Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

2009/11/04 by Jonathan Sebat, Deborah L. Levy, Shane McCarthy +1 · 1 citation
Biochemistry, Genetics and Molecular Biology · Medicine · #Autism #Biology #Copy-number variation #Gene #Genetic Associations and Epidemiology #Genetic architecture #Genetic heterogeneity #Genetics #Genome #Genomic variations and chromosomal abnormalities #Genomics and Rare Diseases #Medicine #Mutation #Neurodevelopmental disorder #Phenotype #Psychiatry #Schizophrenia (object-oriented programming)

paper · doi:10.1016/j.tig.2009.10.004

openalex publication_date 2009/11/04 · crossref created 2009/11/04 · crossref issued 2009/12/01 · crossref published 2009/12/01 · crossref published-print 2009/12/01 · crossref deposited 2023/05/27 · openalex created_date 2025/10/10 · crossref indexed 2026/06/25 · openalex updated_date 2026/08/01

Citations

• Accurate whole human genome sequencing using reversible terminator chemistry
• Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
• The complete genome of an individual by massively parallel DNA sequencing
• Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
• Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors
• Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells
• The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
• Global variation in copy number in the human genome
• XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance.

Cited by

• Paul E. Meehl [wikipedia]