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 | 6 | 4 | 10 |
| 2002 | 6 | 6 | 12 |
| 2003 | 7 | 7 | 14 |
| 2004 | 8 | 10 | 18 |
| 2005 | 25 | 14 | 39 |
| 2006 | 21 | 23 | 44 |
| 2007 | 24 | 28 | 52 |
| 2008 | 35 | 38 | 73 |
| 2009 | 40 | 50 | 90 |
| 2010 | 45 | 64 | 109 |
| 2011 | 49 | 75 | 124 |
| 2012 | 58 | 95 | 153 |
| 2013 | 56 | 69 | 125 |
| 2014 | 39 | 64 | 103 |
| 2015 | 31 | 73 | 104 |
| 2016 | 30 | 74 | 104 |
| 2017 | 39 | 56 | 95 |
| 2018 | 28 | 64 | 92 |
| 2019 | 29 | 66 | 95 |
| 2020 | 20 | 42 | 62 |
| 2021 | 12 | 51 | 63 |
| 2022 | 5 | 39 | 44 |
| 2023 | 3 | 22 | 25 |
| 2024 | 14 | 30 | 44 |
| 2025 | 3 | 7 | 10 |
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Genetic Associations With C-peptide Levels Before Type 1 Diabetes Diagnosis in At-risk Relatives. J Clin Endocrinol Metab. 2025 Mar 17; 110(4):e1046-e1050.
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Clinical and genetic markers of vascular toxicity in glioblastoma patients: Insights from NRG Oncology RTOG-0825. Neuro Oncol. 2025 Mar 07; 27(3):767-778.
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Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants. J Am Heart Assoc. 2025 Feb 18; 14(4):e036499.
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Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis. Nat Genet. 2025 Mar; 57(3):572-582.
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Type 1 Diabetes Genetic Risk Scores: History, Application and Future Directions. Curr Diab Rep. 2025 Feb 08; 25(1):22.
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A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. Nat Comput Sci. 2025 Feb; 5(2):125-143.
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Polygenic Score for Clinicopathologic Features and Survival Outcomes in Papillary Thyroid Carcinoma. JAMA Otolaryngol Head Neck Surg. 2025 Feb 01; 151(2):113-120.
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MYO5B and the Polygenic Landscape of Very Early-Onset Inflammatory Bowel Disease in an Ethnically Diverse Population. Inflamm Bowel Dis. 2025 01 06; 31(1):189-199.
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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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Meta-EA: a gene-specific combination of available computational tools for predicting missense variant effects. Nat Commun. 2025 Jan 02; 16(1):159.