"Genes, 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.
Genes that are located on the X CHROMOSOME.
| Descriptor ID |
D050172
|
| MeSH Number(s) |
G05.360.340.024.340.500 G05.420.457
|
| Concept/Terms |
Genes, X-Linked- Genes, X-Linked
- Genes, X Linked
- Genes, X-Chromosome
- Gene, X-Chromosome
- Genes, X Chromosome
- X-Chromosome Gene
- X-Chromosome Genes
- X Chromosome Genes
- X-Linked Genes
- Gene, X-Linked
- X Linked Genes
- X-Linked Gene
Alleles, X-Linked- Alleles, X-Linked
- Allele, X-Linked
- Alleles, X Linked
- X-Linked Allele
- X-Linked Alleles
X-Linked Traits- X-Linked Traits
- Trait, X-Linked
- X Linked Traits
- X-Linked Trait
- Traits, X-Linked
- Traits, X Linked
|
Below are MeSH descriptors whose meaning is more general than "Genes, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Genes, X-Linked".
This graph shows the total number of publications written about "Genes, X-Linked" by people in this website by year, and whether "Genes, X-Linked" 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 |
|---|
| 2006 | 2 | 2 | 4 |
| 2007 | 2 | 1 | 3 |
| 2008 | 0 | 3 | 3 |
| 2010 | 1 | 1 | 2 |
| 2011 | 1 | 2 | 3 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 2 | 3 |
| 2016 | 0 | 4 | 4 |
| 2017 | 2 | 0 | 2 |
| 2018 | 0 | 1 | 1 |
| 2019 | 1 | 1 | 2 |
| 2020 | 0 | 2 | 2 |
| 2024 | 1 | 2 | 3 |
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Below are the most recent publications written about "Genes, X-Linked" by people in Profiles.
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X-linked genetic associations in sporadic thoracic aortic dissection. Am J Med Genet A. 2024 09; 194(9):e63644.
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Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss. Mol Genet Genomic Med. 2024 Feb; 12(2):e2404.
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Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation. Nat Commun. 2024 Jan 08; 15(1):365.
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De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females. Genet Med. 2021 04; 23(4):645-652.
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Nuclear receptor corepressors in intellectual disability and autism. Mol Psychiatry. 2020 10; 25(10):2220-2236.
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Identification of cancer sex-disparity in the functional integrity of p53 and its X chromosome network. Nat Commun. 2019 11 26; 10(1):5385.
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X-chromosome association studies of congenital heart defects. Am J Med Genet A. 2020 01; 182(1):250-254.
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X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family. Sci Rep. 2018 11 02; 8(1):16280.
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Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A. 2018 06 05; 115(23):E5363-E5372.
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Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability. PLoS One. 2017; 12(4):e0175962.