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ID

45476

Description

Principal Investigator: Todd Lencz, PhD, Feinstein Institute for Medical Research, North Shore - LIJ Health System, Manhasset, NY, USA MeSH: Schizophrenia https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000448 Schizophrenia is characterized by high heritability (~80%), yet the identification of susceptibility genes has proven extremely challenging. The Ashkenazi Jewish population, derived from a limited number of founders, may be enriched for a subset of susceptibility alleles, which may also have higher odds ratios than those detected by previous studies. GWAS was conducted in a large Ashkenazi case-control cohort, derived from the Hebrew University Genetic Resource, using the Illumina HumanOmni1-Quad BeadChip.

Lien

dbGap study = phs000448

Mots-clés

  1. 26/10/2022 26/10/2022 - Simon Heim
  2. 13/12/2022 13/12/2022 - Kristina Keller
Détendeur de droits

Todd Lencz, PhD, Feinstein Institute for Medical Research, North Shore - LIJ Health System, Manhasset, NY, USA

Téléchargé le

13 décembre 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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    dbGaP phs000448 Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort

    Sample ID, subject ID, sample sources, sample source IDs, and sample use variables associated with participants with or without schizophrenia, obtained from the Ashkenazi Jewish population, and involved in the "Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort" project.

    pht002509
    Description

    pht002509

    Subject ID
    Description

    SUBJID

    Type de données

    string

    Alias
    UMLS CUI [1,1]
    C2348585 (Clinical Trial Subject Unique Identifier)
    Sample ID
    Description

    SAMPID

    Type de données

    string

    Alias
    UMLS CUI [1,1]
    C1299222 (Sample identification number)
    SNOMED
    372274003
    Source repository where samples originate [HUGR = Hebrew University Genetic Resource ]
    Description

    SAMP_SOURCE

    Type de données

    string

    Alias
    UMLS CUI [1,1]
    C0449416 (Source)
    SNOMED
    260753009
    LOINC
    LP21212-3
    UMLS CUI [1,2]
    C3847505 (Repository)
    LOINC
    LP182360-0
    Sample ID used in the Source Repository
    Description

    SOURCE_SAMPID

    Type de données

    string

    Alias
    UMLS CUI [1,1]
    C1299222 (Sample identification number)
    SNOMED
    372274003
    UMLS CUI [1,2]
    C0449416 (Source)
    SNOMED
    260753009
    LOINC
    LP21212-3
    UMLS CUI [1,3]
    C3847505 (Repository)
    LOINC
    LP182360-0
    Sample use
    Description

    SAMPLE_USE

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C1524063 (Use of)
    SNOMED
    260676000
    UMLS CUI [1,2]
    C0370003 (Specimen)
    SNOMED
    123038009
    LOINC
    LP7593-9

    Similar models

    Sample ID, subject ID, sample sources, sample source IDs, and sample use variables associated with participants with or without schizophrenia, obtained from the Ashkenazi Jewish population, and involved in the "Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort" project.

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    pht002509
    SUBJID
    Item
    Subject ID
    string
    C2348585 (UMLS CUI [1,1])
    SAMPID
    Item
    Sample ID
    string
    C1299222 (UMLS CUI [1,1])
    SAMP_SOURCE
    Item
    Source repository where samples originate [HUGR = Hebrew University Genetic Resource ]
    string
    C0449416 (UMLS CUI [1,1])
    C3847505 (UMLS CUI [1,2])
    SOURCE_SAMPID
    Item
    Sample ID used in the Source Repository
    string
    C1299222 (UMLS CUI [1,1])
    C0449416 (UMLS CUI [1,2])
    C3847505 (UMLS CUI [1,3])
    Item
    Sample use
    text
    C1524063 (UMLS CUI [1,1])
    C0370003 (UMLS CUI [1,2])
    Code List
    Sample use
    CL Item
    SNP genotypes obtained using standard or custom microarrays (SNP_Array)

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