Polymorphism, Single Nucleotide
"Polymorphism, Single Nucleotide" 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.
A single nucleotide variation in a genetic sequence that occurs at appreciable frequency in the population.
Descriptor ID |
D020641
|
MeSH Number(s) |
G05.365.795.598
|
Concept/Terms |
Polymorphism, Single Nucleotide- Polymorphism, Single Nucleotide
- Nucleotide Polymorphism, Single
- Nucleotide Polymorphisms, Single
- Polymorphisms, Single Nucleotide
- Single Nucleotide Polymorphisms
- SNPs
- Single Nucleotide Polymorphism
|
Below are MeSH descriptors whose meaning is more general than "Polymorphism, Single Nucleotide".
Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Single Nucleotide".
This graph shows the total number of publications written about "Polymorphism, Single Nucleotide" by people in this website by year, and whether "Polymorphism, Single Nucleotide" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1999 | 0 | 1 | 1 |
2000 | 1 | 5 | 6 |
2001 | 3 | 2 | 5 |
2002 | 14 | 8 | 22 |
2003 | 15 | 13 | 28 |
2004 | 13 | 22 | 35 |
2005 | 23 | 22 | 45 |
2006 | 23 | 28 | 51 |
2007 | 35 | 30 | 65 |
2008 | 40 | 45 | 85 |
2009 | 37 | 46 | 83 |
2010 | 51 | 62 | 113 |
2011 | 48 | 88 | 136 |
2012 | 51 | 91 | 142 |
2013 | 35 | 67 | 102 |
2014 | 26 | 74 | 100 |
2015 | 26 | 59 | 85 |
2016 | 19 | 47 | 66 |
2017 | 16 | 47 | 63 |
2018 | 26 | 46 | 72 |
2019 | 12 | 48 | 60 |
2020 | 13 | 33 | 46 |
2021 | 14 | 41 | 55 |
2022 | 4 | 25 | 29 |
2023 | 1 | 18 | 19 |
2024 | 1 | 11 | 12 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Interpreting population- and family-based genome-wide association studies in the presence of confounding. PLoS Biol. 2024 Apr; 22(4):e3002511.
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Novel breast cancer susceptibility loci under linkage peaks identified in African ancestry consortia. Hum Mol Genet. 2024 Apr 08; 33(8):687-697.
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Multi-biobank summary data Mendelian randomisation does not support a causal effect of IL-6 signalling on risk of pulmonary arterial hypertension. Eur Respir J. 2024 Apr; 63(4).
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The Impact of Inherited Genetic Variation on DNA Methylation in Prostate Cancer and Benign Tissues of African American and European American Men. Cancer Epidemiol Biomarkers Prev. 2024 Apr 03; 33(4):557-566.
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Expression- and splicing-based multi-tissue transcriptome-wide association studies identified multiple genes for breast cancer by estrogen-receptor status. Breast Cancer Res. 2024 Mar 21; 26(1):51.
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Integrative cross-omics and cross-context analysis elucidates molecular links underlying genetic effects on complex traits. Nat Commun. 2024 Mar 16; 15(1):2383.
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Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Cell Rep Med. 2024 Feb 20; 5(2):101430.
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Transcriptome-wide association study of the plasma proteome reveals cis and trans regulatory mechanisms underlying complex traits. Am J Hum Genet. 2024 Mar 07; 111(3):445-455.
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Implications of methodologies for integrating empirical kinships into ex situ population management using PMx: A case study of Baer's Pochard (Aythya baeri) in North America. J Hered. 2024 Feb 03; 115(1):19-31.
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Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits. Nat Genet. 2024 Feb; 56(2):336-347.