ID
45650
Description
Principal Investigator: Melissa L. Bondy, PhD, Baylor College of Medicine, Houston, TX, USA MeSH: Glioma https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001319 The main goals of the GICC Study were: 1) to identify novel genetic risk variants for glioma, as well as validate variants implicated by previous genome-wide association studies of glioma; and 2) to explore biologically relevant gene-gene and gene-environment interactions in glioma susceptibility. The GICC Study includes participants from the following centers: Brigham and Women's Hospital (Boston, Massachusetts), Case Western Reserve University (Cleveland, Ohio), Columbia University (New York, New York), the Danish Cancer Society Research Centre (Copenhagen, Denmark), Duke University (Durham, North Carolina), the University of Texas MD Anderson Cancer Center (Houston, Texas), Memorial Sloan Kettering Cancer Center (New York, New York), the Mayo Clinic (Rochester, Minnesota), NorthShore HealthSystem (Chicago, Illinois), Umea University (Umea, Sweden), the University of California, San Francisco (San Francisco, California), the University of Southern California (Los Angeles, California), and the Institute of Cancer Research (London, United Kingdom).
Link
Keywords
Versions (1)
- 20/03/2023 20/03/2023 - Chiara Middel
Copyright Holder
Melissa L. Bondy, PhD, Baylor College of Medicine, Houston, TX, USA
Uploaded on
20 de março de 2023
DOI
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License
Creative Commons BY 4.0
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dbGaP phs001319 Glioma International Case Control Study (GICC)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent groups, and affection status of participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Subject ID, sample ID, and sample use variable obtained from participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Subject ID, race, sex, case or control status of subject, and age of participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Sample ID, analyte type, body site, genotyping center, and tumor status of sample obtained from participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID, consent groups, and affection status of participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Subject ID, sample ID, and sample use variable obtained from participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Subject ID, race, sex, case or control status of subject, and age of participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
- Sample ID, analyte type, body site, genotyping center, and tumor status of sample obtained from participants with or without glioma and involved in the "Glioma International Case Control Study (GICC)" project.
C0680251 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
C1516637 (UMLS CUI [2,1])
C0679557 (UMLS CUI [1,2])
C0441938 (UMLS CUI [1,3])
C3665419 (UMLS CUI [1,4])
C0334582 (UMLS CUI [2,1])
C0334580 (UMLS CUI [3,1])
C0334581 (UMLS CUI [4,1])
C0028945 (UMLS CUI [5,1])
C0547065 (UMLS CUI [6,1])
C0334579 (UMLS CUI [7,1])
C0334590 (UMLS CUI [8,1])
C0431108 (UMLS CUI [9,1])
C0017636 (UMLS CUI [10,1])
C0205276 (UMLS CUI [1,2])
C0023008 (UMLS CUI [1,3])
C4082117 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,4])
C0011008 (UMLS CUI [1,5])
C0008952 (UMLS CUI [1,6])
C0008952 (UMLS CUI [2,1])
C0005834 (UMLS CUI [2,2])
C0444155 (UMLS CUI [2,3])
C0021822 (UMLS CUI [2,4])