"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 |
|---|
| 1994 | 0 | 4 | 4 |
| 1995 | 0 | 5 | 5 |
| 1996 | 0 | 4 | 4 |
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 4 | 4 |
| 1999 | 0 | 8 | 8 |
| 2000 | 0 | 10 | 10 |
| 2001 | 0 | 13 | 13 |
| 2002 | 1 | 13 | 14 |
| 2003 | 0 | 15 | 15 |
| 2004 | 1 | 12 | 13 |
| 2005 | 0 | 20 | 20 |
| 2006 | 0 | 22 | 22 |
| 2007 | 0 | 5 | 5 |
| 2008 | 0 | 16 | 16 |
| 2009 | 0 | 20 | 20 |
| 2010 | 2 | 14 | 16 |
| 2011 | 1 | 13 | 14 |
| 2012 | 2 | 28 | 30 |
| 2013 | 2 | 21 | 23 |
| 2014 | 1 | 31 | 32 |
| 2015 | 0 | 25 | 25 |
| 2016 | 1 | 21 | 22 |
| 2017 | 3 | 27 | 30 |
| 2018 | 1 | 18 | 19 |
| 2019 | 6 | 15 | 21 |
| 2020 | 3 | 19 | 22 |
| 2021 | 2 | 16 | 18 |
| 2022 | 0 | 10 | 10 |
| 2023 | 0 | 3 | 3 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Ancestry-based differences in the immune phenotype are associated with lupus activity. JCI Insight. 2023 08 22; 8(16).
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Maternal Western diet is associated with distinct preclinical pediatric NAFLD phenotypes in juvenile nonhuman primate offspring. Hepatol Commun. 2023 Feb 01; 7(2):e0014.
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Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic disease. Lab Invest. 2021 10; 101(10):1382-1393.
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Neuronal deletion of MnSOD in mice leads to demyelination, inflammation and progressive paralysis that mimics phenotypes associated with progressive multiple sclerosis. Redox Biol. 2023 02; 59:102550.
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A saturated map of common genetic variants associated with human height. Nature. 2022 10; 610(7933):704-712.
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Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Hum Mol Genet. 2022 08 25; 31(17):2845-2856.
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Rare genetic variants explain missing heritability in smoking. Nat Hum Behav. 2022 11; 6(11):1577-1586.
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Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Invest Ophthalmol Vis Sci. 2022 07 08; 63(8):19.
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Transcutaneous Vagus Nerve Stimulation Ameliorates the Phenotype of Heart Failure With Preserved Ejection Fraction Through Its Anti-Inflammatory Effects. Circ Heart Fail. 2022 08; 15(8):e009288.
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The natural history of polycystic ovary syndrome: commentary on a longitudinal study evaluating changes in phenotype with age. Fertil Steril. 2022 05; 117(5):1067-1068.