"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 | 5 | 5 |
| 2011 | 0 | 5 | 5 |
| 2012 | 1 | 6 | 7 |
| 2013 | 2 | 6 | 8 |
| 2014 | 0 | 4 | 4 |
| 2015 | 0 | 10 | 10 |
| 2016 | 2 | 6 | 8 |
| 2017 | 0 | 9 | 9 |
| 2018 | 0 | 3 | 3 |
| 2019 | 0 | 10 | 10 |
| 2020 | 2 | 12 | 14 |
| 2021 | 2 | 9 | 11 |
| 2022 | 0 | 7 | 7 |
| 2023 | 0 | 2 | 2 |
| 2024 | 2 | 3 | 5 |
| 2025 | 0 | 1 | 1 |
| 2026 | 1 | 4 | 5 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Data-Driven Phenotypic Clusters of Gestational Diabetes Mellitus and Associations With Risk of Perinatal Complications and Postpartum Diabetes. Diabetes Care. 2026 Sep 01; 49(9):1557-1566.
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Compound Heterozygous Variants in the Phospholipase Gene PNPLA6 Cause Hypopituitarism and Vision Loss. Hum Mutat. 2026; 2026:4515038.
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Sociodemographic differences in clinical phenotypes among patients with COPD: a latent class analysis. BMJ Open Respir Res. 2026 Mar 02; 13(1).
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Multi-site analysis of COVID-19 and new-onset diabetes reveals need for improved sensitivity of EHR-based COVID-19 phenotypes-a DiCAYA Network analysis. J Am Med Inform Assoc. 2026 Mar 01; 33(3):710-718.
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A Systematic Process for Assessing Fitness-for-Purpose of Health Outcomes for Computable Phenotyping With Electronic Health Record Data. Pharmacoepidemiol Drug Saf. 2026 Mar; 35(3):e70346.
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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.