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The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes
This article provides an overview of (a) issues in definition and diagnosis of specific reading disabilities at the behavioral level that may occur in different constellations of developmental and phenotypic profiles (patterns); (b) rapidly expanding research on genetic heterogeneity and gene candid...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538356/ https://www.ncbi.nlm.nih.gov/pubmed/23308072 http://dx.doi.org/10.3389/fpsyg.2012.00601 |
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author | Raskind, Wendy H. Peter, Beate Richards, Todd Eckert, Mark M. Berninger, Virginia W. |
author_facet | Raskind, Wendy H. Peter, Beate Richards, Todd Eckert, Mark M. Berninger, Virginia W. |
author_sort | Raskind, Wendy H. |
collection | PubMed |
description | This article provides an overview of (a) issues in definition and diagnosis of specific reading disabilities at the behavioral level that may occur in different constellations of developmental and phenotypic profiles (patterns); (b) rapidly expanding research on genetic heterogeneity and gene candidates for dyslexia and other reading disabilities; (c) emerging research on gene-brain relationships; and (d) current understanding of epigenetic mechanisms whereby environmental events may alter behavioral expression of genetic variations. A glossary of genetic terms (denoted by bold font) is provided for readers not familiar with the technical terms. |
format | Online Article Text |
id | pubmed-3538356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35383562013-01-10 The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes Raskind, Wendy H. Peter, Beate Richards, Todd Eckert, Mark M. Berninger, Virginia W. Front Psychol Psychology This article provides an overview of (a) issues in definition and diagnosis of specific reading disabilities at the behavioral level that may occur in different constellations of developmental and phenotypic profiles (patterns); (b) rapidly expanding research on genetic heterogeneity and gene candidates for dyslexia and other reading disabilities; (c) emerging research on gene-brain relationships; and (d) current understanding of epigenetic mechanisms whereby environmental events may alter behavioral expression of genetic variations. A glossary of genetic terms (denoted by bold font) is provided for readers not familiar with the technical terms. Frontiers Media S.A. 2013-01-07 /pmc/articles/PMC3538356/ /pubmed/23308072 http://dx.doi.org/10.3389/fpsyg.2012.00601 Text en Copyright © 2013 Raskind, Peter, Richards, Eckert and Berninger. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Psychology Raskind, Wendy H. Peter, Beate Richards, Todd Eckert, Mark M. Berninger, Virginia W. The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title | The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title_full | The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title_fullStr | The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title_full_unstemmed | The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title_short | The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes |
title_sort | genetics of reading disabilities: from phenotypes to candidate genes |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3538356/ https://www.ncbi.nlm.nih.gov/pubmed/23308072 http://dx.doi.org/10.3389/fpsyg.2012.00601 |
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