"Gene Frequency" 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 proportion of one particular in the total of all ALLELES for one genetic locus in a breeding POPULATION.
| Descriptor ID |
D005787
|
| MeSH Number(s) |
G05.330
|
| Concept/Terms |
Gene Frequency- Gene Frequency
- Frequencies, Gene
- Frequency, Gene
- Gene Frequencies
- Allele Frequency
- Allele Frequencies
- Frequencies, Allele
- Frequency, Allele
|
Below are MeSH descriptors whose meaning is more general than "Gene Frequency".
Below are MeSH descriptors whose meaning is more specific than "Gene Frequency".
This graph shows the total number of publications written about "Gene Frequency" by people in this website by year, and whether "Gene Frequency" 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 | 0 | 8 | 8 |
| 1995 | 0 | 6 | 6 |
| 1996 | 1 | 7 | 8 |
| 1997 | 1 | 6 | 7 |
| 1998 | 2 | 3 | 5 |
| 1999 | 1 | 11 | 12 |
| 2000 | 0 | 19 | 19 |
| 2001 | 2 | 19 | 21 |
| 2002 | 0 | 17 | 17 |
| 2003 | 1 | 29 | 30 |
| 2004 | 3 | 19 | 22 |
| 2005 | 3 | 33 | 36 |
| 2006 | 2 | 36 | 38 |
| 2007 | 2 | 30 | 32 |
| 2008 | 2 | 34 | 36 |
| 2009 | 1 | 29 | 30 |
| 2010 | 1 | 43 | 44 |
| 2011 | 4 | 36 | 40 |
| 2012 | 1 | 46 | 47 |
| 2013 | 0 | 42 | 42 |
| 2014 | 3 | 27 | 30 |
| 2015 | 2 | 32 | 34 |
| 2016 | 0 | 33 | 33 |
| 2017 | 3 | 30 | 33 |
| 2018 | 0 | 21 | 21 |
| 2019 | 4 | 20 | 24 |
| 2020 | 3 | 12 | 15 |
| 2021 | 2 | 12 | 14 |
| 2022 | 0 | 6 | 6 |
| 2023 | 0 | 4 | 4 |
| 2024 | 1 | 7 | 8 |
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Below are the most recent publications written about "Gene Frequency" by people in Profiles.
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Using multiplexed functional data to reduce variant classification inequities in underrepresented populations. Genome Med. 2024 Dec 03; 16(1):143.
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Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion. Blood. 2024 10 17; 144(16):1722-1731.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Nat Commun. 2024 Oct 03; 15(1):8549.
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Extended haplotype with rs41524547-G defines the ancestral origin of SCA10. Hum Mol Genet. 2024 09 03; 33(18):1567-1574.
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Analytical Validation of a Telomerase Reverse Transcriptase (TERT) Promoter Mutation Assay. J Clin Endocrinol Metab. 2024 Aug 13; 109(9):2269-2273.
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Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat Genet. 2024 Jul; 56(7):1397-1411.
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X-linked genetic associations in sporadic thoracic aortic dissection. Am J Med Genet A. 2024 09; 194(9):e63644.
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Characterization of CYP2B6 and CYP2A6 Pharmacogenetic Variation in Sub-Saharan African Populations. Clin Pharmacol Ther. 2024 03; 115(3):576-594.
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Variant allele frequency: a decision-making tool in precision oncology? Trends Cancer. 2023 12; 9(12):1058-1068.