Back to discover
Disease
Chromothripsis
Emerging research
2
Publications
1
Related conditions
2020
Latest publication
Latest activity
betaRecent clinical, regulatory, research and industry developments relating to this disease.
Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing.
Research2020-02-05Nature genetics
Pan-cancer analysis of whole genomes.
Research2020-02-05Nature
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
No activity recorded in this window. Try a wider timeframe.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Most influential
Major themes6
- Genomics2
- Chromothripsis1
- DNA Mutational Analysis1
- Evolution, Molecular1
- Mutation1
- Whole Genome Sequencing1
Leading journals2
- Nature1
- Nature genetics1
Leading researchers8
- Cortés-Ciriano I1
- Gordenin D1
- Jain D1
- Jung YL1
- Klimczak LJ1
- Lee JJ1
- Park PJ1
- Pellman DS1
Affiliations (unnormalised)6
- Broad Institute of MIT and Harvard1
- Centre for Molecular Science Informatics1
- Dana-Farber Cancer Institute1
- Dana-Farber Cancer Institute and Harvard Medical School1
- European Molecular Biology Laboratory1
- Genome Integrity and Structural Biology Laboratory1
Related conditions
Diseases frequently studied alongside this one. Number shows shared papers.
Reference
Authoritative identity, definition & identifiers.
Defined in MeSH
Massive number of chromosomal rearrangements and shattering that occurs in cancer cells. The breakpoints are located within one chromosome or chromosome arm.
Identifiers
References & data sources
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.