Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”

<p dir="ltr">Autism spectrum disorder (ASD), a neurodevelopmental illness that affects children at an early age with a global prevalence of 1%, is diagnosed based on clinical features such as social impairment, repetitive behaviors, and restricted interests. ASD is genetically hetero...

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Main Author: Hyung-Goo Kim (728597) (author)
Published: 2023
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_version_ 1864513509159600128
author Hyung-Goo Kim (728597)
author_facet Hyung-Goo Kim (728597)
author_role author
dc.creator.none.fl_str_mv Hyung-Goo Kim (728597)
dc.date.none.fl_str_mv 2023-06-20T09:00:00Z
dc.identifier.none.fl_str_mv 10.3390/ijms241210394
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Editorial_for_the_IJMS_Special_Issue_on_Molecular_Genetics_of_Autism_and_Intellectual_Disability_/26539396
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biological sciences
Genetics
Biomedical and clinical sciences
Clinical sciences
Autism Spectrum Disorder (ASD)
Neurodevelopmental Disorder
Prevalence
Social Impairment
Repetitive Behaviors
Restricted Interests
Genetic Heterogeneity
dc.title.none.fl_str_mv Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">Autism spectrum disorder (ASD), a neurodevelopmental illness that affects children at an early age with a global prevalence of 1%, is diagnosed based on clinical features such as social impairment, repetitive behaviors, and restricted interests. ASD is genetically heterogeneous, and the genetic etiology of ASD remains unknown in 20–60% of autistic people. ASD subjects commonly have co-occurring comorbidities such as intellectual disability (ID), seizures, sleep problems, or digestive problems, which suggest more complex genetic etiologies. Exome sequencing and other next-generation sequencing (NGS) techniques have been successful in increasing the total number of known ASD genes.</p><h2>Other Information</h2><p dir="ltr">Published in: International Journal of Molecular Sciences<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3390/ijms241210394" target="_blank">https://dx.doi.org/10.3390/ijms241210394</a></p>
eu_rights_str_mv openAccess
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identifier_str_mv 10.3390/ijms241210394
network_acronym_str Manara2
network_name_str Manara2
oai_identifier_str oai:figshare.com:article/26539396
publishDate 2023
repository.mail.fl_str_mv
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rights_invalid_str_mv CC BY 4.0
spelling Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”Hyung-Goo Kim (728597)Biological sciencesGeneticsBiomedical and clinical sciencesClinical sciencesAutism Spectrum Disorder (ASD)Neurodevelopmental DisorderPrevalenceSocial ImpairmentRepetitive BehaviorsRestricted InterestsGenetic Heterogeneity<p dir="ltr">Autism spectrum disorder (ASD), a neurodevelopmental illness that affects children at an early age with a global prevalence of 1%, is diagnosed based on clinical features such as social impairment, repetitive behaviors, and restricted interests. ASD is genetically heterogeneous, and the genetic etiology of ASD remains unknown in 20–60% of autistic people. ASD subjects commonly have co-occurring comorbidities such as intellectual disability (ID), seizures, sleep problems, or digestive problems, which suggest more complex genetic etiologies. Exome sequencing and other next-generation sequencing (NGS) techniques have been successful in increasing the total number of known ASD genes.</p><h2>Other Information</h2><p dir="ltr">Published in: International Journal of Molecular Sciences<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3390/ijms241210394" target="_blank">https://dx.doi.org/10.3390/ijms241210394</a></p>2023-06-20T09:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.3390/ijms241210394https://figshare.com/articles/journal_contribution/Editorial_for_the_IJMS_Special_Issue_on_Molecular_Genetics_of_Autism_and_Intellectual_Disability_/26539396CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/265393962023-06-20T09:00:00Z
spellingShingle Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
Hyung-Goo Kim (728597)
Biological sciences
Genetics
Biomedical and clinical sciences
Clinical sciences
Autism Spectrum Disorder (ASD)
Neurodevelopmental Disorder
Prevalence
Social Impairment
Repetitive Behaviors
Restricted Interests
Genetic Heterogeneity
status_str publishedVersion
title Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
title_full Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
title_fullStr Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
title_full_unstemmed Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
title_short Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
title_sort Editorial for the IJMS Special Issue on “Molecular Genetics of Autism and Intellectual Disability”
topic Biological sciences
Genetics
Biomedical and clinical sciences
Clinical sciences
Autism Spectrum Disorder (ASD)
Neurodevelopmental Disorder
Prevalence
Social Impairment
Repetitive Behaviors
Restricted Interests
Genetic Heterogeneity