"Exome" 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.
That part of the genome that corresponds to the complete complement of EXONS of an organism or cell.
| Descriptor ID |
D059472
|
| MeSH Number(s) |
G05.360.340.011
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Exome".
Below are MeSH descriptors whose meaning is more specific than "Exome".
This graph shows the total number of publications written about "Exome" by people in this website by year, and whether "Exome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2014 | 2 | 0 | 2 |
| 2016 | 3 | 1 | 4 |
| 2017 | 15 | 30 | 45 |
| 2018 | 11 | 15 | 26 |
| 2019 | 2 | 4 | 6 |
| 2020 | 0 | 1 | 1 |
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Exome" by people in Profiles.
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Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. Am J Hum Genet. 2021 07 01; 108(7):1350-1355.
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ACE2 polymorphisms as potential players in COVID-19 outcome. PLoS One. 2020; 15(12):e0243887.
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Factors related to asymptomatic or severe COVID-19 infection. Med Hypotheses. 2020 Nov; 144:110296.
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COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells. Genes (Basel). 2020 08 27; 11(9).
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Whole exome sequencing for personalized hepatology: Expanding applications in adults and challenges. J Hepatol. 2019 10; 71(4):849-850.
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Diagnostic Yield of an Algorithm for Neonatal and Infantile Cholestasis Integrating Next-Generation Sequencing. J Pediatr. 2019 08; 211:54-62.e4.
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Diagnostic Utility of Exome Sequencing for Kidney Disease. N Engl J Med. 2019 05 23; 380(21):2078.
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Germline BMP9 mutation causes idiopathic pulmonary arterial hypertension. Eur Respir J. 2019 03; 53(3).
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Exome sequencing for chronic kidney disease diagnosis. Nat Med. 2019 02; 25(2):197.
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Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a three-generation family with endometriosis. Mol Med Rep. 2019 Mar; 19(3):1716-1720.