ID

45928

Description

Principal Investigator: James P. Evans, MD, PhD, University of North Carolina, Chapel Hill, NC, USA MeSH: Genetic Diseases, Inborn,Neoplasms,Adenomatous Polyposis Coli,Microcephaly,Aortic Aneurysm, Thoracic,Peripheral Nervous System Diseases,Cardiomyopathies,Leukodystrophy, Globoid Cell,Seizures,Mitochondria,Inflammation,Autoimmune Diseases,Progeria,Retina,Muscular Diseases,Rhabdomyolysis,Arrhythmias, Cardiac,Osteochondrodysplasias,Intellectual disability,Autistic Disorder,Neuromuscular Diseases,Paraplegia,Central Nervous System Diseases,Cholestasis,Anemia,Genetic Testing https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000827 North Carolina Clinical Genomic Evaluation by Next-generation Exome Sequencing This study is part of a larger consortium project investigating the validity and best use of next-generation sequencing (in particular, whole exome sequencing, or WES) in clinical care. Participants are patients who were either seen in the UNC Cancer and Adult Genetics Clinic or referred to the study by their physician. They will be approached by their physician or a genetic counselor for recruitment. Once enrolled, a clinical geneticist or genetic counselor will obtain consent and collect blood samples to be analyzed using WES. Results may include information related to a diagnosis and incidental information. Medically actionable incidental findings will be CLIA-certified and returned to participants in a routine genetic counseling session, along with diagnostic findings. Eligible adult participants will be randomized to have the opportunity to choose to get certain types of non-medically actionable incidental findings, as well. Their decisions will be investigated, as will psychosocial and behavioral responses to sequencing and receiving sequencing information. This is a longitudinal, mixed methods study (i.e., multiple assessments pre- and post-return of results, with both quantitative and qualitative methods used to gather data). Because only the quantitative component of the study uses randomization, only measures and procedures associated with that component are included here. The third study release includes data of additional n=189 subjects.

Lien

study_id=phs000827

Mots-clés

  1. 4/3/24 4/3/24 - Dr. Christian Niklas
Détendeur de droits

James P. Evans, MD, PhD, University of North Carolina, Chapel Hill, NC, USA

Téléchargé le

4 de marzo de 2024

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000827 N.C. Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
Study participants represent different clinical phenotypes in which delineation of the molecular etiology might be amenable to genome-scale sequencing. The major areas include:
Description

Elig.phs000827.v3.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C1302261
UMLS CUI [1,2]
C0031437
Hereditary cancer predisposition
Description

Elig.phs000827.v3.p1.2

Type de données

boolean

Alias
UMLS CUI [1,1]
C0314657
UMLS CUI [1,2]
C0006826
Neurological disorders (e.g. neuropathy, myopathy, movement disorders, epilepsy)
Description

Elig.phs000827.v3.p1.3

Type de données

boolean

Alias
UMLS CUI [1,1]
C0027765
Intellectual disability and dysmorphology/birth defects
Description

Elig.phs000827.v3.p1.4

Type de données

boolean

Alias
UMLS CUI [1,1]
C3714756
UMLS CUI [2,1]
C0000768
Cardiovascular conditions (e.g. Long QT syndrome, cardiomyopathy, thoracic aortic aneurysm and dissection)
Description

Elig.phs000827.v3.p1.5

Type de données

boolean

Alias
UMLS CUI [1,1]
C0007222
Retinal disorders
Description

Elig.phs000827.v3.p1.6

Type de données

boolean

Alias
UMLS CUI [1,1]
C0035309
Thrombotic disorders
Description

Elig.phs000827.v3.p1.7

Type de données

boolean

Alias
UMLS CUI [1,1]
C4049573
Eligible patients should have certain hallmarks - including but not limited to, age of onset, severity, family history, or constellation of phenotypic features - suggestive of a monogenic etiology for their presenting signs or symptoms. Excluded: Those with low suspicion of a hereditable disorder.
Description

Elig.phs000827.v3.p1.8

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0332299
UMLS CUI [1,3]
C0439660
UMLS CUI [1,4]
C1314792

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000827.v3.p1.1
Item
Study participants represent different clinical phenotypes in which delineation of the molecular etiology might be amenable to genome-scale sequencing. The major areas include:
boolean
C1302261 (UMLS CUI [1,1])
C0031437 (UMLS CUI [1,2])
Elig.phs000827.v3.p1.2
Item
Hereditary cancer predisposition
boolean
C0314657 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
Elig.phs000827.v3.p1.3
Item
Neurological disorders (e.g. neuropathy, myopathy, movement disorders, epilepsy)
boolean
C0027765 (UMLS CUI [1,1])
Elig.phs000827.v3.p1.4
Item
Intellectual disability and dysmorphology/birth defects
boolean
C3714756 (UMLS CUI [1,1])
C0000768 (UMLS CUI [2,1])
Elig.phs000827.v3.p1.5
Item
Cardiovascular conditions (e.g. Long QT syndrome, cardiomyopathy, thoracic aortic aneurysm and dissection)
boolean
C0007222 (UMLS CUI [1,1])
Elig.phs000827.v3.p1.6
Item
Retinal disorders
boolean
C0035309 (UMLS CUI [1,1])
Elig.phs000827.v3.p1.7
Item
Thrombotic disorders
boolean
C4049573 (UMLS CUI [1,1])
Elig.phs000827.v3.p1.8
Item
Eligible patients should have certain hallmarks - including but not limited to, age of onset, severity, family history, or constellation of phenotypic features - suggestive of a monogenic etiology for their presenting signs or symptoms. Excluded: Those with low suspicion of a hereditable disorder.
boolean
C1512693 (UMLS CUI [1,1])
C0332299 (UMLS CUI [1,2])
C0439660 (UMLS CUI [1,3])
C1314792 (UMLS CUI [1,4])

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