"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 |
|---|
| 1993 | 0 | 3 | 3 |
| 1994 | 1 | 1 | 2 |
| 1995 | 0 | 4 | 4 |
| 1996 | 3 | 4 | 7 |
| 1997 | 2 | 3 | 5 |
| 1998 | 0 | 3 | 3 |
| 1999 | 0 | 3 | 3 |
| 2000 | 0 | 5 | 5 |
| 2001 | 1 | 4 | 5 |
| 2002 | 1 | 3 | 4 |
| 2003 | 1 | 3 | 4 |
| 2004 | 2 | 2 | 4 |
| 2005 | 2 | 5 | 7 |
| 2006 | 3 | 3 | 6 |
| 2007 | 0 | 4 | 4 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 2 | 3 |
| 2010 | 0 | 1 | 1 |
| 2012 | 1 | 2 | 3 |
| 2014 | 0 | 3 | 3 |
| 2015 | 1 | 2 | 3 |
| 2017 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Genes, Dominant" by people in Profiles.
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Germline ETV6 mutations and predisposition to hematological malignancies. Int J Hematol. 2017 Aug; 106(2):189-195.
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Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease. Hum Mutat. 2016 Jan; 37(1):84-97.
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A Brief Review and Update of the Clinicopathologic Diagnosis of Arrhythmogenic Cardiomyopathy. Arch Pathol Lab Med. 2015 Sep; 139(9):1181-6.
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Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing loss. Am J Med Genet A. 2015 Oct; 167A(10):2357-65.
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Critical role of lysine 134 methylation on histone H2AX for ?-H2AX production and DNA repair. Nat Commun. 2014 Dec 09; 5:5691.
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Sumoylated HSP90 is a dominantly inherited plasma cell dyscrasias risk factor. J Clin Invest. 2015 Jan; 125(1):316-23.
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Obesity-associated variants within FTO form long-range functional connections with IRX3. Nature. 2014 Mar 20; 507(7492):371-5.
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Control of vascular permeability by atrial natriuretic peptide via a GEF-H1-dependent mechanism. J Biol Chem. 2014 Feb 21; 289(8):5168-83.
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An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract. Exp Eye Res. 2013 May; 110:136-41.
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Exome sequencing and genetic testing for MODY. PLoS One. 2012; 7(5):e38050.