Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia

10.1038/s41598-017-18214-z

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Main Authors: Han Y., Dorajoo R., Chang X., Wang L., Khor C.-C., Sim X., Cheng C.-Y., Shi Y., Tham Y.C., Zhao W., Chee M.L., Sabanayagam C., Chae M.L., Tan N., Wong T.Y., Tai E.-S., Liu J., Goh D.Y.T., Yuan J.-M., Koh W.-P., Van Dam R.M., Low A.F., Chan M.Y.-Y., Friedlander Y., Heng C.-K.
Other Authors: MEDICINE
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Published: 2020
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Online Access:https://scholarbank.nus.edu.sg/handle/10635/175085
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spelling sg-nus-scholar.10635-1750852024-11-15T00:30:38Z Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia Han Y. Dorajoo R. Chang X. Wang L. Khor C.-C. Sim X. Cheng C.-Y. Shi Y. Tham Y.C. Zhao W. Chee M.L. Sabanayagam C. Chae M.L. Tan N. Wong T.Y. Tai E.-S. Liu J. Goh D.Y.T. Yuan J.-M. Koh W.-P. Van Dam R.M. Low A.F. Chan M.Y.-Y. Friedlander Y. Heng C.-K. MEDICINE DEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL) LIFE SCIENCES INSTITUTE SAW SWEE HOCK SCHOOL OF PUBLIC HEALTH DUKE-NUS MEDICAL SCHOOL PAEDIATRICS APOA5 protein, human apolipoprotein A5 biological marker adult aged case control study coronary artery disease ethnic group ethnology female follow up genetic predisposition genetics genome-wide association study genotype human male metabolism middle aged missense mutation procedures prognosis prospective study single nucleotide polymorphism Southeast Asia very elderly Adult Aged Aged, 80 and over Apolipoprotein A-V Asia, Southeastern Biomarkers Case-Control Studies Coronary Artery Disease Ethnic Groups Female Follow-Up Studies Genetic Predisposition to Disease Genome-Wide Association Study Genotype Humans Male Middle Aged Mutation, Missense Polymorphism, Single Nucleotide Prognosis Prospective Studies 10.1038/s41598-017-18214-z Scientific Reports 7 1 17921 2020-09-09T03:15:23Z 2020-09-09T03:15:23Z 2017 Article Han Y., Dorajoo R., Chang X., Wang L., Khor C.-C., Sim X., Cheng C.-Y., Shi Y., Tham Y.C., Zhao W., Chee M.L., Sabanayagam C., Chae M.L., Tan N., Wong T.Y., Tai E.-S., Liu J., Goh D.Y.T., Yuan J.-M., Koh W.-P., Van Dam R.M., Low A.F., Chan M.Y.-Y., Friedlander Y., Heng C.-K. (2017). Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia. Scientific Reports 7 (1) : 17921. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-017-18214-z 20452322 https://scholarbank.nus.edu.sg/handle/10635/175085 Unpaywall 20200831
institution National University of Singapore
building NUS Library
continent Asia
country Singapore
Singapore
content_provider NUS Library
collection ScholarBank@NUS
topic APOA5 protein, human
apolipoprotein A5
biological marker
adult
aged
case control study
coronary artery disease
ethnic group
ethnology
female
follow up
genetic predisposition
genetics
genome-wide association study
genotype
human
male
metabolism
middle aged
missense mutation
procedures
prognosis
prospective study
single nucleotide polymorphism
Southeast Asia
very elderly
Adult
Aged
Aged, 80 and over
Apolipoprotein A-V
Asia, Southeastern
Biomarkers
Case-Control Studies
Coronary Artery Disease
Ethnic Groups
Female
Follow-Up Studies
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Male
Middle Aged
Mutation, Missense
Polymorphism, Single Nucleotide
Prognosis
Prospective Studies
spellingShingle APOA5 protein, human
apolipoprotein A5
biological marker
adult
aged
case control study
coronary artery disease
ethnic group
ethnology
female
follow up
genetic predisposition
genetics
genome-wide association study
genotype
human
male
metabolism
middle aged
missense mutation
procedures
prognosis
prospective study
single nucleotide polymorphism
Southeast Asia
very elderly
Adult
Aged
Aged, 80 and over
Apolipoprotein A-V
Asia, Southeastern
Biomarkers
Case-Control Studies
Coronary Artery Disease
Ethnic Groups
Female
Follow-Up Studies
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Male
Middle Aged
Mutation, Missense
Polymorphism, Single Nucleotide
Prognosis
Prospective Studies
Han Y.
Dorajoo R.
Chang X.
Wang L.
Khor C.-C.
Sim X.
Cheng C.-Y.
Shi Y.
Tham Y.C.
Zhao W.
Chee M.L.
Sabanayagam C.
Chae M.L.
Tan N.
Wong T.Y.
Tai E.-S.
Liu J.
Goh D.Y.T.
Yuan J.-M.
Koh W.-P.
Van Dam R.M.
Low A.F.
Chan M.Y.-Y.
Friedlander Y.
Heng C.-K.
Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
description 10.1038/s41598-017-18214-z
author2 MEDICINE
author_facet MEDICINE
Han Y.
Dorajoo R.
Chang X.
Wang L.
Khor C.-C.
Sim X.
Cheng C.-Y.
Shi Y.
Tham Y.C.
Zhao W.
Chee M.L.
Sabanayagam C.
Chae M.L.
Tan N.
Wong T.Y.
Tai E.-S.
Liu J.
Goh D.Y.T.
Yuan J.-M.
Koh W.-P.
Van Dam R.M.
Low A.F.
Chan M.Y.-Y.
Friedlander Y.
Heng C.-K.
format Article
author Han Y.
Dorajoo R.
Chang X.
Wang L.
Khor C.-C.
Sim X.
Cheng C.-Y.
Shi Y.
Tham Y.C.
Zhao W.
Chee M.L.
Sabanayagam C.
Chae M.L.
Tan N.
Wong T.Y.
Tai E.-S.
Liu J.
Goh D.Y.T.
Yuan J.-M.
Koh W.-P.
Van Dam R.M.
Low A.F.
Chan M.Y.-Y.
Friedlander Y.
Heng C.-K.
author_sort Han Y.
title Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
title_short Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
title_full Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
title_fullStr Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
title_full_unstemmed Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia
title_sort genome-wide association study identifies a missense variant at apoa5 for coronary artery disease in multi-ethnic cohorts from southeast asia
publishDate 2020
url https://scholarbank.nus.edu.sg/handle/10635/175085
_version_ 1821194350781005824