"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 |
|---|
| 2011 | 4 | 3 | 7 |
| 2012 | 5 | 9 | 14 |
| 2013 | 12 | 12 | 24 |
| 2014 | 14 | 21 | 35 |
| 2015 | 17 | 32 | 49 |
| 2016 | 25 | 44 | 69 |
| 2017 | 13 | 23 | 36 |
| 2018 | 9 | 25 | 34 |
| 2019 | 6 | 21 | 27 |
| 2020 | 6 | 6 | 12 |
| 2021 | 8 | 9 | 17 |
| 2022 | 9 | 11 | 20 |
| 2023 | 5 | 6 | 11 |
| 2024 | 3 | 8 | 11 |
| 2025 | 1 | 6 | 7 |
| 2026 | 1 | 0 | 1 |
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Below are the most recent publications written about "Exome" by people in Profiles.
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Non-Isolated Dandy-Walker Malformation: Exome Sequencing Efficacy and Phenotypic Expansions. Clin Genet. 2026 Jun; 109(6):1029-1037.
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Meta-evolutionary exome analysis identifies novel type 2 diabetes mellitus genes in the UK Biobank and all of us. PLoS Genet. 2025 Sep; 21(9):e1011889.
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De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder. Am J Med Genet A. 2026 01; 200(1):244-252.
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Non-isolated tetralogy of fallot (TOF+): exome sequencing efficacy and phenotypic expansions. Eur J Hum Genet. 2026 Mar; 34(3):333-339.
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Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach. Am J Hum Genet. 2025 07 03; 112(7):1664-1680.
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Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study. Birth Defects Res. 2025 May; 117(5):e2472.
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Diverse ancestral representation improves genetic intolerance metrics. Nat Commun. 2025 Mar 18; 16(1):2648.
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A meta-analysis of diagnostic yield and clinical utility of genome and exome sequencing in pediatric rare and undiagnosed genetic diseases. Genet Med. 2025 Jun; 27(6):101398.
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The "genetic test request": A genomic stewardship intervention for inpatient exome and genome orders at a tertiary pediatric hospital. Genet Med. 2025 Feb; 27(2):101330.
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Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications. Am J Hum Genet. 2024 10 03; 111(10):2219-2231.