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Kyung-ah Lee

Yonsei University · Medicine

About the Lab

Professor Kyung-ah Lee's research lab specializes in translational biomedical research with a focus on clinical biomarkers, cancer genomics, and hematological disorders. The lab investigates novel diagnostic tools such as the delta neutrophil index for sepsis, exosomal nucleic acids for non-small cell lung cancer resistance, and genetic polymorphisms like GSTM1/GSTT1 deletions in aplastic anemia. A key research direction involves developing and validating clinical assessment tools, such as the简易 University Adjustment Scale, to support mental health and student well-being in academic settings. The lab integrates molecular diagnostics, clinical data analysis, and psychosocial assessment to improve patient outcomes and early disease detection.

biomarkerscancer genomicssepsisaplastic anemiaclinical diagnostics

Research Overview

Papers
400
Total Citations
4,606
Papers (5y)
77
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
77total
2021
2022
2023
2024
2025
Citations per year (5y)
401total
20212022202320242025

Selected Papers

15
1
Article|126 citations·2012
Delta Neutrophil Index
Yoonmi Seok, Jong Rak Choi, Juwon Kim, Young Keun Kim, Jong‐Wook Lee, Jaewoo Song, Sue Jeong Kim, Kyung‐A Lee
SJR Q1Shock

Delta neutrophil index (DN) is the immature granulocyte fraction provided by a blood cell analyzer (ADVIA 2120; Siemens Healthcare Diagnostics, Deerfield, Ill), which is determined by subtracting the fraction of mature polymorphonuclear leukocytes from the sum of myeloperoxidase-reactive cells. The purpose of this study was to define the role of DN in differential diagnosis and prognosis prediction of patients with sepsis. Hospital records of 273 patients were retrospectively collected: 47 with

EpidemiologyMedicine
2
Article|114 citations·2008
간편 대학생활적응척도 개발 및 타당화 연구
이경아, 신혜린, 유나현, 이기학

본 연구에서는 대학생들의 학교적응수준을 파악하는데 활용될 수 있는 간편 대학생활적응척도를 제작하기 위해 기존의 대학생활 적응 측정도구와 연구결과를 토대로 상담전문가 및 학생 면담을 거쳐 학생들의 적응상의 문제를 잘 반영하는 문항을 선정하였다. 선정된 문항은 예비연구에서 전문가의 평가 및 탐색적 요인분석을 거쳐 적응수준과 적응자원 차원으로 구분되었다. 또한 고위험군 대학생의 위기 문제 정도를 측정하기 위해 임상 경험 5년 이상인 상담 전문가 5인의 합의를 거쳐 위기문항이 포함되었다. 본연구에서는 구성된 검사의 신뢰도와 타당도를 알아보기 위해 먼저 각 하위척도별로 내적합치도를 살펴보고, 확인적 요인분석을 통해 구성개념 타당도를 검증하였다. 또한 대학생활적응척도의 하위요인들과 U&I 학습유형검사, 정서지능, Brief Symptom Inventory(BSI) 및 Focused Group Interview를 통해 추출된 대학생활적응관련 문항들과의 상관분석을 통해 준거관련 타당도를 알아보았다

3
Article|86 citations·2004
Novel interleukin 1� polymorphism increased the risk of gastric cancer in a Korean population
Kyung‐A Lee, Chang‐Seok Ki, Hye‐Jin Kim, Kwang‐Min Sohn, Jong‐Won Kim, Won Ki Kang, Poong‐Lyul Rhee, Sang Yong Song, Tae Sung Sohn
SJR Q1Journal of GastroenterologyOA
SurgeryMedicine
4
Article|58 citations·2019
A novel approach for tuberculosis diagnosis using exosomal DNA and droplet digital PCR
Sujeong Cho, Saeam Shin, Yoonjung Kim, Wonkeun Song, Yunsop Chong, Seok Hoon Jeong, Myung Seo Kang, Kyung‐A Lee
SJR Q1Clinical Microbiology and InfectionOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
5
Article|55 citations·2011
The frequency of meconium-stained amniotic fluid increases as a function of the duration of labor
Kyung‐A Lee, Seung Mi Lee, Hye Jin Yang, Chan‐Wook Park, Shali Mazaki‐Tovi, Bo Hyun Yoon, Roberto Romero
SJR Q2The Journal of Maternal-Fetal & Neonatal MedicineOA

MSAF was found in only 2.8% (28/1008) of women who delivered before the onset of labor, but in 23.1% (778/3368) of women who delivered after the onset of labor. The longer the duration of labor, the higher the risk of MSAF in term singleton gestation.

EpidemiologyMedicine
6
Article|50 citations·2013
Prevalence of sexually transmitted infections among healthy Korean women: Implications of multiplex PCR pathogen detection on antibiotic therapy
Yoonjung Kim, Juwon Kim, Kyung‐A Lee
SJR Q2Journal of Infection and ChemotherapyOA
MicrobiologyImmunology and Microbiology
7
Article|46 citations·2021
Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy
Yoonjung Kim, Saeam Shin, Kyung‐A Lee
SJR Q1Cancer Cell InternationalOA

BACKGROUND: The exosomal nucleic acid (exoNA) from the plasma and pleural fluid can potentially provide means to identify genomic changes in non-small cell lung cancer (NSCLC) patients who develop resistance to targeted epidermal growth factor receptor (EGFR) inhibitor therapy. METHODS: We compared the performance of the following tools to detect EGFR mutations in 54 plasma samples and 13 pleural fluid using cfDNA, combined TNA (exoTNA + cfTNA), or total cellular DNA: droplet digital PCR (ddPCR)

Pulmonary and Respiratory MedicineMedicine
8
Article|41 citations·2017
Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patients
Saeam Shin, Juwon Kim, Yoonjung Kim, Sun-Mi Cho, Kyung‐A Lee
SJR Q1Clinical Chemistry and Laboratory Medicine (CCLM)OA

BACKGROUND: EGFR mutation is an emerging biomarker for treatment selection in non-small-cell lung cancer (NSCLC) patients. However, optimal mutation detection is hindered by complications associated with the biopsy procedure, tumor heterogeneity and limited sensitivity of test methodology. In this study, we evaluated the diagnostic utility of real-time PCR using malignant pleural effusion samples. METHODS: A total of 77 pleural fluid samples from 77 NSCLC patients were tested using the cobas EGF

Pulmonary and Respiratory MedicineMedicine
9
Article|33 citations·2001
Increased frequencies of glutathione S-transferase(GSTM1 and GSTT1) gene deletions in Korean patients with acquired aplastic anemia
Kyung‐A Lee, Sun Hee Kim, Hee Yeon Woo, Young Joon Hong, Hyoun Chan Cho
SJR Q1BloodOA

Patients with reduced ability to metabolize environmental carcinogens or toxins may be at risk of developing aplastic anemia. Glutathione S-transferase (GST) has been implicated in detoxifying mutagenic electrophilic compounds. This study asked whether the homozygous gene deletions of GSTM1 and GSTT1 affect the likelihood of developing aplastic anemia. The incidence of GSTM1 and GSTT1 gene deletions was significantly higher for aplastic anemia patients (odds ratio [OR]: 3.1, P =.01 and OR: 3.1,

Molecular BiologyBiochemistry, Genetics and Molecular Biology
10
Article|28 citations·2016
Secondhand smoke exposure and susceptibility to initiating cigarette smoking among never-smoking students in selected African countries: Findings from the Global Youth Tobacco Survey
Kyung‐A Lee, Krishna Palipudi, Lorna McLeod English, Nivo Ramanandraibe, Samira Asma
SJR Q1Preventive Medicine
PhysiologyMedicine
11
Article|28 citations·2013
Spectrum of EGFR Gene Copy Number Changes and KRAS Gene Mutation Status in Korean Triple Negative Breast Cancer Patients
Yoonjung Kim, Juwon Kim, Hy De Lee, Joon Jeong, Woochang Lee, Kyung‐A Lee
SJR Q1PLoS ONEOA

Anti-epidermal growth factor receptor (EGFR) therapy has been tried in triple negative breast cancer (TNBC) patients without evaluation of molecular and clinical predictors in several randomized clinical studies. Only fewer than 20% of metastatic TNBCs showed response to anti-EGFR therapy. In order to increase the overall response rate, first step would be to classify TNBC into good or poor responders according to oncogenic mutation profiles. This study provides the molecular characteristics of

Pulmonary and Respiratory MedicineMedicine
12
Article|27 citations·2019
Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients
Yoonjung Kim, Saeam Shin, Boyeon Kim, Kyung‐A Lee
SJR Q1Cancer Cell InternationalOA

Abstract Background Exosomal nucleic acid (exoNA) is a feasible target to improve the sensitivity of EGFR mutation testing in non-small cell lung cancer patients with limited cell-free DNA (cfDNA) mutant copies. However, the type and size of target exoNA related to the sensitivity of EGFR mutation testing has not been explored extensively. Methods The type and size of target exoNA related to the sensitivity of EGFR mutation testing was evaluated using ddPCR. A total of 47 plasma samples was test

Cancer ResearchBiochemistry, Genetics and Molecular Biology
13
Article|27 citations·2007
Association Between a Polymorphism in the Lymphotoxin −a Promoter Region and Migraine
Kyung‐A Lee, Soo Yeon Jang, Kwang‐Min Sohn, Hong‐Hee Won, Min Ji Kim, Jong‐Won Kim, Chin‐Sang Chung
SJR Q1Headache The Journal of Head and Face PainOA

OBJECTIVE: The aim of this study was to determine whether polymorphisms in the lymphotoxin (LTA)-tumor necrosis factor (TNF) region are associated with the risk of migraine. BACKGROUND: Previous studies concerning the role of TNFalpha in migraine have provided conflicting results. It has been reported that LTA could be a susceptibility gene in migraine. It is possible that the TNFalpha polymorphism associated with migraine is in linkage disequilibrium with other functional polymorphisms that inf

Psychiatry and Mental healthMedicine
14
Article|24 citations·2006
Quality Characteristics of Hot-air Dried Radish (Raphanus sativus L.) Leaves
Kyung‐A Lee, Yong‐Ho Kim, Yong‐Woo Lee, 이용환
SJR Q3Journal of the Korean Society of Food Science and Nutrition

무청별 무청의 성분분석과 반응표면 분석법을 이용하여 건조조건에 따른 무청 고유의 색도, 칼슘, 철분, 비타민 등의 성분을 조사하였다. 일반성분의 경우 품종이 다른 미농단백무(RL5)를 제외하고는 품종 간에 회분, 단백질, 지방, 칼슘 및 철분함량에 유의적인 차이가 없었고, 건물량으로 환산한 비타민류, 클로로필 함량, 색도에는 품종 간 유의적인 차이가 있었다. 한편 중심합성 실험계획에 따라 건조한 미농단백무 무청의 품질특성을 조사한 결과 수분함량, 클로로필 함량 및 색도차이를 나타내는 ΔE 값은 건조온도와 시간에 따라 유의적인 차이가 있었고, 칼슘, 철분함량은 각각 31.41~35.80 ㎎, 0.21~0.29 ㎎으로 시료 간 유의성이 없었다. 무청의 건조조건을 독립변수로 하고, 시료 간 유의적인 차이를 보였던 종속변수인 수분, 클로로필 및 색도 값의 상관관계를 나타내는 R²값이 0.97 이상으로 높았다. 또 회귀분석한 모델식중 반응표면 분석법으로 도시한 결과 총 클로로필 함량은 독립변

Food ScienceAgricultural and Biological Sciences
15
Article|23 citations·2021
Effect of sarcomere and mitochondria-related mutations on myocardial fibrosis in patients with hypertrophic cardiomyopathy
Hyemoon Chung, Yoonjung Kim, Chul Hwan Park, Jong‐Youn Kim, Pil‐Ki Min, Young Won Yoon, Tae Hoon Kim, Byoung Kwon Lee, Bum‐Kee Hong, Se‐Joong Rim, Hyuck Moon Kwon, Kyung‐A Lee
SJR Q1Journal of Cardiovascular Magnetic ResonanceOA

BACKGROUND: Myocardial fibrosis is an important prognostic factor in hypertrophic cardiomyopathy (HCM). However, the contribution from a wide spectrum of genetic mutations has not been well defined. We sought to investigate effect of sarcomere and mitochondria-related mutations on myocardial fibrosis in HCM. METHODS: In 133 HCM patients, comprehensive genetic analysis was performed in 82 nuclear DNA (33 sarcomere-associated genes, 5 phenocopy genes, and 44 nuclear genes linked to mitochondrial c

Cardiology and Cardiovascular MedicineMedicine

Research Areas

GeneticsMolecular BiologyHematologyEpidemiologyCardiology and Cardiovascular MedicineSurgery

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