"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 |
|---|
| 1996 | 0 | 19 | 19 |
| 1997 | 0 | 26 | 26 |
| 1998 | 0 | 25 | 25 |
| 1999 | 2 | 33 | 35 |
| 2000 | 0 | 46 | 46 |
| 2001 | 1 | 45 | 46 |
| 2002 | 2 | 59 | 61 |
| 2003 | 2 | 58 | 60 |
| 2004 | 4 | 54 | 58 |
| 2005 | 9 | 63 | 72 |
| 2006 | 4 | 60 | 64 |
| 2007 | 8 | 68 | 76 |
| 2008 | 3 | 81 | 84 |
| 2009 | 6 | 70 | 76 |
| 2010 | 10 | 71 | 81 |
| 2011 | 9 | 86 | 95 |
| 2012 | 11 | 80 | 91 |
| 2013 | 14 | 93 | 107 |
| 2014 | 14 | 94 | 108 |
| 2015 | 19 | 105 | 124 |
| 2016 | 21 | 94 | 115 |
| 2017 | 13 | 107 | 120 |
| 2018 | 8 | 114 | 122 |
| 2019 | 17 | 143 | 160 |
| 2020 | 18 | 106 | 124 |
| 2021 | 15 | 122 | 137 |
| 2022 | 1 | 82 | 83 |
| 2023 | 1 | 83 | 84 |
| 2024 | 29 | 68 | 97 |
| 2025 | 5 | 88 | 93 |
| 2026 | 1 | 55 | 56 |
To return to the timeline,
click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
-
Polygenic Determinants of Arterial Stiffness: Implications for Hypertension. J Am Heart Assoc. 2026 Oct 20; 15(20):e047424.
-
Preclinical models of COPD: a state of the art review. Eur Respir J. 2026 Oct; 68(4).
-
A massively parallel reporter assay of MECP2 cis-regulatory elements reveals genetic candidates for male-biased autism. Am J Hum Genet. 2026 Nov 05; 113(11):2254-2271.
-
Acute Kidney Injury After Extracorporeal Membrane Oxygen in Children: Phenotypes and Prognosis in a Single-Center Cohort, 2020-2023. Pediatr Crit Care Med. 2026 Nov 01; 27(11):1382-1393.
-
Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy. Am J Hum Genet. 2026 Nov 05; 113(11):2291-2309.
-
A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies. Am J Hum Genet. 2026 Oct 01; 113(10):2178-2194.
-
The Childhood Liver Disease Research Network's prospective characterization of pediatric primary sclerosing cholangitis. Hepatol Commun. 2026 Oct 01; 10(10).
-
Androgens mediate sexual dimorphism in Pilarowski-Bjornsson syndrome. Am J Hum Genet. 2026 Sep 03; 113(9):1946-1971.
-
Phenotypic analysis of human and murine endometrial organoids using a machine learning approach. Reproduction. 2026 09 03; 172(3).
-
Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome. Clin Genet. 2026 Dec; 110(6):709-715.