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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...

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Detalles Bibliográficos
Autores principales: Reader, Rose H., Covill, Laura E., Nudel, Ron, Newbury, Dianne F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2014
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.
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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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