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 | 19 | 28 | 47 |
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 | 69 | 110 |
2013 | 45 | 58 | 103 |
2014 | 33 | 51 | 84 |
2015 | 43 | 72 | 115 |
2016 | 40 | 63 | 103 |
2017 | 43 | 80 | 123 |
2018 | 41 | 73 | 114 |
2019 | 59 | 69 | 128 |
2020 | 45 | 48 | 93 |
2021 | 27 | 56 | 83 |
2022 | 11 | 35 | 46 |
2023 | 5 | 20 | 25 |
2024 | 27 | 49 | 76 |
2025 | 18 | 18 | 36 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Genome-Wide Association Studies of Down Syndrome Associated Congenital Heart Defects Suggests a Genetically Heterogeneous Risk for CHD in DS. Genet Epidemiol. 2025 Jun; 49(4):e70010.
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Targeted analysis of dyslexia-associated regions on chromosomes 6, 12 and 15 in large multigenerational cohorts. PLoS One. 2025; 20(5):e0324006.
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Global DNA methylation differences involving germline structural variation impact gene expression in pediatric brain tumors. Nat Commun. 2025 May 21; 16(1):4713.
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Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome. Clin Cancer Res. 2025 May 15; 31(10):1831-1840.
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Genetic, Transcriptomic, and Epigenomic Insights into Sj?gren's Disease: An Integrative Network Investigation and Immune Diseases Comparison. Int J Mol Sci. 2025 May 13; 26(10).
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Human genetic variation determines 24-hour rhythmic gene expression and disease risk. Nat Commun. 2025 May 08; 16(1):4270.
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Update on Retinoblastoma Predisposition and Surveillance Recommendations for Children. Clin Cancer Res. 2025 May 01; 31(9):1573-1579.
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Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study. Birth Defects Res. 2025 May; 117(5):e2472.
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Uncovering shared genetic features between inflammatory bowel disease and systemic lupus erythematosus. Sci Rep. 2025 May 01; 15(1):15309.
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Update on Cancer and Central Nervous System Tumor Surveillance in Pediatric NF2-, SMARCB1-, and LZTR1-Related Schwannomatosis. Clin Cancer Res. 2025 Apr 14; 31(8):1400-1406.