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Genomics publications search

2,677 publications found

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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

Identification of a Late Onset Alzheimer's Disease Candidate Risk Variant at 9q21. 33 in Polish Patients

Variants in the 3′ UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression

PPAR$gamma$2 gene Pro12Ala and PPAR$alpha$ gene Leu162Val SNPs interact with dietary intake of fat in determination of plasma lipid concentrations

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

Oral Abstracts 7: RA ClinicalO37. Long-Term Outcomes of Early RA Patients Initiated with Adalimumab Plus Methotrexate Compared with Methotrexate Alone Following a Targeted Treatment Approach

NCR3/NKp30 contributes to pathogenesis in primary Sjögren's syndrome

Prediction model for knee osteoarthritis incidence, including clinical, genetic and biochemical risk factors

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype

Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy

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

A functional and genetic analysis of SOD2 promoter variants and their contribution to age-related hearing loss

Precursors of Age-Related Macular Degeneration: Associations With Physical Activity, Obesity, and Serum Lipids in the Inter99 Eye Study

A mutation in the start codon of γ-crystallin D leads to nuclear cataracts in the Dahl SS/Jr-Ctr strain

Epidemiology of Aspergillus keratitis at a tertiary care eye hospital in South India and antifungal susceptibilities of the causative agents

Common variation at 3q26. 2, 6p21. 33, 17p11. 2 and 22q13. 1 influences multiple myeloma risk

Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222

Fine mapping of 11q13. 5 identifies regions associated with prostate cancer and prostate cancer death.

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

DNA polymerase ϵ and δ exonuclease domain mutations in endometrial cancer

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

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

Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13. 13

Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients

The TERT variant rs2736100 is associated with colorectal cancer risk

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

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 miRNA binding sites of nucleotide excision repair genes and colorectal cancer risk

Effect of Type 2 Diabetes Predisposing Genetic Variants on Colorectal Cancer Risk

Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer

A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer

Myo9B is associated with an increased risk of Barrett's esophagus and esophageal adenocarcinoma

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