"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 |
|---|
| 1995 | 0 | 24 | 24 |
| 1996 | 0 | 17 | 17 |
| 1997 | 0 | 28 | 28 |
| 1998 | 0 | 27 | 27 |
| 1999 | 2 | 36 | 38 |
| 2000 | 0 | 49 | 49 |
| 2001 | 1 | 44 | 45 |
| 2002 | 2 | 61 | 63 |
| 2003 | 3 | 63 | 66 |
| 2004 | 5 | 56 | 61 |
| 2005 | 9 | 66 | 75 |
| 2006 | 4 | 64 | 68 |
| 2007 | 8 | 69 | 77 |
| 2008 | 3 | 83 | 86 |
| 2009 | 6 | 69 | 75 |
| 2010 | 11 | 73 | 84 |
| 2011 | 9 | 91 | 100 |
| 2012 | 10 | 86 | 96 |
| 2013 | 13 | 92 | 105 |
| 2014 | 13 | 92 | 105 |
| 2015 | 15 | 102 | 117 |
| 2016 | 17 | 90 | 107 |
| 2017 | 14 | 103 | 117 |
| 2018 | 10 | 115 | 125 |
| 2019 | 18 | 134 | 152 |
| 2020 | 16 | 101 | 117 |
| 2021 | 13 | 103 | 116 |
| 2022 | 1 | 81 | 82 |
| 2023 | 1 | 79 | 80 |
| 2024 | 26 | 59 | 85 |
| 2025 | 1 | 28 | 29 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Functional analysis of pathogenic variants in LAMB1-related leukoencephalopathy reveals genotype-phenotype correlations and suggests its role in glial cells. Hum Mol Genet. 2025 May 17; 34(11):990-999.
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Computational modeling of cancer cell metabolism along the catabolic-anabolic axes. NPJ Syst Biol Appl. 2025 May 10; 11(1):46.
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Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18). Hum Mutat. 2025; 2025:3531508.
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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation. Am J Hum Genet. 2025 May 01; 112(5):1139-1157.
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Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational Study. JMIR Res Protoc. 2025 Apr 07; 14:e60587.
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Insights into protection against Mycobacterium tuberculosis infection: time to officially confirm another phenotype? J Clin Invest. 2025 Apr 01; 135(7).
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Why some and not others? Understanding vascular phenotypes in genetic developmental lung diseases. Curr Opin Pediatr. 2025 Jun 01; 37(3):278-288.
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Goal attainment in PMM2-CDG: A new approach measuring meaningful clinical outcomes. Mol Genet Metab. 2025 May; 145(1):109087.
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De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. Am J Hum Genet. 2025 Apr 03; 112(4):846-862.
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Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration. Nat Commun. 2025 Mar 12; 16(1):2479.