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UnknownEpigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study.
Not available
S-EPMC4724884 | biostudies-literature
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GenomicsNHLBI Family Heart Study (FamHS-Visit1 and FamHS-Visit2)
<p>The Family Heart Study (FamHS) was funded by the National Heart, Lung, and Blood Institute (NHLBI). It was begun in 1992 with the ascertainment of 1,200 families, half randomly sampled, and half selected because of an excess of coronary heart disease (CHD) or risk factor abnormalities as compared ...
phs000221.v1.p1 | EGA
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Genomics,MultiomicsFramingham Cohort
<p>Startup of Framingham Heart Study. Cardiovascular disease (CVD) is the leading cause of death and serious illness in the United States. In 1948, the Framingham Heart Study (FHS) -- under the direction of the National Heart Institute (now known as the National Heart, Lung, and Blood Institut...
phs000007.v17.p6 | EGA
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GenomicsGenome wide association study for early onset coronary disease and related phenotypes (ADVANCE)
<p>ADVANCE (Atherosclerotic Disease, VAscular functioN, and genetiC Epidemiology) is a large epidemiological study of genetic and non-genetic determinants of coronary artery disease (CAD) that started in 2000 as a collaborative effort between researchers at Stanford University and Kaiser Pe...
phs000423.v1.p1 | EGA
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TranscriptomicsExpression profiling of Ewing sarcoma samples
Expression profiling of Ewing sarcoma samples in the frame of the CIT program from the french Ligue Nationale Contre le Cancer (http://cit.ligue-cancer.net). Ewing sarcoma a rare pediatric tumor characterized by EWSR1-ETS fusions, is predominantly observed in populations of European ancestry. A genom...
ORGANISM(S): Homo sapiens 
2012-02-11 | E-GEOD-34620 | biostudies-arrayexpress
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TranscriptomicsExpression data for 2 obese subjects from the SibPair cohort with a deletion on 16p11.2
We report a highly-penetrant form of obesity, initially observed in 31 heterozygous carriers of a 593kb or larger deletion at 16p11.2 from amongst subjects ascertained for cognitive deficits. Nineteen similar deletions were identified from GWAS data in 16053 individuals from 8 European cohorts; such ...
ORGANISM(S): Homo sapiens 
2009-12-02 | E-GEOD-19238 | biostudies-arrayexpress
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UnknownExpression of the selenoprotein S (SELS) gene in subcutaneous adipose tissue and SELS genotype are associated with metabolic risk factors.
Not available
S-EPMC3004038 | biostudies-literature
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UnknownPLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women.
Not available
S-EPMC2803169 | biostudies-literature
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UnknownEvaluating the association of common APOA2 variants with type 2 diabetes.
Not available
S-EPMC2650681 | biostudies-literature
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UnknownThe common P446L polymorphism in GCKR inversely modulates fasting glucose and triglyceride levels and reduces type 2 diabetes risk in the DESIR prospective general French population.
Not available
S-EPMC2494697 | biostudies-literature
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