"Genetic Variation" 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.
Genotypic differences observed among individuals in a population.
Descriptor ID |
D014644
|
MeSH Number(s) |
G05.365
|
Concept/Terms |
Genetic Variation- Genetic Variation
- Genetic Variations
- Variations, Genetic
- Variation, Genetic
- Diversity, Genetic
- Diversities, Genetic
- Genetic Diversities
- Genetic Diversity
|
Below are MeSH descriptors whose meaning is more general than "Genetic Variation".
Below are MeSH descriptors whose meaning is more specific than "Genetic Variation".
This graph shows the total number of publications written about "Genetic Variation" by people in this website by year, and whether "Genetic Variation" 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 |
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1995 | 5 | 5 | 10 |
1996 | 3 | 2 | 5 |
1997 | 5 | 5 | 10 |
1998 | 4 | 11 | 15 |
1999 | 4 | 7 | 11 |
2000 | 11 | 8 | 19 |
2001 | 3 | 8 | 11 |
2002 | 10 | 10 | 20 |
2003 | 3 | 16 | 19 |
2004 | 16 | 12 | 28 |
2005 | 7 | 17 | 24 |
2006 | 14 | 15 | 29 |
2007 | 14 | 15 | 29 |
2008 | 18 | 23 | 41 |
2009 | 18 | 21 | 39 |
2010 | 17 | 20 | 37 |
2011 | 20 | 18 | 38 |
2012 | 22 | 14 | 36 |
2013 | 18 | 20 | 38 |
2014 | 20 | 18 | 38 |
2015 | 22 | 23 | 45 |
2016 | 32 | 33 | 65 |
2017 | 27 | 17 | 44 |
2018 | 26 | 32 | 58 |
2019 | 31 | 33 | 64 |
2020 | 21 | 24 | 45 |
2021 | 16 | 18 | 34 |
2022 | 8 | 10 | 18 |
2023 | 1 | 7 | 8 |
2024 | 8 | 18 | 26 |
2025 | 5 | 5 | 10 |
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Below are the most recent publications written about "Genetic Variation" by people in Profiles.
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Human genetic variation determines 24-hour rhythmic gene expression and disease risk. Nat Commun. 2025 May 08; 16(1):4270.
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ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias. JAMA Pediatr. 2025 May 01; 179(5):529-539.
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Genomic and functional analysis of rmp locus variants in Klebsiella pneumoniae. Genome Med. 2025 Apr 09; 17(1):36.
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Diverse ancestral representation improves genetic intolerance metrics. Nat Commun. 2025 Mar 18; 16(1):2648.
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Frequency of variants in Mendelian Alzheimer's disease genes within the Alzheimer's Disease Sequencing Project. J Alzheimers Dis. 2025 Apr; 104(3):841-851.
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Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A. Hum Genet. 2025 Mar; 144(2-3):295-308.
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Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk. Nat Genet. 2025 Mar; 57(3):548-562.
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A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. Nat Comput Sci. 2025 Feb; 5(2):125-143.
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CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs). Hum Genet. 2025 Mar; 144(2-3):227-242.
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Small variant benchmark from a complete assembly of X and Y chromosomes. Nat Commun. 2025 Jan 08; 16(1):497.