"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 | 59 | 61 |
| 2004 | 4 | 54 | 58 |
| 2005 | 9 | 64 | 73 |
| 2006 | 4 | 60 | 64 |
| 2007 | 8 | 69 | 77 |
| 2008 | 3 | 82 | 85 |
| 2009 | 6 | 70 | 76 |
| 2010 | 10 | 72 | 82 |
| 2011 | 9 | 85 | 94 |
| 2012 | 11 | 81 | 92 |
| 2013 | 14 | 93 | 107 |
| 2014 | 14 | 95 | 109 |
| 2015 | 19 | 106 | 125 |
| 2016 | 21 | 94 | 115 |
| 2017 | 13 | 107 | 120 |
| 2018 | 8 | 114 | 122 |
| 2019 | 17 | 143 | 160 |
| 2020 | 18 | 108 | 126 |
| 2021 | 15 | 122 | 137 |
| 2022 | 2 | 83 | 85 |
| 2023 | 1 | 83 | 84 |
| 2024 | 29 | 67 | 96 |
| 2025 | 5 | 87 | 92 |
| 2026 | 1 | 42 | 43 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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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 Jul 23; 148(4):433-449.
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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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Genetics of Cerebrotendinous Xanthomatosis. Mol Diagn Ther. 2026 Jul; 30(4):681-687.
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IMPACT (Immune Monitoring and Phenotype Assessment of Clinical Trajectory) for Patients With Inborn Errors of Immunity From the Primary Immune Deficiency Treatment Consortium (PIDTC). J Allergy Clin Immunol Pract. 2026 Aug; 14(8):1893-1900.
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Rapid phenotypic antimicrobial susceptibility testing of Gram-negative bloodstream isolates: clinical evaluation of the LifeScale AST system. BMC Microbiol. 2026 05 28; 26(1).
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An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice. EBioMedicine. 2026 Jun; 128:106309.
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Low-Abundance and Fragmentary Helicobacter pylori DNA Detected in Phenotypically Negative Gastric Biopsies Using Targeted Sequencing. Biomolecules. 2026 May 22; 16(6).
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A Global Prospective Harmonization Framework for Suicidality, Anhedonia, and Obsessive-Compulsive Symptoms in Psychiatric Genetic Studies: A Cross-Continental Study Within the Ancestral Population Network. Am J Med Genet B Neuropsychiatr Genet. 2026 Sep; 201(6):379-395.
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Natural history of NGLY1 deficiency: motor function & clinical features. Hum Mol Genet. 2026 May 11; 35(8).