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.
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 Harvard Catalyst Profiles by year, and whether "Polymorphism, Single Nucleotide" was a major or minor topic of these publication.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 1 | 1 | 2 |
| 2000 | 7 | 7 | 14 |
| 2001 | 17 | 12 | 29 |
| 2002 | 26 | 21 | 47 |
| 2003 | 28 | 28 | 56 |
| 2004 | 39 | 40 | 79 |
| 2005 | 48 | 78 | 126 |
| 2006 | 81 | 105 | 186 |
| 2007 | 116 | 156 | 272 |
| 2008 | 181 | 221 | 402 |
| 2009 | 193 | 244 | 437 |
| 2010 | 210 | 290 | 500 |
| 2011 | 204 | 357 | 561 |
| 2012 | 175 | 349 | 524 |
| 2013 | 179 | 344 | 523 |
| 2014 | 172 | 335 | 507 |
| 2015 | 198 | 332 | 530 |
| 2016 | 134 | 335 | 469 |
| 2017 | 118 | 300 | 418 |
| 2018 | 116 | 273 | 389 |
| 2019 | 112 | 257 | 369 |
| 2020 | 77 | 213 | 290 |
| 2021 | 60 | 170 | 230 |
| 2022 | 7 | 21 | 28 |
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. Hum Mol Genet. 2022 Mar 31; 31(7):1082-1095.
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Screening for phenotypic outliers identifies an unusually low concentration of a ß-lactoglobulin B protein isoform in bovine milk caused by a synonymous SNP. Genet Sel Evol. 2022 Mar 16; 54(1):22.
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Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes. Am J Hum Genet. 2022 Apr 07; 109(4):692-709.
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Disentangling the association between kidney function and atrial fibrillation: a bidirectional Mendelian randomization study. Int J Cardiol. 2022 May 15; 355:15-22.
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The Role of Mendelian Randomization Studies in Deciphering the Effect of Obesity on Cancer. J Natl Cancer Inst. 2022 03 08; 114(3):361-371.
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Single Nucleotide Variant in FAS Associates With Organ Failure and Soluble Fas Cell Surface Death Receptor in Critical Illness. Crit Care Med. 2022 03 01; 50(3):e284-e293.
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Functional Gly297Ser Variant of the Physiological Dysglycemic Peptide Pancreastatin Is a Novel Risk Factor for Cardiometabolic Disorders. Diabetes. 2022 03 01; 71(3):538-553.
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Cytokine Gene Polymorphisms in Chinese Children with Idiopathic Nephrotic Syndrome. Iran J Immunol. 2022 Mar; 19(1):9.
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Protein prediction for trait mapping in diverse populations. PLoS One. 2022; 17(2):e0264341.
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Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics. 2022 Feb 19; 23(1):148.