"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 | 15 | 15 |
| 1996 | 1 | 22 | 23 |
| 1997 | 0 | 22 | 22 |
| 1998 | 0 | 20 | 20 |
| 1999 | 0 | 25 | 25 |
| 2000 | 0 | 38 | 38 |
| 2001 | 0 | 36 | 36 |
| 2002 | 0 | 36 | 36 |
| 2003 | 3 | 53 | 56 |
| 2004 | 2 | 38 | 40 |
| 2005 | 4 | 47 | 51 |
| 2006 | 5 | 33 | 38 |
| 2007 | 3 | 36 | 39 |
| 2008 | 2 | 63 | 65 |
| 2009 | 2 | 52 | 54 |
| 2010 | 5 | 54 | 59 |
| 2011 | 12 | 66 | 78 |
| 2012 | 5 | 66 | 71 |
| 2013 | 11 | 64 | 75 |
| 2014 | 5 | 82 | 87 |
| 2015 | 8 | 82 | 90 |
| 2016 | 8 | 87 | 95 |
| 2017 | 3 | 63 | 66 |
| 2018 | 10 | 73 | 83 |
| 2019 | 7 | 74 | 81 |
| 2020 | 5 | 66 | 71 |
| 2021 | 8 | 64 | 72 |
| 2022 | 2 | 43 | 45 |
| 2023 | 2 | 41 | 43 |
| 2024 | 11 | 26 | 37 |
| 2025 | 4 | 1 | 5 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Pathogenic de novo variants in PPP2R5C cause a neurodevelopmental disorder within the Houge-Janssens syndrome spectrum. Am J Hum Genet. 2025 Mar 06; 112(3):554-571.
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Heterogeneous clinical phenotypes of sporadic early-onset Alzheimer's disease: a neuropsychological data-driven approach. Alzheimers Res Ther. 2025 Feb 06; 17(1):38.
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Gene and phenome-based analysis of the shared genetic architecture of eye diseases. Am J Hum Genet. 2025 Feb 06; 112(2):318-331.
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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. Am J Hum Genet. 2025 Feb 06; 112(2):276-290.
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Endoscopic Normalization and Transition of J-Pouch Phenotypes Over Time in Patients With Inflammatory Bowel Disease. Inflamm Bowel Dis. 2025 01 06; 31(1):63-71.
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Endophenotype 2.0: updated definitions and criteria for endophenotypes of psychiatric disorders, incorporating new technologies and findings. Transl Psychiatry. 2024 Dec 24; 14(1):502.
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Engineered GM-CSF polarizes protumorigenic tumor-associated macrophages to an antitumorigenic phenotype and potently synergizes with IL-12 immunotherapy. J Immunother Cancer. 2024 Dec 22; 12(12).
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Untargeted metabolome atlas for sleep-related phenotypes in the Hispanic community health study/study of Latinos. EBioMedicine. 2025 Jan; 111:105507.
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Advances in asthma and allergic disease genetics. Curr Opin Allergy Clin Immunol. 2025 Feb 01; 25(1):58-65.
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Body composition and muscle composition phenotypes in patients on waitlist and shortly after liver transplant - results from a pilot study. BMC Gastroenterol. 2024 Oct 09; 24(1):356.