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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Heather J Cordell, Jamie Bentham, Ana Topf, Diana Zelenika, Simon Heath, Chrysovalanto Mamasoula, Catherine Cosgrove, Gillian Blue, Javier Granados-Riveron, Kerry Setchfield, Chris Thornborough, Jeroen Breckpot, Rachel Soemedi, Ruairidh Martin, Thahira J Rahman, Darroch Hall, Klaartje van Engelen, Antoon F M Moorman, Aelko H Zwinderman, Phil Barnett, Tamara T Koopmann, Michiel E Adriaens, Andras Varro, Alfred L George, Christobal dos Remedios, Nanette H Bishopric, Connie R Bezzina, John O'Sullivan, Marc Gewillig, Frances A Bu'Lock, David Winlaw, Shoumo Bhattacharya, Koen Devriendt, J David Brook, Barbara J M Mulder, Seema Mital, Alex V Postma, G Mark Lathrop, Martin Farrall, Judith A Goodship, Bernard D Keavney

Nature Genetics, 2013. DOI 10.1038/ng.2637

Has this study been replicated?

The atlas records 1 replication of this study. Recorded outcomes: 1 successful.

Replications

• Replication of the 4p16 Susceptibility Locus in Congenital Heart Disease in Han Chinese Populations, Zhao et al. (2014). Outcome recorded: successful. Our findings suggest that susceptibility loci of ASD identified from Cordell's European GWAS are generalizable to Chinese population View paper

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