 Autistic Disorder
"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-IV)
| Descriptor ID |
D001321
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| MeSH Number(s) |
F03.550.325.125
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| Concept/Terms |
Autistic Disorder- Autistic Disorder
- Disorder, Autistic
- Disorders, Autistic
- Kanner's Syndrome
- Kanner Syndrome
- Kanners Syndrome
- Syndrome, Kanner's
- Autism, Infantile
- Infantile Autism
- Autism
- Autisms
- Autism, Early Infantile
- Early Infantile Autism
- Infantile Autism, Early
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1986 | 1 | 0 | 1 | | 1988 | 1 | 0 | 1 | | 1990 | 2 | 0 | 2 | | 1991 | 2 | 0 | 2 | | 1992 | 3 | 0 | 3 | | 1993 | 4 | 0 | 4 | | 1994 | 1 | 0 | 1 | | 1996 | 3 | 0 | 3 | | 1997 | 3 | 0 | 3 | | 1998 | 2 | 0 | 2 | | 1999 | 2 | 0 | 2 | | 2000 | 3 | 1 | 4 | | 2001 | 5 | 0 | 5 | | 2002 | 5 | 0 | 5 | | 2003 | 2 | 0 | 2 | | 2004 | 4 | 1 | 5 | | 2005 | 1 | 2 | 3 | | 2006 | 4 | 2 | 6 | | 2007 | 8 | 3 | 11 | | 2008 | 4 | 1 | 5 | | 2009 | 5 | 0 | 5 | | 2010 | 4 | 2 | 6 | | 2011 | 1 | 1 | 2 | | 2012 | 3 | 2 | 5 | | 2013 | 2 | 2 | 4 | | 2014 | 4 | 1 | 5 | | 2015 | 3 | 1 | 4 | | 2016 | 2 | 1 | 3 | | 2018 | 1 | 2 | 3 | | 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Autistic Disorder" by people in Profiles.
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Nambot S, Hevner RF, Dobyns WB. Reply to Hsueh YP et al. Eur J Hum Genet. 2020 08; 28(8):999.
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Ness S, Pandina G, Jagannatha S, Wathen K, Bangerter A, Manyakov NV, Hendren R, Leventhal B, Murphy D, Dawson G, Drevets WC, Manji HK. ASPI: a public-private partnership to develop treatments for autism. Nat Rev Drug Discov. 2020 04; 19(4):219-220.
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Gomez CM. The cerebellum in health and disease. Neurosci Lett. 2019 01 01; 688:1.
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Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies. Am J Hum Genet. 2018 06 07; 102(6):1031-1047.
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Berg KL, Acharya K, Shiu CS, Msall ME. Delayed Diagnosis and Treatment Among Children with Autism Who Experience Adversity. J Autism Dev Disord. 2018 01; 48(1):45-54.
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Hillenmeyer S, Davis LK, Gamazon ER, Cook EH, Cox NJ, Altman RB. STAMS: STRING-assisted module search for genome wide association studies and application to autism. Bioinformatics. 2016 12 15; 32(24):3815-3822.
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Blizinsky KD, Diaz-Castro B, Forrest MP, Schürmann B, Bach AP, Martin-de-Saavedra MD, Wang L, Csernansky JG, Duan J, Penzes P. Reversal of dendritic phenotypes in 16p11.2 microduplication mouse model neurons by pharmacological targeting of a network hub. Proc Natl Acad Sci U S A. 2016 07 26; 113(30):8520-5.
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Berg AT, Dobyns WB. Progress in autism research and postgenomic studies - Authors' reply. Lancet Neurol. 2016 02; 15(2):136-137.
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Kloth AD, Badura A, Li A, Cherskov A, Connolly SG, Giovannucci A, Bangash MA, Grasselli G, Peñagarikano O, Piochon C, Tsai PT, Geschwind DH, Hansel C, Sahin M, Takumi T, Worley PF, Wang SS. Cerebellar associative sensory learning defects in five mouse autism models. Elife. 2015 Jul 09; 4:e06085.
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Hansen J, Snow C, Tuttle E, Ghoneim DH, Yang CS, Spencer A, Gunter SA, Smyser CD, Gurnett CA, Shinawi M, Dobyns WB, Wheless J, Halterman MW, Jansen LA, Paschal BM, Paciorkowski AR. De novo mutations in SIK1 cause a spectrum of developmental epilepsies. Am J Hum Genet. 2015 Apr 02; 96(4):682-90.
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