"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 | 34 | 36 |
| 2000 | 0 | 48 | 48 |
| 2001 | 1 | 46 | 47 |
| 2002 | 2 | 61 | 63 |
| 2003 | 2 | 58 | 60 |
| 2004 | 4 | 56 | 60 |
| 2005 | 9 | 65 | 74 |
| 2006 | 4 | 61 | 65 |
| 2007 | 8 | 71 | 79 |
| 2008 | 3 | 83 | 86 |
| 2009 | 6 | 70 | 76 |
| 2010 | 10 | 73 | 83 |
| 2011 | 9 | 88 | 97 |
| 2012 | 11 | 84 | 95 |
| 2013 | 14 | 96 | 110 |
| 2014 | 14 | 98 | 112 |
| 2015 | 19 | 110 | 129 |
| 2016 | 22 | 98 | 120 |
| 2017 | 14 | 110 | 124 |
| 2018 | 8 | 119 | 127 |
| 2019 | 18 | 147 | 165 |
| 2020 | 19 | 112 | 131 |
| 2021 | 15 | 124 | 139 |
| 2022 | 2 | 84 | 86 |
| 2023 | 1 | 82 | 83 |
| 2024 | 29 | 67 | 96 |
| 2025 | 5 | 86 | 91 |
| 2026 | 1 | 28 | 29 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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An Adnp frameshift variant disrupts Wnt signalling inducing chromatocytoskeletal defects and autism-related behaviour in male mice. EBioMedicine. 2026 Jun; 128:106309.
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Natural history of NGLY1 deficiency: motor function & clinical features. Hum Mol Genet. 2026 May 11; 35(8).
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Multimodal Noninvasive Biomarker Characterization of Structural and Functional Alterations in ADSS1-Deficient Myopathy. J Inherit Metab Dis. 2026 May; 49(3):e70193.
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Meal-Related Symptoms Define Distinct and Clinically Significant Phenotypes in Children With Pain-Related Disorders of Gut-Brain Interaction. Neurogastroenterol Motil. 2026 May; 38(5):e70349.
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Inherited TBX4 frameshifting variants predicted to escape nonsense mediated decay in two families with variable phenotypes, including lethal lung developmental disorders. Hum Genomics. 2026 Apr 30; 20(1).
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INS-17 acts as a nutrient deprivation signal to mediate adult IIS-regulated associative behaviors in C. elegans. PLoS Genet. 2026 Apr; 22(4):e1012130.
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Brain-Derived Neurotrophic Factor in Acute Coronary Syndromes: Beyond Diagnosis Toward Biological Phenotyping and Risk Stratification. Int J Mol Sci. 2026 Apr 25; 27(9).
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New genotype-phenotype correlations and management recommendations for individuals with RERE variants. Genet Med. 2026 Jun; 28(6):102580.
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Saturation editing of RNU4-2 reveals distinct dominant and recessive disorders. Nature. 2026 Jun; 654(8118):429-436.
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Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes. Nat Genet. 2026 Apr; 58(4):761-773.