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 this website by year, and whether "Polymorphism, Single Nucleotide" was a major or minor topic of these publications.
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Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
Physical Activity and Insulin Sensitivity Independently Attenuate the Effect of FTO rs9939609 on Obesity. Diabetes Care. 2023 05 01; 46(5):985-992.
Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome. BMC Genomics. 2023 Feb 16; 24(1):75.
Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing. Nat Genet. 2023 02; 55(2):291-300.
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome Med. 2023 01 26; 15(1):7.
Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations. PLoS Genet. 2023 01; 19(1):e1010588.
Probabilistic integration of transcriptome-wide association studies and colocalization analysis identifies key molecular pathways of complex traits. Am J Hum Genet. 2023 01 05; 110(1):44-57.
Single-neuron whole genome sequencing identifies increased somatic mutation burden in Alzheimer's disease related genes. Neurobiol Aging. 2023 03; 123:222-232.
Novel genotyping algorithms for rare variants significantly improve the accuracy of Applied Biosystems? Axiom? array genotyping calls: Retrospective evaluation of UK Biobank array data. PLoS One. 2022; 17(11):e0277680.
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Leukemia. 2022 12; 36(12):2835-2844.
New Insights Relating Gasdermin B to the Onset of Childhood Asthma. Am J Respir Cell Mol Biol. 2022 Oct; 67(4):430-437.