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Rahman TJ

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of fallot
A common variant in the PTPN11 gene contributes to the risk of tetralogy of fallot

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