Work

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities

Year: 2014

Type: article

Study design: Observational Study

Source: Molecular Psychiatry

DOI: 10.1038/mp.2013.189

Authors: R E Gur, J J Yi, D M McDonald-McGinn, S X Tang, M E Calkins, D Whinna, M C Souders, A Savitt, E H Zackai, P J Moberg, B S Emanuel, R C Gur

Institutions: University of Pennsylvania, Children's Hospital of Philadelphia

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funder: National Institute of Mental Health

Awards: Neurodevelopmental Genomics: Trajectories of Complex Phenotypes, G17793626, 1/2-Brain-Behavior and Genetic Studies of the 22q11DS, 2/2 Brain, Behavior and Genetic Studies of the 22q11 Deletion Studies, G4945665992, 2/2 Neurodevelopmental Genomics: Trajectories of Complex Phenotypes, G5992877304, G741339269, Psychosis: A Convergent Neuroscience Perspective, A Prospective Study of Endophenotypes in At-Risk Youths and Their Siblings

OpenAlex ID: W2122361375

FWCI: 7.225

Cites: 59

Cited by: 97

Related to: 10