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Genomics publications search

2,677 publications found

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Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study

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

TFAP2B influences the effect of dietary fat on weight loss under energy restriction

Glucokinase links Krüppel‐like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease

PCSK1 rs6232 is associated with childhood and adult class III obesity in the Mexican population

COL1A1 association and otosclerosis: A meta-analysis

Polymorphisms Related to the Serum 25-Hydroxyvitamin D Level and Risk of Myocardial Infarction, Diabetes, Cancer and Mortality. The Tromsø Study

Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies

Significant association between body composition phenotypes and the osteocalcin genomic region in normative human population

Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Pharmacogenetic studies of change in cortisol on ecstasy (MDMA) consumption

Use of a predictive model derived from in vivo endophenotype measurements to demonstrate associations with a complex locus, CYP2A6

WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk

Effects of genetic variation in the P2RX7 gene on pharmacodynamics of a P2X7 receptor antagonist: a prospective genotyping approach

Assessment of the value of a genetic risk score in improving the estimation of coronary risk

Influence of Genetic Variants in Type I Interferon Genes on Melanoma Survival and Therapy

Tumor suppressor TNFAIP3 (A20) is frequently deleted in Sézary syndrome

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot

Interleukin-6 receptor pathways in abdominal aortic aneurysm

P21-Activated Kinase 1 (PAK1) as a therapeutic target in BrAF Wild-type Melanoma

Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population

Sequencing of the ANKYRIN 3 gene (ANK3) encoding ankyrin G in bipolar disorder reveals a non‐conservative amino acid change in a short isoform of ankyrin G

Maternal Depression and Child and Adolescent Depression Symptoms: An Exploratory Test for Moderation by CRHR1, FKBP5 and NR3C1 Gene Variants

Multigene interactions and the prediction of depression in the Wisconsin Longitudinal Study

An acenocoumarol dosing algorithm using clinical and pharmacogenetic data in Spanish patients with thromboembolic disease

Genetic variation in DNMT3B and increased global DNA methylation is associated with suicide attempts in psychiatric patients

rs12512631 on the Group Specific Complement (Vitamin D-Binding Protein GC) Implicated in Melanoma Susceptibility

Are myocardial infarction–associated single-nucleotide polymorphisms associated with ischemic stroke?

Lack of replication of seven pancreatic cancer susceptibility loci identified in two Asian populations

Variations of CHI3L1, Levels of the Encoded Glycoprotein YKL-40 and Prediction of Fatal and Non-fatal Ischemic Stroke

ABO blood groups and pancreatic cancer risk and survival: Results from the PANcreatic Disease ReseArch (PANDoRA) consortium

Durable Remission of Renal Cell Carcinoma in Conjuncture with Graft versus Host Disease following Allogeneic Stem Cell Transplantation and Donor Lymphocyte Infusion: Rule or Exception?

The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma

An Epistatic Interaction between the PAX8 and STK17B Genes in Papillary Thyroid Cancer Susceptibility

Genome-wide association study on differentiated thyroid cancer

CSReport: A New Computational Tool Designed for Automatic Analysis of Class Switch Recombination Junctions Sequenced by High-Throughput Sequencing

Protein tyrosine phosphatase 1B (PTP1B) is dispensable for IgE-mediated cutaneous reaction in vivo

Down into the Earth: microbial diversity of the deepest cave of the world

Fluorescence in situ hybridization for the identification of Treponema pallidum in tissue sections

Emerging prion disease drives host selection in a wildlife population

Indoor air pollution from gas cooking and infant neurodevelopment

Genome-Wide Association Study on Plasma Levels of Midregional-Proadrenomedullin and C-Terminal-Pro-Endothelin-1Novelty and Significance

A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation

Genetic and environmental factors influencing the placental growth factor (PGF) variation in two populations

Genetic variants associated with protein C levels

The impact of susceptibility loci for coronary artery disease on other vascular domains and recurrence risk

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