Mental Retardation, X-Linked
"Mental Retardation, X-Linked" 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 class of genetic disorders resulting in INTELLECTUAL DISABILITY that is associated either with mutations of GENES located on the X CHROMOSOME or aberrations in the structure of the X chromosome (SEX CHROMOSOME ABERRATIONS).
MeSH Number(s)
C10.597.606.643.455
C16.320.322.500
C16.320.400.525
Concept/Terms
Mental Retardation, X-Linked- Mental Retardation, X-Linked
- Mental Retardation, X Linked
- Retardation, X-Linked Mental
- X-Linked Mental Retardations
- X-Linked Mental Retardation Disorders
- X Linked Mental Retardation Disorders
- X-Linked Mental Retardation Syndromes
- X Linked Mental Retardation Syndromes
- X-Linked Mental Retardation
- X Linked Mental Retardation
Below are MeSH descriptors whose meaning is more general than "Mental Retardation, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Mental Retardation, X-Linked".
This graph shows the total number of publications written about "Mental Retardation, X-Linked" by people in Harvard Catalyst Profiles by year, and whether "Mental Retardation, X-Linked" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 2 | 0 | 2 |
| 2008 | 0 | 2 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 1 | 2 |
| 2015 | 0 | 1 | 1 |
| 2017 | 3 | 0 | 3 |
| 2018 | 2 | 0 | 2 |
| 2019 | 2 | 0 | 2 |
| 2020 | 3 | 1 | 4 |
| 2021 | 3 | 0 | 3 |
| 2022 | 2 | 1 | 3 |
Below are the most recent publications written about "Mental Retardation, X-Linked" by people in Profiles.
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Increased Reliability of Visually-Evoked Activity in Area V1 of the MECP2-Duplication Mouse Model of Autism. J Neurosci. 2022 08 17; 42(33):6469-6482.
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Rare pathogenic variants in WNK3 cause X-linked intellectual disability. Genet Med. 2022 09; 24(9):1941-1951.
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Exploration of group II metabotropic glutamate receptor modulation in mouse models of Rett syndrome and MECP2 Duplication syndrome. Neuropharmacology. 2022 05 15; 209:109022.
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Maternal mosaicism for a missense variant in the SMS gene that causes Snyder-Robinson syndrome. Cold Spring Harb Mol Case Stud. 2021 12; 7(6).
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Inhibition of Elevated Ras-MAPK Signaling Normalizes Enhanced Motor Learning and Excessive Clustered Dendritic Spine Stabilization in the MECP2-Duplication Syndrome Mouse Model of Autism. eNeuro. 2021 Jul-Aug; 8(4).
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Excessive Formation and Stabilization of Dendritic Spine Clusters in the MECP2-Duplication Syndrome Mouse Model of Autism. eNeuro. 2021 Jan-Feb; 8(1).
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Person Ability Scores as an Alternative to Norm-Referenced Scores as Outcome Measures in Studies of Neurodevelopmental Disorders. Am J Intellect Dev Disabil. 2020 11 01; 125(6):475-480.
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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation. Thyroid. 2021 05; 31(5):713-720.
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MCT8 deficiency: collaborative rare disease phenotyping for care and research. Lancet Diabetes Endocrinol. 2020 07; 8(7):555-557.
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Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation. Commun Biol. 2020 06 01; 3(1):278.