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 | 6 | 10 |
| 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 | 15 | 30 |
| 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 |
| 2024 | 1 | 4 | 5 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Contribution of circulating Mfge8 to human T2DM and cardiovascular disease. Gene. 2024 Nov 15; 927:148712.
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Bridging the Divide: From Universal Germline Testing Guidance to Real-World Implementation in Pancreatic Cancer Care. JCO Oncol Pract. 2024 Aug; 20(8):1012-1015.
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Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions. Nat Genet. 2024 May; 56(5):809-818.
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Genetic variant rs1205 is associated with COVID-19 outcomes: The Strong Heart Study and Strong Heart Family Study. PLoS One. 2024; 19(4):e0302464.
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The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner. Front Immunol. 2024; 15:1349601.
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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.