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 44 publications over 14 distinct years, with a maximum of 6 publications in 2012

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	3	0	3
2012	1	5	6
2013	1	4	5
2014	1	4	5
2015	1	1	2
2016	0	2	2
2017	1	2	3
2018	2	2	4
2019	1	3	4
2020	3	1	4
2021	0	1	1
2022	0	1	1

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

Patel SA. Functional genomic approaches in acute myeloid leukemia: Insights into disease models and the therapeutic potential of reprogramming. Cancer Lett. 2022 05 01; 533:215579.

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Wang P, Castellani CA, Yao J, Huan T, Bielak LF, Zhao W, Haessler J, Joehanes R, Sun X, Guo X, Longchamps RJ, Manson JE, Grove ML, Bressler J, Taylor KD, Lappalainen T, Kasela S, Van Den Berg DJ, Hou L, Reiner A, Liu Y, Boerwinkle E, Smith JA, Peyser PA, Fornage M, Rich SS, Rotter JI, Kooperberg C, Arking DE, Levy D, Liu C. Epigenome-wide association study of mitochondrial genome copy number. Hum Mol Genet. 2021 12 27; 31(2):309-319.

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Gortakowski M, Feghali K, Osakwe I. Single Institution Experience with Afirma and Thyroseq Testing in Indeterminate Thyroid Nodules. Thyroid. 2021 09; 31(9):1376-1382.

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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.

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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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