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Genome-Wide Studies of Specific Language Impairment
Specific language impairment (SLI) is a multifactorial neurodevelopmental disorder which occurs unexpectedly and without an obvious cause. Over a decade of research suggests that SLI is highly heritable. Several genes and loci have already been implicated in SLI through linkage and targeted associat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228195/ https://www.ncbi.nlm.nih.gov/pubmed/25411653 http://dx.doi.org/10.1007/s40473-014-0024-z |
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author | Reader, Rose H. Covill, Laura E. Nudel, Ron Newbury, Dianne F. |
author_facet | Reader, Rose H. Covill, Laura E. Nudel, Ron Newbury, Dianne F. |
author_sort | Reader, Rose H. |
collection | PubMed |
description | Specific language impairment (SLI) is a multifactorial neurodevelopmental disorder which occurs unexpectedly and without an obvious cause. Over a decade of research suggests that SLI is highly heritable. Several genes and loci have already been implicated in SLI through linkage and targeted association methods. Recently, genome-wide association studies (GWAS) of SLI and language traits in the general population have been reported and, consequently, new candidate genes have been identified. This review aims to summarise the literature concerning genome-wide studies of SLI. In addition, this review highlights the methodologies that have been used to research the genetics of SLI to date, and also considers the current, and future, contributions that GWAS can offer. |
format | Online Article Text |
id | pubmed-4228195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-42281952014-11-17 Genome-Wide Studies of Specific Language Impairment Reader, Rose H. Covill, Laura E. Nudel, Ron Newbury, Dianne F. Curr Behav Neurosci Rep Genetics & Neuroscience (P Gejman, Section Editor) Specific language impairment (SLI) is a multifactorial neurodevelopmental disorder which occurs unexpectedly and without an obvious cause. Over a decade of research suggests that SLI is highly heritable. Several genes and loci have already been implicated in SLI through linkage and targeted association methods. Recently, genome-wide association studies (GWAS) of SLI and language traits in the general population have been reported and, consequently, new candidate genes have been identified. This review aims to summarise the literature concerning genome-wide studies of SLI. In addition, this review highlights the methodologies that have been used to research the genetics of SLI to date, and also considers the current, and future, contributions that GWAS can offer. Springer International Publishing 2014-09-26 2014 /pmc/articles/PMC4228195/ /pubmed/25411653 http://dx.doi.org/10.1007/s40473-014-0024-z Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Genetics & Neuroscience (P Gejman, Section Editor) Reader, Rose H. Covill, Laura E. Nudel, Ron Newbury, Dianne F. Genome-Wide Studies of Specific Language Impairment |
title | Genome-Wide Studies of Specific Language Impairment |
title_full | Genome-Wide Studies of Specific Language Impairment |
title_fullStr | Genome-Wide Studies of Specific Language Impairment |
title_full_unstemmed | Genome-Wide Studies of Specific Language Impairment |
title_short | Genome-Wide Studies of Specific Language Impairment |
title_sort | genome-wide studies of specific language impairment |
topic | Genetics & Neuroscience (P Gejman, Section Editor) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228195/ https://www.ncbi.nlm.nih.gov/pubmed/25411653 http://dx.doi.org/10.1007/s40473-014-0024-z |
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