Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart DiseaseRachel Soemedi, Bernard Keavney, Catherine Cosgrove et al.|The American Journal of Human Genetics|2012Cited by 338
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16Heather J. Cordell, Bernard Keavney, Jamie Bentham et al.|Nature Genetics|2013Cited by 165
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRachel Soemedi, Bernard Keavney, Ana Töpf et al.|Human Molecular Genetics|2011Cited by 165