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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1994 | 1 | 3 | 4 |
1995 | 0 | 3 | 3 |
1996 | 0 | 1 | 1 |
1997 | 2 | 3 | 5 |
1998 | 1 | 5 | 6 |
1999 | 4 | 5 | 9 |
2000 | 7 | 8 | 15 |
2001 | 9 | 13 | 22 |
2002 | 8 | 20 | 28 |
2003 | 10 | 20 | 30 |
2004 | 20 | 22 | 42 |
2005 | 21 | 27 | 48 |
2006 | 24 | 31 | 55 |
2007 | 25 | 34 | 59 |
2008 | 42 | 41 | 83 |
2009 | 26 | 28 | 54 |
2010 | 39 | 45 | 84 |
2011 | 35 | 53 | 88 |
2012 | 42 | 60 | 102 |
2013 | 26 | 36 | 62 |
2014 | 33 | 51 | 84 |
2015 | 21 | 46 | 67 |
2016 | 28 | 46 | 74 |
2017 | 31 | 58 | 89 |
2018 | 45 | 46 | 91 |
2019 | 37 | 50 | 87 |
2020 | 28 | 37 | 65 |
2021 | 25 | 52 | 77 |
2022 | 7 | 33 | 40 |
2023 | 4 | 26 | 30 |
2024 | 17 | 20 | 37 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Germline CDH1 Variants and Lifetime Cancer Risk. JAMA. 2024 Sep 03; 332(9):722-729.
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency. Nat Genet. 2024 Sep; 56(9):1804-1810.
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No evidence that ACE2 or TMPRSS2 drive population disparity in COVID risks. BMC Med. 2024 Aug 26; 22(1):337.
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Genetics and Genomics of Pulmonary Fibrosis: Charting the Molecular Landscape and Shaping Precision Medicine. Am J Respir Crit Care Med. 2024 Aug 15; 210(4):401-423.
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Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer. Cancer Res. 2024 Aug 01; 84(15):2533-2548.
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An integrative multi-context Mendelian randomization method for identifying risk genes across human tissues. Am J Hum Genet. 2024 Aug 08; 111(8):1736-1749.
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Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease. Nat Commun. 2024 Jul 09; 15(1):5748.
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Evaluation of the genetic basis of familial-associated early-onset hematologic cancers in an ancestral/ethnically diverse population. Haematologica. 2024 07 01; 109(7):2085-2091.
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Multi-tissue transcriptome-wide association studies identified 235 genes for intrinsic subtypes of breast cancer. J Natl Cancer Inst. 2024 Jul 01; 116(7):1105-1115.
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Association of ESR1 Germline Variants with TP53 Somatic Variants in Breast Tumors in a Genome-wide Study. Cancer Res Commun. 2024 Jun 27; 4(6):1597-1608.