"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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 3 | 10 | 13 |
| 2013 | 5 | 9 | 14 |
| 2014 | 1 | 8 | 9 |
| 2015 | 5 | 11 | 16 |
| 2016 | 6 | 9 | 15 |
| 2017 | 4 | 3 | 7 |
| 2018 | 1 | 9 | 10 |
| 2019 | 1 | 3 | 4 |
| 2020 | 0 | 2 | 2 |
| 2021 | 1 | 3 | 4 |
| 2022 | 2 | 1 | 3 |
| 2023 | 1 | 1 | 2 |
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Below are the most recent publications written about "Exome" by people in Profiles.
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Gene-based burden scores identify rare variant associations for 28 blood biomarkers. BMC Genom Data. 2023 09 04; 24(1):50.
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Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation. Biomolecules. 2023 07 13; 13(7).
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Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. PLoS Genet. 2022 11; 18(11):e1010367.
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Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank. BMC Med Genomics. 2022 05 21; 15(1):119.
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A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies. Prenat Diagn. 2022 06; 42(7):901-910.
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Distinct gene-set burden patterns underlie common generalized and focal epilepsies. EBioMedicine. 2021 Oct; 72:103588.
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Homozygous nonsense mutation of WNT10B gene in a Moroccan family with split-hand foot malformation identified by exome sequencing: a case report. Pan Afr Med J. 2021; 39:21.
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Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. J Gerontol A Biol Sci Med Sci. 2021 04 30; 76(5):786-795.
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Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clin Genet. 2021 07; 100(1):59-78.
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QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrum. Clin Genet. 2021 01; 99(1):199-207.
MeSH information
