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
Allelic variations in superoxide dismutase-1 (< i> SOD1) gene and renal and cardiovascular morbidity and mortality in type 2 diabetic subjects
Genetic predisposition to type 2 diabetes is associated with impaired insulin secretion but does not modify insulin resistance or secretion in response to an intervention to lower dietary saturated fat
Genetic polymorphisms in homologous recombination repair genes in healthy Slovenian population and their influence on DNA damage
Association between autoantibodies to the Arginine variant of the Zinc transporter 8 (ZnT8) and stimulated C‐peptide levels in Danish children and adolescents with newly diagnosed type 1 diabetes
Zinc transporter 8 autoantibodies and their association with SLC30A8 and HLA-DQ genes differ between immigrant and Swedish patients with newly diagnosed type 1 diabetes in the better diabetes diagnosis study
Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population
Multiple genetic variants explain measurable variance in type 2 diabetes-related traits in Pakistanis
Reduced insulin secretion correlates with decreased expression of exocytotic genes in pancreatic islets from patients with type 2 diabetes
The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals
Maternal and offspring fasting glucose and type 2 diabetes-associated genetic variants and cognitive function at age 8: a Mendelian randomization study in the Avon Longitudinal Study of Parents and Children
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
Polymorphisms Related to the Serum 25-Hydroxyvitamin D Level and Risk of Myocardial Infarction, Diabetes, Cancer and Mortality. The Troms{o} Study
Nco I TNF-$beta$ gene polymorphism and TNF expression are associated with an increased risk of developing Barrett's esophagus and esophageal adenocarcinoma
IL28B polymorphisms influence stage of fibrosis and spontaneous or interferon-induced viral clearance in thalassemia patients with hepatitis C virus infection
Hepatitis C viral load, genotype 3 and interleukin-28B CC genotype predict mortality in HIV and hepatitis C-coinfected individuals
The pan-genotype specificity of the hepatitis C virus anti-core monoclonal antibody C7-50 is contingent on the quasispecies profile of a population
Potent immune activation in chronic hepatitis C patients upon administration of an oral inducer of endogenous interferons that acts via Toll-like receptor 7
Negative regulation of hepatitis C virus specific immunity is highly heterogeneous and modulated by pegylated interferon-alpha/ribavirin therapy
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
Interaction of a 17q12 variant with both fetal and infant smoke exposure in the development of childhood asthma‐like symptoms.
A role for PACE4 in osteoarthritis pain: evidence from human genetic association and null mutant phenotype
Effects of polymorphisms in TRAILR1 and TNFR1A on the response to anti-TNF therapies in patients with rheumatoid and psoriatic arthritis
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.
TGFβ receptor gene variants in systemic sclerosis-related pulmonary arterial hypertension: results from a multicentre EUSTAR study of European Caucasian patients
Polymorphisms in the Interleukin 4, Interleukin 13, and Corresponding Receptor Genes Are Not Associated with Systemic Sclerosis and Do Not Influence Gene Expression
TRAF Family Member-Associated NF-KB Activator (TANK) Gene Polymorphism in Chronic Periodontitis and Peri-implantitis Patients
Tests of linkage and allelic association between markers in the 1p36 PRKCZ (Protein Kinase C Zeta) gene region and bipolar affective disorder},
Identification of polymorphisms in the malic enzyme 1, NADP (+)-dependent, cytosolic and nuclear receptor subfamily 0, group B, member 2 genes and their associations with meat and carcass quality traits in commercial Angus cattle
