"Genes, Dominant" 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 influence the PHENOTYPE both in the homozygous and the heterozygous state.
Descriptor ID |
D005799
|
MeSH Number(s) |
G05.360.340.024.340.240 G05.420.320
|
Concept/Terms |
Genetic Conditions, Dominant- Genetic Conditions, Dominant
- Conditions, Dominant Genetic
- Condition, Dominant Genetic
- Dominant Genetic Condition
- Genetic Condition, Dominant
- Dominant Genetic Conditions
|
Below are MeSH descriptors whose meaning is more general than "Genes, Dominant".
Below are MeSH descriptors whose meaning is more specific than "Genes, Dominant".
This graph shows the total number of publications written about "Genes, Dominant" by people in this website by year, and whether "Genes, Dominant" 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 |
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1997 | 0 | 1 | 1 |
2000 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2005 | 1 | 0 | 1 |
2007 | 1 | 1 | 2 |
2008 | 0 | 1 | 1 |
2010 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2014 | 0 | 1 | 1 |
2015 | 0 | 2 | 2 |
2016 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2019 | 1 | 1 | 2 |
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Below are the most recent publications written about "Genes, Dominant" by people in Profiles.
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Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2. PLoS One. 2019; 14(12):e0225943.
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Two females with hair loss. J Dtsch Dermatol Ges. 2019 08; 17(8):845-847.
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Investigation of dominant and recessive inheritance models in genome-wide association studies data of nonsyndromic cleft lip with or without cleft palate. Birth Defects Res. 2018 03 01; 110(4):336-341.
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Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations. Muscle Nerve. 2016 09; 54(3):496-500.
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Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR. Acta Derm Venereol. 2015 Nov; 95(8):1005-7.
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A specific IFIH1 gain-of-function mutation causes Singleton-Merten syndrome. Am J Hum Genet. 2015 Feb 05; 96(2):275-82.
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Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Brain. 2014 Mar; 137(Pt 3):683-92.
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Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegia. Hum Mutat. 2013 Jun; 34(6):860-3.
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Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature. Eur J Pediatr. 2011 Jun; 170(6):741-6.
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Interference with PPARgamma signaling causes cerebral vascular dysfunction, hypertrophy, and remodeling. Hypertension. 2008 Apr; 51(4):867-71.