"Mutation" 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.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
| Descriptor ID |
D009154
|
| MeSH Number(s) |
G05.365.590
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Mutation".
Below are MeSH descriptors whose meaning is more specific than "Mutation".
This graph shows the total number of publications written about "Mutation" by people in this website by year, and whether "Mutation" 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 | 14 | 18 | 32 |
| 1997 | 16 | 35 | 51 |
| 1998 | 23 | 23 | 46 |
| 1999 | 22 | 51 | 73 |
| 2000 | 19 | 53 | 72 |
| 2001 | 21 | 47 | 68 |
| 2002 | 22 | 63 | 85 |
| 2003 | 32 | 69 | 101 |
| 2004 | 31 | 69 | 100 |
| 2005 | 31 | 86 | 117 |
| 2006 | 26 | 80 | 106 |
| 2007 | 42 | 83 | 125 |
| 2008 | 38 | 66 | 104 |
| 2009 | 39 | 70 | 109 |
| 2010 | 27 | 75 | 102 |
| 2011 | 39 | 98 | 137 |
| 2012 | 44 | 83 | 127 |
| 2013 | 38 | 102 | 140 |
| 2014 | 72 | 111 | 183 |
| 2015 | 76 | 116 | 192 |
| 2016 | 79 | 100 | 179 |
| 2017 | 76 | 139 | 215 |
| 2018 | 76 | 137 | 213 |
| 2019 | 65 | 132 | 197 |
| 2020 | 45 | 172 | 217 |
| 2021 | 41 | 136 | 177 |
| 2022 | 4 | 129 | 133 |
| 2023 | 3 | 106 | 109 |
| 2024 | 34 | 93 | 127 |
| 2025 | 32 | 102 | 134 |
| 2026 | 7 | 26 | 33 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Clinicogenomic and Histopathologic Analyses of Supermassive Intrahepatic Cholangiocarcinoma and the Role of Ablative Radiotherapy. Clin Cancer Res. 2026 May 15; 32(10):2079-2087.
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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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Dolutegravir developmental toxicity is mitigated by magnesium and folate in zebrafish embryos. Dis Model Mech. 2026 May 01; 19(5).
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Genetic Characterization of First-Line Drug-Resistance Mutations in Multidrug-Resistant Mycobacterium tuberculosis. Pathogens. 2026 Apr 22; 15(5).
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Multi-site DMS probing reveals higher-order structure of RNA-protein complexes in living cells. Mol Cell. 2026 May 07; 86(9):1815-1830.e9.
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POD24 is a novel determinant of prognosis in patients with Waldenstr?m macroglobulinemia. Blood Adv. 2026 Apr 14; 10(7):2322-2327.
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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.
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Important role in transcription start site selection for the RNA polymerase II-TFIIE-TFIIH interface in Saccharomyces cerevisiae. Genetics. 2026 04 04; 232(4).
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Defective DNA Damage Response Is a Targetable Therapeutic Vulnerability in ESR1-Mutant Breast Cancer. Cancer Res. 2026 Apr 02; 86(7):1707-1723.
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DICER1-mutated renal neoplasia: A series of 5 cases demonstrating the spectrum of cystic nephroma, Wilms tumor, and anaplastic sarcoma. Hum Pathol. 2026 Jun; 172:106110.