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Additional evidence supports association of common genetic variants in VTI1A and ETFA with increased risk of glioma susceptibility
A complex association between ABCA7 genotypes and blood lipid levels in Southern Chinese Han patients of sporadic Alzheimer’s disease
Dysfunction of Myosin Light‐Chain 4 (MYL 4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From …
Polymorphism of neuropeptide Y gene rs16147 modifies the response to a hypocaloric diet on cardiovascular risk biomarkers and adipokines
The impact of a panel of 18 SNPs on breast cancer risk in women attending a UK familial screening clinic: a case–control study
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome
The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study
Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population
Nine differentially expressed genes from a post mortem study and their association with suicidal status in a sample of suicide completers, attempters and controls
CYP genetic variants, CYP metabolite levels, and neurologic deterioration in acute ischemic stroke in Chinese population