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Paper Details

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Nat Genet
271
2016
CDK13, CHD, CHD-associated genes, CHD4, CHDs, Congenital heart defects, NS-CHD, PRKD1, PTVs, S-CHD, S-CHD disorders, humans, mice, monogenic CHD, nonsyndromic CHD, patients, protein-truncating variants, syndromic CHD, syndromic and nonsyndromic congenital heart defects, syndromic'
Author NameAffiliation
Tarjinder SinghWellcome Trust Sanger Institute
Ganesh J SwaminathanWellcome Trust Sanger Institute
Siddharth BankaInstitute of Human Development, University of Manchester
Siddharth BankaSt Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust
John DaneshWellcome Trust Sanger Institute
John DaneshUniversity of Cambridge
John DaneshNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Willem H OuwehandWellcome Trust Sanger Institute
Willem H Ouwehand
Willem H OuwehandUniversity of Cambridge
Willem H OuwehandNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Willem H OuwehandWellcome Trust Sanger Institute
Willem H OuwehandNIHR Blood and Transplant Research Unit in Donor Health and Genomics, University of Cambridge
Willem H OuwehandUniversity of Cambridge
Willem H Ouwehand
Soo-Mi ParkCambridge University Hospitals NHS Foundation Trust
Leema RobertGuy's and St Thomas' NHS Foundation Trust, Guy's Hospital
Jennifer SambrookUniversity of Cambridge
Jennifer SambrookUniversity of Cambridge
Hugh WatkinsUniversity of Oxford
Seema MitalHospital for Sick Children
Bernard KeavneyInstitute of Cardiovascular Sciences, University of Manchester
Caroline F WrightWellcome Trust Sanger Institute
Helen V FirthCambridge University Hospitals NHS Foundation Trust
Jeffrey C BarrettWellcome Trust Sanger Institute
David R FitzPatrickMedical Research Council (MRC) Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine (IGMM), University of Edinburgh, Western General Hospital
Matthew E HurlesWellcome Trust Sanger Institute
Matthew E HurlesWellcome Trust Sanger Institute
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