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The genetic relationship between handedness and neurodevelopmental disorders
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dc.contributor.author | Brandler, William M. | |
dc.contributor.author | Paracchini, Silvia | |
dc.date.accessioned | 2014-02-03T14:31:03Z | |
dc.date.available | 2014-02-03T14:31:03Z | |
dc.date.issued | 2014-02 | |
dc.identifier.citation | Brandler , W M & Paracchini , S 2014 , ' The genetic relationship between handedness and neurodevelopmental disorders ' , Trends in Molecular Medicine , vol. 20 , no. 2 , pp. 83-90 . https://doi.org/10.1016/j.molmed.2013.10.008 | en |
dc.identifier.issn | 1471-4914 | |
dc.identifier.other | PURE: 82992634 | |
dc.identifier.other | PURE UUID: 9a00ed94-e52d-4dba-825f-27e8f7141e39 | |
dc.identifier.other | RIS: urn:AA9AA7B91012D876AED96EF75E990B4F | |
dc.identifier.other | Scopus: 84893705609 | |
dc.identifier.other | ORCID: /0000-0001-9934-8602/work/60428088 | |
dc.identifier.other | WOS: 000331589300004 | |
dc.identifier.uri | https://hdl.handle.net/10023/4427 | |
dc.description.abstract | Handedness and brain asymmetry have been linked to neurodevelopmental disorders such as dyslexia and schizophrenia. The genetic nature of this correlation is not understood. Recent discoveries have shown handedness is determined in part by the biological pathways that establish left/right (LR) body asymmetry during development. Cilia play a key role in this process, and candidate genes for dyslexia have also been recently shown to be involved in cilia formation. Defective cilia result not only in LR body asymmetry phenotypes but also brain midline phenotypes such as an absent corpus callosum. These findings suggest that the mechanisms for establishing LR asymmetry in the body are reused for brain midline development, which in turn influences traits such as handedness and reading ability. | |
dc.language.iso | eng | |
dc.relation.ispartof | Trends in Molecular Medicine | en |
dc.rights | (c) 2013 The Authors. Published by Elsevier Ltd. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. | en |
dc.subject | Cerebral asymmetry | en |
dc.subject | Ciliogenesis | en |
dc.subject | Corpus callosum | en |
dc.subject | Dyslexia | en |
dc.subject | Handedness | en |
dc.subject | Schizophrenia | en |
dc.subject | QH426 Genetics | en |
dc.subject.lcc | QH426 | en |
dc.title | The genetic relationship between handedness and neurodevelopmental disorders | en |
dc.type | Journal article | en |
dc.description.version | Publisher PDF | en |
dc.contributor.institution | University of St Andrews. School of Medicine | en |
dc.contributor.institution | University of St Andrews. Biomedical Sciences Research Complex | en |
dc.identifier.doi | https://doi.org/10.1016/j.molmed.2013.10.008 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S1471491413001937 | en |
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