ID

45495

Description

Principal Investigator: Isaac S. Kohane, MD, PhD, Boston Children's Hospital, Boston, MA, USA MeSH: Autistic Disorder,Heart Defects, Congenital,Asthma,Attention Deficit Disorders,Diabetes Mellitus, Type 1,Diabetes Mellitus, Type 2,Epilepsy,Gastrointestinal Diseases,Hypersensitivity,Autoimmune Diseases,Hematologic Diseases,Neoplasms,Arrhythmias, Cardiac,Chromosome Aberrations,Congenital Abnormalities,Dermatology,Developmental Disabilities,Endocrine System,Otolaryngology,Syndrome,Urogenital System,Hearing Loss,Immune System Diseases,Musculoskeletal Abnormalities,Nervous System Diseases,Neuromuscular Diseases,Metabolic Diseases,Nutrition Disorders,Vision Disorders,Mouth Diseases,Mental Disorders,Kidney Diseases,Respiration Disorders,Thyroid Diseases,Vascular Diseases https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000495 The Gene Partnership (TGP) is a prospective longitudinal registry at Boston Children's Hospital (BCH) to study the genetic and environmental contributions to childhood health and disease, collect genetic information on a large number of children who have been phenotyped, and implement the Informed Cohort and the Informed Cohort Oversight Board (ICOB). The term "*The Gene Partnership*" reflects a partnership between researchers and participants. Children seen at BCH are offered enrollment, as are their parents and siblings. DNA is collected on all enrollees. BCH has a comprehensive EMR system, and virtually all inpatient and outpatient data are captured electronically. Clinical data in the BCH EMR is loaded in the i2b2 data warehouse which is available to investigators. Cases, phenotypes, and covariates are ascertained using the i2b2 database. Participants at BCH in TGP have consented to receive any research result and/or incidental finding that arises from studies using TGP that is approved by the Informed Cohort Oversight Board (ICOB) and is in accordance with the participants' preferences; results are returned through the Personally Controlled Health Record (PCHR). BCH and Cincinnati Children's Hospital Medical Center (CCHMC) have partnered as the *P*ediatric *A*lliance for *G*enomic and *E*lectronic Medical Record (EMR) *R*esearch (*PAGER*) site for the eMERGE Phase II network for pediatric institutions, and the cohort for eMERGE at BCH is TGP.

Lien

dbGap study = phs000495

Mots-clés

  1. 16/11/2022 16/11/2022 - Kristina Keller
  2. 13/12/2022 13/12/2022 - Kristina Keller
Détendeur de droits

Isaac S. Kohane, MD, PhD, Boston Children's Hospital, Boston, MA, USA

Téléchargé le

13 décembre 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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dbGaP phs000495 The Gene Partnership (TGP) - eMERGE Data

Sample Attribute Information

pht002867
Description

pht002867

De-identified sample id
Description

SAMPID

Type de données

string

Alias
UMLS CUI [1,1]
C1299222
UMLS CUI [1,2]
C4684638
Gender of sample - as indicated by genotype analysis
Description

GENDER

Type de données

text

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C1303103
UMLS CUI [1,3]
C1285573
Type of sample obtained
Description

COLLECTION TYPE

Type de données

text

Alias
UMLS CUI [1,1]
C2347029
Analytye type
Description

ANALYTE TYPE

Type de données

text

Alias
UMLS CUI [1,1]
C4744818

Similar models

Sample Attribute Information

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
pht002867
SAMPID
Item
De-identified sample id
string
C1299222 (UMLS CUI [1,1])
C4684638 (UMLS CUI [1,2])
Item
Gender of sample - as indicated by genotype analysis
text
C0079399 (UMLS CUI [1,1])
C1303103 (UMLS CUI [1,2])
C1285573 (UMLS CUI [1,3])
Code List
Gender of sample - as indicated by genotype analysis
CL Item
Male (M)
C0086582 (UMLS CUI [1,1])
CL Item
Female (F)
C0086287 (UMLS CUI [1,1])
CL Item
Missing (.)
C1705492 (UMLS CUI [1,1])
CL Item
Unknown (99)
C0439673 (UMLS CUI [1,1])
Item
Type of sample obtained
text
C2347029 (UMLS CUI [1,1])
Code List
Type of sample obtained
CL Item
Saliva (1)
C0438730 (UMLS CUI [1,1])
CL Item
Blood (2)
C0005834 (UMLS CUI [1,1])
CL Item
Missing (.)
C1705492 (UMLS CUI [1,1])
CL Item
Unknown (99)
C0439673 (UMLS CUI [1,1])
Item
Analytye type
text
C4744818 (UMLS CUI [1,1])
Code List
Analytye type
CL Item
DNA (1)
C0012854 (UMLS CUI [1,1])
CL Item
Missing (.)
C1705492 (UMLS CUI [1,1])
CL Item
Unknown (99)
C0439673 (UMLS CUI [1,1])

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