"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 | 5 | 5 |
| 1995 | 0 | 1 | 1 |
| 1997 | 0 | 2 | 2 |
| 1998 | 0 | 2 | 2 |
| 1999 | 0 | 3 | 3 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 4 | 4 |
| 2002 | 0 | 5 | 5 |
| 2003 | 0 | 7 | 7 |
| 2004 | 1 | 1 | 2 |
| 2005 | 1 | 4 | 5 |
| 2006 | 0 | 4 | 4 |
| 2007 | 1 | 9 | 10 |
| 2008 | 1 | 8 | 9 |
| 2009 | 1 | 6 | 7 |
| 2010 | 1 | 6 | 7 |
| 2011 | 2 | 12 | 14 |
| 2012 | 0 | 14 | 14 |
| 2013 | 0 | 16 | 16 |
| 2014 | 0 | 10 | 10 |
| 2015 | 3 | 12 | 15 |
| 2016 | 2 | 14 | 16 |
| 2017 | 0 | 12 | 12 |
| 2018 | 0 | 6 | 6 |
| 2019 | 3 | 17 | 20 |
| 2020 | 2 | 6 | 8 |
| 2021 | 2 | 14 | 16 |
| 2022 | 0 | 5 | 5 |
| 2023 | 0 | 7 | 7 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Impact of vaccination and variants of concern on long COVID clinical phenotypes. BMC Infect Dis. 2023 Nov 16; 23(1):804.
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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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Differential gene expression analysis based on linear mixed model corrects false positive inflation for studying quantitative traits. Sci Rep. 2023 10 03; 13(1):16570.
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Tobacco Smoking and Pack-Years Are Associated With Frailty Among People With HIV. J Acquir Immune Defic Syndr. 2023 10 01; 94(2):135-142.
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Elevated cerebrospinal fluid ubiquitin C-terminal hydrolase-L1 levels correlate with phenotypic severity and therapeutic response in Niemann-Pick disease, type C1. Mol Genet Metab. 2023 11; 140(3):107656.
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Updated consensus guidelines on the management of Phelan-McDermid syndrome. Am J Med Genet A. 2023 08; 191(8):2015-2044.
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Memory Phenotypes In Early, De Novo Parkinson's Disease Patients with Mild Cognitive Impairment. Mov Disord. 2023 08; 38(8):1461-1472.
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Correlated decline of cognitive and motor phenotypes and ADRD pathologies in old age. Alzheimers Dement. 2023 09; 19(9):4150-4162.
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Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature. Mol Genet Genomic Med. 2023 07; 11(7):e2166.
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Prediction of lumbar disc herniation resorption in symptomatic patients: a prospective, multi-imaging and clinical phenotype study. Spine J. 2023 02; 23(2):247-260.