Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
GWA analysis for milk production traits in dairy sheep and genetic support for a QTN influencing milk protein percentage in the LALBA gene
Identification of Single Nucleotide Polymorphisms in the Nicastrese Goat and Sardinia Sheep Mannose-Binding Lectin
Effect of PRNP gene polymorphism on reproductive performance of mother sheep and their offspring growth
Photoperiod effects on the expression of kisspeptin and gonadotropin genes in Atlantic cod,< i> Gadus morhua, during first maturation
Characterisation of QTL-linked and genome-wide restriction site-associated DNA (RAD) markers in farmed Atlantic salmon
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
Single nucleotide polymorphism discovery in cutthroat trout subspecies using genome reduction, barcoding, and 454 pyro-sequencing
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
Associations between oxytocin receptor gene (< i> OXTR) polymorphisms and self-reported aggressive behavior and anger: Interactions with alcohol consumption
Alcohol and aggressive behavior in men–moderating effects of oxytocin receptor gene (OXTR) polymorphisms
Risk and protective genetic variants in suicidal behaviour: association with SLC1A2, SLC1A3, 5-HTR1B & NTRK2 polymorphisms
Subcongenic analyses reveal complex interactions between distal chromosome 4 genes controlling diabetogenic B cells and CD4 T cells in nonobese diabetic mice
Overexpression of TGF-ss1 in macrophages reduces and stabilizes atherosclerotic plaques in ApoE-deficient mice
Are single nucleotide polymorphisms in the oxytocin and vasopressin 1A/1B receptor genes likely candidates for variation in ejaculatory function?
A Study of Possible Associations Between Single Nucleotide Polymorphisms in the Serotonin Receptor 1A, 1B, and 2C Genes and Self‐Reported Ejaculation Latency Time.
Genetic polymorphisms in homologous recombination repair genes in healthy Slovenian population and their influence on DNA damage
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
Genetic divergences and intraspecific variation in corvids of the genus Corvus (Aves: Passeriformes: Corvidae)--a first survey based on museum specimens
Where is the line? Phylogeography and secondary contact of western Palearctic coal tits (Periparus ater: Aves, Passeriformes, Paridae)
Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese C
From genes to phenotypes–Evaluation of two methods for the SNP analysis in archaeological remains: Pyrosequencing and competitive allele specific PCR (KASPar)
Parallelism in the oxygen transport system of the lake whitefish: the role of physiological divergence in ecological speciation
i> IL28B and< i> PNPLA3 polymorphisms affect histological liver damage in patients with non-alcoholic fatty liver disease
MAP3K7 and GSTZ1 are associated with human longevity: a two-stage case--control study using a multilocus genotyping
Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programme
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
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.
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