"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 | 1 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 2 | 2 |
| 2002 | 0 | 1 | 1 |
| 2004 | 0 | 2 | 2 |
| 2005 | 0 | 4 | 4 |
| 2006 | 0 | 1 | 1 |
| 2007 | 1 | 5 | 6 |
| 2008 | 0 | 6 | 6 |
| 2009 | 0 | 3 | 3 |
| 2010 | 0 | 6 | 6 |
| 2011 | 0 | 5 | 5 |
| 2012 | 1 | 5 | 6 |
| 2013 | 2 | 6 | 8 |
| 2014 | 0 | 4 | 4 |
| 2015 | 0 | 11 | 11 |
| 2016 | 2 | 7 | 9 |
| 2017 | 0 | 9 | 9 |
| 2018 | 0 | 3 | 3 |
| 2019 | 0 | 10 | 10 |
| 2020 | 2 | 11 | 13 |
| 2021 | 2 | 9 | 11 |
| 2022 | 0 | 7 | 7 |
| 2023 | 0 | 2 | 2 |
| 2024 | 3 | 2 | 5 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Genotype-Phenotype Spectrum of eyeGENE Patients With Familial Exudative Vitreoretinopathy: Novel Variants in Norrin/?-Catenin Signaling Pathway Genes. Invest Ophthalmol Vis Sci. 2025 Feb 03; 66(2):9.
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Racial and Ethnic Disease Phenotype Differences Are Driven by Genetics: No. Mult Scler. 2024 Dec; 30(5_suppl):9-11.
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Expanding the genetic landscape of Usher syndrome type IV caused by pathogenic ARSG variants. Clin Genet. 2025 Jan; 107(1):44-55.
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Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders. Brain. 2024 Jun 03; 147(6):2085-2097.
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Computable phenotype for diagnostic error: developing the data schema for application of symptom-disease pair analysis of diagnostic error (SPADE). Diagnosis (Berl). 2024 Aug 01; 11(3):295-302.
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Centralized Interactive Phenomics Resource: an integrated online phenomics knowledgebase for health data users. J Am Med Inform Assoc. 2024 04 19; 31(5):1126-1134.
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Framework of the Centralized Interactive Phenomics Resource (CIPHER) standard for electronic health data-based phenomics knowledgebase. J Am Med Inform Assoc. 2023 04 19; 30(5):958-964.
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Characterizing variability of electronic health record-driven phenotype definitions. J Am Med Inform Assoc. 2023 Feb 16; 30(3):427-437.
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Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network. Sci Rep. 2023 Feb 03; 13(1):1971.
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Genotype-Phenotype Association in ABCA4-Associated Retinopathy. Adv Exp Med Biol. 2023; 1415:289-295.