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TBXAS1 Gene Polymorphism Is Associated with the Risk of Ischemic Stroke of Metabolic Syndrome in a Chinese Han Population
Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population
Hippocampal and motor regions contribute to memory benefits after enacted encoding: cross-sectional and longitudinal evidence
Examining the common and specific grey matter abnormalities in childhood maltreatment and peer victimisation
A probable cis-acting genetic modifier of Huntington disease frequent in individuals with African ancestry
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures
Genetic variants in CYP11B1 influence the susceptibility to coronary heart disease
Role of PAX7 Gene rs766325 and rs4920520 Polymorphisms in the Etiology of Non-syndromic Cleft Lip and Palate: A Genetic Study
Association of Maternal Betaine-Homocysteine Methyltransferase (BHMT) and BHMT2 Genes Polymorphisms with Congenital Heart Disease in Offspring
Detection of enterovirus RNA in peripheral blood mononuclear cells correlates with the presence of the predisposing allele of the type 1 diabetes risk gene IFIH1 and with disease stage