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Paper Details

Congenital heart disease risk loci identified by genome-wide association study in European patients.
J Clin Invest
41
2021
ATAV, CHD, Congenital heart disease, GOSR2, GOSR2 locus, MACROD2, MACROD2 locus, MSX1, SNP-carrying genes, TGA, WNT3, anomalies of thoracic arteries and veins, chromosome 17q21, chromosome 20p12, chromosome 5q22, congenital heart disease, human, human and murine induced pluripotent stem cells, induced pluripotent stem cells, murine, patients, risk loci, risk variants, rs870142, septal defects, transposition of the great arteries
Author NameAffiliation
Bernard KeavneyThe University of Manchester
Bernard KeavneyManchester University NHS Foundation Trust
Peter LichtnerInstitute of Human Genetics, German Research Center for Environmental Health
James R PriestStanford University School of Medicine
Thomas MeitingerInstitute of Human Genetics, German Research Center for Environmental Health
Thomas MeitingerDZHK (German Center for Cardiovascular Research) - Partner Site Munich Heart Alliance
Thomas MeitingerInstitute of Human Genetics, Technical University of Munich
Thomas MeitingerInstitute of Human Genetics, German Research Center for Environmental Health
Thomas MeitingerInstitute of Human Genetics, Technical University of Munich
Thomas MeitingerDZHK (German Center for Cardiovascular Research) - Partner Site Munich Heart Alliance
Heather J CordellPopulation Health Sciences Institute, Newcastle University, International Centre for Life
Bertram M??ller-MyhsokMax Planck Institute of Psychiatry Munich
Bertram M??ller-Myhsok
Bertram M??ller-MyhsokInstitute of Translational Medicine, University of Liverpool
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