Chromosome Aberrations

"Chromosome Aberrations" 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

Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.

Descriptor ID	D002869
MeSH Number(s)	C23.550.210 G05.365.590.175
Concept/Terms	Chromosome Aberrations Chromosome Aberrations Aberration, Chromosome Aberrations, Chromosome Chromosome Aberration Abnormalities, Chromosome Abnormality, Chromosome Chromosome Abnormality Cytogenetic Abnormalities Abnormalities, Cytogenetic Abnormality, Cytogenetic Cytogenetic Abnormality Chromosome Abnormalities Cytogenetic Aberrations Aberration, Cytogenetic Aberrations, Cytogenetic Cytogenetic Aberration Abnormalities, Chromosomal Abnormality, Chromosomal Chromosomal Abnormalities Chromosomal Abnormality Chromosomal Aberrations Aberration, Chromosomal Aberrations, Chromosomal Chromosomal Aberration Autosome Abnormalities Autosome Abnormalities Abnormality, Autosome Autosome Abnormality Abnormalities, Autosome

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

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

Below are MeSH descriptors whose meaning is related to "Chromosome Aberrations".

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

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Chromosome Aberrations" by people in this website by year, and whether "Chromosome Aberrations" was a major or minor topic of these publications.

Bar chart showing 134 publications over 29 distinct years, with a maximum of 9 publications in 2011

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

Year	Major Topic	Minor Topic	Total
1996	4	0	4
1997	5	3	8
1998	2	1	3
1999	4	1	5
2000	0	2	2
2001	4	2	6
2002	1	2	3
2003	3	2	5
2004	2	1	3
2005	1	6	7
2006	2	5	7
2007	5	2	7
2008	4	3	7
2009	0	4	4
2010	5	1	6
2011	5	4	9
2012	2	5	7
2013	2	6	8
2014	0	1	1
2015	3	1	4
2016	2	3	5
2017	4	3	7
2018	0	2	2
2019	3	1	4
2020	1	0	1
2021	2	1	3
2022	1	2	3
2023	0	2	2
2024	0	1	1

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

Kirschen GW, Blakemore K, Al-Kouatly HB, Fridkis G, Baschat A, Gearhart J, Jelin AC. The genetic etiologies of bilateral renal agenesis. Prenat Diagn. 2024 02; 44(2):205-221.

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Dhital B, Rodriguez-Bravo V. Mechanisms of chromosomal instability (CIN) tolerance in aggressive tumors: surviving the genomic chaos. Chromosome Res. 2023 04 14; 31(2):15.

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Pasvolsky O, Gaballa MR, Milton DR, Masood A, Sami SS, Tanner MR, Bashir Q, Srour S, Saini N, Ramdial J, Nieto Y, Tang G, Lin P, Lee HC, Patel KK, Kebriaei P, Thomas SK, Weber DM, Orlowski RZ, Shpall EJ, Champlin RE, Qazilbash MH. Autologous Stem Cell Transplantation for Patients with Multiple Myeloma with Translocation (4;14): The MD Anderson Cancer Center Experience. Transplant Cell Ther. 2023 04; 29(4):260.e1-260.e6.

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Davidow K, Mumanachit S, Mangum DS. The two-hit hypothesis in practice: Monozygotic twins with simultaneous hyperdiploid acute lymphoblastic leukemia. Pediatr Blood Cancer. 2022 10; 69(10):e29885.

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Gaballa MR, Ma J, Rauf M, Bassett R, Pasvolsky O, Tanner MR, Bashir Q, Srour SA, Saini N, Ramdial J, Nieto Y, Murphy R, Rezvani K, Tang G, Lin P, Lee HC, Patel KK, Ullah MR, Kaufman GP, Manasanch EE, Kebriaei P, Thomas SK, Weber DM, Shpall EJ, Champlin RE, Orlowski RZ, Qazilbash MH. KRD vs. VRD as induction before autologous hematopoietic progenitor cell transplantation for high-risk multiple myeloma. Bone Marrow Transplant. 2022 07; 57(7):1142-1149.

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Bi X, French Z, Palmisiano N, Wen KY, Wilde L. The prognostic impact of cigarette smoking on survival in acute myeloid leukemia with TP53 mutations and/or 17p deletions. Ann Hematol. 2022 Jun; 101(6):1251-1259.

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Wierenga APA, Brouwer NJ, Gelmi MC, Verdijk RM, Stern MH, Bas Z, Malkani K, van Duinen SG, Ganguly A, Kroes WGM, Marinkovic M, Luyten GPM, Shields CL, Jager MJ. Chromosome 3 and 8q Aberrations in Uveal Melanoma Show Greater Impact on Survival in Patients with Light Iris versus Dark Iris Color. Ophthalmology. 2022 04; 129(4):421-430.

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Pei J, Flieder DB, Talarchek JN, Cooper HS, Patchefsky AS, Wei S. Clinical Application of Chromosome Microarray Analysis in the Diagnosis of Lipomatous Tumors. Appl Immunohistochem Mol Morphol. 2021 09 01; 29(8):592-598.

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Wang JW, Lyu YN, Qiao B, Li Y, Zhang Y, Dhanyamraju PK, Bamme Y, Yu MD, Yang D, Tong YQ. Cell-free fetal DNA testing and its correlation with prenatal indications. BMC Pregnancy Childbirth. 2021 Aug 24; 21(1):585.

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Levy AT, Berghella V, Al-Kouatly HB. Outcome of 45,X fetuses with cystic hygroma: A systematic review. Am J Med Genet A. 2021 01; 185(1):26-32.

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