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 | 35 | 30 | 65 |
| 2008 | 40 | 45 | 85 |
| 2009 | 37 | 45 | 82 |
| 2010 | 51 | 62 | 113 |
| 2011 | 47 | 88 | 135 |
| 2012 | 50 | 90 | 140 |
| 2013 | 34 | 66 | 100 |
| 2014 | 28 | 76 | 104 |
| 2015 | 26 | 62 | 88 |
| 2016 | 21 | 49 | 70 |
| 2017 | 17 | 50 | 67 |
| 2018 | 27 | 49 | 76 |
| 2019 | 14 | 50 | 64 |
| 2020 | 14 | 38 | 52 |
| 2021 | 15 | 44 | 59 |
| 2022 | 5 | 27 | 32 |
| 2023 | 2 | 21 | 23 |
| 2024 | 14 | 36 | 50 |
| 2025 | 0 | 35 | 35 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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PICALM Alzheimer's risk allele causes aberrant lipid droplets in microglia. Nature. 2025 Oct; 646(8087):1178-1186.
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The African-Specific Variant in the Duffy Antigen Receptor for Chemokines Gene, CD8+ T-Cell Density, and Aggressive Breast Cancer Subtypes in Black Women. Cancer Epidemiol Biomarkers Prev. 2025 Sep 02; 34(9):1509-1515.
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Genetic variation in the FMO and GSTO gene clusters impacts arsenic metabolism in humans. PLoS Genet. 2025 Sep; 21(9):e1011826.
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Genetic characterization of preschool wheeze phenotypes. J Allergy Clin Immunol. 2025 Dec; 156(6):1537-1546.
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Association of 17q12-q21 Asthma Risk Locus with Clinical Severity of Infant Respiratory Syncytial Virus Infection. Biomolecules. 2025 Jul 22; 15(8).
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Integrating multi-ancestry genomic and proteomic data to identify blood risk biomarkers and target proteins for breast cancer genetic risk loci. Int J Cancer. 2025 Nov 15; 157(10):2071-2080.
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Haplotype analysis reveals pleiotropic disease associations in the HLA region. Am J Hum Genet. 2025 Aug 07; 112(8):1833-1851.
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The evolution of separate sexes in waterhemp is associated with surprising chromosomal diversity and complexity. PLoS Biol. 2025 Jun; 23(6):e3003254.
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Genetic relationships between systemic lupus erythematosus and a positive antinuclear antibody test in the absence of autoimmune disease. Lupus Sci Med. 2025 Jun 12; 12(1).
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PTPN2 and Leukopenia in Individuals With Normal TPMT and NUDT15 Metabolizer Status Taking Azathioprine. Clin Transl Sci. 2025 Jun; 18(6):e70220.