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Insufficient Evidence for “Autism-Specific” Genes

Despite evidence that deleterious variants in the same genes are implicated across multiple neurodevelopmental and neuropsychiatric disorders, there has been considerable interest in identifying genes that, when mutated, confer risk that is largely specific for autism spectrum disorder (ASD). Here,...

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Autores principales: Myers, Scott M., Challman, Thomas D., Bernier, Raphael, Bourgeron, Thomas, Chung, Wendy K., Constantino, John N., Eichler, Evan E., Jacquemont, Sebastien, Miller, David T., Mitchell, Kevin J., Zoghbi, Huda Y., Martin, Christa Lese, Ledbetter, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212289/
https://www.ncbi.nlm.nih.gov/pubmed/32359473
http://dx.doi.org/10.1016/j.ajhg.2020.04.004
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author Myers, Scott M.
Challman, Thomas D.
Bernier, Raphael
Bourgeron, Thomas
Chung, Wendy K.
Constantino, John N.
Eichler, Evan E.
Jacquemont, Sebastien
Miller, David T.
Mitchell, Kevin J.
Zoghbi, Huda Y.
Martin, Christa Lese
Ledbetter, David H.
author_facet Myers, Scott M.
Challman, Thomas D.
Bernier, Raphael
Bourgeron, Thomas
Chung, Wendy K.
Constantino, John N.
Eichler, Evan E.
Jacquemont, Sebastien
Miller, David T.
Mitchell, Kevin J.
Zoghbi, Huda Y.
Martin, Christa Lese
Ledbetter, David H.
author_sort Myers, Scott M.
collection PubMed
description Despite evidence that deleterious variants in the same genes are implicated across multiple neurodevelopmental and neuropsychiatric disorders, there has been considerable interest in identifying genes that, when mutated, confer risk that is largely specific for autism spectrum disorder (ASD). Here, we review the findings and limitations of recent efforts to identify relatively “autism-specific” genes, efforts which focus on rare variants of large effect size that are thought to account for the observed phenotypes. We present a divergent interpretation of published evidence; discuss practical and theoretical issues related to studying the relationships between rare, large-effect deleterious variants and neurodevelopmental phenotypes; and describe potential future directions of this research. We argue that there is currently insufficient evidence to establish meaningful ASD specificity of any genes based on large-effect rare-variant data.
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spelling pubmed-72122892020-10-09 Insufficient Evidence for “Autism-Specific” Genes Myers, Scott M. Challman, Thomas D. Bernier, Raphael Bourgeron, Thomas Chung, Wendy K. Constantino, John N. Eichler, Evan E. Jacquemont, Sebastien Miller, David T. Mitchell, Kevin J. Zoghbi, Huda Y. Martin, Christa Lese Ledbetter, David H. Am J Hum Genet Commentary Despite evidence that deleterious variants in the same genes are implicated across multiple neurodevelopmental and neuropsychiatric disorders, there has been considerable interest in identifying genes that, when mutated, confer risk that is largely specific for autism spectrum disorder (ASD). Here, we review the findings and limitations of recent efforts to identify relatively “autism-specific” genes, efforts which focus on rare variants of large effect size that are thought to account for the observed phenotypes. We present a divergent interpretation of published evidence; discuss practical and theoretical issues related to studying the relationships between rare, large-effect deleterious variants and neurodevelopmental phenotypes; and describe potential future directions of this research. We argue that there is currently insufficient evidence to establish meaningful ASD specificity of any genes based on large-effect rare-variant data. Elsevier 2020-05-07 2020-04-30 /pmc/articles/PMC7212289/ /pubmed/32359473 http://dx.doi.org/10.1016/j.ajhg.2020.04.004 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Commentary
Myers, Scott M.
Challman, Thomas D.
Bernier, Raphael
Bourgeron, Thomas
Chung, Wendy K.
Constantino, John N.
Eichler, Evan E.
Jacquemont, Sebastien
Miller, David T.
Mitchell, Kevin J.
Zoghbi, Huda Y.
Martin, Christa Lese
Ledbetter, David H.
Insufficient Evidence for “Autism-Specific” Genes
title Insufficient Evidence for “Autism-Specific” Genes
title_full Insufficient Evidence for “Autism-Specific” Genes
title_fullStr Insufficient Evidence for “Autism-Specific” Genes
title_full_unstemmed Insufficient Evidence for “Autism-Specific” Genes
title_short Insufficient Evidence for “Autism-Specific” Genes
title_sort insufficient evidence for “autism-specific” genes
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7212289/
https://www.ncbi.nlm.nih.gov/pubmed/32359473
http://dx.doi.org/10.1016/j.ajhg.2020.04.004
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