"Chromosome Breakpoints" 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.
The locations in specific DNA sequences where CHROMOSOME BREAKS have occurred.
Concept/Terms
Chromosome Breakpoints- Chromosome Breakpoints
- Chromosome Breakpoint
- Breakpoints, Chromosome
- Breakpoint, Chromosome
Chromosome Breakpoint Sequence- Chromosome Breakpoint Sequence
- Breakpoint Sequence, Chromosome
- Breakpoint Sequences, Chromosome
- Chromosome Breakpoint Sequences
- Sequence, Chromosome Breakpoint
- Sequences, Chromosome Breakpoint
Below are MeSH descriptors whose meaning is more general than "Chromosome Breakpoints".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Breakpoints".
This graph shows the total number of publications written about "Chromosome Breakpoints" by people in Harvard Catalyst Profiles by year, and whether "Chromosome Breakpoints" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2009 | 0 | 1 | 1 |
2010 | 1 | 2 | 3 |
2011 | 0 | 2 | 2 |
2012 | 0 | 7 | 7 |
2013 | 1 | 7 | 8 |
2014 | 3 | 3 | 6 |
2015 | 0 | 1 | 1 |
2016 | 0 | 2 | 2 |
2017 | 1 | 4 | 5 |
2018 | 0 | 3 | 3 |
2019 | 0 | 2 | 2 |
2020 | 1 | 3 | 4 |
2021 | 0 | 1 | 1 |
Below are the most recent publications written about "Chromosome Breakpoints" by people in Profiles.
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Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Genetics. 2021 02 09; 217(2).
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Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing. Curr Protoc Hum Genet. 2020 12; 108(1):e107.
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Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics. 2020 Jun 29; 21(1):446.
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Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition. JAMA Psychiatry. 2020 04 01; 77(4):420-430.
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HiNT: a computational method for detecting copy number variations and translocations from Hi-C data. Genome Biol. 2020 03 23; 21(1):73.
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Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency. Mol Genet Genomic Med. 2020 04; 8(4):e1154.
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome. Hum Mutat. 2020 01; 41(1):150-168.
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A New Next-Generation Sequencing Strategy for the Simultaneous Analysis of Mutations and Chromosomal Rearrangements at DNA Level in Acute Myeloid Leukemia Patients. J Mol Diagn. 2020 01; 22(1):60-71.
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Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks. Genome Res. 2019 04; 29(4):576-589.
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PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome. Eur J Med Genet. 2019 Dec; 62(12):103587.