"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 | 25 | 25 |
| 1999 | 2 | 33 | 35 |
| 2000 | 0 | 46 | 46 |
| 2001 | 1 | 45 | 46 |
| 2002 | 2 | 59 | 61 |
| 2003 | 2 | 58 | 60 |
| 2004 | 4 | 54 | 58 |
| 2005 | 9 | 63 | 72 |
| 2006 | 4 | 60 | 64 |
| 2007 | 8 | 68 | 76 |
| 2008 | 3 | 81 | 84 |
| 2009 | 6 | 70 | 76 |
| 2010 | 10 | 71 | 81 |
| 2011 | 9 | 86 | 95 |
| 2012 | 11 | 80 | 91 |
| 2013 | 14 | 93 | 107 |
| 2014 | 14 | 94 | 108 |
| 2015 | 19 | 105 | 124 |
| 2016 | 21 | 94 | 115 |
| 2017 | 13 | 107 | 120 |
| 2018 | 8 | 114 | 122 |
| 2019 | 17 | 143 | 160 |
| 2020 | 18 | 106 | 124 |
| 2021 | 15 | 122 | 137 |
| 2022 | 1 | 82 | 83 |
| 2023 | 1 | 83 | 84 |
| 2024 | 29 | 68 | 97 |
| 2025 | 5 | 88 | 93 |
| 2026 | 1 | 55 | 56 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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The Childhood Liver Disease Research Network's prospective characterization of pediatric primary sclerosing cholangitis. Hepatol Commun. 2026 Oct 01; 10(10).
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Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome. Am J Hum Genet. 2026 Sep 03; 113(9):1946-1971.
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Phenotypic analysis of human and murine endometrial organoids using a machine learning approach. Reproduction. 2026 Sep 03; 172(3).
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Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations. Hum Mol Genet. 2026 Aug 10; 35(17).
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Complex Genomic Rearrangement Involving the TBX4 Promoter Manifesting With Variable Expressivity in a Five-Generation Family. Hum Mutat. 2026; 2026:7278477.
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Pathogenic myeloid phenotypes drive disease pathology in a novel human neurohistiocytosis model. Blood. 2026 07 23; 148(4):433-449.
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Multi-generational mitochondrial complex V deficiency due to the recurrent ATP5F1A c.620G>A?(p.Arg207His) pathogenic variant: A novel family and a review of the literature. Mol Genet Metab. 2026 Sep-Oct; 149(1-2):110207.
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Uncovering phenotypic expansion in AXIN2-related disorders through precision animal modeling. Genet Med. 2026 Sep; 28(9):102648.
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Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants. Clin Genet. 2026 Sep; 110(3):325-335.
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Natural History of C3 Glomerulopathy and Immune Complex-Associated Membranoproliferative Glomerulonephritis in Children. Clin J Am Soc Nephrol. 2026 Sep 01; 21(9):1606-1620.