Sort   by:  
 Page size 
GenomicsGenome wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
We conducted GWAS of sporadic CJD, variant CJD, iatrogenic CJD, inherited prion disease, kuru and resistance to kuru despite attendance at mortuary feasts. After quality control we analysed 2000 samples and 6015 control individuals (provided by the Wellcome Trust Case Control Consortium and KORA-gen...
EGAS00000000097 | EGA
GenomicsCase samples (660K/670K) - samples
Case samples (Illumina_660K & Illumina_670K)
EGAD00010000202 | EGA
GenomicsMRC Prion Unit Data Access Committee
Data Access Committee EGAC01000000007
EGAC01000000007 | EGA
TranscriptomicsTranscription profiling by array of epidermal shave samples taken from lesional and non-lesional skin from German atopic dermatitis patients and from healthy skin from German controls
Epigenetic alterations are increasingly recognized as mechanisms for disease-associated changes in genome function and important risk factors for complex diseases. The epigenome differs between cell types and so far has been characterized in few human tissues only. In order to identify disease-assoc...
ORGANISM(S): Homo sapiens 
2014-08-26 | E-GEOD-60709 | biostudies-arrayexpress
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
Sort   by:  
 Page size