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Mamasoula C

Latest

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Novel blood pressure locus and gene discovery using genome-wide association study and expression data sets from blood and the kidney
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Antidepressant augmentation with metyrapone for treatment-resistant depression (the ADD study): A double-blind, randomised, placebo-controlled trial
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
Common variation neighbouring micro-RNA 22 is sssociated with increased left ventricular mass
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
Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data

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