ID

45035

Descripción

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.

Link

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

Palabras clave

  1. 29/7/22 29/7/22 - Simon Heim
  2. 12/10/22 12/10/22 - Adrian Schulz
Titular de derechos de autor

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

Subido en

29 de julio de 2022

DOI

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Licencia

Creative Commons BY 4.0

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dbGaP phs000431 IgA Nephropathy GWAS (IGANGWAS)

Eligibility Criteria

Inclusion and exclusion criteria
Descripción

Inclusion and exclusion criteria

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

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

Tipo de datos

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.
Descripción

Control participants were healthy blood donors.

Tipo de datos

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
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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