"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 |
|---|
| 2000 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 2 | 2 | 4 |
| 2007 | 2 | 5 | 7 |
| 2008 | 8 | 7 | 15 |
| 2009 | 14 | 8 | 22 |
| 2010 | 16 | 8 | 24 |
| 2011 | 13 | 6 | 19 |
| 2012 | 14 | 20 | 34 |
| 2013 | 18 | 12 | 30 |
| 2014 | 8 | 14 | 22 |
| 2015 | 22 | 11 | 33 |
| 2016 | 15 | 15 | 30 |
| 2017 | 18 | 21 | 39 |
| 2018 | 17 | 18 | 35 |
| 2019 | 18 | 14 | 32 |
| 2020 | 9 | 15 | 24 |
| 2021 | 12 | 19 | 31 |
| 2022 | 2 | 19 | 21 |
| 2023 | 3 | 6 | 9 |
To return to the timeline,
click here.
Below are the most recent publications written about "Genetic Predisposition to Disease" by people in Profiles.
-
Gene-based burden scores identify rare variant associations for 28 blood biomarkers. BMC Genom Data. 2023 09 04; 24(1):50.
-
Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients. Eur J Hum Genet. 2023 10; 31(10):1139-1146.
-
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.
-
A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children. Genet Med. 2023 08; 25(8):100875.
-
A TMC8 splice variant causes epidermodysplasia verruciformis in a Pakistani family. Clin Exp Dermatol. 2023 03 22; 48(4):434-437.
-
A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies. Brain. 2023 03 01; 146(3):977-990.
-
Functional damaging germline variants in ETV6, IKZF1, PAX5 and RUNX1 predisposing to B-cell precursor acute lymphoblastic leukemia. Eur J Med Genet. 2023 Apr; 66(4):104725.
-
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome Med. 2023 01 26; 15(1):7.
-
Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Schizophr Res. 2023 02; 252:161-171.
-
The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients. Int J Cancer. 2023 04 01; 152(7):1388-1398.
MeSH information
