"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 | 6 | 3 | 9 |
| 2012 | 9 | 14 | 23 |
| 2013 | 14 | 20 | 34 |
| 2014 | 17 | 25 | 42 |
| 2015 | 19 | 36 | 55 |
| 2016 | 28 | 59 | 87 |
| 2017 | 13 | 31 | 44 |
| 2018 | 9 | 31 | 40 |
| 2019 | 7 | 24 | 31 |
| 2020 | 5 | 12 | 17 |
| 2021 | 10 | 9 | 19 |
| 2022 | 10 | 12 | 22 |
| 2023 | 5 | 8 | 13 |
| 2024 | 2 | 7 | 9 |
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Below are the most recent publications written about "Exome" by people in Profiles.
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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 Oct 03; 111(10):2219-2231.
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Comparing the Diagnostic Yield of Germline Exome Versus Panel Sequencing in the Diverse Population of the Texas KidsCanSeq Pediatric Cancer Study. JCO Precis Oncol. 2024 Sep; 8:e2400187.
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Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study. Birth Defects Res. 2024 Jul; 116(7):e2384.
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Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. Genet Med. 2024 Oct; 26(10):101199.
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Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension. JCI Insight. 2024 May 08; 9(9).
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Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic-ischemic encephalopathy: A retrospective analysis. Clin Genet. 2024 Jul; 106(1):95-101.
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Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis. Genet Med. 2024 06; 26(6):101115.
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
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Genetic architecture and biology of youth-onset type 2 diabetes. Nat Metab. 2024 Feb; 6(2):226-237.
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Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child? Genet Med. 2024 02; 26(2):101033.