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 519 publications over 14 distinct years, with a maximum of 53 publications in 2012

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

Year	Major Topic	Minor Topic	Total
2009	3	3	6
2010	7	10	17
2011	19	13	32
2012	22	31	53
2013	24	19	43
2014	18	22	40
2015	16	35	51
2016	19	26	45
2017	19	28	47
2018	17	26	43
2019	13	28	41
2020	17	32	49
2021	15	30	45
2022	1	6	7

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

Gibitova EA, Dobrynin PV, Pomerantseva EA, Musatova EV, Kostareva A, Evsyukov I, Rychkov SY, Zhukova OV, Naumova OY, Grigorenko EL. A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing. Genes (Basel). 2022 May 20; 13(5).

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Zhang Y, Chen F, Chandrashekar DS, Varambally S, Creighton CJ. Proteogenomic characterization of 2002 human cancers reveals pan-cancer molecular subtypes and associated pathways. Nat Commun. 2022 May 13; 13(1):2669.

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Wu LR, Dai P, Wang MX, Chen SX, Cohen EN, Jayachandran G, Zhang JX, Serrano AV, Xie NG, Ueno NT, Reuben JM, Barcenas CH, Zhang DY. Ensemble of nucleic acid absolute quantitation modules for copy number variation detection and RNA profiling. Nat Commun. 2022 04 04; 13(1):1791.

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Ramani NS, Morani AC, Zhang S. MET Gene High Copy Number (Amplification/Polysomy) Identified in Melanoma for Potential Targeted Therapy. Am J Clin Pathol. 2022 04 01; 157(4):502-505.

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Barinka J, Hu Z, Wang L, Wheeler DA, Rahbarinia D, McLeod C, Gu Z, Mullighan CG. RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data. Leukemia. 2022 06; 36(6):1492-1498.

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Scott DA, Gofin Y, Berry AM, Adams AD. Underlying genetic etiologies of congenital diaphragmatic hernia. Prenat Diagn. 2022 Mar; 42(3):373-386.

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Dong X, Chen G, Huang X, Li Z, Peng F, Chen H, Zhou Y, He L, Qiu L, Cai Z, Liu J, Liu X. Copy number profiling of circulating free DNA predicts transarterial chemoembolization response in advanced hepatocellular carcinoma. Mol Oncol. 2022 05; 16(10):1986-1999.

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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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Baslan T, Kovaka S, Sedlazeck FJ, Zhang Y, Wappel R, Tian S, Lowe SW, Goodwin S, Schatz MC. High resolution copy number inference in cancer using short-molecule nanopore sequencing. Nucleic Acids Res. 2021 12 02; 49(21):e124.

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Chen M, Chen R, Jin Y, Li J, Hu X, Zhang J, Fujimoto J, Hubert SM, Gay CM, Zhu B, Tian Y, McGranahan N, Lee WC, George J, Hu X, Chen Y, Wu M, Behrens C, Chow CW, Pham HHN, Fukuoka J, Wu J, Parra ER, Little LD, Gumbs C, Song X, Wu CJ, Diao L, Wang Q, Cardnell R, Zhang J, Wang J, Le X, Gibbons DL, Heymach JV, Jack Lee J, William WN, Cheng C, Glisson B, Wistuba I, Andrew Futreal P, Thomas RK, Reuben A, Byers LA, Zhang J. Cold and heterogeneous T cell repertoire is associated with copy number aberrations and loss of immune genes in small-cell lung cancer. Nat Commun. 2021 11 17; 12(1):6655.

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