"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 | 24 | 24 |
| 1996 | 0 | 19 | 19 |
| 1997 | 0 | 28 | 28 |
| 1998 | 0 | 27 | 27 |
| 1999 | 2 | 34 | 36 |
| 2000 | 0 | 50 | 50 |
| 2001 | 1 | 47 | 48 |
| 2002 | 2 | 62 | 64 |
| 2003 | 3 | 63 | 66 |
| 2004 | 5 | 57 | 62 |
| 2005 | 10 | 68 | 78 |
| 2006 | 4 | 62 | 66 |
| 2007 | 8 | 71 | 79 |
| 2008 | 3 | 85 | 88 |
| 2009 | 6 | 70 | 76 |
| 2010 | 11 | 76 | 87 |
| 2011 | 9 | 95 | 104 |
| 2012 | 10 | 88 | 98 |
| 2013 | 14 | 99 | 113 |
| 2014 | 14 | 105 | 119 |
| 2015 | 17 | 111 | 128 |
| 2016 | 20 | 100 | 120 |
| 2017 | 14 | 111 | 125 |
| 2018 | 9 | 125 | 134 |
| 2019 | 18 | 151 | 169 |
| 2020 | 20 | 115 | 135 |
| 2021 | 14 | 125 | 139 |
| 2022 | 2 | 84 | 86 |
| 2023 | 1 | 87 | 88 |
| 2024 | 27 | 66 | 93 |
| 2025 | 2 | 63 | 65 |
To return to the timeline,
click here.
Below are the most recent publications written about "Phenotype" by people in Profiles.
-
Multiomic and electrophysiologic analyses reveal that an inherited MRC2 variant causes fibroblast dysfunction and increased atrial fibrillation susceptibility. Am J Physiol Heart Circ Physiol. 2025 Nov 01; 329(5):H1055-H1071.
-
Genome-wide association study provides novel insight into the genetic architecture of severe obesity. PLoS Genet. 2025 Sep; 21(9):e1011842.
-
A clinical and genotype-phenotype analysis of MACF1 variants. Am J Hum Genet. 2025 Oct 02; 112(10):2363-2380.
-
ADSL deficiency is a secondary mitochondrial disease affecting organelle homeostasis and ERK2/AKT signaling in a linear genotype-phenotype relation. Cell Rep. 2025 Sep 23; 44(9):116230.
-
TPI deficiency: A case report and review of the literature. Mol Genet Metab. 2025 Sep-Oct; 146(1-2):109227.
-
CSWG-SCAI Stages Combined With Machine Learning-Based Phenotypes for Serial Risk Stratification in Cardiogenic Shock. JACC Heart Fail. 2025 Oct; 13(10):102611.
-
Improving automated deep phenotyping through large language models using retrieval-augmented generation. Genome Med. 2025 Aug 18; 17(1):91.
-
Clinical phenotype and outcomes in autoimmune encephalitis after herpes simplex virus encephalitis: A systematic review and meta-analysis. J Infect. 2025 Sep; 91(3):106566.
-
Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism. Brain. 2025 Aug 01; 148(8):2812-2826.
-
Development and Adaptive Function in Individuals With SCN2A-Related Disorders. Neurology. 2025 Aug 12; 105(3):e213868.