"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 |
|---|
| 1999 | 0 | 2 | 2 |
| 2001 | 0 | 1 | 1 |
| 2002 | 0 | 4 | 4 |
| 2003 | 0 | 3 | 3 |
| 2004 | 0 | 1 | 1 |
| 2005 | 1 | 2 | 3 |
| 2006 | 0 | 4 | 4 |
| 2007 | 0 | 5 | 5 |
| 2008 | 0 | 4 | 4 |
| 2009 | 0 | 2 | 2 |
| 2010 | 1 | 5 | 6 |
| 2011 | 1 | 7 | 8 |
| 2012 | 0 | 4 | 4 |
| 2013 | 0 | 8 | 8 |
| 2014 | 0 | 3 | 3 |
| 2015 | 1 | 3 | 4 |
| 2016 | 1 | 9 | 10 |
| 2017 | 0 | 8 | 8 |
| 2018 | 0 | 4 | 4 |
| 2019 | 2 | 6 | 8 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 7 | 8 |
| 2022 | 0 | 2 | 2 |
| 2023 | 0 | 1 | 1 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational Study. JMIR Res Protoc. 2025 Apr 07; 14:e60587.
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The molecular genetic landscape of human brain size variation. Cell Rep. 2023 Nov 28; 42(11):113439.
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Intramembranous bone regeneration in diversity outbred mice is heritable. Bone. 2022 11; 164:116524.
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Comparison of motor, non-motor, and quality of life phenotype in Black and White patients with Parkinson's disease. Parkinsonism Relat Disord. 2022 03; 96:18-21.
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Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants. PLoS Genet. 2021 11; 17(11):e1009918.
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Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes. Neurobiol Aging. 2022 03; 111:95-106.
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Behavioral circadian phenotypes are associated with the risk of elevated body mass index. Eat Weight Disord. 2022 May; 27(4):1395-1403.
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The association of epigenetic clocks in brain tissue with brain pathologies and common aging phenotypes. Neurobiol Dis. 2021 09; 157:105428.
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Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation. Fertil Steril. 2021 09; 116(3):843-854.
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The Modic-endplate-complex phenotype in cervical spine patients: Association with symptoms and outcomes. J Orthop Res. 2022 Feb; 40(2):449-459.