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Genomics publications search

2,677 publications found

Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB–FKBPL–NOTCH4 region of chromosome 6p21.3

Hearing in 44–45 year olds with m. 1555A> G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study

COL1A1 association and otosclerosis: A meta‐analysis

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

Leukotriene B4 receptor locus gene characterisation and association studies in asthma

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

Single nucleotide polymorphisms in the HIF‑1α gene and chemoradiotherapy of locally advanced rectal cancer

Peptide-mediated targeting of liposomes to TrkB receptor-expressing cells

Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer

CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 Trial

SNP discovery using Paired‐End RAD‐tag sequencing on pooled genomic DNA of Sisymbrium austriacum (Brassicaceae)

Application of real-time PCR-based SNP detection for mapping of Net2, a causal D-genome gene for hybrid necrosis in interspecific crosses between tetraploid wheat and Aegilops tauschii

Targeted re‐sequencing of the allohexaploid wheat exome

Combining SNP discovery from next-generation sequencing data with bulked segregant analysis (BSA) to fine-map genes in polyploid wheat

Impaired auxin biosynthesis in the defective endosperm18 mutant is due to mutational loss of expression in the ZmYuc1 gene encoding endosperm-specific YUCCA1 protein in maize

New Insights into the Genetics of in Vivo Induction of Maternal Haploids, the Backbone of Doubled Haploid Technology in Maize

Outcrossing Study and Heterozygosity-Hunt Study in Cheatgrass

Copy number variation affecting the Photoperiod-B1 and Vernalization-A1 genes is associated with altered flowering time in wheat (Triticum aestivum)

Nutrients, technological properties and genetic relationships among twenty cowpea landraces cultivated in West Africa

Heterozygosity and diversity analysis using mapped single nucelotide polymorphisms in a faba bean inbreeding programme

Quality control genotyping for assessment of genetic identity and purity in diverse tropical maize inbred lines

Identification of 4 novel HLA-B* 40: 01 restricted minor histocompatibility antigens and their potential as targets for graft-versus-leukemia reactivity

CYP3A variation, premenopausal estrone levels, and breast cancer risk

FGFR2 genotype and risk of radiation-associated breast cancer in Hodgkin lymphoma

Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families

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

Genomic Resources for Evolutionary Studies in the Large, Diverse, Tropical Genus, Begonia

The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives

Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation

Genome wide linkage disequilibrium in Chinese asparagus bean (Vigna. unguiculata ssp. sesquipedialis) germplasm: implications for domestication history and genome wide association studies

Nco I TNF-β gene polymorphism and TNF expression are associated with an increased risk of developing Barrett's esophagus and esophageal adenocarcinoma

The PNPLA3 rs738409 G-allele associates with reduced fasting serum triglyceride and serum cholesterol in Danes with impaired glucose regulation

Common variants at the MHC locus and at chromosome 16q24. 1 predispose to Barrett's esophagus

Common variation at 6p21. 31 (BAK1) influences the risk of chronic lymphocytic leukemia

genetic variants involved in melanoma susceptibility in Southern European populations: Results from a Meta-analysis

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

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

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

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

The Novel Sigma Factor-Like Regulator RpoQ Controls Luminescence, Chitinase Activity, and Motility in Vibrio fischeri

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

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

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