Common genetic variants at the 11q13. 3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression
An acenocoumarol dosing algorithm using clinical and pharmacogenetic data in Spanish patients with thromboembolic disease
Genetic Variant SCL2A2 Is Associated with Risk of Cardiovascular Disease–Assessing the Individual and Cumulative Effect of 46 Type 2 Diabetes Related Genetic Variants
Are myocardial infarction–associated single-nucleotide polymorphisms associated with ischemic stroke?
The association between genetic variations of CHI3L1, levels of the encoded glycoprotein YKL-40 and the lipid profile in a danish population
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease
A Multi-Cohort Study of Polymorphisms in the GH/IGF Axis and Physical Capability: The HALCyon Programme
A pilot study of the association between genetic polymorphisms involved in estrogen signaling and infant male genital phenotypes
The frequent UCP2- 866G> A polymorphism protects against insulin resistance and is associated with obesity: a study of obesity and related metabolic traits among 17 636 Danes
An association analysis between OXT genotype and milk yield and flow in Italian Mediterranean river buffalo
Identification of a Short Region on Chromosome 6 Affecting Direct Calving Ease in Piedmontese Cattle Breed
High Dietary Saturated Fat Intake Accentuates Obesity Risk Associated with the Fat Mass and Obesity–Associated Gene in Adults
PPARγ2 gene Pro12Ala and PPARα gene Leu162Val SNPs interact with dietary intake of fat in determination of plasma lipid concentrations
Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa
Functional characterization of TLR4+ 3725 G/C polymorphism and association with protection against overweight
Glucokinase links Krüppel‐like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease
Effect of PRNP gene polymorphism on reproductive performance of mother sheep and their offspring growth
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population
PWE-166 Increasing VacA toxin activity alters Helicobacter pylori colonisation density and the nature of the acquired immune response in a mouse model of infection
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases
Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B & NTRK2 polymorphisms
The pan-genotype specificity of the hepatitis C virus anti-core monoclonal antibody C7-50 is contingent on the quasispecies profile of a population
Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patients
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis
Continuous interferon-α2b infusion in combination with ribavirin for chronic hepatitis C in treatment-experienced patients
PM10-induced hospital admissions for asthma and chronic obstructive pulmonary disease: the modifying effect of individual characteristics
Interaction of a 17q12 variant with both fetal and infant smoke exposure in the development of childhood asthma-like symptoms: Epidemiology and Genetics
The Zebrafish Mutation Project: Systematic Genome-wide Identification of Knockout Alleles in the Zebrafish Using Whole Exome Enrichment and Illumina Sequencing
Interaction of a 17q12 variant with both fetal and infant smoke exposure in the development of childhood asthma‐like symptoms.
Effets des polymorphismes des gènes< i> TRAILR1 et< i> TNFR1A sur la réponse au traitement anti-TNF chez les patients atteints de polyarthrite rhumatoïde et de rhumatisme psoriasique.
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese C
