(Q34217081)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

title

Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

author

Avinash V Dharmadhikari

6

1 reference

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12 February 2020

Feng Zhang

9

1 reference

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12 February 2020

Lane Strathearn

23

1 reference

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12 February 2020

30

James R Lupski

1 reference

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12 February 2020

11

Carlos A Bacino

1 reference

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12 February 2020

29

Paweł Stankiewicz

1 reference

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12 February 2020

22

Fernando Scaglia

1 reference

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12 February 2020

26

Ankita Patel

1 reference

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12 February 2020

19

Seema R Lalani

1 reference

12 February 2020

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25

Sung-Hae L Kang

1 reference

12 February 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

16

Theresa A Grebe

1 reference

12 February 2020

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27

Sau Wai Cheung

1 reference

12 February 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

14

Debra Freedenberg

1 reference

12 February 2020

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Pengfei Liu

1

1 reference

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12 February 2020

Ayelet Erez

2

1 reference

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12 February 2020

Sandesh C Sreenath Nagamani

3

1 reference

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12 February 2020

Shweta U Dhar

4

1 reference

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12 February 2020

Katarzyna E Kołodziejska

5

1 reference

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12 February 2020

M Lance Cooper

7

1 reference

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12 February 2020

Joanna Wiszniewska

8

1 reference

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12 February 2020

Marjorie A Withers

10

1 reference

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12 February 2020

Luis Daniel Campos-Acevedo

12

1 reference

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12 February 2020

Mauricio R Delgado

13

1 reference

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12 February 2020

Adolfo Garnica

15

1 reference

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12 February 2020

Dolores Hernández-Almaguer

17

1 reference

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12 February 2020

LaDonna Immken

18

1 reference

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12 February 2020

Scott D McLean

20

1 reference

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12 February 2020

Hope Northrup

21

1 reference

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12 February 2020

Pamela Trapane

24

1 reference

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12 February 2020

P J Hastings

28

1 reference

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12 February 2020

Weimin Bi

31

1 reference

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12 February 2020

language of work or name

English

0 references

publication date

1 September 2011

1 reference

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12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

volume

146

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

page(s)

889-903

1 reference

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12 February 2020

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome

12 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Evidence for disease penetrance relating to CNV size: Pelizaeus-Merzbacher disease and manifesting carriers with a familial 11 Mb duplication at Xq22

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Break-induced replication is highly inaccurate

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Massive genomic rearrangement acquired in a single catastrophic event during cancer development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Detection of clinically relevant exonic copy-number changes by array CGH.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Loss of DNA replication control is a potent inducer of gene amplification

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Increased mutagenesis and unique mutation signature associated with mitotic gene conversion

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Genomic rearrangements in inherited disease and cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Leaping forks at inverted repeats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Mechanisms of change in gene copy number

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Complex human chromosomal and genomic rearrangements

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Replicon dynamics, dormant origin firing, and terminal fork integrity after double-strand break formation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

A microhomology-mediated break-induced replication model for the origin of human copy number variation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Increased LIS1 expression affects human and mouse brain development

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Segmental duplications arise from Pol32-dependent repair of broken forks through two alternative replication-based mechanisms

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

On the mechanism of gene amplification induced under stress in Escherichia coli

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Genome architecture catalyzes nonrecurrent chromosomal rearrangements

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Recent segmental duplications in the human genome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Genome architecture, rearrangements and genomic disorders

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

"Break copy" duplication: a model for chromosome fragment formation in Saccharomyces cerevisiae

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Template switching during break-induced replication

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardation.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3242451

Copy number amplification of the 2 micron circle plasmid of Saccharomyces cerevisiae

28 October 2018

1 reference

12 December 2020

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

12 December 2020

New mutations and intellectual function

1 reference

12 December 2020

Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1016/J.CELL.2011.07.042

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21925314%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference