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Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF)
Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2
Genetic Variants in the LEPR, CRY1, RNASEL, IL4, and ARVCF Genes Are Prognostic Markers of Prostate Cancer-Specific Mortality
Common polymorphisms in the adiponectin and its receptor genes, adiponectin levels and the risk of prostate cancer
Association between genome-wide association studies reported SNPs and pediatric-onset CrohnÂ´s disease in Canadian children
Susceptibility loci reported in genome-wide association studies are associated with CrohnÂ´s disease in Canadian children
RIPK1 and CASP7 polymorphism as prognostic markers for survival in patients with colorectal cancer after complete resection
Association of common DNA sequence variants at 33 genetic loci with blood lipids in individuals of African ancestry from Jamaica