Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features

Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens

(2014) Haoyang Cai et al.   BMC GENOMICS

Prevalence and clinical implications of chromothripsis in cancer genomes

(2013) Wigard P. Kloosterman et al.   CURRENT OPINION IN ONCOLOGY

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2

(2013) Lusine Nazaryan et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism

(2013) Anne Frühmesser et al.   European Journal of Medical Genetics

Pan-cancer patterns of somatic copy number alteration

(2013) Travis I Zack et al.   NATURE GENETICS

A Familial Cri-du-Chat/5p Deletion Syndrome Resulted from Rare Maternal Complex Chromosomal Rearrangements (CCRs) and/or Possible Chromosome 5p Chromothripsis

(2013) Heng Gu et al.   PLoS One

Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event

(2013) Rita Genesio et al.   Molecular Cytogenetics

Chromothripsis and Human Disease: Piecing Together the Shattering Process

(2012) Christopher A. Maher et al.   CELL

Poly-gene fusion transcripts and chromothripsis in prostate cancer

(2012) Chunxiao Wu et al.   GENES CHROMOSOMES & CANCER

Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients

(2011) F. Magrangeas et al.   BLOOD

Massive Genomic Rearrangement Acquired in a Single Catastrophic Event during Cancer Development

(2011) Philip J. Stephens et al.   CELL

Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements

(2011) Pengfei Liu et al.   CELL

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline†

(2011) Wigard P. Kloosterman et al.   HUMAN MOLECULAR GENETICS

Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

(2011) Wigard P Kloosterman et al.   GENOME BIOLOGY

The Mechanism of Double-Strand DNA Break Repair by the Nonhomologous DNA End-Joining Pathway

(2010) Michael R. Lieber   Annual Review of Biochemistry

Chromosome 6 between-arm intrachromosomal insertion with intrasegmental double inversion: A four-break model

(2009) Jia-Chi Wang et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

(2009) P. J. Hastings et al.   PLoS Genetics

A complex submicroscopic chromosomal imbalance in 19p13.11 with one microduplication and two microtriplications

(2008) Bernard Thienpont et al.   European Journal of Medical Genetics