ID
45618
Beskrivning
Principal Investigator: James B. Potash, MD, Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA MeSH: Bipolar Disorder,Schizoaffective disorder https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001358 Bipolar disorder is a complex psychiatric disease for which few causative genes have been discovered. Targeted sequencing of bipolar cases and unaffected controls was performed to elucidate the contribution of rare variants to bipolar disorder. This study included the standard exome targets as well as genes involved in synaptic function and genes previously implicated in bipolar disorder.
Länk
Nyckelord
Versioner (1)
- 2023-02-26 2023-02-26 - Simon Heim
Rättsinnehavare
James B. Potash, MD, Department of Psychiatry, University of Iowa Carver College of Medicine, Iowa City, IA, USA
Uppladdad den
26 februari 2023
DOI
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Licens
Creative Commons BY 4.0
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dbGaP phs001358 RareBliss: Rare Bipolar Loci Identification Through Sequencing Study
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and case control status of the subject for bipolar disorder.
- The subject pedigree table contains family ID, subject ID, mother ID, father ID, and sex.
- This data table contains 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 use.
- This subject phenotype table contains subject IDs, sex, and race.
- This sample attributes table contains sample IDs, body type, analyte type, histological type, and tumor status.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and case control status of the subject for bipolar disorder.
- The subject pedigree table contains family ID, subject ID, mother ID, father ID, and sex.
- This data table contains 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 use.
- This subject phenotype table contains subject IDs, sex, and race.
- This sample attributes table contains sample IDs, body type, analyte type, histological type, and tumor status.
C0680251 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,2])
C0080105 (UMLS CUI [1,3])
C2827447 (UMLS CUI [1,4])
C0683462 (UMLS CUI [1,5])
C0025102 (UMLS CUI [1,6])
C4321457 (UMLS CUI [1,7])
C0811741 (UMLS CUI [1,8])
C0027466 (UMLS CUI [1,9])
C3847505 (UMLS CUI [1,10])
C0451085 (UMLS CUI [1,11])
C5142702 (UMLS CUI [1,12])
C0455498 (UMLS CUI [1,13])
C0009932 (UMLS CUI [1,14])
C0021430 (UMLS CUI [1,15])