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 |
|---|
| 1996 | 0 | 2 | 2 |
| 1998 | 1 | 1 | 2 |
| 1999 | 1 | 2 | 3 |
| 2000 | 1 | 1 | 2 |
| 2001 | 2 | 3 | 5 |
| 2002 | 0 | 1 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 2 | 3 | 5 |
| 2005 | 5 | 6 | 11 |
| 2006 | 2 | 4 | 6 |
| 2007 | 8 | 13 | 21 |
| 2008 | 6 | 12 | 18 |
| 2009 | 4 | 9 | 13 |
| 2010 | 6 | 15 | 21 |
| 2011 | 12 | 14 | 26 |
| 2012 | 4 | 10 | 14 |
| 2013 | 8 | 11 | 19 |
| 2014 | 3 | 17 | 20 |
| 2015 | 13 | 13 | 26 |
| 2016 | 3 | 8 | 11 |
| 2017 | 9 | 7 | 16 |
| 2018 | 2 | 6 | 8 |
| 2019 | 7 | 4 | 11 |
| 2020 | 12 | 8 | 20 |
| 2021 | 8 | 6 | 14 |
| 2022 | 2 | 9 | 11 |
| 2023 | 0 | 7 | 7 |
| 2024 | 1 | 2 | 3 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Population-Level Identification of Patients With Lynch Syndrome for Clinical Care, Quality Improvement, and Research. JCO Clin Cancer Inform. 2024 Jun; 8:e2300157.
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Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants. JAMA Netw Open. 2024 Apr 01; 7(4):e247421.
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Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature. 2024 Mar; 627(8003):347-357.
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Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study. Public Health Genomics. 2024; 27(1):16-22.
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European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nat Commun. 2023 10 04; 14(1):6172.
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Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. Nat Commun. 2023 10 02; 14(1):6147.
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Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system. Breast Cancer Res Treat. 2023 Oct; 201(3):461-470.
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Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nat Genet. 2023 07; 55(7):1116-1125.
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Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine. HGG Adv. 2023 Jul 13; 4(3):100211.
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MiXcan: a framework for cell-type-aware transcriptome-wide association studies with an application to breast cancer. Nat Commun. 2023 Jan 23; 14(1):377.