"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 |
|---|
| 1995 | 0 | 41 | 41 |
| 1996 | 1 | 33 | 34 |
| 1997 | 0 | 46 | 46 |
| 1998 | 0 | 55 | 55 |
| 1999 | 2 | 65 | 67 |
| 2000 | 0 | 80 | 80 |
| 2001 | 2 | 73 | 75 |
| 2002 | 2 | 87 | 89 |
| 2003 | 5 | 103 | 108 |
| 2004 | 4 | 93 | 97 |
| 2005 | 9 | 96 | 105 |
| 2006 | 6 | 97 | 103 |
| 2007 | 11 | 105 | 116 |
| 2008 | 4 | 128 | 132 |
| 2009 | 7 | 110 | 117 |
| 2010 | 12 | 115 | 127 |
| 2011 | 15 | 135 | 150 |
| 2012 | 17 | 116 | 133 |
| 2013 | 16 | 142 | 158 |
| 2014 | 17 | 134 | 151 |
| 2015 | 16 | 151 | 167 |
| 2016 | 18 | 153 | 171 |
| 2017 | 14 | 160 | 174 |
| 2018 | 12 | 163 | 175 |
| 2019 | 21 | 159 | 180 |
| 2020 | 16 | 141 | 157 |
| 2021 | 13 | 125 | 138 |
| 2022 | 2 | 95 | 97 |
| 2023 | 1 | 93 | 94 |
| 2024 | 28 | 72 | 100 |
| 2025 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
-
Ganglioside GD2 Contributes to a Stem-Like Phenotype in Intrahepatic Cholangiocarcinoma. Liver Int. 2025 Jan; 45(1):e16208.
-
Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression. Genome Med. 2024 Dec 18; 16(1):146.
-
SPACe: an open-source, single-cell analysis of Cell Painting data. Nat Commun. 2024 Nov 23; 15(1):10170.
-
Desmoplakin Cardiomyopathy in Pediatric Patients: A Distinct, Underrecognized Cohort of Arrhythmogenic Cardiomyopathy. Circ Arrhythm Electrophysiol. 2024 Nov; 17(11):e013114.
-
Uncovering cell-type-specific immunomodulatory variants and molecular phenotypes in COVID-19 using structurally resolved protein networks. Cell Rep. 2024 Nov 26; 43(11):114930.
-
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia. Am J Hum Genet. 2024 Nov 07; 111(11):2566-2581.
-
Neurodevelopmental Disorder Caused by Deletion of CHASERR, a lncRNA Gene. N Engl J Med. 2024 Oct 24; 391(16):1511-1518.
-
Pathogenic SATB2 missense variants affecting p.Gly392 have variable functional implications and result in diverse clinical phenotypes. J Med Genet. 2024 Oct 23; 61(11):1062-1067.
-
Mice with lymphatic dysfunction develop pathogenic lung tertiary lymphoid organs that model an autoimmune emphysema phenotype of COPD. Am J Physiol Lung Cell Mol Physiol. 2025 Jan 01; 328(1):L1-L14.
-
Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium. J Am Heart Assoc. 2024 Nov 05; 13(21):e036274.