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Töpf A

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
Increased power for detection of parent-of-origin effects via the use of haplotype estimation
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
Aetiological role of folate deficiency in congenital cardiovascular malformation: Evidence from 'mendelian randomisation' and meta-analysis
A common variant in the PTPN11 gene contributes to the risk of tetralogy of fallot

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