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GenomicsNational Institute of Arthritis and Musculoskeletal and Skin Diseases and Istanbul Faculty of Medicine Genome wide Association Study of Behçet's Disease (Turkish)

Introduction
Behçet's disease (BD) is a genetically complex multisystem disease of unknown etiology, characterized by recurrent inflammatory attacks affecting orogenital mucosa, eyes, skin, joints, blood vessels, and less frequently, the central nervous system and gastroint...

phs000272.v1.p1 | EGA
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GenomicsThe Genetic Analysis of multiple sclerosis
We created these data in order to identify genetic variants associated with increased susceptibility to multiple sclerosis. Cases from many parts of the world were genotyped with the Illumina 660 chip along with Swedish controls. In our analysis we also used control data from the WTCCC2 common UK con...
EGAS00000000101 | EGA
0
GenomicsMS
WTCCC2 project Multiple Sclerosis (MS) samples
EGAD00000000120 | EGA
0
UnknownIdentifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics.
Not available
S-EPMC8357785 | biostudies-literature
0
Genomics58C
WTCCC2 project samples from 1958 British Birth Cohort
EGAD00000000022 | EGA
0
GenomicsNBS
WTCCC2 project samples from National Blood Donors (NBS) Cohort
EGAD00000000024 | EGA
0
Genomics58C
WTCCC2 project samples from 1958 British Birth Cohort
EGAD00000000021 | EGA
0
GenomicsNBS
WTCCC2 project samples from National Blood Donors (NBS) Cohort
EGAD00000000023 | EGA
1K
OtherWellcome Trust Case Control Consortium
The Wellcome Trust Case Control Consortium (WTCCC) is a collaboration of 24 leading human geneticists, who will analyse thousands of DNA samples from patients suffering with different diseases to identify common genetic variations for each condition.
EGAO00000000001 | EGA
0
Genomics,MultiomicsWellcome Trust Sanger Institute
Wellcome Trust Sanger Institute
EGAC00001000205 | EGA
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