"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 | 3 | 3 |
| 1996 | 0 | 3 | 3 |
| 1997 | 0 | 4 | 4 |
| 1998 | 0 | 4 | 4 |
| 1999 | 0 | 3 | 3 |
| 2000 | 0 | 1 | 1 |
| 2001 | 0 | 2 | 2 |
| 2002 | 0 | 3 | 3 |
| 2003 | 0 | 7 | 7 |
| 2004 | 0 | 7 | 7 |
| 2005 | 1 | 4 | 5 |
| 2006 | 0 | 14 | 14 |
| 2007 | 0 | 5 | 5 |
| 2008 | 0 | 9 | 9 |
| 2009 | 1 | 12 | 13 |
| 2010 | 0 | 12 | 12 |
| 2011 | 0 | 10 | 10 |
| 2012 | 0 | 7 | 7 |
| 2013 | 0 | 9 | 9 |
| 2014 | 0 | 9 | 9 |
| 2015 | 0 | 3 | 3 |
| 2016 | 0 | 6 | 6 |
| 2017 | 0 | 5 | 5 |
| 2018 | 0 | 4 | 4 |
| 2019 | 0 | 3 | 3 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 2 | 2 |
To return to the timeline,
click here.
Below are the most recent publications written about "Gene Frequency" by people in Profiles.
-
The Spectrum of ?-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study. Hemoglobin. 2021 Nov; 45(6):365-370.
-
Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features. Circ Genom Precis Med. 2021 04; 14(2):e003097.
-
Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus. Genome Biol. 2020 11 19; 21(1):281.
-
The immunoglobulin ? marker 17 allotype and KIR/HLA genes prevent the development of chronic hepatitis B in humans. Immunology. 2020 02; 159(2):178-182.
-
Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis. Circulation. 2019 10 15; 140(16):1331-1341.
-
Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome. Kidney Int. 2019 10; 96(4):883-889.
-
No major role for rare plectin variants in arrhythmogenic right ventricular cardiomyopathy. PLoS One. 2018; 13(8):e0203078.
-
Profile of drug resistance mutations in nucleos(t)ide analogue-experienced chronic hepatitis B patients in Tianjin, China. Int J Antimicrob Agents. 2018 Nov; 52(5):735-736.
-
Genome-Wide Mapping of Gene-Phenotype Relationships in Experimentally Evolved Populations. Mol Biol Evol. 2018 08 01; 35(8):2085-2095.
-
Genetics of hypertension: Implications of single nucleotide polymorphism(s) in African populations and beyond. J Clin Hypertens (Greenwich). 2018 03; 20(3):496-498.