채효진 부교수
#임상 화학#유전 진단
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학력
1997~2004
가톨릭대학교 의학 학사
2006~2011
가톨릭대학교 진단검사의학과 의학박사
가톨릭대학교 의학 학사
2006~2011
가톨릭대학교 진단검사의학과 의학박사
경력
2019~현재
서울성모병원 진단검사의학과 부교수
2015~2018
서울성모병원 진단검사의학과 조교수
2013~2015
서울성모병원 진단검사의학과 임상조교수
2012~2013
여의도성모병원 진단검사의학과 임상강사
2009~2012
서울성모병원 진단검사의학과 임상강사
2005~2009
가톨릭중앙의료원 진단검사의학과 레지던트
2004~2005
가톨릭중앙의료원 인턴
서울성모병원 진단검사의학과 부교수
2015~2018
서울성모병원 진단검사의학과 조교수
2013~2015
서울성모병원 진단검사의학과 임상조교수
2012~2013
여의도성모병원 진단검사의학과 임상강사
2009~2012
서울성모병원 진단검사의학과 임상강사
2005~2009
가톨릭중앙의료원 진단검사의학과 레지던트
2004~2005
가톨릭중앙의료원 인턴
논문
019 Oct
JOURNAL OF LABORATORY MEDICINE 제1저자
Analysis of a 6-year pilot external quality assurance survey of free light chain using Sigma metrics
2019 Sep
ANNALS OF LABORATORY MEDICINE 제1저자
Use of Liquid Chromatography-Tandem Mass Spectrometry for Clinical Testing in Korean Laboratories: a Questionnaire Survey
2019 Aug
JOURNAL OF CLINICAL MEDICINE 공동저자
A Mutation in ZNF143 as a Novel Candidate Gene for Endothelial Corneal Dystrophy
2019 Aug
INTERNATIONAL JOURNAL OF HEMATOLOGY 공동저자
Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing
2019 May
ANNALS OF LABORATORY MEDICINE 공동저자
Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea
2019 Jan
EXPERIMENTAL AND MOLECULAR MEDICINE 공동저자
CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia
2018 Dec
ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM(2012년부터 게재) 공동저자
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
2018 Jul
LABORATORY MEDICINE ONLINE 공동저자
높은 침투도를 보인 BMPR2 Intron 3 Splice Site Pathogenic Variant와 연관된 폐동맥고혈압 한국인 가족 증례 보고
2018 Jul
PEDIATRIC BLOOD & CANCER 공동저자
Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing
2018 Jun
THERAPEUTIC DRUG MONITORING 제1저자
Measurement of Teicoplanin Concentration With Liquid Chromatography-Tandem Mass Spectrometry Method Demonstrates the Usefulness of Therapeutic Drug Monitoring in Hematologic Patient Populations
2018 Apr
CLINICA CHIMICA ACTA 제1저자
Heavy/light chain assay as a biomarker for diagnosis and follow-up of multiple myeloma
2018 Jan
CELL DEATH & DISEASE 공동저자
Ubiquitin C decrement plays a pivotal role in replicative senescence of bone marrow mesenchymal stromal cells
2017 Oct
대한흉부외과학회 공동저자
Birt-Hogg-Dube Syndrome Manifesting as Spontaneous Pneumothorax: A Novel Mutation of the Folliculin Gene
2017 Jul
KOREAN SOC LABORATORY MEDICINE 공동저자
Hemoglobin Kansas: First Korean Family and Literature Review
2017 Apr
대한안과학회 공동저자
COL8A2 유전자 돌연변이 유무에 따른 푹스이상증의 임상적 특징 및 예후
2017 Apr
THE KOREAN SOCIETY FOR LABORATORY MEDICINE(대한진단검사의학회) 공동저자
GNAS 메틸화 이상으로 인한 거짓부갑상선기능저하증 Ib 1예
2017 Mar
KOREAN SOC LABORATORY MEDICINE 공동저자
Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency
2017 Jan
THE KOREAN SOCIETY FOR LABORATORY MEDICINE(대한진단검사의학회) 공동저자
FLT3-ITD 검출을 위한 절편분석법: 일반 중합효소연쇄반응 및 직접염기서열분석법과의 비교
외 다수
JOURNAL OF LABORATORY MEDICINE 제1저자
Analysis of a 6-year pilot external quality assurance survey of free light chain using Sigma metrics
2019 Sep
ANNALS OF LABORATORY MEDICINE 제1저자
Use of Liquid Chromatography-Tandem Mass Spectrometry for Clinical Testing in Korean Laboratories: a Questionnaire Survey
2019 Aug
JOURNAL OF CLINICAL MEDICINE 공동저자
A Mutation in ZNF143 as a Novel Candidate Gene for Endothelial Corneal Dystrophy
2019 Aug
INTERNATIONAL JOURNAL OF HEMATOLOGY 공동저자
Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing
2019 May
ANNALS OF LABORATORY MEDICINE 공동저자
Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea
2019 Jan
EXPERIMENTAL AND MOLECULAR MEDICINE 공동저자
CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia
2018 Dec
ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM(2012년부터 게재) 공동저자
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
2018 Jul
LABORATORY MEDICINE ONLINE 공동저자
높은 침투도를 보인 BMPR2 Intron 3 Splice Site Pathogenic Variant와 연관된 폐동맥고혈압 한국인 가족 증례 보고
2018 Jul
PEDIATRIC BLOOD & CANCER 공동저자
Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing
2018 Jun
THERAPEUTIC DRUG MONITORING 제1저자
Measurement of Teicoplanin Concentration With Liquid Chromatography-Tandem Mass Spectrometry Method Demonstrates the Usefulness of Therapeutic Drug Monitoring in Hematologic Patient Populations
2018 Apr
CLINICA CHIMICA ACTA 제1저자
Heavy/light chain assay as a biomarker for diagnosis and follow-up of multiple myeloma
2018 Jan
CELL DEATH & DISEASE 공동저자
Ubiquitin C decrement plays a pivotal role in replicative senescence of bone marrow mesenchymal stromal cells
2017 Oct
대한흉부외과학회 공동저자
Birt-Hogg-Dube Syndrome Manifesting as Spontaneous Pneumothorax: A Novel Mutation of the Folliculin Gene
2017 Jul
KOREAN SOC LABORATORY MEDICINE 공동저자
Hemoglobin Kansas: First Korean Family and Literature Review
2017 Apr
대한안과학회 공동저자
COL8A2 유전자 돌연변이 유무에 따른 푹스이상증의 임상적 특징 및 예후
2017 Apr
THE KOREAN SOCIETY FOR LABORATORY MEDICINE(대한진단검사의학회) 공동저자
GNAS 메틸화 이상으로 인한 거짓부갑상선기능저하증 Ib 1예
2017 Mar
KOREAN SOC LABORATORY MEDICINE 공동저자
Genetic Profiles of Korean Patients With Glucose-6-Phosphate Dehydrogenase Deficiency
2017 Jan
THE KOREAN SOCIETY FOR LABORATORY MEDICINE(대한진단검사의학회) 공동저자
FLT3-ITD 검출을 위한 절편분석법: 일반 중합효소연쇄반응 및 직접염기서열분석법과의 비교
외 다수
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