"Age of Onset" 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.
The age, developmental stage, or period of life at which a disease or the initial symptoms or manifestations of a disease appear in an individual.
| Descriptor ID |
D017668
|
| MeSH Number(s) |
N05.715.350.075.100 N06.850.490.250.100
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Age of Onset".
Below are MeSH descriptors whose meaning is more specific than "Age of Onset".
This graph shows the total number of publications written about "Age of Onset" by people in this website by year, and whether "Age of Onset" 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 |
|---|
| 2000 | 0 | 1 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 0 | 3 | 3 |
| 2009 | 0 | 1 | 1 |
| 2011 | 0 | 2 | 2 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 2 | 2 |
| 2014 | 1 | 4 | 5 |
| 2015 | 0 | 3 | 3 |
| 2016 | 0 | 1 | 1 |
| 2017 | 0 | 3 | 3 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 7 | 7 |
| 2020 | 0 | 2 | 2 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Age of Onset" by people in Profiles.
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Nat Commun. 2021 06 07; 12(1):3417.
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The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME. Neurology. 2020 12 15; 95(24):e3163-e3179.
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Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles. Brain. 2020 08 01; 143(8):2406-2420.
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Alzheimer's disease-associated (hydroxy)methylomic changes in the brain and blood. Clin Epigenetics. 2019 11 27; 11(1):164.
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Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women. BMC Cancer. 2019 Aug 08; 19(1):787.
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How I approach hereditary cancer predisposition in a child with cancer. Pediatr Blood Cancer. 2019 11; 66(11):e27916.
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Novel mutations in KMT2B offer pathophysiological insights into childhood-onset progressive dystonia. J Hum Genet. 2019 Aug; 64(8):803-813.
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Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer. Breast Cancer Res. 2019 04 29; 21(1):55.
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Variant PADI3 in Central Centrifugal Cicatricial Alopecia. N Engl J Med. 2019 02 28; 380(9):833-841.
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Association between breast cancer risk factors and molecular type in postmenopausal patients with hormone receptor-positive early breast cancer. Breast Cancer Res Treat. 2019 Apr; 174(2):453-461.
MeSH information
