐Woo Seong, Anna Cho, Hyunwoong Park, Soo Hyun Seo, Byung Chan Lim, Dong-soo Seol, S.I. Cho, Sung Sup Park, Jong‐Hee Chae
SJR Q2FWCI 2.0Clinical Genetics

Muscular dystrophy (MD) is a genetically and clinically heterogeneous group of disorders. Here, we performed targeted sequencing of 18 limb-girdle MD (LGMD)-related genes in 35 patients who were highly suspected of having MD. We identified one or more pathogenic variants in 23 of 35 patients (65.7%), and a genetic diagnosis was performed in 20 patients (57.1%). LGMD2B was the most common LGMD type, followed by LGMD1B, LGMD2A, and LGMD2G. Among the three major LGMD types in this group, LGMD1B was

Molecular BiologyBiochemistry, Genetics and Molecular Biology
3
논문|인용수 44·2021
Longitudinal proteomic profiling provides insights into host response and proteome dynamics in COVID‐19 progression
Jee‐Soo Lee, Dohyun Han, So Yeon Kim, Ki Ho Hong, Myoung‐jin Jang, Man Jin Kim, Young‐Gon Kim, Jae Hyeon Park, Sung Im Cho, Wan Beom Park, Kyungbok Lee, Ho Seob Shin
SJR Q2FWCI 2.5PROTEOMICSOA

In managing patients with coronavirus disease 2019 (COVID-19), early identification of those at high risk and real-time monitoring of disease progression to severe COVID-19 is a major challenge. We aimed to identify potential early prognostic protein markers and to expand understanding of proteome dynamics during clinical progression of the disease. We performed in-depth proteome profiling on 137 sera, longitudinally collected from 25 patients with COVID-19 (non-severe patients, n = 13; patients

Infectious DiseasesMedicine
4
논문|인용수 43·2008
Molecular characterization of Leber congenital amaurosis in Koreans.
Moon‐Woo Seong, Seong Yeon Kim, Young Suk Yu, Jeong‐Min Hwang, Kim J, Sung Sup Park
FWCI 1.0PubMedOA

This comprehensive mutational analysis shows marked genetic heterogeneity in Korean LCA patients and reveals a mutation spectrum that differs from those previously reported. In turn, this suggests that a different strategy should be used for the molecular diagnosis of LCA in Koreans.

Molecular BiologyBiochemistry, Genetics and Molecular Biology
5
논문|인용수 38·2015
Microevolution of Outbreak-Associated Middle East Respiratory Syndrome Coronavirus, South Korea, 2015
Moon‐Woo Seong, So Yeon Kim, Victor M. Corman, Taek Soo Kim, Sung Im Cho, Man Jin Kim, Seung Jun Lee, Hyukmin Lee, Soo Hyun Seo, Ji Soo Ahn, Byeong Su Yu, Nare Park
SJR Q1FWCI 4.3Emerging infectious diseasesOA

During the 2015 Middle East respiratory syndrome coronavirus outbreak in South Korea, we sequenced full viral genomes of strains isolated from 4 patients early and late during infection. Patients represented at least 4 generations of transmission. We found no evidence of changes in the evolutionary rate and no reason to suspect adaptive changes in viral proteins.

Infectious DiseasesMedicine
6
논문|인용수 33·2009
Comprehensive mutational analysis of <i>BRCA1/BRCA2</i> for Korean breast cancer patients: evidence of a founder mutation
Moon‐Woo Seong, SI Cho, D‐Y Noh, Wonshik Han, S‐W Kim, C. Park, Hyunwoong Park, SY Kim, Kim J, Sung Sup Park
SJR Q2FWCI 1.2Clinical GeneticsOA

The BRCA1 and BRCA2 genes are the strongest susceptibility genes identified for breast cancer worldwide. However, BRCA1/BRCA2 have been incompletely investigated due to their large size and the genomic rearrangements that occasionally occur within them. Here we performed a comprehensive mutational analysis for BRCA1/BRCA2 in 206 Korean patients with breast cancer. We analyzed all exons and flanking regions of BRCA1/BRCA2 by direct sequencing and screened deletions or duplications involving BRCA1

GeneticsBiochemistry, Genetics and Molecular Biology
7
논문|인용수 33·2018
Reclassification of <i>BRCA1</i> and <i>BRCA2</i> variants of uncertain significance: a multifactorial analysis of multicentre prospective cohort
Hyukmin Lee, Sohee Oh, Sue K. Park, Min-Hyuk Lee, Jong Won Lee, Sung‐Won Kim, Byung Ho Son, Dong‐Young Noh, Jeong Eon Lee, Hai‐Lin Park, Man Jin Kim, Sung Im Cho
SJR Q1FWCI 3.4Journal of Medical Genetics

The classification in this study would minimise the 'uncertainty' in clinical interpretation, and this validated multifactorial model can be used for the reliable annotation of <i>BRCA1/2</i> VUSs.

GeneticsBiochemistry, Genetics and Molecular Biology
8
논문|인용수 31·2018
Diagnostic challenge for the rare lysosomal storage disease: Late infantile GM1 gangliosidosis
Jin Sook Lee, Jong-Moon Choi, Moses Lee, Soo Yeon Kim, Sangmoon Lee, Byung Chan Lim, Jung‐Eun Cheon, In-One Kim, Ki Joong Kim, Murim Choi, Moon‐Woo Seong, Jong‐Hee Chae
SJR Q2FWCI 2.9Brain and Development
PhysiologyMedicine
9
논문|인용수 27·2014
A multi-institutional study of the prevalence of BRCA1 and BRCA2 large genomic rearrangements in familial breast cancer patients
Moon‐Woo Seong, Sung Im Cho, Hyun‐Ah Kim, Il Yong Chung, Eunyoung Kang, Jong Won Lee, Hai‐Lin Park, Min Hyuk Lee, Doo Ho Choi, Cha Kyong Yom, Woo-Chul Noh, Myung Chul Chang
SJR Q2FWCI 2.8BMC CancerOA

In this study, we showed that LGRs were found in 3.7% (3/81) of the patients who had mutations in BRCA1 or BRCA2, and 7.5% (3/40) of patients with mutations in BRCA1. This suggests that the contribution of LGRs to familial breast cancer in this population might be comparable to that in other ethnic populations. Given these findings, an MLPA to screen for mutations in the BRCA1 gene is recommended as an initial screening test in highly selective settings.

GeneticsBiochemistry, Genetics and Molecular Biology
10
논문|인용수 25·2008
Neonatal Hair Nicotine Levels and Fetal Exposure to Paternal Smoking at Home
Moon‐Woo Seong, Joyce Hyunjoo Hwang, Jin Soo Moon, Hye-Jung Ryu, Sun‐Young Kong, Tae Hyun Um, J-G Park, Do Hoon Lee
SJR Q1FWCI 2.2American Journal of EpidemiologyOA

Exposure to environmental tobacco smoke (ETS) is a major risk to human health, and the home is the greatest single source of ETS for children. The authors investigated fetal exposure to paternal smoking at home during pregnancy. Korean families were included as trios of fathers, mothers, and neonates identified in 2005-2007. Sixty-three trios were finally enrolled in this study after exclusion of those in which the mother was a smoker or was regularly exposed to ETS at places other than the home

PhysiologyMedicine
11
논문|인용수 22·2009
Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population
Moon‐Woo Seong, Sung Im Cho, Dong‐Young Noh, Wonshik Han, Sung‐Won Kim, Chulmin Park, Hyunwoong Park, So Yeon Kim, Kim J, Sung Sup Park
SJR Q2FWCI 1.2Familial Cancer
GeneticsBiochemistry, Genetics and Molecular Biology
12
논문|인용수 20·2015
Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia
Hyunwoong Park, Seong-Ho Kang, Seungman Park, So Yeon Kim, Soo Hyun Seo, Seung Jun Lee, Jung Ae Lee, Sung Im Cho, Jung‐Joon Sung, Kwang Woo Lee, Kim J, Sung Sup Park
SJR Q1FWCI 0.4Journal of the Neurological Sciences
Cellular and Molecular NeuroscienceNeuroscience
13
논문|인용수 20·2022
SARS-CoV-2 shedding dynamics and transmission in immunosuppressed patients
Jee‐Soo Lee, Ki Wook Yun, Hyeonju Jeong, Boram Kim, Man Jin Kim, Jae Hyeon Park, Ho Seob Shin, Hyeon Sae Oh, Hobin Sung, Myung Gi Song, Sung Im Cho, So Yeon Kim
SJR Q1FWCI 2.0VirulenceOA

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern have been emerging. However, knowledge of temporal and spatial dynamics of SARS-CoV-2 is limited. This study characterized SARS-CoV-2 evolution in immunosuppressed patients with long-term SARS-CoV-2 shedding for 73-250 days, without specific treatment. We conducted whole-genome sequencing of 27 serial samples, including 26 serial samples collected from various anatomic sites of two patients and the first positive sa

Infectious DiseasesMedicine
14
논문|인용수 19·2014
Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene
Hyunwoong Park, S.y. Hong, Sung Im Cho, Tae‐Joon Cho, In Ho Choi, Dong‐Kyu Jin, Young Bae Sohn, Sung Won Park, Hyun‐Hae Cho, Jung‐Eun Cheon, So Yeon Kim, Kim J
SJR Q2FWCI 1.0European Journal of Medical Genetics
Molecular BiologyBiochemistry, Genetics and Molecular Biology
15
논문|인용수 17·2014
Diagnostic Application of an Extensive Gene Panel for Leber Congenital Amaurosis with Severe Genetic Heterogeneity
Moon‐Woo Seong, Soo Hyun Seo, Young Suk Yu, Jeong‐Min Hwang, Sung Im Cho, Eun Kyung, Hyunwoong Park, Seung Jun Lee, Kim J, Sung Sup Park
SJR Q1FWCI 0.9Journal of Molecular Diagnostics
Molecular BiologyBiochemistry, Genetics and Molecular Biology

대표 연구 분야

GeneticsMolecular BiologyInfectious DiseasesEpidemiologyPhysiologySurgery

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