Sort   by:  
 Page size 
GenomicsAlzheimer's Disease Sequencing Project (ADSP)

The overarching goals of the ADSP are to: (1) identify new genomic variants contributing to increased risk of developing AD, (2) identify new genomic variants contributing to protection against developing AD, and (3) provide insight as to why individuals with known risk factor variants escape fro...

phs000572.v1.p1 | EGA
GenomicsDNA methylation and the adverse metabolic outcomes of adiposity
Overweight and obesity affect ~1.5 billion people worldwide, and are major risk factors for type-2 diabetes (T2D), cardiovascular disease and related metabolic and inflammatory disturbances.1,2 Although the mechanisms linking adiposity to its clinical sequelae are poorly understood, recent studies s...
EGAS00001001922 | EGA
GenomicsBMI EWAS summary stats
Summary statistics for a multi-cohort epigenome-wide association study. This includes summary statistics (effect-size, standard error, p-value) for 470,000 methylation markers.
EGAD00010001029 | EGA
GenomicsGenome wide association study of Coeliac Disease
We performed a second-generation genome-wide association study of 4,533 individuals with celiac disease (cases) and 10,750 control subjects. We genotyped 113 selected SNPs with P(GWAS) < 10(-4) and 18 SNPs from 14 known loci in a further 4,918 cases and 5,684 controls. Variants from 13 new regions r...
EGAS00000000057 | EGA
UnknownDissecting the causal genetic mechanisms of coronary heart disease.
Not available
S-EPMC4015632 | biostudies-literature
UnknownTM6SF2-rs58542926 Genetic Variant Modifies the Protective Effect of a "Prudent" Dietary Pattern on Serum Triglyceride Levels.
Not available
S-EPMC10005630 | biostudies-literature
UnknownEpigenome-wide DNA methylation in hearing ability: new mechanisms for an old problem.
Not available
S-EPMC4153547 | biostudies-literature
UnknownCOVID-19 susceptibility variants associate with blood clots, thrombophlebitis and circulatory diseases.
Not available
S-EPMC8415605 | biostudies-literature
TranscriptomicsFAIRE-chip in CHRF-288-11 and K562 cells
Maps of open chromatin in a megakaryocytic (CHRF-288-11) and an erythroblastoid (K562) cell line using the formaldehyde-assisted isolation of regulatory elements (FAIRE) method. We profiled chromatin structure at 62 non-redundant genetic loci representing all known associations (as of November 2009,...
ORGANISM(S): Homo sapiens 
2011-07-01 | E-GEOD-25716 | biostudies-arrayexpress
UnknownDNA sequence and structural properties as predictors of human and mouse promoters.
Not available
S-EPMC2672154 | biostudies-literature
Sort   by:  
 Page size