 Mutation Rate
"Mutation Rate" 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 number of mutations that occur in a specific sequence, GENE, or GENOME over a specified period of time such as years, CELL DIVISIONS, or generations.
| Descriptor ID |
D059645
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| MeSH Number(s) |
G05.355.044.250.750 G05.365.590.612 G16.100.178.250.750
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| Concept/Terms |
Mutation Rate- Mutation Rate
- Mutation Rates
- Rate, Mutation
- Rates, Mutation
- Mutation Frequency
- Frequencies, Mutation
- Frequency, Mutation
- Mutation Frequencies
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Below are MeSH descriptors whose meaning is more general than "Mutation Rate".
Below are MeSH descriptors whose meaning is more specific than "Mutation Rate".
This graph shows the total number of publications written about "Mutation Rate" by people in this website by year, and whether "Mutation Rate" 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 |
|---|
| 2010 | 0 | 1 | 1 | | 2012 | 1 | 5 | 6 | | 2013 | 0 | 4 | 4 | | 2014 | 1 | 2 | 3 | | 2015 | 1 | 1 | 2 | | 2016 | 3 | 3 | 6 | | 2017 | 2 | 1 | 3 | | 2018 | 1 | 4 | 5 | | 2019 | 0 | 3 | 3 | | 2020 | 2 | 1 | 3 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mutation Rate" by people in Profiles.
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Milligan WR, Amster G, Sella G. The impact of genetic modifiers on variation in germline mutation rates within and among human populations. Genetics. 2022 07 30; 221(4).
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Wu FL, Strand AI, Cox LA, Ober C, Wall JD, Moorjani P, Przeworski M. A comparison of humans and baboons suggests germline mutation rates do not track cell divisions. PLoS Biol. 2020 08; 18(8):e3000838.
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Amster G, Murphy DA, Milligan WR, Sella G. Changes in life history and population size can explain the relative neutral diversity levels on X and autosomes in extant human populations. Proc Natl Acad Sci U S A. 2020 08 18; 117(33):20063-20069.
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Amster G, Sella G. Life History Effects on Neutral Diversity Levels of Autosomes and Sex Chromosomes. Genetics. 2020 08; 215(4):1133-1142.
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Sasani TA, Pedersen BS, Gao Z, Baird L, Przeworski M, Jorde LB, Quinlan AR. Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. Elife. 2019 09 24; 8.
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Lin JJ, Bhattacharjee MJ, Yu CP, Tseng YY, Li WH. Many human RNA viruses show extraordinarily stringent selective constraints on protein evolution. Proc Natl Acad Sci U S A. 2019 09 17; 116(38):19009-19018.
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Zhao S, Liu J, Nanga P, Liu Y, Cicek AE, Knoblauch N, He C, Stephens M, He X. Detailed modeling of positive selection improves detection of cancer driver genes. Nat Commun. 2019 07 30; 10(1):3399.
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Kang H, Pettinga D, Schubert AD, Ladenson PW, Ball DW, Chung JH, Schrock AB, Madison R, Frampton GM, Stephens PJ, Ross JS, Miller VA, Ali SM. Genomic Profiling of Parathyroid Carcinoma Reveals Genomic Alterations Suggesting Benefit from Therapy. Oncologist. 2019 06; 24(6):791-797.
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McGinnis LM, Nybakken G, Ma L, Arber DA. Frequency of MAP2K1, TP53, and U2AF1 Mutations in BRAF-mutated Langerhans Cell Histiocytosis: Further Characterizing the Genomic Landscape of LCH. Am J Surg Pathol. 2018 07; 42(7):885-890.
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Liu Y, Liang Y, Cicek AE, Li Z, Li J, Muhle RA, Krenzer M, Mei Y, Wang Y, Knoblauch N, Morrison J, Zhao S, Jiang Y, Geller E, Ionita-Laza I, Wu J, Xia K, Noonan JP, Sun ZS, He X. A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies. Am J Hum Genet. 2018 06 07; 102(6):1031-1047.
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