ID
45984
Description
Principal Investigator: Gerald Nestadt, Johns Hopkins University, Baltimore, MD, USA MeSH: Obsessive-Compulsive Disorder https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000903 The OCD Collaborative Genetics Association Study Group (OCGAS) was funded by NIMH to conduct a genome-wide association study to identify disease susceptibility loci of early-onset obsessive-compulsive disorder (OCD). Collaborators at Johns Hopkins, Brown, Columbia, MGH, UCLA, and NIMH evaluated 2,000 individuals with OCD and collected DNA from these individuals and both their parents. The genotyping and analyses was performed in two stages. In the first stage 1,065 families (comprising 1406 patients with OCD and 2895 individuals in total) were genotyped on the Illumina OmniExpress GWA (SNPs) panel at the JHU SNP Center.
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Mots-clés
Versions (1)
- 06/04/2024 06/04/2024 - Madita Rudolph
Détendeur de droits
Gerald Nestadt, Johns Hopkins University, Baltimore, MD, USA
Téléchargé le
6 avril 2024
DOI
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Licence
Creative Commons BY 4.0
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dbGaP phs000903 OCD Collaborative Genetic Association Study (OCGAS)
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for early-onset obsessive-compulsive disorder (OCD).
- This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and sex of subject.
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample aliases and sample use.
- This subject phenotype data table includes early-onset obsessive-compulsive disorder (OCD) evaluation and age of OCD onset.
- This sample attributes data table includes body site where sample was collected, analyte type, histological type, and tumor status.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent data table contains subject IDs, consent group information, subject aliases, and affection status for early-onset obsessive-compulsive disorder (OCD).
- This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, and sex of subject.
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes sample aliases and sample use.
- This subject phenotype data table includes early-onset obsessive-compulsive disorder (OCD) evaluation and age of OCD onset.
- This sample attributes data table includes body site where sample was collected, analyte type, histological type, and tumor status.
C0680251 (UMLS CUI [1,2])
C0028768 (UMLS CUI [1,2])
C0206132 (UMLS CUI [1,3])
C1385010 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C0036341 (UMLS CUI [2,2])
C0680251 (UMLS CUI [3,1])
C0025362 (UMLS CUI [3,2])
C0205082 (UMLS CUI [3,3])
C0680251 (UMLS CUI [4,1])
C0040517 (UMLS CUI [4,2])
C0680251 (UMLS CUI [5,1])
C0028768 (UMLS CUI [5,2])
C0175668 (UMLS CUI [5,3])
C0011581 (UMLS CUI [5,4])