"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.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 7 | 8 |
| 1996 | 4 | 7 | 11 |
| 1997 | 1 | 8 | 9 |
| 1998 | 4 | 15 | 19 |
| 1999 | 3 | 16 | 19 |
| 2000 | 5 | 24 | 29 |
| 2001 | 5 | 11 | 16 |
| 2002 | 8 | 23 | 31 |
| 2003 | 4 | 32 | 36 |
| 2004 | 4 | 26 | 30 |
| 2005 | 3 | 21 | 24 |
| 2006 | 8 | 10 | 18 |
| 2007 | 5 | 20 | 25 |
| 2008 | 6 | 19 | 25 |
| 2009 | 4 | 8 | 12 |
| 2010 | 2 | 11 | 13 |
| 2011 | 1 | 9 | 10 |
| 2012 | 1 | 9 | 10 |
| 2013 | 6 | 9 | 15 |
| 2014 | 5 | 4 | 9 |
| 2015 | 3 | 7 | 10 |
| 2016 | 2 | 8 | 10 |
| 2017 | 1 | 2 | 3 |
| 2018 | 6 | 4 | 10 |
| 2019 | 0 | 1 | 1 |
| 2020 | 2 | 4 | 6 |
| 2021 | 3 | 4 | 7 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
| 2024 | 0 | 4 | 4 |
Below are the most recent publications written about "Genes, Dominant" by people in Profiles.
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Constraining models of dominance for nonsynonymous mutations in the human genome. PLoS Genet. 2024 Sep; 20(9):e1011198.
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Revisiting Dominance in Population Genetics. Genome Biol Evol. 2024 Aug 05; 16(8).
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Autosomal Dominant Osteopetrosis (ADO) Caused by a Missense Variant in the TCIRG1 Gene. J Clin Endocrinol Metab. 2024 Jun 17; 109(7):1726-1732.
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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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Autosomal dominant osteopetrosis. Bone. 2023 05; 170:116723.
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Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome. J Hum Genet. 2022 Sep; 67(9):553-556.
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Enhanced prime editing systems by manipulating cellular determinants of editing outcomes. Cell. 2021 10 28; 184(22):5635-5652.e29.
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Active site variants in STT3A cause a dominant type I congenital disorder of glycosylation with neuromusculoskeletal findings. Am J Hum Genet. 2021 11 04; 108(11):2130-2144.
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Allele-specific gene editing to rescue dominant CRX-associated LCA7 phenotypes in a retinal organoid model. Stem Cell Reports. 2021 11 09; 16(11):2690-2702.
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Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nat Genet. 2021 07; 53(7):1006-1021.