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 |
| 1996 | 0 | 1 | 1 |
| 1998 | 1 | 1 | 2 |
| 1999 | 2 | 1 | 3 |
| 2000 | 4 | 3 | 7 |
| 2001 | 5 | 4 | 9 |
| 2002 | 4 | 5 | 9 |
| 2003 | 1 | 5 | 6 |
| 2004 | 4 | 5 | 9 |
| 2005 | 5 | 4 | 9 |
| 2006 | 2 | 10 | 12 |
| 2007 | 9 | 4 | 13 |
| 2008 | 5 | 13 | 18 |
| 2009 | 15 | 14 | 29 |
| 2010 | 9 | 11 | 20 |
| 2011 | 15 | 14 | 29 |
| 2012 | 12 | 12 | 24 |
| 2013 | 11 | 19 | 30 |
| 2014 | 14 | 21 | 35 |
| 2015 | 11 | 11 | 22 |
| 2016 | 7 | 20 | 27 |
| 2017 | 7 | 16 | 23 |
| 2018 | 6 | 10 | 16 |
| 2019 | 9 | 9 | 18 |
| 2020 | 8 | 3 | 11 |
| 2021 | 6 | 6 | 12 |
| 2022 | 0 | 8 | 8 |
| 2023 | 1 | 1 | 2 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Multiple Correspondence Analysis and HLA-Associations of Organ Involvement in a Large Cohort of African-American and European-American Patients with Sarcoidosis. Lung. 2023 06; 201(3):297-302.
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Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. PLoS One. 2023; 18(1):e0276700.
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Rare germline deleterious variants increase susceptibility for lung cancer. Hum Mol Genet. 2022 Oct 10; 31(20):3558-3565.
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Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies. Ann Rheum Dis. 2023 Feb; 82(2):235-245.
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Defining novel causal SNPs and linked phenotypes at melanoma-associated loci. Hum Mol Genet. 2022 08 25; 31(17):2845-2856.
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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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Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells. Nat Commun. 2022 07 27; 13(1):4287.
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Novel HLA associations with outcomes of Mycobacterium tuberculosis exposure and sarcoidosis in individuals of African ancestry using nearest-neighbor feature selection. Genet Epidemiol. 2022 10; 46(7):463-474.
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Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1. Hum Mol Genet. 2022 03 21; 31(6):863-874.
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Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms with Coronary Artery Disease in North Indian Punjabi Population. Biochem Genet. 2022 Dec; 60(6):2120-2136.