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.
Polymorphism, Single Nucleotide
- Polymorphism, Single Nucleotide
- Nucleotide Polymorphism, Single
- Nucleotide Polymorphisms, Single
- Polymorphisms, Single Nucleotide
- Single Nucleotide Polymorphisms
- 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 Harvard Catalyst Profiles by year, and whether "Polymorphism, Single Nucleotide" was a major or minor topic of these publication.
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|Year||Major Topic||Minor Topic||Total|
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nat Genet. 2023 Mar; 55(3):410-422.
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring. Sleep. 2023 Mar 09; 46(3).
Genome-wide Interaction Study with Smoking for Colorectal Cancer Risk Identifies Novel Genetic Loci Related to Tumor Suppression, Inflammation, and Immune Response. Cancer Epidemiol Biomarkers Prev. 2023 03 06; 32(3):315-328.
Optimized high-throughput screening of non-coding variants identified from genome-wide association studies. Nucleic Acids Res. 2023 02 22; 51(3):e18.
Leveraging GWAS data derived from a large cooperative group trial to assess the risk of taxane-induced peripheral neuropathy (TIPN) in patients being treated for breast cancer: Part 2-functional implications of a SNP cluster associated with TIPN risk in patients being treated for breast cancer. Support Care Cancer. 2023 Feb 21; 31(3):178.
Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Circulation. 2023 Mar 21; 147(12):942-955.
Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India. Int J Environ Res Public Health. 2023 Feb 20; 20(4).
Systolic Blood Pressure and Cardiovascular Risk: Straightening the Evidence. Hypertension. 2023 03; 80(3):577-579.
Reassessing the causal role of obesity in breast cancer susceptibility: a comprehensive multivariable Mendelian randomization investigating the distribution and timing of exposure. Int J Epidemiol. 2023 02 08; 52(1):58-70.
No Association of IFNL4 Genotype With Opportunistic Infections and Cancers Among Men With Human Immunodeficiency Virus 1 Infection. Clin Infect Dis. 2023 02 08; 76(3):521-527.