Inglês

Eligibility Criteria

6 Formulários  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This pedigree data table includes family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, sex of subjects, and twin IDs for monozygotic twins. Please note that if a couple did not have children, the submitters created a dummy child to link the couple in a pedigree. The gender of a dummy child was set as missing.
    4. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. 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. Several subjects gave permission to share their DNA results, but not their phenotypes.
    5. This subject phenotype table includes sociodemographic information (n=7 variables), medical history (n=12 variables; historical height, self-reported history, and reproductive physiological processes), physical observations (n=12 variables; subject's age, blood pressure, anthropometric measurements, hearing, eyesight, physical status, lung spirometry), disease diagnosis (n=33 variables), laboratory measurements (n=17 variables), Mini-Mental State Exam (MMSE) (n=9 variables), level of physical activity (n=3 variables), surgery and treatment (n=5 variables), and smoking status (n=7 variables). Several subjects gave permission to share their DNA results, but not their phenotypes.
    6. The sample attributes table includes the body site, analyte type, and tumor status.
Inclusion and exclusion criteria
Descrição

Inclusion and exclusion criteria

Families must have Family Longevity Selection Scores (FLOSS) of 7 or more, as defined in Sebastiani et al., 2009 (PMID: 19910380).
Descrição

Families must have Family Longevity Selection Scores (FLOSS) of 7 or more

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0241889
UMLS CUI [1,3]
C0449820
UMLS CUI [1,4]
C3846158
Families consist of at least a sibling pair in the upper generation, plus the entire second generation (including children of deceased), and the children's spouses.
Descrição

Elig.phs000397.v3.p3.2

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C0205435
UMLS CUI [1,3]
C0079411
UMLS CUI [1,4]
C0037047
UMLS CUI [1,5]
C1709450
UMLS CUI [1,6]
C1512693
UMLS CUI [2,1]
C0015576
UMLS CUI [2,2]
C0205436
UMLS CUI [2,3]
C0079411
UMLS CUI [2,4]
C0205197
UMLS CUI [2,5]
C0162409
UMLS CUI [2,6]
C1512693
Minimum family size is 3, with at least a pair in the upper generation and one child.
Descrição

Elig.phs000397.v3.p3.3

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1524031
UMLS CUI [1,2]
C0015576
UMLS CUI [1,3]
C0456389
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Similar models

Eligibility Criteria

6 Formulários
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This pedigree data table includes family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, sex of subjects, and twin IDs for monozygotic twins. Please note that if a couple did not have children, the submitters created a dummy child to link the couple in a pedigree. The gender of a dummy child was set as missing.
    4. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. 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. Several subjects gave permission to share their DNA results, but not their phenotypes.
    5. This subject phenotype table includes sociodemographic information (n=7 variables), medical history (n=12 variables; historical height, self-reported history, and reproductive physiological processes), physical observations (n=12 variables; subject's age, blood pressure, anthropometric measurements, hearing, eyesight, physical status, lung spirometry), disease diagnosis (n=33 variables), laboratory measurements (n=17 variables), Mini-Mental State Exam (MMSE) (n=9 variables), level of physical activity (n=3 variables), surgery and treatment (n=5 variables), and smoking status (n=7 variables). Several subjects gave permission to share their DNA results, but not their phenotypes.
    6. The sample attributes table includes the body site, analyte type, and tumor status.
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion and exclusion criteria
Families must have Family Longevity Selection Scores (FLOSS) of 7 or more
Item
Families must have Family Longevity Selection Scores (FLOSS) of 7 or more, as defined in Sebastiani et al., 2009 (PMID: 19910380).
boolean
C1512693 (UMLS CUI [1,1])
C0241889 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C3846158 (UMLS CUI [1,4])
Elig.phs000397.v3.p3.2
Item
Families consist of at least a sibling pair in the upper generation, plus the entire second generation (including children of deceased), and the children's spouses.
boolean
C0015576 (UMLS CUI [1,1])
C0205435 (UMLS CUI [1,2])
C0079411 (UMLS CUI [1,3])
C0037047 (UMLS CUI [1,4])
C1709450 (UMLS CUI [1,5])
C1512693 (UMLS CUI [1,6])
C0015576 (UMLS CUI [2,1])
C0205436 (UMLS CUI [2,2])
C0079411 (UMLS CUI [2,3])
C0205197 (UMLS CUI [2,4])
C0162409 (UMLS CUI [2,5])
C1512693 (UMLS CUI [2,6])
Elig.phs000397.v3.p3.3
Item
Minimum family size is 3, with at least a pair in the upper generation and one child.
boolean
C1524031 (UMLS CUI [1,1])
C0015576 (UMLS CUI [1,2])
C0456389 (UMLS CUI [1,3])
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