Mamasoula

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease

*Circulation: Cardiovascular Genetics* 2013; 6(4):347-353

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

*Nature Genetics* 2013; 45(7):822-824

Common variation neighbouring micro-RNA 22 is sssociated with increased left ventricular mass

*PLoS ONE* 2013; 8(1):e55061

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of fallot

*Human Molecular Genetics* 2013; 22(7):1473–1481

Aetiological role of folate deficiency in congenital cardiovascular malformation: Evidence from 'mendelian randomisation' and meta-analysis

*Genetic Epidemiology* 2012; 36(2):118-171

A common variant in the PTPN11 gene contributes to the risk of tetralogy of fallot

*Circulation: Cardiovascular Genetics* 2012; 5(3):287-292

Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data

*BMC Proceedings* 2011; 5(S9):S92