"Genes, Recessive" 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 only in the homozygous state.
| Descriptor ID |
D005808
|
| MeSH Number(s) |
G05.360.340.024.340.415 G05.420.325
|
| Concept/Terms |
Conditions, Recessive Genetic- Conditions, Recessive Genetic
- Condition, Recessive Genetic
- Genetic Condition, Recessive
- Recessive Genetic Condition
- Recessive Genetic Conditions
- Genetic Conditions, Recessive
|
Below are MeSH descriptors whose meaning is more general than "Genes, Recessive".
Below are MeSH descriptors whose meaning is more specific than "Genes, Recessive".
This graph shows the total number of publications written about "Genes, Recessive" by people in this website by year, and whether "Genes, Recessive" 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 |
|---|
| 1997 | 1 | 4 | 5 |
| 1998 | 0 | 2 | 2 |
| 1999 | 1 | 3 | 4 |
| 2000 | 1 | 2 | 3 |
| 2001 | 0 | 3 | 3 |
| 2002 | 0 | 3 | 3 |
| 2003 | 0 | 5 | 5 |
| 2004 | 0 | 2 | 2 |
| 2005 | 1 | 3 | 4 |
| 2006 | 1 | 1 | 2 |
| 2007 | 2 | 3 | 5 |
| 2008 | 1 | 2 | 3 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 3 | 4 |
| 2011 | 1 | 1 | 2 |
| 2012 | 1 | 1 | 2 |
| 2013 | 1 | 6 | 7 |
| 2014 | 0 | 2 | 2 |
| 2015 | 2 | 1 | 3 |
| 2016 | 4 | 5 | 9 |
| 2017 | 1 | 2 | 3 |
| 2018 | 2 | 7 | 9 |
| 2019 | 4 | 2 | 6 |
| 2020 | 0 | 3 | 3 |
| 2021 | 1 | 6 | 7 |
| 2022 | 0 | 1 | 1 |
| 2024 | 0 | 3 | 3 |
| 2025 | 1 | 0 | 1 |
| 2026 | 1 | 2 | 3 |
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click here.
Below are the most recent publications written about "Genes, Recessive" by people in Profiles.
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Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome. Am J Hum Genet. 2016 08 04; 99(2):318-36.
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A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism. J Allergy Clin Immunol. 2016 08; 138(2):599-601.e3.
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A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2014 Dec 04; 56(1):150-5.
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Potentially functional variants in the core nucleotide excision repair genes predict survival in Japanese gastric cancer patients. Carcinogenesis. 2014 Sep; 35(9):2031-8.
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De novo anti-type VII collagen antibodies in patients with recessive dystrophic epidermolysis bullosa. J Invest Dermatol. 2014 Apr; 134(4):1138-1140.
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Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements. Hum Genet. 2014 Mar; 133(3):331-45.
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A probabilistic disease-gene finder for personal genomes. Genome Res. 2011 Sep; 21(9):1529-42.
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Signatures of mutation and selection in the cancer genome. Nature. 2010 Feb 18; 463(7283):893-8.
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A pocket on the surface of the N-terminal BRCT domain of Mcph1 is required to prevent abnormal chromosome condensation. J Mol Biol. 2010 Feb 05; 395(5):908-15.
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New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene. Hum Mol Genet. 2009 Jan 01; 18(1):178-92.