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 |
---|
1999 | 0 | 1 | 1 |
2000 | 1 | 5 | 6 |
2001 | 3 | 2 | 5 |
2002 | 14 | 8 | 22 |
2003 | 15 | 13 | 28 |
2004 | 13 | 22 | 35 |
2005 | 23 | 22 | 45 |
2006 | 23 | 28 | 51 |
2007 | 35 | 30 | 65 |
2008 | 40 | 45 | 85 |
2009 | 37 | 46 | 83 |
2010 | 51 | 62 | 113 |
2011 | 48 | 88 | 136 |
2012 | 51 | 91 | 142 |
2013 | 35 | 67 | 102 |
2014 | 26 | 74 | 100 |
2015 | 26 | 59 | 85 |
2016 | 19 | 47 | 66 |
2017 | 16 | 47 | 63 |
2018 | 26 | 46 | 72 |
2019 | 12 | 48 | 60 |
2020 | 13 | 33 | 46 |
2021 | 14 | 41 | 55 |
2022 | 4 | 25 | 29 |
2023 | 1 | 17 | 18 |
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.
-
Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Cell Rep Med. 2024 Feb 20; 5(2):101430.
-
Implications of methodologies for integrating empirical kinships into ex situ population management using PMx: A case study of Baer's Pochard (Aythya baeri) in North America. J Hered. 2024 Feb 03; 115(1):19-31.
-
Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits. Nat Genet. 2024 Feb; 56(2):336-347.
-
Addition of polygenic risk score to a risk calculator for prediction of breast cancer in US Black women. Breast Cancer Res. 2024 01 02; 26(1):2.
-
The evolutionary tale of lactase persistence in humans. Nat Rev Genet. 2024 Jan; 25(1):7.
-
Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nat Genet. 2023 Dec; 55(12):2082-2093.
-
BRASS: Permutation methods for binary traits in genetic association studies with structured samples. PLoS Genet. 2023 Nov; 19(11):e1011020.
-
Systematic differences in discovery of genetic effects on gene expression and complex traits. Nat Genet. 2023 Nov; 55(11):1866-1875.
-
GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors. Am J Psychiatry. 2023 10 01; 180(10):723-738.
-
Predicted Proteome Association Studies of Breast, Prostate, Ovarian, and Endometrial Cancers Implicate Plasma Protein Regulation in Cancer Susceptibility. Cancer Epidemiol Biomarkers Prev. 2023 09 01; 32(9):1198-1207.