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 | 19 | 27 |
2003 | 10 | 20 | 30 |
2004 | 21 | 22 | 43 |
2005 | 21 | 27 | 48 |
2006 | 24 | 32 | 56 |
2007 | 24 | 34 | 58 |
2008 | 42 | 42 | 84 |
2009 | 26 | 27 | 53 |
2010 | 39 | 44 | 83 |
2011 | 34 | 52 | 86 |
2012 | 42 | 60 | 102 |
2013 | 26 | 36 | 62 |
2014 | 32 | 50 | 82 |
2015 | 20 | 45 | 65 |
2016 | 28 | 42 | 70 |
2017 | 30 | 57 | 87 |
2018 | 45 | 45 | 90 |
2019 | 35 | 50 | 85 |
2020 | 25 | 37 | 62 |
2021 | 25 | 51 | 76 |
2022 | 5 | 32 | 37 |
2023 | 1 | 21 | 22 |
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Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
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Sex and Gene Influence Arrhythmia Susceptibility in Murine Models of Calmodulinopathy. Circ Arrhythm Electrophysiol. 2023 Sep; 16(9):e010891.
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Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C. Cancer Res. 2023 08 01; 83(15):2557-2571.
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Retrospective Cohort Study on the Limitations of Direct-to-Consumer Genetic Screening in Hereditary Breast and Ovarian Cancer. JCO Precis Oncol. 2023 08; 7:e2200695.
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Germline Variants Incidentally Detected via Tumor-Only Genomic Profiling of Patients With Mesothelioma. JAMA Netw Open. 2023 08 01; 6(8):e2327351.
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Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival. Cancer Med. 2023 08; 12(15):16142-16162.
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Clinical guideline variability in the diagnosis of hereditary hematopoietic malignancy syndromes. Leuk Lymphoma. 2023 Sep; 64(9):1562-1565.
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Rare penetrant mutations confer severe risk of common diseases. Science. 2023 06 02; 380(6648):eabo1131.
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Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups. Nat Commun. 2023 06 02; 14(1):3202.
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A joint transcriptome-wide association study across multiple tissues identifies candidate breast cancer susceptibility genes. Am J Hum Genet. 2023 06 01; 110(6):950-962.
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Physical Activity and Insulin Sensitivity Independently Attenuate the Effect of FTO rs9939609 on Obesity. Diabetes Care. 2023 05 01; 46(5):985-992.