"Autistic Disorder" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V)
Descriptor ID |
D001321
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MeSH Number(s) |
F03.625.164.113.500
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Concept/Terms |
Autistic Disorder- Autistic Disorder
- Disorder, Autistic
- Disorders, Autistic
- Kanner's Syndrome
- Kanner Syndrome
- Kanners Syndrome
- Autism, Infantile
- Infantile Autism
- Autism
- Autism, Early Infantile
- Early Infantile Autism
- Infantile Autism, Early
|
Below are MeSH descriptors whose meaning is more general than "Autistic Disorder".
Below are MeSH descriptors whose meaning is more specific than "Autistic Disorder".
This graph shows the total number of publications written about "Autistic Disorder" by people in this website by year, and whether "Autistic Disorder" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 |
2015 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
2018 | 1 | 2 | 3 |
2019 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Autistic Disorder" by people in Profiles.
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Inherited cases of CNOT3-associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clin Genet. 2020 10; 98(4):408-412.
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De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures. Brain. 2019 11 01; 142(11):3351-3359.
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Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Environ Mol Mutagen. 2019 01; 60(1):17-28.
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Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia. Mol Psychiatry. 2020 03; 25(3):584-602.
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Rare gene deletions in genetic generalized and Rolandic epilepsies. PLoS One. 2018; 13(8):e0202022.
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Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism. Hum Genet. 2017 02; 136(2):179-192.
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Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans. Nat Commun. 2015 Sep 01; 6:8086.
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Importance measures for epistatic interactions in case-parent trios. Ann Hum Genet. 2011 Jan; 75(1):122-32.