"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 | 4 | 4 |
| 1995 | 0 | 4 | 4 |
| 1996 | 2 | 4 | 6 |
| 1997 | 0 | 5 | 5 |
| 1998 | 0 | 2 | 2 |
| 1999 | 1 | 10 | 11 |
| 2000 | 0 | 12 | 12 |
| 2001 | 1 | 9 | 10 |
| 2002 | 0 | 16 | 16 |
| 2003 | 2 | 10 | 12 |
| 2004 | 4 | 22 | 26 |
| 2005 | 2 | 25 | 27 |
| 2006 | 2 | 21 | 23 |
| 2007 | 3 | 28 | 31 |
| 2008 | 1 | 17 | 18 |
| 2009 | 3 | 21 | 24 |
| 2010 | 1 | 28 | 29 |
| 2011 | 4 | 26 | 30 |
| 2012 | 2 | 21 | 23 |
| 2013 | 0 | 16 | 16 |
| 2014 | 2 | 11 | 13 |
| 2015 | 2 | 14 | 16 |
| 2016 | 1 | 12 | 13 |
| 2017 | 2 | 13 | 15 |
| 2018 | 0 | 14 | 14 |
| 2019 | 1 | 7 | 8 |
| 2020 | 1 | 7 | 8 |
| 2021 | 0 | 14 | 14 |
| 2022 | 0 | 4 | 4 |
| 2023 | 1 | 6 | 7 |
| 2024 | 0 | 8 | 8 |
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Below are the most recent publications written about "Gene Frequency" by people in Profiles.
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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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Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies. Am J Hum Genet. 2024 Nov 07; 111(11):2444-2457.
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Selection with two alleles of X-linkage and its application to the fitness component analysis of OdsH in Drosophila. G3 (Bethesda). 2024 Sep 04; 14(9).
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
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Evaluation of the genetic basis of familial-associated early-onset hematologic cancers in an ancestral/ethnically diverse population. Haematologica. 2024 07 01; 109(7):2085-2091.
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Known pathogenic gene variants and new candidates detected in sudden unexpected infant death using whole genome sequencing. Am J Med Genet A. 2024 Nov; 194(11):e63596.
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Biotic interactions promote local adaptation to soil in plants. Nat Commun. 2024 Jun 18; 15(1):5186.
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The evolutionary tale of lactase persistence in humans. Nat Rev Genet. 2024 Jan; 25(1):7.
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TP53 variant allele frequency and therapy-related setting independently predict survival in myelodysplastic syndromes with del(5q). Br J Haematol. 2024 Apr; 204(4):1243-1248.
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Scaling the discrete-time Wright-Fisher model to biobank-scale datasets. Genetics. 2023 11 01; 225(3).