Work

Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity

Year: 2018

Type: article

Study design: Observational Study

Source: Schizophrenia Research

DOI: 10.1016/j.schres.2018.02.034

Authors: Fayeza F. Khan, Phillip E. Melton, Nina S. McCarthy, Bharti Morar, John Blangero, Eric K. Moses, Assen Jablensky

Institutions: The University of Western Australia, Curtin University, Cooperative Research Centre for Mental Health, Harry Perkins Institute of Medical Research, The University of Texas Rio Grande Valley

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

Funders: Society for Mental Health Research, National Health and Medical Research Council, National Institute of Mental Health, Medical Research Foundation

Awards: 2/3: Pedigree-Based Whole Genome Sequencing of Affective and Psychotic Disorders, Schizophrenia under the genomic lens: next generation sequencing of Western Australian families with schizophrenia

OpenAlex ID: W2791189474

FWCI: 1.073

Cites: 40

Cited by: 17

Related to: 10