"Phenotype" 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.
The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment.
| Descriptor ID |
D010641
|
| MeSH Number(s) |
G05.695
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Phenotype".
Below are MeSH descriptors whose meaning is more specific than "Phenotype".
This graph shows the total number of publications written about "Phenotype" by people in this website by year, and whether "Phenotype" 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 |
|---|
| 1996 | 0 | 19 | 19 |
| 1997 | 0 | 26 | 26 |
| 1998 | 0 | 24 | 24 |
| 1999 | 2 | 34 | 36 |
| 2000 | 0 | 48 | 48 |
| 2001 | 1 | 46 | 47 |
| 2002 | 2 | 61 | 63 |
| 2003 | 2 | 57 | 59 |
| 2004 | 4 | 55 | 59 |
| 2005 | 9 | 64 | 73 |
| 2006 | 4 | 60 | 64 |
| 2007 | 8 | 70 | 78 |
| 2008 | 3 | 79 | 82 |
| 2009 | 5 | 69 | 74 |
| 2010 | 10 | 73 | 83 |
| 2011 | 9 | 87 | 96 |
| 2012 | 11 | 84 | 95 |
| 2013 | 14 | 94 | 108 |
| 2014 | 14 | 94 | 108 |
| 2015 | 17 | 107 | 124 |
| 2016 | 19 | 95 | 114 |
| 2017 | 14 | 110 | 124 |
| 2018 | 8 | 116 | 124 |
| 2019 | 18 | 141 | 159 |
| 2020 | 17 | 111 | 128 |
| 2021 | 14 | 121 | 135 |
| 2022 | 2 | 81 | 83 |
| 2023 | 1 | 79 | 80 |
| 2024 | 27 | 58 | 85 |
| 2025 | 4 | 58 | 62 |
| 2026 | 0 | 4 | 4 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Expanding the phenotypic spectrum of MECOM-associated syndrome: rare variants are associated with syndromic pulmonary arterial hypertension. J Med Genet. 2026 Mar 20; 63(4):225-234.
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Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes. Nature. 2026 04; 652(8110):675-685.
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Host- and pathogen-related determinants of pulmonary versus extrapulmonary tuberculosis. Eur Respir Rev. 2026 01; 35(179).
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De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disorders. Nat Commun. 2026 Jan 23; 17(1):1569.
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The biomedical landscape of genomic structural variation in the qatari population. Nat Commun. 2026 Jan 13; 17(1):1019.
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To jump or not to jump: comparing effects of phenotypic plasticity on the visual responses and escape behavior of locusts and grasshoppers. J Neurophysiol. 2026 Jan 01; 135(1):312-323.
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Mutations in the ?-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypes. Nat Commun. 2025 Nov 27; 16(1):10637.
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Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia. Am J Hum Genet. 2025 Dec 04; 112(12):2961-2972.
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Association of metabolomics measurements with blood cell phenotypes. Blood Cells Mol Dis. 2026 Mar; 117:102966.
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Information Theory Analysis of CTX Shows Consistent Clinical Presentation. J Inherit Metab Dis. 2025 Nov; 48(6):e70098.