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 |
|---|
| 2000 | 3 | 4 | 7 |
| 2001 | 7 | 5 | 12 |
| 2002 | 6 | 7 | 13 |
| 2003 | 10 | 9 | 19 |
| 2004 | 11 | 16 | 27 |
| 2005 | 32 | 24 | 56 |
| 2006 | 32 | 33 | 65 |
| 2007 | 42 | 46 | 88 |
| 2008 | 64 | 66 | 130 |
| 2009 | 66 | 82 | 148 |
| 2010 | 86 | 107 | 193 |
| 2011 | 87 | 114 | 201 |
| 2012 | 94 | 144 | 238 |
| 2013 | 87 | 127 | 214 |
| 2014 | 59 | 92 | 151 |
| 2015 | 50 | 100 | 150 |
| 2016 | 46 | 103 | 149 |
| 2017 | 57 | 88 | 145 |
| 2018 | 37 | 88 | 125 |
| 2019 | 32 | 91 | 123 |
| 2020 | 27 | 52 | 79 |
| 2021 | 18 | 60 | 78 |
| 2022 | 6 | 46 | 52 |
| 2023 | 4 | 29 | 33 |
| 2024 | 20 | 39 | 59 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation. Genome Res. 2024 Nov 20; 34(11):2061-2073.
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Investigating p.Ala1035Val in NPC1: New Cellular Models for Niemann-Pick Type C Disease. Int J Mol Sci. 2024 Nov 13; 25(22).
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Genetic variants in canonical Wnt signaling pathway associated with pediatric immune thrombocytopenia. Blood Adv. 2024 11 12; 8(21):5529-5538.
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Investigation of the a9-nicotinic receptor single nucleotide polymorphisms induced oncogenic properties and molecular mechanisms in breast cancer. Hum Mol Genet. 2024 11 08; 33(22):1948-1965.
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Fidaxomicin resistance in Clostridioides difficile: a systematic review and predictive modeling with RNA polymerase binding sites. Antimicrob Agents Chemother. 2024 Dec 05; 68(12):e0120624.
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Body composition in recurrent prostate cancer and the role of steroidogenic genotype. Endocr Relat Cancer. 2024 Dec 01; 31(12).
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Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk. BMC Med Genomics. 2024 10 24; 17(1):255.
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Chemogenetic targeting TRPV1 in obesity-induced depression: Unveiling therapeutic potential of eicosapentaenoic acid and acupuncture. Brain Behav Immun. 2025 Jan; 123:771-783.
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An ancient ecospecies of Helicobacter pylori. Nature. 2024 Nov; 635(8037):178-185.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.