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dc.contributor.authorMitchell, Kevin
dc.contributor.authorChallman, Thomas D.
dc.contributor.authorBernier, Raphael
dc.contributor.authorBourgeron, Thomas
dc.contributor.authorChung, Wendy K.
dc.contributor.authorConstantino, John N.
dc.contributor.authorEichler, Evan E.
dc.contributor.authorJacquemont, Sebastien
dc.contributor.authorMiller, David T.
dc.contributor.authorZoghbi, Huda Y.
dc.contributor.authorMartin, Christa Lese
dc.contributor.authorLedbetter, David H.
dc.date.accessioned2020-06-17T09:00:46Z
dc.date.available2020-06-17T09:00:46Z
dc.date.issued2020
dc.date.submitted2020en
dc.identifier.citationMyers, S.M., Challman, T.D., Bernier, R., Bourgeron, T., Chung, W.K., Constantino, J.N., Eichler, E.E., Jacquemont, S., Miller, D.T., Mitchell, K.J., Zoghbi, H.Y., Martin, C.L., & Ledbetter, D.H., Insufficient Evidence for "Autism-Specific" Genes, American Journal of Human Genetics, 106, 5, 2020, 587 - 595en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractDespite 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.en
dc.format.extent587en
dc.format.extent595en
dc.language.isoenen
dc.relation.ispartofseriesAmerican Journal of Human Genetics;
dc.relation.ispartofseries106;
dc.relation.ispartofseries5;
dc.rightsYen
dc.subjectAutism spectrum disorderen
dc.subjectAutismen
dc.subjectNeurodevelopmental disordersen
dc.subjectGeneticsen
dc.titleInsufficient Evidence for "Autism-Specific" Genesen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/kemitche
dc.identifier.rssinternalid217108
dc.identifier.doi10.1016/j.ajhg.2020.04.004
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDThemeNeuroscienceen
dc.status.accessibleNen
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0002929720301130
dc.identifier.urihttp://hdl.handle.net/2262/92780


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