ID

45194

Descripción

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.

Link

dbGaP study = phs000367

Palabras clave

  1. 19/8/22 19/8/22 - Simon Heim
  2. 12/10/22 12/10/22 - Adrian Schulz
Titular de derechos de autor

Steven R. Brant, MD, Johns Hopkins University, Baltimore, MD, USA

Subido en

12 de octubre de 2022

DOI

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Licencia

Creative Commons BY 4.0

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dbGaP phs000367 Genome Wide Association Study in Familial Crohn's Disease

Eligibility Criteria

Inclusion and exclusion criteria
Descripción

Inclusion and exclusion criteria

Inclusion Criteria:
Descripción

Inclusion Criteria

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1512693
Proper consent and IRB approval for release of data to dbGaP
Descripción

Proper consent and IRB approval for release of data to dbGaP

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0021430
Non-Hispanic Caucasian
Descripción

Non-Hispanic Caucasian

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1518424
UMLS CUI [1,3]
C0043157
Confirm diagnosis of IBD and relatives/family members
Descripción

Confirm diagnosis of IBD and relatives/family members

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C0022104
UMLS CUI [1,3]
C0086282

Similar models

Eligibility Criteria

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion and exclusion criteria
Inclusion Criteria
Item
Inclusion Criteria:
boolean
C1512693 (UMLS CUI [1,1])
Proper consent and IRB approval for release of data to dbGaP
Item
Proper consent and IRB approval for release of data to dbGaP
boolean
C1512693 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Non-Hispanic Caucasian
Item
Non-Hispanic Caucasian
boolean
C1512693 (UMLS CUI [1,1])
C1518424 (UMLS CUI [1,2])
C0043157 (UMLS CUI [1,3])
Confirm diagnosis of IBD and relatives/family members
Item
Confirm diagnosis of IBD and relatives/family members
boolean
C0011900 (UMLS CUI [1,1])
C0022104 (UMLS CUI [1,2])
C0086282 (UMLS CUI [1,3])

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