Genomic

Dataset Information

0

OCD Collaborative Genetic Association Study (OCGAS)


ABSTRACT:

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.

PROVIDER: phs000903 | dbGaP |

SECONDARY ACCESSION(S): PRJNA281971PRJNA281970

REPOSITORIES: dbGaP

Dataset's files

Source:
Action DRS
phs000903.pha003885.txt Txt
GapExchange_phs000903.v1.p1.xml Xml
dbGaPEx2.1.5.xsd Other
Study_Report.phs000903.OCGAS.v1.p1.MULTI.pdf Pdf
manifest_phs000903.OCGAS.v1.p1.c1.DS-OCD-OPC.pdf Pdf
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