"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 |
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1995 | 0 | 1 | 1 |
2004 | 0 | 3 | 3 |
2006 | 1 | 1 | 2 |
2009 | 0 | 2 | 2 |
2013 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
2017 | 1 | 4 | 5 |
2018 | 3 | 9 | 12 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Genes, Recessive" by people in Profiles.
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LINE-1-Mediated AluYa5 Insertion Underlying Complete Autosomal Recessive IFN-?R1 Deficiency. J Clin Immunol. 2019 10; 39(7):739-742.
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Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability. Hum Genet. 2018 Sep; 137(9):735-752.
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Mutations in WDR4 as a new cause of Galloway-Mowat syndrome. Am J Med Genet A. 2018 11; 176(11):2460-2465.
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A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children. Clin Genet. 2018 10; 94(3-4):393-395.
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Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function. Am J Hum Genet. 2018 07 05; 103(1):100-114.
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A novel in-frame deletion in ZMPSTE24 is associated with autosomal recessive acrogeria (Gottron type) in an extended consanguineous family. Clin Dysmorphol. 2018 Jul; 27(3):88-90.
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ZNF341 controls STAT3 expression and thereby immunocompetence. Sci Immunol. 2018 06 15; 3(24).
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A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
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A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome. Am J Med Genet A. 2018 06; 176(6):1427-1431.
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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi003-A from a patient affected by an autosomal recessive form of Long QT Syndrome type 1. Stem Cell Res. 2018 05; 29:170-173.