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.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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1999 | 1 | 1 | 2 |
2000 | 7 | 7 | 14 |
2001 | 16 | 12 | 28 |
2002 | 27 | 18 | 45 |
2003 | 28 | 24 | 52 |
2004 | 39 | 41 | 80 |
2005 | 46 | 73 | 119 |
2006 | 78 | 105 | 183 |
2007 | 113 | 149 | 262 |
2008 | 179 | 217 | 396 |
2009 | 190 | 237 | 427 |
2010 | 205 | 283 | 488 |
2011 | 197 | 354 | 551 |
2012 | 174 | 340 | 514 |
2013 | 172 | 326 | 498 |
2014 | 175 | 324 | 499 |
2015 | 189 | 326 | 515 |
2016 | 137 | 328 | 465 |
2017 | 116 | 279 | 395 |
2018 | 114 | 271 | 385 |
2019 | 111 | 257 | 368 |
2020 | 79 | 213 | 292 |
2021 | 61 | 183 | 244 |
2022 | 24 | 158 | 182 |
2023 | 7 | 137 | 144 |
2024 | 1 | 19 | 20 |
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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An immunogenetic basis for lung cancer risk. Science. 2024 Feb 23; 383(6685):eadi3808.
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HDL levels modulate the impact of type 2 diabetes susceptibility alleles in older adults. Lipids Health Dis. 2024 Feb 22; 23(1):56.
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Genetic investigation into the broad health implications of caffeine: evidence from phenome-wide, proteome-wide and metabolome-wide Mendelian randomization. BMC Med. 2024 Feb 20; 22(1):81.
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The genetic basis of autoimmunity seen through the lens of T cell functional traits. Nat Commun. 2024 Feb 08; 15(1):1204.
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Birth weight influences cardiac structure, function, and disease risk: evidence of a causal association. Eur Heart J. 2024 Feb 07; 45(6):443-454.
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Convergence of coronary artery disease genes onto endothelial cell programs. Nature. 2024 Feb; 626(8000):799-807.
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Novel functional insights into ischemic stroke biology provided by the first genome-wide association study of stroke in indigenous Africans. Genome Med. 2024 Feb 05; 16(1):25.
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Biological basis of extensive pleiotropy between blood traits and cancer risk. Genome Med. 2024 Feb 02; 16(1):21.
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Cell-type deconvolution of bulk-blood RNA-seq reveals biological insights into neuropsychiatric disorders. Am J Hum Genet. 2024 Feb 01; 111(2):323-337.
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Genetic architecture of alcohol consumption identified by a genotype-stratified GWAS and impact on esophageal cancer risk in Japanese people. Sci Adv. 2024 Jan 26; 10(4):eade2780.