ID
45194
Descrição
Principal Investigator: Steven R. Brant, MD, Johns Hopkins University, Baltimore, MD, USA MeSH: Crohn Disease,Colitis, Ulcerative,Inflammatory Bowel Diseases https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000367 The National Institute of Diabetes and Digestive and Kidney Diseases Inflammatory Bowel Disease Genetics Consortium (NIDDK - IBDGC) conducted a genome wide association study (GWAS) using the Human Omni2.5-Quad beadchip from Illumina to identify disease variants associated with familial Crohn's disease. This study includes a subset of individuals from an original cohort of affected subjects and affected/unaffected relatives from a previous linkage scan which showed increased linkage evidence at three novel risk loci. A total of 708 samples were selected based on various criteria for inclusion from the 6 Genetic Research Centers (GRC) in North America that participate in the IBDGC. This project was supported by an ancillary R01 grant from the NIDDK with resources made available through the IBDGC.
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Versões (2)
- 19/08/2022 19/08/2022 - Simon Heim
- 12/10/2022 12/10/2022 - Adrian Schulz
Titular dos direitos
Steven R. Brant, MD, Johns Hopkins University, Baltimore, MD, USA
Transferido a
12 de outubro de 2022
DOI
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Licença
Creative Commons BY 4.0
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dbGaP phs000367 Genome Wide Association Study in Familial Crohn's Disease
Subject ID, sample ID, sample source, sample source ID, and sample use of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent group, subject source, and subject source ID of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Family ID, subject ID, mother ID, father ID, and sex of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Subject ID, sample ID, sample source, sample source ID, and sample use of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Subject ID, sex, race, affection status, and diagnosis of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Sample ID, body site where sample was collected, genomic data, analyte data, tumor status, and histological type of samples of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
Similar models
Subject ID, sample ID, sample source, sample source ID, and sample use of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent group, subject source, and subject source ID of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Family ID, subject ID, mother ID, father ID, and sex of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Subject ID, sample ID, sample source, sample source ID, and sample use of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Subject ID, sex, race, affection status, and diagnosis of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
- Sample ID, body site where sample was collected, genomic data, analyte data, tumor status, and histological type of samples of participants with or without Crohn's disease and involved in the "NIDDK Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease" project.
C0370003 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,2])
C1299222 (UMLS CUI [1,2])