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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 |
| 2005 | 2 | 3 | 5 |
| 2006 | 4 | 4 | 8 |
| 2007 | 14 | 11 | 25 |
| 2008 | 13 | 12 | 25 |
| 2009 | 13 | 13 | 26 |
| 2010 | 12 | 12 | 24 |
| 2011 | 10 | 16 | 26 |
| 2012 | 5 | 9 | 14 |
| 2013 | 11 | 12 | 23 |
| 2014 | 13 | 7 | 20 |
| 2015 | 11 | 16 | 27 |
| 2016 | 4 | 15 | 19 |
| 2017 | 6 | 10 | 16 |
| 2018 | 2 | 8 | 10 |
| 2019 | 1 | 9 | 10 |
| 2020 | 3 | 19 | 22 |
| 2021 | 2 | 5 | 7 |
| 2022 | 0 | 7 | 7 |
| 2023 | 0 | 5 | 5 |
| 2024 | 1 | 4 | 5 |
To return to the timeline,
click here.
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
-
Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries. Nat Genet. 2024 Dec; 56(12):2659-2671.
-
Structural framework to address variant-gene relationship in primary open-angle glaucoma. Vision Res. 2025 Jan; 226:108505.
-
Commonly used genomic arrays may lose information due to imperfect coverage of discovered variants for autism spectrum disorder. J Neurodev Disord. 2024 Sep 12; 16(1):54.
-
Mammographic density mediates the protective effect of early-life body size on breast cancer risk. Nat Commun. 2024 May 13; 15(1):4021.
-
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma. Commun Biol. 2024 01 05; 7(1):33.
-
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nat Commun. 2023 10 04; 14(1):6172.
-
Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. Nat Commun. 2023 10 02; 14(1):6147.
-
Association of Behavioral and Clinical Risk Factors With Cataract: A Two-Sample Mendelian Randomization Study. Invest Ophthalmol Vis Sci. 2023 07 03; 64(10):19.
-
Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nat Genet. 2023 07; 55(7):1116-1125.
-
MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer. Nat Commun. 2023 Jan 23; 14(1):377.