"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 | 60 | 62 |
| 2003 | 3 | 63 | 66 |
| 2004 | 5 | 56 | 61 |
| 2005 | 9 | 66 | 75 |
| 2006 | 4 | 63 | 67 |
| 2007 | 8 | 68 | 76 |
| 2008 | 3 | 83 | 86 |
| 2009 | 6 | 69 | 75 |
| 2010 | 11 | 73 | 84 |
| 2011 | 9 | 91 | 100 |
| 2012 | 10 | 85 | 95 |
| 2013 | 13 | 93 | 106 |
| 2014 | 13 | 92 | 105 |
| 2015 | 15 | 99 | 114 |
| 2016 | 17 | 89 | 106 |
| 2017 | 14 | 104 | 118 |
| 2018 | 10 | 116 | 126 |
| 2019 | 18 | 134 | 152 |
| 2020 | 16 | 102 | 118 |
| 2021 | 13 | 102 | 115 |
| 2022 | 1 | 82 | 83 |
| 2023 | 1 | 78 | 79 |
| 2024 | 29 | 56 | 85 |
| 2025 | 6 | 9 | 15 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Molecular Testing for the World Health Organization Classification of Central Nervous System Tumors: A Review. JAMA Oncol. 2025 Mar 01; 11(3):317-328.
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Emerging Clostridioides difficile ribotypes have divergent metabolic phenotypes. mSystems. 2025 Mar 18; 10(3):e0107524.
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MBNL overexpression rescues cardiac phenotypes in a myotonic dystrophy type 1 heart mouse model. J Clin Invest. 2025 Feb 11; 135(7).
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Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
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Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variants. Ann Clin Transl Neurol. 2025 Mar; 12(3):602-614.
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A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. Nat Comput Sci. 2025 Feb; 5(2):125-143.
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Causes of mortality in the congenital disorders of glycosylation. Mol Genet Metab. 2025 Mar; 144(3):109052.
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Sequence variants in HECTD1 result in a variable neurodevelopmental disorder. Am J Hum Genet. 2025 Mar 06; 112(3):537-553.
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Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease: results from the Montalcino Aortic Consortium. J Med Genet. 2025 Jan 27; 62(2):82-88.
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TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies. J Med Genet. 2025 Jan 27; 62(2):126-137.