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UnknownComprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume.
Not available
S-EPMC9213584 | biostudies-literature
TranscriptomicsFactors underlying variable DNA methylation in a human community cohort
Epigenetics is emerging as an attractive mechanism to explain the persistent genomic embedding of early-life experiences. Tightly linked to chromatin, which packages DNA into chromosomes, epigenetic marks primarily serve to regulate the activity of genes. DNA methylation is the most accessible and c...
ORGANISM(S): Homo sapiens 
2012-10-10 | E-GEOD-37008 | biostudies-arrayexpress
UnknownIncremental Value of Aortomitral Continuity Calcification for Risk Assessment after Transcatheter Aortic Valve Replacement.
Not available
S-EPMC7977784 | biostudies-literature
UnknownSocial determinants of hazardous alcohol use in a Ugandan population cohort.
Not available
S-EPMC11986868 | biostudies-literature
TranscriptomicsWidespread Discordance of DNA Methylation Between two Accessible Human Tissues
Inter-individual variability in DNA methylation has been hypothesized to contribute to complex phenotypes through epigenetic modulation of gene expression levels. Population epigenetic studies have been examining differences in DNA methylation in a variety of accessible tissues for association with ...
ORGANISM(S): Homo sapiens 
2014-05-31 | E-GEOD-53396 | biostudies-arrayexpress
UnknownAlzheimer's disease genetic risk and cognitive reserve in relationship to long-term cognitive trajectories among cognitively normal individuals.
Not available
S-EPMC10045505 | biostudies-literature
UnknownThe Canadian Healthy Infant Longitudinal Development (CHILD) birth cohort study: assessment of environmental exposures.
Not available
S-EPMC4611361 | biostudies-literature
UnknownAn IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer's disease.
Not available
S-EPMC10154240 | biostudies-literature
UnknownAssociation of APOL1 Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program.
Not available
S-EPMC6754626 | biostudies-literature
UnknownGenome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease.
Not available
S-EPMC6858581 | biostudies-literature
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