"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 | 62 | 66 |
| 2007 | 8 | 69 | 77 |
| 2008 | 3 | 83 | 86 |
| 2009 | 6 | 68 | 74 |
| 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 | 92 | 109 |
| 2017 | 14 | 104 | 118 |
| 2018 | 9 | 114 | 123 |
| 2019 | 18 | 137 | 155 |
| 2020 | 16 | 102 | 118 |
| 2021 | 13 | 105 | 118 |
| 2022 | 1 | 80 | 81 |
| 2023 | 1 | 79 | 80 |
| 2024 | 25 | 60 | 85 |
| 2025 | 1 | 33 | 34 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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A novel cardiomyopathy phenotype linked to a CHD7 missense variant. Sci Rep. 2025 Jun 03; 15(1):19429.
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Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range. Am J Hum Genet. 2025 Jun 05; 112(6):1415-1429.
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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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Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder. Am J Hum Genet. 2025 Jun 05; 112(6):1388-1414.
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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.