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 |
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1995 | 0 | 5 | 5 |
1996 | 0 | 4 | 4 |
1997 | 1 | 8 | 9 |
1998 | 1 | 4 | 5 |
1999 | 9 | 8 | 17 |
2000 | 9 | 13 | 22 |
2001 | 11 | 24 | 35 |
2002 | 18 | 22 | 40 |
2003 | 18 | 28 | 46 |
2004 | 21 | 24 | 45 |
2005 | 19 | 27 | 46 |
2006 | 17 | 41 | 58 |
2007 | 28 | 49 | 77 |
2008 | 32 | 50 | 82 |
2009 | 27 | 53 | 80 |
2010 | 44 | 50 | 94 |
2011 | 38 | 51 | 89 |
2012 | 41 | 68 | 109 |
2013 | 45 | 59 | 104 |
2014 | 33 | 51 | 84 |
2015 | 43 | 72 | 115 |
2016 | 40 | 61 | 101 |
2017 | 43 | 80 | 123 |
2018 | 41 | 73 | 114 |
2019 | 59 | 70 | 129 |
2020 | 45 | 48 | 93 |
2021 | 28 | 56 | 84 |
2022 | 11 | 35 | 46 |
2023 | 5 | 21 | 26 |
2024 | 26 | 49 | 75 |
2025 | 6 | 5 | 11 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Genetic Associations With C-peptide Levels Before Type 1 Diabetes Diagnosis in At-risk Relatives. J Clin Endocrinol Metab. 2025 Mar 17; 110(4):e1046-e1050.
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Molecular Testing for the World Health Organization Classification of Central Nervous System Tumors: A Review. JAMA Oncol. 2025 Mar 01; 11(3):317-328.
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Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes. Am J Hum Genet. 2025 Mar 06; 112(3):693-708.
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Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases. Nat Commun. 2025 Feb 19; 16(1):1779.
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Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants. J Am Heart Assoc. 2025 Feb 18; 14(4):e036499.
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Long-read sequencing of 945 Han individuals identifies structural variants associated with phenotypic diversity and disease susceptibility. Nat Commun. 2025 Feb 10; 16(1):1494.
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Type 1 Diabetes Genetic Risk Scores: History, Application and Future Directions. Curr Diab Rep. 2025 Feb 08; 25(1):22.
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Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene Poll. Invest Ophthalmol Vis Sci. 2025 Feb 03; 66(2):12.
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Polygenic Score for Clinicopathologic Features and Survival Outcomes in Papillary Thyroid Carcinoma. JAMA Otolaryngol Head Neck Surg. 2025 Feb 01; 151(2):113-120.
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Aortic and arterial manifestations and clinical features in TGFB3-related heritable thoracic aortic disease: results from the Montalcino Aortic Consortium. J Med Genet. 2025 Jan 27; 62(2):82-88.