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 | 44 | 83 |
2011 | 35 | 53 | 88 |
2012 | 42 | 60 | 102 |
2013 | 26 | 35 | 61 |
2014 | 33 | 51 | 84 |
2015 | 21 | 46 | 67 |
2016 | 28 | 45 | 73 |
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 | 24 | 26 | 50 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Update on Recommendations for Cancer Screening and Surveillance in Children with Genomic Instability Disorders. Clin Cancer Res. 2024 Nov 15; 30(22):5009-5020.
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Gene-based burden tests of rare germline variants identify six cancer susceptibility genes. Nat Genet. 2024 Nov; 56(11):2422-2433.
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Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition. Blood. 2024 10 24; 144(17):1765-1780.
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A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations. PLoS Genet. 2024 Oct; 20(10):e1011322.
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The Black and African American Connections to Parkinson's Disease (BLAAC PD) study protocol. BMC Neurol. 2024 Oct 21; 24(1):403.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Cross-ancestry analysis of brain QTLs enhances interpretation of schizophrenia genome-wide association studies. Am J Hum Genet. 2024 Nov 07; 111(11):2444-2457.
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Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy. Clin Cancer Res. 2024 Oct 01; 30(19):4286-4295.
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Comprehensive investigation of long non-coding RNA HOTAIR polymorphisms and cancer risk: a current meta-analysis encompassing 96,458 participants. Sci Rep. 2024 09 30; 14(1):22670.
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Sequence variants influencing the regulation of serum IgG subclass levels. Nat Commun. 2024 Sep 14; 15(1):8054.