 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 | 3 | 1 | 4 | | 2009 | 5 | 0 | 5 | | 2010 | 4 | 2 | 6 | | 2011 | 1 | 1 | 2 | | 2012 | 3 | 2 | 5 | | 2013 | 1 | 2 | 3 | | 2014 | 4 | 1 | 5 | | 2015 | 3 | 1 | 4 | | 2016 | 2 | 1 | 3 | | 2018 | 1 | 2 | 3 | | 2020 | 5 | 0 | 5 | | 2021 | 2 | 0 | 2 | | 2022 | 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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Grant JE, Chamberlain SR. Autistic traits in trichotillomania. Brain Behav. 2022 07; 12(7):e2663.
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Guerrero MGB, Sobotka SA. Understanding the Barriers to Receiving Autism Diagnoses for Hispanic and Latinx Families. Pediatr Ann. 2022 Apr; 51(4):e167-e171.
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Vysotskiy M, Zhong X, Miller-Fleming TW, Zhou D. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Med. 2021 10 29; 13(1):172.
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Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, Soucy A, Genetti CA, Suslovitch V, Rodan LH, Tiller GE, Lesca G, Gripp KW, Asadollahi R, Hamosh A, Applegate CD, Turnpenny PD, Simon MEH, Volker-Touw CML, Gassen KLIV, Binsbergen EV, Pfundt R, Gardeitchik T, Vries BBA, Immken LL, Buchanan C, Willing M, Toler TL, Fassi E, Baker L, Vansenne F, Wang X, Ambrus JL, Fannemel M, Posey JE, Agolini E, Novelli A, Rauch A, Boonsawat P, Fagerberg CR, Larsen MJ, Kibaek M, Labalme A, Poisson A, Payne KK, Walsh LE, Aldinger KA, Balciuniene J, Skraban C, Gray C, Murrell J, Bupp CP, Pascolini G, Grammatico P, Broly M, Küry S, Nizon M, Rasool IG, Zahoor MY, Kraus C, Reis A, Iqbal M, Uguen K, Audebert-Bellanger S, Ferec C, Redon S, Baker J, Wu Y, Zampino G, Syrbe S, Brosse I, Jamra RA, Dobyns WB, Cohen LL, Blomhoff A, Mignot C, Keren B, Courtin T, Agrawal PB, Beggs AH, Yu TW. Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior. Genet Med. 2021 06; 23(6):1028-1040.
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Bilaver LA, Sobotka SA, Mandell DS. Understanding Racial and Ethnic Disparities in Autism-Related Service Use Among Medicaid-Enrolled Children. J Autism Dev Disord. 2021 Sep; 51(9):3341-3355.
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Simmons DH, Titley HK, Hansel C, Mason P. Behavioral Tests for Mouse Models of Autism: An Argument for the Inclusion of Cerebellum-Controlled Motor Behaviors. Neuroscience. 2021 05 10; 462:303-319.
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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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Nambot S, Faivre L, Mirzaa G, Thevenon J, Bruel AL, Mosca-Boidron AL, Masurel-Paulet A, Goldenberg A, Le Meur N, Charollais A, Mignot C, Petit F, Rossi M, Metreau J, Layet V, Amram D, Boute-Bénéjean O, Bhoj E, Cousin MA, Kruisselbrink TM, Lanpher BC, Klee EW, Fiala E, Grange DK, Meschino WS, Hiatt SM, Cooper GM, Olivié H, Smith WE, Dumas M, Lehman A. De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature. Eur J Hum Genet. 2020 06; 28(6):770-782.
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Gomez CM. The cerebellum in health and disease. Neurosci Lett. 2019 01 01; 688:1.
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