ID

45035

Description

Principal Investigator: Ali G. Gharavi, MD, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY, USA MeSH: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000431 In this second study version, we report a genome-wide association study of IgA nephropathy performed in individuals of European ancestry (US and Italian cohorts), followed by a meta-analysis with the existing GWAS cohorts (Han Chinese [study version 1] and French cohorts). Genomic DNA was extracted from whole blood and genotyped with the HumanHap550-2v3, Human610-Quadv1and HumanOmni1-Quad_v1 platforms. This GWAS also utilized pre-genotyped population controls from other studies.

Lien

https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000431

Mots-clés

  1. 29/07/2022 29/07/2022 - Simon Heim
  2. 12/10/2022 12/10/2022 - Adrian Schulz
Détendeur de droits

Ali G. Gharavi, MD, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY, USA

Téléchargé le

29 juillet 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000431 IgA Nephropathy GWAS (IGANGWAS)

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

The inclusion criterion for cases was confirmation of affected status by renal biopsy.
Description

The inclusion criterion for cases was confirmation of affected status by renal biopsy.

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1706256
UMLS CUI [1,3]
C0522476
UMLS CUI [1,4]
C0194073
Control participants were healthy blood donors.
Description

Control participants were healthy blood donors.

Type de données

boolean

Alias
UMLS CUI [1,1]
C0009932
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C3898900
UMLS CUI [1,4]
C0005795

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
The inclusion criterion for cases was confirmation of affected status by renal biopsy.
Item
The inclusion criterion for cases was confirmation of affected status by renal biopsy.
boolean
C1512693 (UMLS CUI [1,1])
C1706256 (UMLS CUI [1,2])
C0522476 (UMLS CUI [1,3])
C0194073 (UMLS CUI [1,4])
Control participants were healthy blood donors.
Item
Control participants were healthy blood donors.
boolean
C0009932 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C3898900 (UMLS CUI [1,3])
C0005795 (UMLS CUI [1,4])

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