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 |
|---|
| 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 | 21 | 44 |
| 2006 | 23 | 28 | 51 |
| 2007 | 34 | 30 | 64 |
| 2008 | 40 | 45 | 85 |
| 2009 | 37 | 45 | 82 |
| 2010 | 51 | 62 | 113 |
| 2011 | 47 | 87 | 134 |
| 2012 | 50 | 90 | 140 |
| 2013 | 34 | 66 | 100 |
| 2014 | 26 | 74 | 100 |
| 2015 | 25 | 61 | 86 |
| 2016 | 21 | 48 | 69 |
| 2017 | 17 | 47 | 64 |
| 2018 | 27 | 47 | 74 |
| 2019 | 12 | 48 | 60 |
| 2020 | 13 | 36 | 49 |
| 2021 | 14 | 43 | 57 |
| 2022 | 5 | 27 | 32 |
| 2023 | 2 | 19 | 21 |
| 2024 | 13 | 30 | 43 |
| 2025 | 5 | 1 | 6 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genome-wide association study of prostate-specific antigen levels in 392,522 men identifies new loci and improves prediction across ancestry groups. Nat Genet. 2025 Feb; 57(2):334-344.
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A cost-effective, high-throughput, highly accurate genotyping method for outbred populations. G3 (Bethesda). 2025 Feb 05; 15(2).
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Genome-wide association study on chronic postsurgical pain in the UK Biobank. Br J Anaesth. 2025 Mar; 134(3):783-792.
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ADELLE: A global testing method for trans-eQTL mapping. PLoS Genet. 2025 Jan; 21(1):e1011563.
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Genomic analysis of surgical patients to identify patients at risk for postoperative sepsis and surgical site infection. J Trauma Acute Care Surg. 2025 Mar 01; 98(3):385-392.
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Refining breast cancer genetic risk and biology through multi-ancestry fine-mapping analyses of 192 risk regions. Nat Genet. 2025 Jan; 57(1):80-87.
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Genome-wide meta-analysis associates donor-recipient non-HLA genetic mismatch with acute cellular rejection post-liver transplantation. Hepatol Commun. 2025 Jan 01; 9(1).
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A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations. PLoS Genet. 2024 Oct; 20(10):e1011322.
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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.