Work

Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

Year: 2012

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2012.05.011

Authors: Rui Luo, Stephan J. Sanders, Yuan Tian, Irina Voineagu, Ni Huang, Su H. Chu, Lambertus Klei, Chaochao Cai, Jing Ou, Jennifer K. Lowe, Matthew E. Hurles, Bernie Devlin, Matthew W. State, Daniel H. Geschwind

Institutions: University of California, Los Angeles, Yale University, Wellcome Sanger Institute, Carnegie Mellon University, University of Pittsburgh

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: bronze

Funders: Wellcome Trust, National Institute of Mental Health

Awards: A Comprehensive Approach to Identification of Autism Susceptibility Genes, G7487573014

OpenAlex ID: W2093773663

FWCI: 13.68

Cites: 84

Cited by: 167

Related to: 10