The Zebrafish Mutation Project: Systematic Genome-wide Identification of Knockout Alleles in the Zebrafish Using Whole Exome Enrichment and Illumina Sequencing
Identity of Pelodiscus sinensis revealed by DNA sequences of an approximately 180-year-old type specimen and a taxonomic reappraisal of Pelodiscus species (Testudines: Trionychidae)
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
The Genetic Consequences of Spatially Varying Selection in the Panmictic American Eel (Anguilla rostrata)
Comparison of IKKI Gene Polymorphisms (rs1539243 and rs12728136) between Chronic Periodontitis and Peri-implantitis Patients in an Iranian Population (A Cross-Sectional Study)
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
Hearing in 44–45 year olds with m. 1555A> G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study
APOE E4 carriers show prospective memory enhancement under nicotine, and evidence for specialisation within medial BA10
Dominant optic atrophy in Denmark–report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90%
Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood
DNA repair polymorphisms and treatment outcomes of patients with malignant mesothelioma treated with gemcitabine-platinum combination chemotherapy
Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy
The influence of gemcitabine pathway polymorphisms on treatment outcome in patients with malignant mesothelioma
Single nucleotide polymorphisms in the HIF‑1α gene and chemoradiotherapy of locally advanced rectal cancer
CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 Trial
Estimating causal effects of genetic risk variants for breast cancer using marker data from bilateral and familial cases
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
Comprehensive Evaluation of the Impact of 14 Genetic Variants on Colorectal Cancer Phenotype and Risk
Identification of candidate genes carrying polymorphisms associated with the risk of colorectal cancer by analyzing the colorectal mutome and microRNAome
Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer
Large-Scale Development of Cost-Effective Single-Nucleotide Polymorphism Marker Assays for Genetic Mapping in Pigeonpea and Comparative Mapping in Legumes
A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer
