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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2023
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| _version_ | 1864513509159600128 |
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| 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 |
| id | Manara2_06bcf460b0527e3d4c913e1a0c9e4aa9 |
| 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 | |
| repository.name.fl_str_mv | |
| repository_id_str | |
| 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 |