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Genomics publications search

2,677 publications found

A genetic risk factor for low serum ferritin levels in Danish blood donors

A common variant highly associated with plasma VEGFA levels also contributes to the variation of both LDL-C and HDL-C

PREVALENCE OF ANEMIA IN ADOLESCENT GIRLS

Associations between Polymorphisms Related to Calcium Metabolism and Human Height: The Troms{o} Study

Common variants in SOCS7 gene predict obesity, disturbances in lipid metabolism and insulin resistance

Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

Vitamin B-12 Status during Pregnancy and Child's IQ at Age 8: A Mendelian Randomization Study in the Avon Longitudinal Study of Parents and Children

PPARγ2 Gene Pro12Ala and PPARα Gene Leu162Val Single Nucleotide Polymorphisms Interact with Dietary Intake of Fat in Determination of Plasma Lipid Concentrations

Dietary saturated fat, gender and genetic variation at the< i> TCF7L2 locus predict the development of metabolic syndrome

Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer’s Disease in Women with Down Syndrome

Bitter taste receptor polymorphisms and human aging

Residues of E. coli topoisomerase I conserved for interaction with a specific cytosine base to facilitate DNA cleavage

Ultrasensitive Measurement of Hotspot Mutations in Tumor DNA in Blood Using Error-Suppressed Multiplexed Deep Sequencing.

Alteration of gene expression in human cumulus cells as a potential indicator of oocyte aneuploidy.

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

Variants at chromosome 20 (ASIP locus) and melanoma risk

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

Investigation of the genetic architecture of a bone carcass weight QTL on BTA6

Novel SNP Discovery in African Buffalo, Syncerus caffer, Using High-Throughput Sequencing

Variation in the ovocalyxin‐32 gene in commercial egg‐laying chickens and its relationship with egg production and egg quality traits

Gene test to elucidate the ETEC F4ab/F4ac receptor status in pigs

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

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

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

Characterisation of QTL-linked and genome-wide restriction site-associated DNA (RAD) markers in farmed Atlantic salmon

Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot

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

Development and evaluation of 200 novel SNP assays for population genetic studies of westslope cutthroat trout and genetic identification of related taxa

RAD sequencing yields a high success rate for westslope cutthroat and rainbow trout species-diagnostic SNP assays

Tests of linkage and allelic association between markers in the 1p36 PRKCZ (Protein Kinase C Zeta) gene region and bipolar affective disorder},

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

TFPI gene variation and ischemic stroke

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

Blood Pressure Loci Identified with a Gene-Centric Array

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

An oxytocin receptor gene variant predicts attachment anxiety in females and autism-spectrum traits in males

Genetic and Molecular Insights Into the Role of PROX1 in Glucose Metabolism

WNT2 Locus Is Involved in Genetic Susceptibility of Peyronie's Disease

A Multi-Cohort Study of Polymorphisms in the GH/IGF Axis and Physical Capability: The HALCyon Programme

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

Fetal alcohol exposure and IQ at age 8: evidence from a population-based birth-cohort study

Allelic variations in superoxide dismutase-1 (< i> SOD1) gene and renal and cardiovascular morbidity and mortality in type 2 diabetic subjects

Overexpression of TGF-ss1 in macrophages reduces and stabilizes atherosclerotic plaques in ApoE-deficient mice

Proteins involved in extracellular matrix dynamics are associated with respiratory syncytial virus disease severity

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

Protective role for CCR5 in murine lupus nephritis

Evaluation of IL-28B Polymorphisms and Serum IP-10 in Hepatitis C Infected Chimpanzees

Identification of a new soybean rust resistance gene in PI 567102B

Genetic polymorphisms in homologous recombination repair genes in healthy Slovenian population and their influence on DNA damage

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