"Translocation, Genetic" 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.
A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome.
| Descriptor ID |
D014178
|
| MeSH Number(s) |
C23.550.210.870 G05.365.590.175.870 G05.558.860
|
| Concept/Terms |
Translocation, Genetic- Translocation, Genetic
- Genetic Translocation
- Genetic Translocations
- Translocations, Genetic
- Chromosomal Translocation
- Chromosomal Translocations
- Translocations, Chromosomal
- Translocation, Chromosomal
|
Below are MeSH descriptors whose meaning is more general than "Translocation, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Translocation, Genetic".
This graph shows the total number of publications written about "Translocation, Genetic" by people in this website by year, and whether "Translocation, Genetic" was a major or minor topic of these publications.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 16 | 4 | 20 |
| 1996 | 6 | 8 | 14 |
| 1997 | 5 | 12 | 17 |
| 1998 | 14 | 9 | 23 |
| 1999 | 11 | 4 | 15 |
| 2000 | 6 | 5 | 11 |
| 2001 | 4 | 8 | 12 |
| 2002 | 5 | 9 | 14 |
| 2003 | 12 | 12 | 24 |
| 2004 | 11 | 13 | 24 |
| 2005 | 11 | 13 | 24 |
| 2006 | 9 | 10 | 19 |
| 2007 | 13 | 13 | 26 |
| 2008 | 8 | 12 | 20 |
| 2009 | 9 | 7 | 16 |
| 2010 | 9 | 9 | 18 |
| 2011 | 7 | 13 | 20 |
| 2012 | 14 | 10 | 24 |
| 2013 | 10 | 12 | 22 |
| 2014 | 8 | 18 | 26 |
| 2015 | 8 | 10 | 18 |
| 2016 | 11 | 13 | 24 |
| 2017 | 11 | 4 | 15 |
| 2018 | 7 | 8 | 15 |
| 2019 | 5 | 8 | 13 |
| 2020 | 7 | 6 | 13 |
| 2021 | 8 | 12 | 20 |
| 2022 | 0 | 6 | 6 |
| 2023 | 1 | 7 | 8 |
| 2024 | 5 | 4 | 9 |
Below are the most recent publications written about "Translocation, Genetic" by people in Profiles.
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Long read sequencing identifies complex structural variant landscape and recurrent TERT rearrangements in mucoepidermoid carcinoma. Oral Oncol. 2024 Dec; 159:107108.
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Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly. Am J Hum Genet. 2024 Dec 05; 111(12):2693-2706.
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The Four Core Genotypes mouse model: evaluating the impact of a recently discovered translocation. Biol Sex Differ. 2024 Oct 31; 15(1):90.
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Recurrent Xp22.31-Yq11 Unbalanced Translocations: Molecular Diagnosis and Clinical Implications in Three Families. Am J Med Genet A. 2025 Mar; 197(3):e63913.
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Interchromosomal segmental duplication drives translocation and loss of P. falciparum histidine-rich protein 3. Elife. 2024 Oct 07; 13.
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Increased AID results in mutations at the CRLF2 locus implicated in Latin American ALL health disparities. Nat Commun. 2024 Jul 27; 15(1):6331.
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The RNA tether model for human chromosomal translocation fragile zones. Trends Biochem Sci. 2024 May; 49(5):391-400.
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ASPSCR1-TFE3 reprograms transcription by organizing enhancer loops around hexameric VCP/p97. Nat Commun. 2024 Feb 07; 15(1):1165.
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COL1A1::PDGFB fusion-associated uterine fibrosarcoma: A case report and review of the literature. Cancer Rep (Hoboken). 2024 02; 7(2):e1969.
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The incidence of translocation t(11;14) among patients with multiple myeloma in a single clinic. Am J Clin Pathol. 2024 Jan 04; 161(1):16-23.