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
|
| MeSH Number(s) |
F03.625
|
| 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,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 0 | 1 | 1 |
| 2015 | 6 | 2 | 8 |
| 2016 | 8 | 3 | 11 |
| 2017 | 6 | 3 | 9 |
| 2018 | 12 | 5 | 17 |
| 2019 | 19 | 3 | 22 |
| 2020 | 24 | 5 | 29 |
| 2021 | 29 | 3 | 32 |
| 2022 | 22 | 1 | 23 |
| 2023 | 19 | 0 | 19 |
| 2024 | 20 | 11 | 31 |
| 2025 | 37 | 4 | 41 |
| 2026 | 9 | 0 | 9 |
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Below are the most recent publications written about "Neurodevelopmental Disorders" by people in Profiles.
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes. Nat Genet. 2026 Apr; 58(4):761-773.
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Bi-allelic variants in NRDC cause a neurodevelopmental disorder characterized by neonatal lethality, microcephaly, and brain abnormalities. Am J Hum Genet. 2026 Mar 05; 113(3):548-561.
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Leveraging clinical sleep data across multiple pediatric cohorts for insights into neurodevelopment: the Retrospective Analysis of Sleep in Pediatric (RASP) cohorts study. Sleep. 2026 Feb 10; 49(2).
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Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders. Mol Cell. 2026 Feb 19; 86(4):604-624.e16.
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Association between fetal brain diffusion-weighted imaging and postnatal neurodevelopmental outcome after prenatal myelomeningocele repair. Ultrasound Obstet Gynecol. 2026 Mar; 67(3):329-340.
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De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders. Nat Commun. 2026 Jan 23; 17(1):1569.
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Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder. Genet Med. 2026 Apr; 28(4):101685.
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Bi-allelic variants in neuronal adhesion molecule astrotactin 1 gene ASTN1 cause diverse neurodevelopmental disorders. Am J Hum Genet. 2026 02 05; 113(2):362-379.
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Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia. Brain. 2026 Jan 08; 149(1):252-261.
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Automated EEG Background Analysis and 2-Year Outcomes in Neonatal Hypoxic-Ischemic Encephalopathy. JAMA Netw Open. 2025 Dec 01; 8(12):e2548321.