"Chromosome Aberrations" 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.
Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.
| Descriptor ID |
D002869
|
| MeSH Number(s) |
C23.550.210 G05.365.590.175
|
| Concept/Terms |
Chromosome Aberrations- Chromosome Aberrations
- Aberration, Chromosome
- Aberrations, Chromosome
- Chromosome Aberration
- Abnormalities, Chromosome
- Abnormality, Chromosome
- Chromosome Abnormality
- Cytogenetic Abnormalities
- Abnormalities, Cytogenetic
- Abnormality, Cytogenetic
- Cytogenetic Abnormality
- Chromosome Abnormalities
- Cytogenetic Aberrations
- Aberration, Cytogenetic
- Aberrations, Cytogenetic
- Cytogenetic Aberration
- Abnormalities, Chromosomal
- Abnormality, Chromosomal
- Chromosomal Abnormalities
- Chromosomal Abnormality
- Chromosomal Aberrations
- Aberration, Chromosomal
- Aberrations, Chromosomal
- Chromosomal Aberration
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Aberrations".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Aberrations".
This graph shows the total number of publications written about "Chromosome Aberrations" by people in this website by year, and whether "Chromosome Aberrations" 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 |
|---|
| 2001 | 0 | 1 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 2 | 3 |
| 2016 | 1 | 0 | 1 |
| 2017 | 8 | 8 | 16 |
| 2018 | 7 | 9 | 16 |
| 2019 | 3 | 0 | 3 |
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Below are the most recent publications written about "Chromosome Aberrations" by people in Profiles.
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Evaluation of a genetic risk score for severity of COVID-19 using human chromosomal-scale length variation. Hum Genomics. 2020 10 09; 14(1):36.
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Congenital Heart Disease in Asymptomatic Neonates with Extra-Cardiac Malformations and Genetic Disorders Balkan Med J. 2019 10 28; 36(6):366-366.
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A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature. J Matern Fetal Neonatal Med. 2021 Sep; 34(17):2918-2922.
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Long-term Prognostic Impact of Chromosome Abnormalities in Clear Cell Renal Cell Carcinoma. Anticancer Res. 2019 Jun; 39(6):2757-2765.
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Genomic changes of chromosomes 8p23.1 and 1q21: Novel mutations in malignant mesothelioma. Lung Cancer. 2018 12; 126:106-111.
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Prognostic factors for multiple myeloma in the era of novel therapies. Expert Rev Hematol. 2018 11; 11(11):863-879.
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Staphylococcus aureus Bacteremia in Children Aged 5-18 Years-Risk Factors in the New Millennium. J Pediatr. 2018 12; 203:108-115.e3.
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Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events. Leuk Res. 2018 10; 73:86-94.
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Challenges in Diagnosing Myelodysplastic Syndromes in the Era of Genetic Testing: Proceedings of the 13th Workshop of the European Bone Marrow Working Group. Pathobiology. 2019; 86(1):62-75.
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[Expression of Insulin-like Growth Factor Recepter Type I in CD34+ Cells of Patients with Myelodysplastic Syndromes]. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2018 Jun; 26(3):849-853.