Copy number variation at 1q21.1 associated with neuroblastoma (Q24642330)

15

0 references

Hakon Hakonarson

26

0 references

Kai Wang

14

Kai Wang

0 references

Joseph Glessner

3

Joseph T Glessner

1 reference

ORCID Public Data File 2021

Struan F.A. Grant

22

Struan F A Grant

0 references

Andrew R Wood

9

Andrew Wood

0 references

Tamim H Shaikh

20

Tamim H Shaikh

0 references

Jonathan P Bradfield

21

Jonathan Bradfield

0 references

Eric F Rappaport

25

Eric R Rappaport

0 references

Cuiping Hou

2

Cuiping Hou

0 references

John M. Maris

27

John M Maris

0 references

Sharon J Diskin

1

Sharon J Diskin

0 references

Edward F. Attiyeh

4

Edward F Attiyeh

0 references

Marci Laudenslager

5

Marci Laudenslager

0 references

Kristopher Bosse

6

Kristopher Bosse

0 references

Kristina A Cole

7

Kristina Cole

0 references

Yaël P. Mossé

8

Yaël P Mossé

0 references

Maura A Diamond

12

Maura Diamond

0 references

Cynthia Winter

13

Cynthia Winter

0 references

Wendy B London

19

Wendy B London

0 references

author name string

Jill E Lynch

10

0 references

Katlyn Pecor

11

0 references

Elizabeth A Geiger

16

0 references

Patrick W McGrady

17

0 references

Alexandra I F Blakemore

18

0 references

Hongzhe Li

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

23

0 references

language of work or name

English

0 references

publication date

18 June 2009

0 references

published in

Nature

0 references

volume

459

0 references

issue

7249

0 references

page(s)

987-91

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Large recurrent microdeletions associated with schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Rare chromosomal deletions and duplications increase risk of schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Strong association of de novo copy number mutations with autism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

BLAT—The BLAST-Like Alignment Tool

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Human lineage-specific amplification, selection, and neuronal expression of DUF1220 domains

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

A novel gene family NBPF: intricate structure generated by gene duplications during primate evolution

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Suppression subtractive hybridization and expression profiling identifies a unique set of genes overexpressed in non-small-cell lung cancer

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

A greedy algorithm for aligning DNA sequences

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Relative impact of nucleotide and copy number variation on gene expression phenotypes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

A constitutional translocation t(1;17)(p36.2;q11.2) in a neuroblastoma patient disrupts the human NBPF1 and ACCN1 genes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Psoriasis is associated with increased beta-defensin genomic copy number

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Copy-number variation in control population cohorts

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Detection of MYCN gene amplification in neuroblastoma by fluorescence in situ hybridization: a pediatric oncology group study.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

The International Neuroblastoma Pathology Classification (the Shimada system).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Whole-genome genotyping with the single-base extension assay

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

A genome-wide scalable SNP genotyping assay using microarray technology

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

Positional cloning identifies a novel cyclophilin as a candidate amplified oncogene in 1q21.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2755253

A high-resolution survey of deletion polymorphism in the human genome

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19536264

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/19536264

12 December 2020

inferred from PubMed ID database lookup

Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19536264

12 December 2020

inferred from PubMed ID database lookup

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

1 reference

Crossref

https://api.crossref.org/works/10.1038/NATURE08035

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NATURE08035

1 reference

Dimensions Publication ID

1014011076

0 references

1 reference

1 reference

PubMed publication ID

19536264

1 reference