"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 |
|---|
| 1995 | 15 | 25 | 40 |
| 1996 | 24 | 21 | 45 |
| 1997 | 26 | 16 | 42 |
| 1998 | 23 | 35 | 58 |
| 1999 | 14 | 33 | 47 |
| 2000 | 27 | 40 | 67 |
| 2001 | 15 | 47 | 62 |
| 2002 | 21 | 49 | 70 |
| 2003 | 19 | 76 | 95 |
| 2004 | 20 | 61 | 81 |
| 2005 | 23 | 80 | 103 |
| 2006 | 25 | 72 | 97 |
| 2007 | 27 | 56 | 83 |
| 2008 | 26 | 67 | 93 |
| 2009 | 25 | 70 | 95 |
| 2010 | 33 | 66 | 99 |
| 2011 | 35 | 83 | 118 |
| 2012 | 45 | 69 | 114 |
| 2013 | 42 | 68 | 110 |
| 2014 | 43 | 82 | 125 |
| 2015 | 47 | 95 | 142 |
| 2016 | 41 | 94 | 135 |
| 2017 | 33 | 78 | 111 |
| 2018 | 43 | 104 | 147 |
| 2019 | 51 | 72 | 123 |
| 2020 | 38 | 95 | 133 |
| 2021 | 25 | 88 | 113 |
| 2022 | 8 | 81 | 89 |
| 2023 | 3 | 86 | 89 |
| 2024 | 33 | 60 | 93 |
| 2025 | 13 | 17 | 30 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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The distribution of highly deleterious variants across human ancestry groups. Proc Natl Acad Sci U S A. 2025 May 27; 122(21):e2503857122.
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Genetic Mutations and Small Bowel Ulcerating Disease: Role in Diagnosis? Curr Gastroenterol Rep. 2025 May 21; 27(1):33.
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Validation of the 5th edition of the World Health Organization and International Consensus Classification guidelines for TP53-mutated myeloid neoplasm in an independent international cohort. Blood Cancer J. 2025 May 07; 15(1):88.
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Prevalence and Clinical Impact of BRAF p.V600E Mutation in Papillary Thyroid Carcinoma. Endocr Pathol. 2025 Apr 16; 36(1):13.
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Outcomes of patients with relapsed/refractory lymphoplasmacytic lymphoma/waldenström macroglobulinemia treated with venetoclax: a multicenter retrospective analysis. Blood Cancer J. 2025 Apr 15; 15(1):65.
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Energy landscape of a Kv channel revealed by temperature steps while perturbing its electromechanical coupling. Nat Commun. 2025 Apr 09; 16(1):3379.
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Robustness of Ancestral Sequence Reconstruction to Among-site and Among-lineage Evolutionary Heterogeneity. Mol Biol Evol. 2025 Apr 01; 42(4).
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Tet Methylcytosine Dioxygenase 2 (TET2) Mutation Drives a Global Hypermethylation Signature in Patients With Pulmonary Arterial Hypertension (PAH): Correlation With Altered Gene Expression Relevant to a Common T Cell Phenotype. Compr Physiol. 2025 Apr; 15(2):e70011.
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Dual inhibition of ATR and DNA-PKcs radiosensitizes ATM-mutant prostate cancer. Oncogene. 2025 Jun; 44(22):1746-1760.
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TP53 mutations and TET2 deficiency cooperate to drive leukemogenesis and establish an immunosuppressive environment. J Clin Invest. 2025 May 15; 135(10).