"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 |
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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 |
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1997 | 0 | 3 | 3 |
1998 | 0 | 3 | 3 |
1999 | 0 | 1 | 1 |
2000 | 0 | 2 | 2 |
2001 | 1 | 0 | 1 |
2002 | 0 | 3 | 3 |
2003 | 1 | 1 | 2 |
2004 | 0 | 1 | 1 |
2006 | 0 | 4 | 4 |
2007 | 1 | 2 | 3 |
2008 | 0 | 5 | 5 |
2009 | 0 | 6 | 6 |
2010 | 0 | 2 | 2 |
2011 | 0 | 2 | 2 |
2012 | 0 | 5 | 5 |
2013 | 1 | 4 | 5 |
2014 | 0 | 5 | 5 |
2015 | 0 | 1 | 1 |
2016 | 0 | 6 | 6 |
2017 | 0 | 6 | 6 |
2018 | 1 | 12 | 13 |
2019 | 0 | 8 | 8 |
2020 | 0 | 5 | 5 |
2021 | 1 | 4 | 5 |
2022 | 0 | 4 | 4 |
2023 | 0 | 2 | 2 |
2024 | 0 | 5 | 5 |
2025 | 1 | 1 | 2 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Obesity phenotypes and dyslipidemia in adults from four African countries: An H3Africa AWI-Gen study. PLoS One. 2025; 20(1):e0316527.
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Resistance mutations that distinguish HIV-1 envelopes with discordant VRC01 phenotypes from multi-lineage infections in the HVTN703/HPTN081 trial: implications for cross-resistance. J Virol. 2025 Feb 25; 99(2):e0173024.
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Thymidine Analogue Mutations with M184V Significantly Decrease Phenotypic Susceptibility of HIV-1 Subtype C Reverse Transcriptase to Islatravir. Viruses. 2024 12 06; 16(12).
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The PRIMED Consortium: Reducing disparities in polygenic risk assessment. Am J Hum Genet. 2024 Dec 05; 111(12):2594-2606.
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K103N, V106M and Y188L Significantly Reduce HIV-1 Subtype C Phenotypic Susceptibility to Doravirine. Viruses. 2024 Sep 20; 16(9).
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Evolocumab Treatment in Pediatric Patients With Homozygous Familial Hypercholesterolemia: Pooled Data From Three Open-Label Studies. Arterioscler Thromb Vasc Biol. 2024 May; 44(5):1156-1164.
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Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype. Mol Genet Genomic Med. 2024 Jan; 12(1):e2342.
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Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Commun Biol. 2023 03 27; 6(1):328.
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Reclassifying hemophilia to include the definition of outcomes and phenotype as new targets. J Thromb Haemost. 2023 07; 21(7):1737-1740.
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biol. 2022 12 27; 23(1):268.