Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub mutant mice
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
Tests of linkage and allelic association between markers in the 1p36 PRKCZ (Protein Kinase C Zeta) gene region and bipolar affective disorder},
Maternal Depression and Child and Adolescent Depression Symptoms: An Exploratory Test for Moderation by CRHR1, FKBP5 and NR3C1 Gene Variants
ESR1 Polymorphisms, Daily Hassles, Anger Expression, and Depressive Symptoms in Adolescent Boys and Girls
ARMS2 Increases the Risk of Early and Late Age-related Macular Degeneration in the European Eye Study
Prevalence and audiological features in carriers of GJB2 mutations, c. 35delG and c. 101T> C (p. M34T), in a UK population study
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
Simultaneous monitoring of two fungal genotypes on plant roots by single nucleotide polymorphism quantification with an innovative KASPar quantitative PCR
Identification of 4 novel HLA-B* 40: 01 restricted minor histocompatibility antigens and their potential as targets for graft-versus-leukemia reactivity
Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13. 13
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 the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
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
genetic variants involved in melanoma susceptibility in Southern European populations: Results from a Meta-analysis
Evaluation of diagnostic molecular markers for DUS phenotypic assessment in the cereal crop, barley (Hordeum vulgare ssp. vulgare L.)
Single nucleotide polymorphisms identification, characterization and linkage mapping in Chenopodium quinoa
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
Coverage-based consensus calling (CbCC) of short sequence reads and comparison of CbCC results to identify SNPs in chickpea (Cicer arietinum; Fabaceae), a crop species without a reference genome
The Novel Sigma Factor-Like Regulator RpoQ Controls Luminescence, Chitinase Activity, and Motility in Vibrio fischeri
