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 |
|---|
| 2001 | 1 | 1 | 2 |
| 2002 | 0 | 4 | 4 |
| 2003 | 2 | 5 | 7 |
| 2004 | 1 | 2 | 3 |
| 2005 | 3 | 3 | 6 |
| 2006 | 2 | 0 | 2 |
| 2007 | 1 | 6 | 7 |
| 2008 | 7 | 3 | 10 |
| 2009 | 3 | 6 | 9 |
| 2010 | 2 | 10 | 12 |
| 2011 | 4 | 16 | 20 |
| 2012 | 5 | 6 | 11 |
| 2013 | 6 | 7 | 13 |
| 2014 | 4 | 3 | 7 |
| 2015 | 3 | 3 | 6 |
| 2016 | 4 | 4 | 8 |
| 2017 | 6 | 12 | 18 |
| 2018 | 6 | 9 | 15 |
| 2019 | 4 | 4 | 8 |
| 2020 | 1 | 1 | 2 |
| 2021 | 4 | 6 | 10 |
| 2022 | 0 | 5 | 5 |
| 2023 | 1 | 2 | 3 |
| 2024 | 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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Inositol 1,4,5-Trisphosphate Receptor 1 Gain-of-Function Increases the Risk for Cardiac Arrhythmias in Mice and Humans. Circulation. 2025 Mar 25; 151(12):847-862.
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The molecular genetic landscape of human brain size variation. Cell Rep. 2023 Nov 28; 42(11):113439.
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Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study. Lancet Neurol. 2023 11; 22(11):1015-1025.
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Screening Practices for Breast and Nonbreast Cancers in High-Risk Mutation Carriers. J Surg Res. 2023 11; 291:388-395.
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Impact of the 2018 ACR Supplemental Screening Recommendations on MRI Eligibility in Breast Cancer Survivors. J Am Coll Radiol. 2023 01; 20(1):71-78.
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CCR5-?32 polymorphism-a possible protective factor from gait impairment amongst post-stroke patients. Eur J Neurol. 2023 03; 30(3):692-701.
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The Caribbean-Hispanic Alzheimer's disease brain transcriptome reveals ancestry-specific disease mechanisms. Neurobiol Dis. 2023 01; 176:105938.
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Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease. Brain. 2022 07 29; 145(7):2541-2554.
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Adherence to MIND Diet, Genetic Susceptibility, and Incident Dementia in Three US Cohorts. Nutrients. 2022 Jul 03; 14(13).
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Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants. PLoS Genet. 2021 11; 17(11):e1009918.