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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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
MeSH Number(s)	G05.365.795.297.500
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 DNA Copy Number Changes DNA Copy Number Changes DNA Copy Number Change Copy Number Changes, DNA

Below are MeSH descriptors whose meaning is more general than "DNA Copy Number Variations".

Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Polymorphism, Genetic [G05.365.795]
Genomic Structural Variation [G05.365.795.297]
DNA Copy Number Variations [G05.365.795.297.500]

Below are MeSH descriptors whose meaning is related to "DNA Copy Number Variations".

Below are MeSH descriptors whose meaning is more specific than "DNA Copy Number Variations".

publications

Timeline | Most Recent

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.

Bar chart showing 39 publications over 12 distinct years, with a maximum of 5 publications in 2012 and 2014

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2009	2	1	3
2010	1	0	1
2011	4	0	4
2012	1	4	5
2013	0	3	3
2014	1	4	5
2015	1	1	2
2016	0	2	2
2017	1	1	2
2018	2	2	4
2019	1	3	4
2020	3	1	4

Below are the most recent publications written about "DNA Copy Number Variations" by people in Profiles.

Oluwayiose OA, Josyula S, Houle E, Marcho C, Rahil T, Sites CK, Pilsner JR. Association between sperm mitochondarial DNA copy number and nuclear DNA methylation. Epigenomics. 2020 12; 12(24):2141-2153.

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Kim J, Zhao B, Huang AY, Miller MB, Lodato MA, Walsh CA, Lee EA. APP gene copy number changes reflect exogenous contamination. Nature. 2020 08; 584(7821):E20-E28.

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Liu Y, Smith CE, Parnell LD, Lee YC, An P, Straka RJ, Tiwari HK, Wood AC, Kabagambe EK, Hidalgo B, Hopkins PN, Province MA, Arnett DK, Tucker KL, Ordovas JM, Lai CQ. Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk. Clin Chem. 2020 05 01; 66(5):718-726.

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Singh K, Singh IN, Diggins E, Connors SL, Karim MA, Lee D, Zimmerman AW, Frye RE. Developmental regression and mitochondrial function in children with autism. Ann Clin Transl Neurol. 2020 05; 7(5):683-694.

View in: PubMed
Fotiou E, Williams S, Martin-Geary A, Robertson DL, Tenin G, Hentges KE, Keavney B. Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease. Circ Genom Precis Med. 2019 10; 12(10):442-451.

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Qiu Y, Arbogast T, Lorenzo SM, Li H, Tang SC, Richardson E, Hong O, Cho S, Shanta O, Pang T, Corsello C, Deutsch CK, Chevalier C, Davis EE, Iakoucheva LM, Herault Y, Katsanis N, Messer K, Sebat J. Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development. Cell Rep. 2019 09 24; 28(13):3320-3328.e4.

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Zhao Y, Huang W, Kim TM, Jung Y, Menon LG, Xing H, Li H, Carroll RS, Park PJ, Yang HW, Johnson MD. MicroRNA-29a activates a multi-component growth and invasion program in glioblastoma. J Exp Clin Cancer Res. 2019 Jan 25; 38(1):36.

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Wu H, Whitcomb BW, Huffman A, Brandon N, Labrie S, Tougias E, Lynch K, Rahil T, Sites CK, Pilsner JR. Associations of sperm mitochondrial DNA copy number and deletion rate with fertilization and embryo development in a clinical setting. Hum Reprod. 2019 Jan 01; 34(1):163-170.

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Chun K, Wenger GD, Chaubey A, Dash DP, Kanagal-Shamanna R, Kantarci S, Kolhe R, Van Dyke DL, Wang L, Wolff DJ, Miron PM. Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia. Cancer Genet. 2018 12; 228-229:236-250.

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Sherman MA, Barton AR, Lodato MA, Vitzthum C, Coulter ME, Walsh CA, Park PJ. PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Res. 2018 02 28; 46(4):e20.

View in: PubMed

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