"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 | 12 | 18 | 30 |
| 1997 | 15 | 37 | 52 |
| 1998 | 23 | 23 | 46 |
| 1999 | 22 | 48 | 70 |
| 2000 | 19 | 53 | 72 |
| 2001 | 21 | 48 | 69 |
| 2002 | 21 | 62 | 83 |
| 2003 | 32 | 64 | 96 |
| 2004 | 30 | 68 | 98 |
| 2005 | 31 | 85 | 116 |
| 2006 | 26 | 81 | 107 |
| 2007 | 41 | 82 | 123 |
| 2008 | 36 | 65 | 101 |
| 2009 | 39 | 69 | 108 |
| 2010 | 27 | 72 | 99 |
| 2011 | 39 | 100 | 139 |
| 2012 | 44 | 82 | 126 |
| 2013 | 37 | 97 | 134 |
| 2014 | 68 | 107 | 175 |
| 2015 | 72 | 111 | 183 |
| 2016 | 79 | 97 | 176 |
| 2017 | 75 | 135 | 210 |
| 2018 | 74 | 133 | 207 |
| 2019 | 66 | 130 | 196 |
| 2020 | 43 | 165 | 208 |
| 2021 | 42 | 133 | 175 |
| 2022 | 3 | 130 | 133 |
| 2023 | 3 | 105 | 108 |
| 2024 | 34 | 90 | 124 |
| 2025 | 33 | 98 | 131 |
| 2026 | 12 | 51 | 63 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Baseline and placebo-related imaging, cerebrospinal fluid, plasma biomarker, and cognitive findings in unimpaired PSEN1 E280A mutation carriers and non-carriers in the Alzheimer's Prevention Initiative Autosomal Dominant Alzheimer's Disease Colombia Trial. EBioMedicine. 2026 Aug; 130:106390.
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Clonal hematopoiesis in Alzheimer's brain: Protective, pathogenic, and context-dependent? Trends Mol Med. 2026 Oct; 32(10):963-965.
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Targeted next-generation sequencing implementation in Eswatini identifies rifampicin and bedaquiline resistance undetected by routine diagnostic testing. Nat Commun. 2026 Jun 11; 17(1).
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COXFA4L2 upregulation preserves residual cytochrome c oxidase activity in COXFA4-related Leigh-like encephalopathy. Nat Commun. 2026 May 30; 17(1).
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[Loss of CHC1 or CHC2 in Arabidopsis compromises autophagy pathway and leads to enhanced disease resistance]. Sheng Wu Gong Cheng Xue Bao. 2026 May 25; 42(5):2129-2139.
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H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs. Nat Genet. 2026 Jun; 58(6):1368-1382.
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Reduced catalytic activity of KPC ?-lactamase can increase ceftazidime resistance. Commun Biol. 2026 Apr 07; 9(1).
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Venetoclax or Pirtobrutinib in Relapsed/Refractory Waldenstr?m Macroglobulinemia: Clinical and Molecular Predictors and Sequencing Implications. Am J Hematol. 2026 May; 101(5):1045-1055.
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Non-Isolated Dandy-Walker Malformation: Exome Sequencing Efficacy and Phenotypic Expansions. Clin Genet. 2026 06; 109(6):1029-1037.
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Mutational analysis of human norovirus VP2 elucidates critical molecular interactions for virus assembly. J Virol. 2026 02 17; 100(2):e0142025.