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Interaction of Multiple Gene Variants and their Effects on Schizophrenia Phenotypes
Association Between Single Nucleotide Polymorphisms in NFATC1 Signaling Pathway Genes and Susceptibility to Congenital Heart Disease in the Chinese Population
Polymorphisms in UGT1A1 gene predispose South Indians to pigmentous gallstones
Lack of association between SREBF-1c gene polymorphisms and risk of non-alcoholic fatty liver disease in a Chinese Han population
IGF2BP2 rs11705701 polymorphisms are associated with prediabetes in a Chinese population: A population-based case-control study
Whole exome sequencing of extreme age-related macular degeneration phenotype
Loss-of-function variants influence the human serum metabolome
Genetic Testing as a New Standard for Clinical Diagnosis of Color Vision Deficiencies
Association of DYRK1A polymorphisms with sporadic Parkinson’s disease in Chinese Han population
A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease