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.
Descriptor ID |
D056915
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MeSH Number(s) |
G05.365.795.297.500
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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 this website by year, and whether "DNA Copy Number Variations" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2009 | 3 | 3 | 6 |
2010 | 6 | 10 | 16 |
2011 | 18 | 13 | 31 |
2012 | 21 | 29 | 50 |
2013 | 23 | 18 | 41 |
2014 | 19 | 20 | 39 |
2015 | 17 | 35 | 52 |
2016 | 20 | 27 | 47 |
2017 | 18 | 27 | 45 |
2018 | 18 | 25 | 43 |
2019 | 13 | 27 | 40 |
2020 | 17 | 33 | 50 |
2021 | 15 | 30 | 45 |
2022 | 4 | 18 | 22 |
2023 | 2 | 9 | 11 |
2024 | 2 | 1 | 3 |
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Below are the most recent publications written about "DNA Copy Number Variations" by people in Profiles.
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HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data. Nucleic Acids Res. 2024 Feb 28; 52(4):e18.
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A statistical learning method for simultaneous copy number estimation and subclone clustering with single-cell sequencing data. Genome Res. 2024 Feb 07; 34(1):85-93.
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Etiologic Evaluation of Children with Autism Spectrum Disorder. Pediatr Clin North Am. 2024 Apr; 71(2):179-197.
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The Landscape of Alterations from 1407 Ultra-Rare Sarcomas from the AACR GENIE Database: Clinical Implications. Clin Cancer Res. 2023 11 14; 29(22):4669-4678.
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Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk. J Am Heart Assoc. 2023 10 17; 12(20):e029090.
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COMPASS: joint copy number and mutation phylogeny reconstruction from amplicon single-cell sequencing data. Nat Commun. 2023 08 15; 14(1):4921.
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Pan-cancer proteogenomics connects oncogenic drivers to functional states. Cell. 2023 08 31; 186(18):3921-3944.e25.
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HER2/ ERBB2 Immunohistochemical Expression and Copy Number Status in Ovarian Mucinous Tumors. Int J Gynecol Pathol. 2024 Mar 01; 43(2):134-139.
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Interferon signaling promotes tolerance to chromosomal instability during metastatic evolution in renal cancer. Nat Cancer. 2023 07; 4(7):984-1000.
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Hotspot of de novo telomere addition stabilizes linear amplicons in yeast grown in sulfate-limiting conditions. Genetics. 2023 05 26; 224(2).