"Quantitative Trait Loci" 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.
Genetic loci associated with a QUANTITATIVE TRAIT.
| Descriptor ID |
D040641
|
| MeSH Number(s) |
G05.360.340.024.380.937
|
| Concept/Terms |
Quantitative Trait Loci- Quantitative Trait Loci
- Loci, Quantitative Trait
- Locus, Quantitative Trait
- Quantitative Trait Locus
- Trait Loci, Quantitative
- Trait Locus, Quantitative
|
Below are MeSH descriptors whose meaning is more general than "Quantitative Trait Loci".
Below are MeSH descriptors whose meaning is more specific than "Quantitative Trait Loci".
This graph shows the total number of publications written about "Quantitative Trait Loci" by people in this website by year, and whether "Quantitative Trait Loci" 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 |
|---|
| 2002 | 0 | 1 | 1 |
| 2003 | 3 | 0 | 3 |
| 2004 | 2 | 2 | 4 |
| 2005 | 8 | 4 | 12 |
| 2006 | 9 | 5 | 14 |
| 2007 | 4 | 4 | 8 |
| 2008 | 5 | 3 | 8 |
| 2009 | 6 | 3 | 9 |
| 2010 | 3 | 6 | 9 |
| 2011 | 1 | 2 | 3 |
| 2012 | 6 | 2 | 8 |
| 2013 | 5 | 6 | 11 |
| 2014 | 7 | 5 | 12 |
| 2015 | 1 | 6 | 7 |
| 2016 | 5 | 10 | 15 |
| 2017 | 4 | 15 | 19 |
| 2018 | 5 | 12 | 17 |
| 2019 | 8 | 15 | 23 |
| 2020 | 8 | 6 | 14 |
| 2021 | 6 | 5 | 11 |
| 2022 | 2 | 5 | 7 |
| 2023 | 2 | 4 | 6 |
| 2024 | 0 | 3 | 3 |
| 2025 | 2 | 4 | 6 |
| 2026 | 0 | 6 | 6 |
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Below are the most recent publications written about "Quantitative Trait Loci" by people in Profiles.
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Mapping epigenetic gene variant dynamics: comparative analysis of frequency, functional impact and trait associations in African and European populations. Sci Rep. 2026 Mar 06; 16(1).
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Epigenome-wide association study of blood proteome in the Atherosclerosis Risk in Communities study. HGG Adv. 2026 Apr 09; 7(2):100585.
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Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes. Nature. 2026 04; 652(8110):675-685.
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Unravelling the molecular mechanisms causal to type 2 diabetes across global populations and disease-relevant tissues. Nat Metab. 2026 Feb; 8(2):506-520.
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Single-cell atlas of the transcriptome and chromatin accessibility in the human retina. Nat Genet. 2026 Feb; 58(2):418-433.
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Whole genome sequence analysis of pulmonary function and COPD in 44,287 multi-ancestry participants. Genome Biol. 2026 Jan 15; 27(1):28.
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Integrative exome sequencing and machine learning identify MICB and interferon pathway genes as contributors to SSc risk. Ann Rheum Dis. 2025 Aug; 84(8):1363-1374.
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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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Regulation of MCCC1 expression by a Parkinson's disease-associated intronic variant: implications for pathogenesis. J Hum Genet. 2025 Jul; 70(7):371-374.
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Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis. Nat Commun. 2025 Apr 01; 16(1):3101.