"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 | 29 | 29 |
| 1995 | 0 | 41 | 41 |
| 1996 | 1 | 33 | 34 |
| 1997 | 0 | 46 | 46 |
| 1998 | 0 | 55 | 55 |
| 1999 | 2 | 65 | 67 |
| 2000 | 0 | 81 | 81 |
| 2001 | 2 | 73 | 75 |
| 2002 | 2 | 88 | 90 |
| 2003 | 5 | 104 | 109 |
| 2004 | 4 | 94 | 98 |
| 2005 | 9 | 96 | 105 |
| 2006 | 6 | 97 | 103 |
| 2007 | 11 | 107 | 118 |
| 2008 | 4 | 128 | 132 |
| 2009 | 7 | 110 | 117 |
| 2010 | 12 | 115 | 127 |
| 2011 | 15 | 135 | 150 |
| 2012 | 17 | 117 | 134 |
| 2013 | 16 | 145 | 161 |
| 2014 | 17 | 136 | 153 |
| 2015 | 16 | 150 | 166 |
| 2016 | 18 | 154 | 172 |
| 2017 | 14 | 161 | 175 |
| 2018 | 12 | 163 | 175 |
| 2019 | 21 | 160 | 181 |
| 2020 | 17 | 141 | 158 |
| 2021 | 13 | 126 | 139 |
| 2022 | 2 | 95 | 97 |
| 2023 | 1 | 93 | 94 |
| 2024 | 26 | 66 | 92 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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SPACe: an open-source, single-cell analysis of Cell Painting data. Nat Commun. 2024 Nov 23; 15(1):10170.
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Desmoplakin Cardiomyopathy in Pediatric Patients: A Distinct, Underrecognized Cohort of Arrhythmogenic Cardiomyopathy. Circ Arrhythm Electrophysiol. 2024 Nov; 17(11):e013114.
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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.
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Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia. Am J Hum Genet. 2024 Nov 07; 111(11):2566-2581.
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Neurodevelopmental Disorder Caused by Deletion of CHASERR, a lncRNA Gene. N Engl J Med. 2024 Oct 24; 391(16):1511-1518.
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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.
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Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium. J Am Heart Assoc. 2024 Nov 05; 13(21):e036274.
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Integrated Clinical Genotype-Phenotype Characteristics of STAT3-Mutated Myeloid Neoplasms. Clin Cancer Res. 2024 Oct 15; 30(20):4681-4689.
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Nat Commun. 2024 Oct 03; 15(1):8549.
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A genome-wide Association study of the Count of Codeine prescriptions. Sci Rep. 2024 10 01; 14(1):22780.