"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 |
|---|
| 1993 | 2 | 15 | 17 |
| 1994 | 0 | 19 | 19 |
| 1995 | 0 | 16 | 16 |
| 1996 | 1 | 22 | 23 |
| 1997 | 0 | 23 | 23 |
| 1998 | 0 | 21 | 21 |
| 1999 | 0 | 25 | 25 |
| 2000 | 0 | 38 | 38 |
| 2001 | 0 | 36 | 36 |
| 2002 | 0 | 36 | 36 |
| 2003 | 3 | 52 | 55 |
| 2004 | 2 | 38 | 40 |
| 2005 | 4 | 45 | 49 |
| 2006 | 4 | 30 | 34 |
| 2007 | 3 | 36 | 39 |
| 2008 | 2 | 58 | 60 |
| 2009 | 2 | 52 | 54 |
| 2010 | 4 | 54 | 58 |
| 2011 | 12 | 64 | 76 |
| 2012 | 5 | 67 | 72 |
| 2013 | 11 | 60 | 71 |
| 2014 | 5 | 79 | 84 |
| 2015 | 7 | 75 | 82 |
| 2016 | 6 | 84 | 90 |
| 2017 | 2 | 57 | 59 |
| 2018 | 9 | 71 | 80 |
| 2019 | 7 | 69 | 76 |
| 2020 | 5 | 59 | 64 |
| 2021 | 7 | 59 | 66 |
| 2022 | 2 | 39 | 41 |
| 2023 | 1 | 5 | 6 |
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Below are the most recent publications written about "Phenotype" by people in Profiles.
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Dual Functions of labial Resolve the Hox Logic of Chelicerate Head Segments. Mol Biol Evol. 2023 Mar 04; 40(3).
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The endogenous repertoire harbors self-reactive CD4+ T cell clones that adopt a follicular helper T cell-like phenotype at steady state. Nat Immunol. 2023 Mar; 24(3):487-500.
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A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes. Nat Metab. 2023 02; 5(2):237-247.
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FinnGen provides genetic insights from a well-phenotyped isolated population. Nature. 2023 01; 613(7944):508-518.
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Relating pathogenic loss-of-function mutations in humans to their evolutionary fitness costs. Elife. 2023 Jan 17; 12.
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Cancer Risk Associated With PTEN Pathogenic Variants Identified Using Multigene Hereditary Cancer Panel Testing. JCO Precis Oncol. 2023 01; 7:e2200415.
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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies. Nat Genet. 2023 01; 55(1):154-164.
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Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization. Circulation. 2023 Mar 07; 147(10):824-840.
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Addressing the challenges of polygenic scores in human genetic research. Am J Hum Genet. 2022 12 01; 109(12):2095-2100.
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Cross-trait assortative mating is widespread and inflates genetic correlation estimates. Science. 2022 11 18; 378(6621):754-761.