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 | 36 | 71 |
| 2009 | 40 | 50 | 90 |
| 2010 | 44 | 64 | 108 |
| 2011 | 49 | 76 | 125 |
| 2012 | 59 | 96 | 155 |
| 2013 | 55 | 69 | 124 |
| 2014 | 39 | 64 | 103 |
| 2015 | 33 | 74 | 107 |
| 2016 | 30 | 77 | 107 |
| 2017 | 40 | 57 | 97 |
| 2018 | 28 | 63 | 91 |
| 2019 | 29 | 66 | 95 |
| 2020 | 20 | 43 | 63 |
| 2021 | 12 | 51 | 63 |
| 2022 | 5 | 39 | 44 |
| 2023 | 3 | 21 | 24 |
| 2024 | 14 | 30 | 44 |
| 2025 | 3 | 16 | 19 |
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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 Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS. Genet Epidemiol. 2025 Jun; 49(4):e70010.
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Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts. PLoS One. 2025; 20(5):e0324006.
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Human genetic variation determines 24-hour rhythmic gene expression and disease risk. Nat Commun. 2025 May 08; 16(1):4270.
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Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication. Mol Neurodegener. 2025 May 03; 20(1):51.
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Uncovering shared genetic features between inflammatory bowel disease and systemic lupus erythematosus. Sci Rep. 2025 May 01; 15(1):15309.
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Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele. Nat Commun. 2025 Apr 11; 16(1):3470.
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Computational and functional prioritization identifies genes that rescue behavior and reduce tau protein in fly and human cell models of Alzheimer disease. Am J Hum Genet. 2025 May 01; 112(5):1081-1096.
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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.