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Resequencing of the CCL5 and CCR5 genes and investigation of variants for association with diabetic nephropathy
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
Origins and functional impact of copy number variation in the human genome
The Wellcome Trust Case Control Consortium, Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Single-Nucleotide Polymorphisms of NKX2.5 Found in Congenital Heart Disease Patients of Mysore, South India
Candidate malaria susceptibility/protective SNPs in hospital and population-based studies: the effect of sub-structuring
KCNN4 Gene variant is associated with ileal CrohnÂ´s disease in the Australian and New Zealand population
Genetic analysis of six SNPs in candidate genes associated with high cross-race risk of development of thoracic aortic aneurysms and dissections in Chinese Han population
Testing replication of a 5-SNP set for general cognitive ability in six population samples
Genome-wide scan identifies a quantitative trait locus at 4p15.3 for serum urate