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Imprinted gene alterations in the kidneys of growth restricted offspring may be mediated by a long non-coding RNA
Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population
17 variants interaction of Wnt/β-catenin pathway associated with development of osteonecrosis of femoral head in Chinese Han population
Predisposing factors for adrenal crisis in chronic adrenal insufficiency: a case–control study.
Single nucleotide polymorphisms in cytokine genes and their association with primary Sjögren’s syndrome in Saudi patients: A cross-sectional study.
Association study for the role of MMP8 gene polymorphisms in Colorectal cancer susceptibility
Classifying Alzheimer’s disease and normal subjects using machine learning techniques and genetic-environmental features
Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients
Gene polymorphisms of molecules of the cGAS-STING signalling pathway are associated with AML in Chinese patients
Peripheral amyloid-β clearance mediates cognitive impairment in non-alcoholic fatty liver disease