"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 | 28 | 28 |
| 1998 | 0 | 27 | 27 |
| 1999 | 2 | 34 | 36 |
| 2000 | 0 | 50 | 50 |
| 2001 | 1 | 47 | 48 |
| 2002 | 2 | 60 | 62 |
| 2003 | 2 | 62 | 64 |
| 2004 | 5 | 56 | 61 |
| 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 | 92 | 101 |
| 2012 | 10 | 89 | 99 |
| 2013 | 14 | 99 | 113 |
| 2014 | 14 | 104 | 118 |
| 2015 | 17 | 111 | 128 |
| 2016 | 20 | 100 | 120 |
| 2017 | 14 | 111 | 125 |
| 2018 | 9 | 124 | 133 |
| 2019 | 18 | 152 | 170 |
| 2020 | 20 | 117 | 137 |
| 2021 | 15 | 126 | 141 |
| 2022 | 2 | 83 | 85 |
| 2023 | 1 | 87 | 88 |
| 2024 | 27 | 66 | 93 |
| 2025 | 4 | 67 | 71 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Further phenotypical delineation of DLG3-related neurodevelopmental disorders. Eur J Hum Genet. 2025 Dec; 33(12):1585-1595.
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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.
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Genome-wide association study provides novel insight into the genetic architecture of severe obesity. PLoS Genet. 2025 Sep; 21(9):e1011842.
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De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder. Am J Med Genet A. 2026 Jan; 200(1):244-252.
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A clinical and genotype-phenotype analysis of MACF1 variants. Am J Hum Genet. 2025 Oct 02; 112(10):2363-2380.
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Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+). Eur J Hum Genet. 2025 Dec; 33(12):1606-1615.
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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.
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TPI deficiency: A case report and review of the literature. Mol Genet Metab. 2025 Sep-Oct; 146(1-2):109227.
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Case Series of Nizon-Isidor Syndrome by Heterozygous Variants in MED12L With Further Evidence of Mitotic Instability in One Case With Diploid-Triploid Mosaicism. Am J Med Genet A. 2026 Jan; 200(1):205-214.
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CSWG-SCAI Stages Combined With Machine Learning-Based Phenotypes for Serial Risk Stratification in Cardiogenic Shock. JACC Heart Fail. 2025 Oct; 13(10):102611.