"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 |
|---|
| 1994 | 12 | 31 | 43 |
| 1995 | 15 | 26 | 41 |
| 1996 | 24 | 22 | 46 |
| 1997 | 26 | 16 | 42 |
| 1998 | 23 | 37 | 60 |
| 1999 | 14 | 34 | 48 |
| 2000 | 27 | 41 | 68 |
| 2001 | 15 | 48 | 63 |
| 2002 | 21 | 49 | 70 |
| 2003 | 20 | 77 | 97 |
| 2004 | 19 | 61 | 80 |
| 2005 | 23 | 80 | 103 |
| 2006 | 25 | 72 | 97 |
| 2007 | 27 | 56 | 83 |
| 2008 | 25 | 68 | 93 |
| 2009 | 25 | 69 | 94 |
| 2010 | 34 | 66 | 100 |
| 2011 | 35 | 83 | 118 |
| 2012 | 45 | 69 | 114 |
| 2013 | 42 | 69 | 111 |
| 2014 | 44 | 79 | 123 |
| 2015 | 47 | 88 | 135 |
| 2016 | 39 | 93 | 132 |
| 2017 | 34 | 77 | 111 |
| 2018 | 42 | 105 | 147 |
| 2019 | 48 | 67 | 115 |
| 2020 | 26 | 88 | 114 |
| 2021 | 25 | 84 | 109 |
| 2022 | 8 | 80 | 88 |
| 2023 | 2 | 82 | 84 |
| 2024 | 17 | 36 | 53 |
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Below are the most recent publications written about "Mutation" by people in Profiles.
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Predictors of clinical outcome in myeloproliferative neoplasm, unclassifiable: A Bone Marrow Pathology Group study. Am J Clin Pathol. 2024 Sep 03; 162(3):233-242.
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Clinical and molecular correlates of tumor aneuploidy in metastatic non-small cell lung cancer. Sci Rep. 2024 08 21; 14(1):19375.
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Comprehensive analysis of the functional impact of single nucleotide variants of human CHEK2. PLoS Genet. 2024 Aug; 20(8):e1011375.
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Crohn's Disease-Associated Pathogenic Mutation in the Manganese Transporter ZIP8 Shifts the Ileal and Rectal Mucosal Microbiota Implicating Aberrant Bile Acid Metabolism. Inflamm Bowel Dis. 2024 Aug 01; 30(8):1379-1388.
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Prognostic impact of SF3B1 mutation and multilineage dysplasia in myelodysplastic syndromes with ring sideroblasts: a Mayo Clinic study of 170 informative cases. Haematologica. 2024 08 01; 109(8):2525-2532.
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Exploring markers of immunoresponsiveness in papillary thyroid carcinoma and future treatment strategies. J Immunother Cancer. 2024 Jul 29; 12(7).
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Association of KRAS Mutation and Gene Pathways in Colorectal Carcinoma: A Transcriptome- and Methylome-Wide Study and Potential Implications for Therapy. Int J Mol Sci. 2024 Jul 25; 25(15).
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Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. Nat Commun. 2024 Jul 11; 15(1):5837.
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Cell free DNA in patients with pancreatic adenocarcinoma: clinicopathologic correlations. Sci Rep. 2024 07 08; 14(1):15744.
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Bayesian estimation of gene constraint from an evolutionary model with gene features. Nat Genet. 2024 Aug; 56(8):1632-1643.