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,
click here.
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 | 284 | 489 |
2011 | 197 | 353 | 550 |
2012 | 175 | 340 | 515 |
2013 | 172 | 328 | 500 |
2014 | 175 | 325 | 500 |
2015 | 189 | 325 | 514 |
2016 | 139 | 327 | 466 |
2017 | 116 | 278 | 394 |
2018 | 113 | 269 | 382 |
2019 | 112 | 254 | 366 |
2020 | 80 | 214 | 294 |
2021 | 60 | 187 | 247 |
2022 | 24 | 161 | 185 |
2023 | 7 | 142 | 149 |
2024 | 1 | 25 | 26 |
Below are the most recent publications written about "Polymorphism, Single Nucleotide" by people in Profiles.
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Ancestry-specific high-risk gene variant profiling unmasks diabetes-associated genes. Hum Mol Genet. 2024 Apr 08; 33(8):655-666.
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Heterogeneous associations between interleukin-6 receptor variants and phenotypes across ancestries and implications for therapy. Sci Rep. 2024 04 05; 14(1):8021.
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A noncoding regulatory variant in IKZF1 increases acute lymphoblastic leukemia risk in Hispanic/Latino children. Cell Genom. 2024 Apr 10; 4(4):100526.
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Lipid levels and risk of acute pancreatitis using bidirectional Mendelian randomization. Sci Rep. 2024 03 15; 14(1):6267.
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Assessing the impact of post-mortem damage and contamination on imputation performance in ancient DNA. Sci Rep. 2024 03 14; 14(1):6227.
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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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Phenome-wide Mendelian randomization analysis reveals multiple health comorbidities of coeliac disease. EBioMedicine. 2024 Mar; 101:105033.
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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.