"Genetic Testing" 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.
Detection of a MUTATION; GENOTYPE; KARYOTYPE; or specific ALLELES associated with genetic traits, heritable diseases, or predisposition to a disease, or that may lead to the disease in descendants. It includes prenatal genetic testing.
Descriptor ID |
D005820
|
MeSH Number(s) |
E01.370.225.562 E05.200.562 E05.393.435 N02.421.308.430 N02.421.726.233.221
|
Concept/Terms |
Testing, Genetic Predisposition- Testing, Genetic Predisposition
- Predisposition Testing, Genetic
- Predictive Testing, Genetic
- Genetic Predictive Testing
- Testing, Genetic Predictive
- Predictive Genetic Testing
- Genetic Testing, Predictive
- Testing, Predictive Genetic
- Genetic Predisposition Testing
Genetic Screening- Genetic Screening
- Genetic Screenings
- Screening, Genetic
- Screenings, Genetic
|
Below are MeSH descriptors whose meaning is more general than "Genetic Testing".
Below are MeSH descriptors whose meaning is more specific than "Genetic Testing".
This graph shows the total number of publications written about "Genetic Testing" by people in this website by year, and whether "Genetic Testing" 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 | 2 | 3 | 5 |
1995 | 3 | 2 | 5 |
1996 | 3 | 4 | 7 |
1997 | 7 | 7 | 14 |
1998 | 3 | 7 | 10 |
1999 | 5 | 3 | 8 |
2000 | 7 | 9 | 16 |
2001 | 8 | 6 | 14 |
2002 | 7 | 11 | 18 |
2003 | 3 | 14 | 17 |
2004 | 4 | 4 | 8 |
2005 | 13 | 14 | 27 |
2006 | 14 | 12 | 26 |
2007 | 9 | 14 | 23 |
2008 | 8 | 8 | 16 |
2009 | 7 | 10 | 17 |
2010 | 15 | 14 | 29 |
2011 | 10 | 20 | 30 |
2012 | 13 | 13 | 26 |
2013 | 17 | 21 | 38 |
2014 | 22 | 18 | 40 |
2015 | 20 | 22 | 42 |
2016 | 23 | 21 | 44 |
2017 | 27 | 27 | 54 |
2018 | 33 | 25 | 58 |
2019 | 28 | 39 | 67 |
2020 | 24 | 28 | 52 |
2021 | 13 | 38 | 51 |
2022 | 10 | 29 | 39 |
2023 | 9 | 16 | 25 |
2024 | 26 | 24 | 50 |
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Below are the most recent publications written about "Genetic Testing" by people in Profiles.
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Pediatric Cancer Screening in Hereditary Gastrointestinal Cancer Risk Syndromes: An Update from the AACR Childhood Cancer Predisposition Working Group. Clin Cancer Res. 2024 Oct 15; 30(20):4566-4571.
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The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants. Am J Hum Genet. 2024 Oct 03; 111(10):2094-2106.
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Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance. Clin Cancer Res. 2024 Sep 13; 30(18):3983-3989.
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Hereditary hemorrhagic telangiectasia - pediatric review. Curr Opin Pediatr. 2024 Dec 01; 36(6):592-598.
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Developing a scoring system for gene curation prioritization in lysosomal diseases. Mol Genet Metab. 2024 Sep-Oct; 143(1-2):108572.
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Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions. Prenat Diagn. 2024 Oct; 44(11):1296-1303.
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BRCA-mutated breast cancer: the unmet need, challenges and therapeutic benefits of genetic testing. Br J Cancer. 2024 Nov; 131(9):1400-1414.
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Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy. J Peripher Nerv Syst. 2024 Sep; 29(3):363-367.
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Measuring perceived utility of genomic sequencing: Development and validation of the GENEtic Utility (GENE-U) scale for adult screening. Genet Med. 2024 Nov; 26(11):101240.
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Diagnostic utility of DNA methylation analysis in genetically unsolved pediatric epilepsies and CHD2 episignature refinement. Nat Commun. 2024 Aug 06; 15(1):6524.