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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
A common BACE1 polymorphism is a risk factor for sporadic Creutzfeldt-Jakob disease
A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control
A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS
Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.
Association of CD14 rs2569190 polymorphism with mortality in shock septic patients who underwent major cardiac or abdominal surgery: A retrospective study
ATA homozigosity in the IL-10 gene promoter is a risk factor for schizophrenia in Spanish females: a case control study
Characterization of LEDGF/p75 genetic variants and association with HIV-1 disease progression
Characterization of the Plasmodium falciparum sarcoplasmic/endoplasmic reticulum Ca2+-ATPase gene in samples from Equatorial Guinea before implementation of artemisinin-based combination therapy
CLOCK 3111 T/C SNP interacts with emotional eating behavior for weight-loss in a Mediterranean population
Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
Evaluating the Impact of Functional Genetic Variation on HIV-1 Control
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
Genes Interacting with Occupational Exposures to Low Molecular Weight Agents and Irritants on Adult-Onset Asthma in Three European Studies
Genetic variants in CCNB1 associated with differential gene transcription and risk of coronary in-stent restenosis
Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.