Chromosome Duplication

"Chromosome Duplication" 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

An aberration in which an extra chromosome or a chromosomal segment is made.

Descriptor ID

D058674

MeSH Number(s)

C23.550.210.182

G05.355.600.164

G05.365.590.175.183

Concept/Terms

Chromosome Duplication

Below are MeSH descriptors whose meaning is more general than "Chromosome Duplication".

Diseases [C]
Pathological Conditions, Signs and Symptoms [C23]
Pathologic Processes [C23.550]
Chromosome Aberrations [C23.550.210]
Chromosome Duplication [C23.550.210.182]
Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Processes [G05.355]
Mutagenesis [G05.355.600]
Chromosome Duplication [G05.355.600.164]
Genetic Variation [G05.365]
Mutation [G05.365.590]
Chromosome Aberrations [G05.365.590.175]
Chromosome Duplication [G05.365.590.175.183]

Below are MeSH descriptors whose meaning is more specific than "Chromosome Duplication".

Chromosome Duplication
Tetrasomy
Trisomy

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Chromosome Duplication" by people in Harvard Catalyst Profiles by year, and whether "Chromosome Duplication" was a major or minor topic of these publication.

Bar chart showing 44 publications over 12 distinct years, with a maximum of 7 publications in 2016

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

Year	Major Topic	Minor Topic	Total
2010	1	1	2
2011	1	2	3
2012	2	2	4
2013	1	1	2
2014	4	2	6
2015	2	2	4
2016	3	4	7
2017	1	1	2
2018	3	2	5
2019	4	2	6
2020	1	1	2
2023	0	1	1

Below are the most recent publications written about "Chromosome Duplication" by people in Profiles.

Genetic Profiling Uncovers Genome-Wide Loss of Heterozygosity and Provides Insight into Mechanisms of Sarcomatoid Transformation in Chromophobe Renal Cell Carcinoma. Mod Pathol. 2024 Feb; 37(2):100396.

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Language characterization in 16p11.2 deletion and duplication syndromes. Am J Med Genet B Neuropsychiatr Genet. 2020 09; 183(6):380-391.

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Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features. Hum Mutat. 2020 07; 41(7):1238-1249.

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Psychotic symptoms in 16p11.2 copy-number variant carriers. Autism Res. 2020 02; 13(2):187-198.

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Duplication 2p16 is associated with perisylvian polymicrogyria. Am J Med Genet A. 2019 12; 179(12):2343-2356.

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Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials. Am J Med Genet A. 2020 01; 182(1):71-84.

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The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals. Am J Hum Genet. 2019 11 07; 105(5):947-958.

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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations. Neuroimage. 2019 12; 203:116155.

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Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa. J Psychiatr Res. 2019 06; 113:34-38.

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Psychiatric disorders in children with 16p11.2 deletion and duplication. Transl Psychiatry. 2019 01 16; 9(1):8.

View in: PubMed

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