Please use this identifier to cite or link to this item:
https://hdl.handle.net/1959.11/22046
Title: | Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor | Contributor(s): | Keller, Matthew C (author); Simonson, Matthew A (author); Ripke, Stephan (author); Neale, Ben M (author); Gejman, Pablo V (author); Howrigan, Daniel P (author); Lee, Sang Hong (author); Lencz, Todd (author); Levinson, Douglas F (author); Sullivan, Patrick F (author) | Corporate Author: | Psychiatric Genomics Consortium, Schizophrenia Working Group (PGC SCZ) | Publication Date: | 2012 | Open Access: | Yes | DOI: | 10.1371/journal.pgen.1002656![]() |
Handle Link: | https://hdl.handle.net/1959.11/22046 | Abstract: | Autozygosity occurs when two chromosomal segments that are identical from a common ancestor are inherited from each parent. This occurs at high rates in the offspring of mates who are closely related (inbreeding), but also occurs at lower levels among the offspring of distantly related mates. Here, we use runs of homozygosity in genome-wide SNP data to estimate the proportion of the autosome that exists in autozygous tracts in 9,388 cases with schizophrenia and 12,456 controls. We estimate that the odds of schizophrenia increase by ∼17% for every 1% increase in genome-wide autozygosity. This association is not due to one or a few regions, but results from many autozygous segments spread throughout the genome, and is consistent with a role for multiple recessive or partially recessive alleles in the etiology of schizophrenia. Such a bias towards recessivity suggests that alleles that increase the risk of schizophrenia have been selected against over evolutionary time. | Publication Type: | Journal Article | Source of Publication: | PLoS Genetics, 8(4), p. 1-11 | Publisher: | Public Library of Science | Place of Publication: | United States of America | ISSN: | 1553-7404 1553-7390 |
Fields of Research (FoR) 2008: | 060405 Gene Expression (incl. Microarray and other genome-wide approaches) | Fields of Research (FoR) 2020: | 310505 Gene expression (incl. microarray and other genome-wide approaches) | Socio-Economic Objective (SEO) 2008: | 920110 Inherited Diseases (incl. Gene Therapy) | Socio-Economic Objective (SEO) 2020: | 200101 Diagnosis of human diseases and conditions | Peer Reviewed: | Yes | HERDC Category Description: | C1 Refereed Article in a Scholarly Journal |
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Appears in Collections: | Journal Article |
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