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 |
|---|
| 2000 | 3 | 4 | 7 |
| 2001 | 6 | 4 | 10 |
| 2002 | 6 | 6 | 12 |
| 2003 | 7 | 7 | 14 |
| 2004 | 8 | 10 | 18 |
| 2005 | 24 | 13 | 37 |
| 2006 | 21 | 23 | 44 |
| 2007 | 24 | 27 | 51 |
| 2008 | 34 | 36 | 70 |
| 2009 | 41 | 49 | 90 |
| 2010 | 44 | 64 | 108 |
| 2011 | 49 | 73 | 122 |
| 2012 | 57 | 94 | 151 |
| 2013 | 55 | 69 | 124 |
| 2014 | 39 | 64 | 103 |
| 2015 | 30 | 73 | 103 |
| 2016 | 30 | 74 | 104 |
| 2017 | 38 | 56 | 94 |
| 2018 | 29 | 65 | 94 |
| 2019 | 29 | 66 | 95 |
| 2020 | 20 | 42 | 62 |
| 2021 | 12 | 49 | 61 |
| 2022 | 5 | 38 | 43 |
| 2023 | 3 | 22 | 25 |
| 2024 | 13 | 30 | 43 |
| 2025 | 1 | 5 | 6 |
To return to the timeline,
click here.
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
-
Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants. J Am Heart Assoc. 2025 Feb 18; 14(4):e036499.
-
Type 1 Diabetes Genetic Risk Scores: History, Application and Future Directions. Curr Diab Rep. 2025 Feb 08; 25(1):22.
-
Polygenic Score for Clinicopathologic Features and Survival Outcomes in Papillary Thyroid Carcinoma. JAMA Otolaryngol Head Neck Surg. 2025 Feb 01; 151(2):113-120.
-
MYO5B and the Polygenic Landscape of Very Early-Onset Inflammatory Bowel Disease in an Ethnically Diverse Population. Inflamm Bowel Dis. 2025 Jan 06; 31(1):189-199.
-
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.
-
Meta-EA: a gene-specific combination of available computational tools for predicting missense variant effects. Nat Commun. 2025 Jan 02; 16(1):159.
-
General Kernel Machine Methods for Multi-Omics Integration and Genome-Wide Association Testing With Related Individuals. Genet Epidemiol. 2025 Jan; 49(1):e22610.
-
Refinement of a Published Gene-Physical Activity Interaction Impacting HDL-Cholesterol: Role of Sex and Lipoprotein Subfractions. Genet Epidemiol. 2025 Jan; 49(1):e22607.
-
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.
-
Investigating p.Ala1035Val in NPC1: New Cellular Models for Niemann-Pick Type C Disease. Int J Mol Sci. 2024 Nov 13; 25(22).