"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 |
|---|
| 1994 | 2 | 7 | 9 |
| 1995 | 1 | 5 | 6 |
| 1996 | 3 | 2 | 5 |
| 1997 | 4 | 4 | 8 |
| 1998 | 2 | 0 | 2 |
| 1999 | 3 | 6 | 9 |
| 2000 | 1 | 14 | 15 |
| 2001 | 2 | 11 | 13 |
| 2002 | 2 | 11 | 13 |
| 2003 | 2 | 14 | 16 |
| 2004 | 1 | 14 | 15 |
| 2005 | 2 | 7 | 9 |
| 2006 | 1 | 7 | 8 |
| 2007 | 2 | 7 | 9 |
| 2008 | 3 | 6 | 9 |
| 2009 | 2 | 2 | 4 |
| 2010 | 0 | 3 | 3 |
| 2011 | 0 | 7 | 7 |
| 2012 | 0 | 2 | 2 |
| 2013 | 2 | 7 | 9 |
| 2014 | 0 | 3 | 3 |
| 2015 | 0 | 4 | 4 |
| 2016 | 2 | 2 | 4 |
| 2017 | 1 | 3 | 4 |
| 2018 | 1 | 2 | 3 |
| 2019 | 1 | 2 | 3 |
| 2020 | 2 | 5 | 7 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Dominant" by people in Profiles.
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Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases. Hum Mol Genet. 2024 05 18; 33(11):945-957.
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Recurrent Breast Abscesses in a Female with Autosomal Dominant Hyper-IgE Syndrome. J Clin Immunol. 2022 05; 42(4):889-891.
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Molecular basis of ETV6-mediated predisposition to childhood acute lymphoblastic leukemia. Blood. 2021 01 21; 137(3):364-373.
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Vertical transmission of a large calvarial ossification defect due to heterozygous variants of ALX4 and TWIST1. Am J Med Genet A. 2021 03; 185(3):916-922.
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Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study. Brain. 2020 12 01; 143(12):3589-3602.
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Craniofacial phenotypes associated with Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3606-3612.
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BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms. Am J Hum Genet. 2020 12 03; 107(6):1096-1112.
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Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. Am J Med Genet A. 2021 12; 185(12):3593-3600.
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Phenotypic expansion in KIF1A-related dominant disorders: A description of novel variants and review of published cases. Hum Mutat. 2020 12; 41(12):2094-2104.
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Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome. J Exp Med. 2020 06 01; 217(6).