Atlas Logo
Philadelphia Neurodevelopmental Cohort (PNC)
BACK
Sample details

The PNC initiative focuses on characterizing brain and behavior interaction with genetics. It includes a population-based sample of approximately 9,500 individuals from the greater Philadelphia area, ages 8-21 years who received medical care at the Children’s Hospital of Philadelphia (CHOP) network. The participants presented for diverse medical conditions, ranging from a well child visit and minor problems to chronic condition management to potentially life threatening health problems, but not ascertained through psychiatric services. They were initially enrolled in the genetic study at CHOP’s Center for Applied Genomics (CAG). Upon assent or consent, participants were genotyped during the time of their clinical visit and provided written permission to be recontacted for studies of complex pediatric disorders. The PNC participants were selected at random after stratification by sex, age and ethnicity, and a total of 1,445 participants also received neuroimaging.

Study design
Cohort - clinical

Number of participants at first data collection

9,498 (participants)

Age at first data collection

8 - 21 years (participants)

Participant year of birth

Varied (participants)

Participant sex
All

Representative sample at baseline?
No

Sample features

Children and young people
Patients and clinical populations
Dataset details

Country

United States of America

Year of first data collection

2009

Primary Institutions

Children's Hospital of Philadelphia (CHOP)

University of Pennsylvania

Links

med.upenn.edu/bbl/philadelphianeurodevelopmentalcohort.html

nitrc.org/projects/pnc

omicsdi.org/dataset/dbgap/phs000607

Funders

National Institute of Mental Health (NIMH)

Ongoing?
Yes

Data types collected

neuroImagingData
mentalHealthData
qualitativeData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – face-to-face
  • Secondary data
Qualitative data collection
  • Ethnography or participant observation
Neuroimaging data collection
  • Diffusion Tensor Imaging (DTI)
  • Functional magnetic resonance imaging (fMRI)
  • Magnetic Resonance Imaging (MRI)
Linked or secondary data
  • Healthcare data
Features

Engagement

  • None
  • Keywords

    Behaviour
    Brain functioning
    Education
    Genetics
    Medical history
    Neurodevelopment
    Neurodevelopmental disorders
    Neuroimaging
    Psychology and psychopathology
    Stressful life events

    Consortia and dataset groups

    FAMILY Consortium
    Harmonization of At Risk Multisite Observational Networks for Youth (HARMONY) collaboration
    Contact us

    |

    FAQS

    |

    Privacy

    |

    © 2024 Louise Arseneault

    Platform by Delosis