Genetic Predisposition to Disease
"Genetic Predisposition to Disease" 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.
A latent susceptibility to disease at the genetic level, which may be activated under certain conditions.
| Descriptor ID |
D020022
|
| MeSH Number(s) |
C23.550.291.687.500 G05.380.355
|
| Concept/Terms |
Genetic Predisposition to Disease- Genetic Predisposition to Disease
- Genetic Susceptibility
- Genetic Susceptibilities
- Susceptibilities, Genetic
- Susceptibility, Genetic
- Genetic Predisposition
- Genetic Predispositions
- Predispositions, Genetic
- Predisposition, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Genetic Predisposition to Disease".
Below are MeSH descriptors whose meaning is more specific than "Genetic Predisposition to Disease".
This graph shows the total number of publications written about "Genetic Predisposition to Disease" by people in this website by year, and whether "Genetic Predisposition to Disease" 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 |
|---|
| 1995 | 0 | 1 | 1 |
| 1997 | 1 | 2 | 3 |
| 1998 | 1 | 2 | 3 |
| 1999 | 4 | 5 | 9 |
| 2000 | 2 | 4 | 6 |
| 2001 | 1 | 4 | 5 |
| 2002 | 3 | 2 | 5 |
| 2003 | 7 | 11 | 18 |
| 2004 | 13 | 13 | 26 |
| 2005 | 8 | 11 | 19 |
| 2006 | 6 | 14 | 20 |
| 2007 | 4 | 21 | 25 |
| 2008 | 12 | 25 | 37 |
| 2009 | 14 | 22 | 36 |
| 2010 | 17 | 29 | 46 |
| 2011 | 26 | 26 | 52 |
| 2012 | 18 | 30 | 48 |
| 2013 | 21 | 26 | 47 |
| 2014 | 14 | 23 | 37 |
| 2015 | 13 | 22 | 35 |
| 2016 | 7 | 20 | 27 |
| 2017 | 10 | 21 | 31 |
| 2018 | 7 | 12 | 19 |
| 2019 | 5 | 19 | 24 |
| 2020 | 2 | 7 | 9 |
| 2021 | 5 | 8 | 13 |
| 2022 | 0 | 5 | 5 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Implementation Mapping for Managing Patients at High Risk for Hereditary Cancer. Am J Prev Med. 2024 Mar; 66(3):503-515.
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Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Nat Genet. 2023 01; 55(1):89-99.
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Rare copy number variation in posttraumatic stress disorder. Mol Psychiatry. 2022 12; 27(12):5062-5069.
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Heritable cancer predisposition testing in pediatric cancer patients excluding retinoblastoma in a middle-income country. Pediatr Blood Cancer. 2022 11; 69(11):e29982.
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Loss-of-function variants in SAT1 cause X-linked childhood-onset systemic lupus erythematosus. Ann Rheum Dis. 2022 Dec; 81(12):1712-1721.
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Polymorphism rs3742330 in microRNA Biogenesis Gene DICER1 Is Associated with Pseudoexfoliation Glaucoma in Saudi Cohort. Genes (Basel). 2022 03 10; 13(3).
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Vancomycin-induced drug reactions with eosinophilia and systemic symptoms syndrome in a patient with positive family history. Dermatol Online J. 2021 Nov 15; 27(11).
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Targeted Therapy for BRAF Mutant Brain Tumors. Curr Treat Options Oncol. 2021 10 06; 22(11):105.
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Pain Experience in Pancreatitis: Strong Association of Genetic Risk Loci for Anxiety and PTSD in Patients With Severe, Constant, and Constant-Severe Pain. Am J Gastroenterol. 2021 10 01; 116(10):2128-2136.
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Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants. Circulation. 2021 11 16; 144(20):1600-1611.