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Increased female autosomal burden of rare copy number variants in human populations and in autism families

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Year: 2015
Type: article
Source: Molecular Psychiatry
DOI: 10.1038/mp.2014.179
Authors: G Desachy, L A Croen, A R Torres, M Kharrazi, G N Delorenze, G C Windham, C K Yoshida, L A Weiss
Institutions: University of California, San Francisco, Kaiser Permanente, Kaiser Permanente Northern California, Utah State University, California Department of Public Health
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: closed

Funders: National Institute of Environmental Health Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: A Sex-Specific Dissection of Autism Genetics, Prenatal and Neonatal Biologic Markers for Autism
OpenAlex ID: W2018982295
FWCI: 4.931
Cites: 30
Cited by: 54
Related to: 10
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