Neurodevelopmental Disorders
"Neurodevelopmental Disorders" 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.
These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-V).
Descriptor ID |
D065886
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MeSH Number(s) |
F03.625
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Concept/Terms |
Neurodevelopmental Disorders- Neurodevelopmental Disorders
- Disorder, Neurodevelopmental
- Disorders, Neurodevelopmental
- Neurodevelopmental Disorder
- Disorders Usually Diagnosed in Infancy, Childhood or Adolescence
- Child Mental Disorders
- Child Mental Disorder
- Disorder, Child Mental
- Disorders, Child Mental
- Mental Disorder, Child
- Mental Disorders, Child
- Mental Disorders Diagnosed in Childhood
|
Below are MeSH descriptors whose meaning is more general than "Neurodevelopmental Disorders".
Below are MeSH descriptors whose meaning is more specific than "Neurodevelopmental Disorders".
This graph shows the total number of publications written about "Neurodevelopmental Disorders" by people in this website by year, and whether "Neurodevelopmental Disorders" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2014 | 0 | 1 | 1 |
2015 | 4 | 2 | 6 |
2016 | 8 | 3 | 11 |
2017 | 7 | 2 | 9 |
2018 | 11 | 4 | 15 |
2019 | 19 | 3 | 22 |
2020 | 23 | 5 | 28 |
2021 | 31 | 4 | 35 |
2022 | 22 | 1 | 23 |
2023 | 20 | 0 | 20 |
2024 | 12 | 7 | 19 |
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Below are the most recent publications written about "Neurodevelopmental Disorders" by people in Profiles.
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Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder. Pediatr Neurol. 2024 Nov; 160:45-53.
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Mechanisms of neurodevelopmental toxicity of topiramate. Crit Rev Toxicol. 2024 Aug; 54(7):465-475.
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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release. Sci Adv. 2024 Jul 12; 10(28):eadk5462.
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Mortality and neurodevelopmental outcomes at 2?years' corrected age of very preterm infants with necrotising enterocolitis or spontaneous intestinal perforation: The EPIPAGE-2 cohort study. Eur J Pediatr. 2024 Sep; 183(9):4019-4028.
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Nutrition and the gut-brain axis in neonatal brain injury and development. Semin Perinatol. 2024 Aug; 48(5):151927.
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PSMD11 loss-of-function variants correlate with a neurobehavioral phenotype, obesity, and increased interferon response. Am J Hum Genet. 2024 07 11; 111(7):1352-1369.
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Late Preterm Corticosteroids Exposure and Neurodevelopmental Outcomes. JAMA. 2024 05 21; 331(19):1626-1627.
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Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes. Brain. 2024 May 03; 147(5):1837-1855.
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Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals. Eur J Hum Genet. 2024 Aug; 32(8):928-937.