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GenomicsType 1 Diabetes Genetics Consortium (T1DGC): Genome-Wide Association Study in Type 1 Diabetes, 2008

Cases with Type 1 Diabetes (T1D) in the UK, were part of the Wellcome Trust Case Control Consortium (WTCCC) - http://www.wtccc.org.uk - that first reported in 2007:

Wellcome Trust Case Control Consortium (2007) Genome-wide association s...

phs000180.v2.p2 | EGA
UnknownQuiet quitting among healthcare professionals in hospital environments: a concept analysis and scoping review protocol.
Not available
S-EPMC10660974 | biostudies-literature
MetabolomicsRare and common genetic determinants of metabolic individuality and their effects on human health (INTERVAL study assays)

Garrod’s concept of “chemical individuality” has contributed to comprehension of the molecular origins of human diseases. Untargeted high-throughput metabolomic technologies provide an in-depth snapshot of human metabolism at scale. We studied the genetic architecture of the human plasma metabolo...

2022-09-09 | MTBLS834 | MetaboLights
UnknownUnderstanding the value of brain donation for research to donors, next-of-kin and clinicians: A systematic review.
Not available
S-EPMC10732432 | biostudies-literature
UnknownBiomechanical effectiveness of controlled ankle motion boots: A systematic review and narrative synthesis.
Not available
S-EPMC11633339 | biostudies-literature
UnknownRole and responsibilities of a forensic mental health nurse: a scoping review protocol.
Not available
S-EPMC12265835 | biostudies-literature
UnknownHDAC6-Dependent Deacetylation of SAE2 enhances SUMO1 Conjugation for Mitotic Integrity.
Not available
S-SCDT-10_1038-S44318-025-00532-Y | biostudies-other
Genomicsena-DATASET-GoT2D/T2D-GENES-09-07-2016-02:03:47:226-1135 - samples
The GoT2D study includes ~2800 samples, half T2D cases and half T2D controls, of Northern European ancestry sequenced over 3 three technologies: deep whole exome sequencing, low-pass (4x) whole genome sequencing, and OMNI 2.5M genotyping. Samples were ascertained to be phenotypically "extreme" (e.g....
EGAD00001002247 | EGA
GenomicsImputation analysis file
This data set includes the following summary level data file used for the imputation data: imputation.sv.assoc.txt: results from single variant association analysis in imputed samples
EGAD00010001184 | EGA
Genomics13K T2D-GENES analysis files
This data set includes the following summary level data files used for the 13k analysis of T2D-GENES data: wes.variants.list: list of variants to keep for any analysis of the exomes data wes.assoc.samples.list: list of samples to keep for association analysis wes.assoc.variants.list: list of variant...
EGAD00010001188 | EGA
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