DNA Copy Number Variations
"DNA Copy Number Variations" 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.
Stretches of genomic DNA that exist in different multiples between individuals. Many copy number variations have been associated with susceptibility or resistance to disease.
Concept/Terms
DNA Copy Number Variations- DNA Copy Number Variations
- DNA Copy Number Variation
- DNA Copy Number Variants
- Copy Number Variants, DNA
- Copy Number Variation, DNA
DNA Copy Number Polymorphisms- DNA Copy Number Polymorphisms
- DNA Copy Number Polymorphism
- Copy Number Polymorphisms
- Copy Number Polymorphism
- Polymorphism, Copy Number
- Polymorphisms, Copy Number
Below are MeSH descriptors whose meaning is more general than "DNA Copy Number Variations".
Below are MeSH descriptors whose meaning is more specific than "DNA Copy Number Variations".
This graph shows the total number of publications written about "DNA Copy Number Variations" by people in Harvard Catalyst Profiles by year, and whether "DNA Copy Number Variations" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2009 | 2 | 2 | 4 |
| 2010 | 15 | 11 | 26 |
| 2011 | 35 | 16 | 51 |
| 2012 | 22 | 36 | 58 |
| 2013 | 35 | 42 | 77 |
| 2014 | 25 | 45 | 70 |
| 2015 | 31 | 33 | 64 |
| 2016 | 33 | 47 | 80 |
| 2017 | 21 | 37 | 58 |
| 2018 | 32 | 53 | 85 |
| 2019 | 24 | 44 | 68 |
| 2020 | 23 | 50 | 73 |
| 2021 | 24 | 49 | 73 |
| 2022 | 14 | 32 | 46 |
| 2023 | 0 | 2 | 2 |
Below are the most recent publications written about "DNA Copy Number Variations" by people in Profiles.
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Sperm mitochondrial DNA copy number mediates the association between seminal plasma selenium concentrations and semen quality among healthy men. Ecotoxicol Environ Saf. 2023 Feb; 251:114532.
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Obesity Is Associated with Altered Tumor Metabolism in Metastatic Melanoma. Clin Cancer Res. 2023 01 04; 29(1):154-164.
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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience. BMC Med Genomics. 2022 12 21; 15(1):268.
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16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up. BMC Pregnancy Childbirth. 2022 Dec 07; 22(1):913.
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Molecular Diagnostic Yield of Exome Sequencing and Chromosomal Microarray in Cerebral Palsy: A Systematic Review and Meta-analysis. JAMA Neurol. 2022 12 01; 79(12):1287-1295.
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Retrospective analysis of genetic etiology and obstetric outcome of fetal cystic hygroma: A single-center study. Medicine (Baltimore). 2022 Nov 25; 101(47):e31689.
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Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci. J Natl Cancer Inst. 2022 11 14; 114(11):1533-1544.
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Blood trihalomethane concentrations in relation to sperm mitochondrial DNA copy number and telomere length among 958 healthy men. Environ Res. 2023 01 01; 216(Pt 4):114737.
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Circulating tumour DNA characterisation of invasive lobular carcinoma in patients with metastatic breast cancer. EBioMedicine. 2022 Dec; 86:104316.
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Influences of rare copy-number variation on human complex traits. Cell. 2022 10 27; 185(22):4233-4248.e27.