(Q37642520)

21 August 2017

1 reference

retracted paper

2 references

Dataset for "Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine"

Continued use of retracted papers: Temporal trends in citations and (lack of) awareness of retractions shown in citation contexts in biomedicine

title

Copy number variations and cancer susceptibility (English)

1 reference

21 August 2017

2

David Malkin

0 references

author name string

Adam Shlien

series ordinal

1

1 reference

21 August 2017

publication date

1 January 2010

1 reference

Current Opinion in Oncology

21 August 2017

published in

1 reference

21 August 2017

volume

22

1 reference

21 August 2017

issue

1

1 reference

21 August 2017

page(s)

55-63

1 reference

Global variation in copy number in the human genome

21 August 2017

cites work

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE05329

Two cases of 5q deletions in patients with familial adenomatous polyposis: possible link with Caroli's disease

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Integrated detection and population-genetic analysis of SNPs and copy number variation

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Structural variation in the human genome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Long-range control of gene expression: emerging mechanisms and disruption in disease

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large genomic deletions of SMAD4, BMPR1A and PTEN in juvenile polyposis

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Human MHC architecture and evolution: implications for disease association studies

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

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

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Detection of large-scale variation in the human genome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large recurrent microdeletions associated with schizophrenia

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Segmental copy number variation shapes tissue transcriptomes.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Distribution and functional impact of DNA copy number variation in the rat.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Copy number variation at 1q21.1 associated with neuroblastoma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

CancerGenes: a gene selection resource for cancer genome projects

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Constitutional translocation t(1;17)(p36;q12-21) in a patient with neuroblastoma.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Comparison of polymorphisms in the alpha7 nicotinic receptor gene and its partial duplication in schizophrenic and control subjects

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Deletion of RB exons 24 and 25 causes low-penetrance retinoblastoma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Highly penetrant hereditary cancer syndromes.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large-scale copy number polymorphism in the human genome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Molecular mechanisms for genomic disorders

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Genomic rearrangements of the APC tumor-suppressor gene in familial adenomatous polyposis.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large deletions of the PRKAR1A gene in Carney complex

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Smith-Magenis syndrome

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

The contribution of germline rearrangements to the spectrum of BRCA2 mutations

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

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

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

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

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Characterizing the cancer genome in lung adenocarcinoma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Screening for TP53 rearrangements in families with the Li-Fraumeni syndrome reveals a complete deletion of the TP53 gene

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

A census of human cancer genes

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

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

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

The fine-scale and complex architecture of human copy-number variation

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Personal genomes: The case of the missing heritability

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Copy-number variation and association studies of human disease

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

NF1 microdeletion syndrome: refined FISH characterization of sporadic and familial deletions with locus-specific probes.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Germline novel MSH2 deletions and a founder MSH2 deletion associated with anticipation effects in HNPCC.

1 reference

30 December 2023

https://opencitations.net/index/api/v1/references/10.1097/CCO.0B013E328333DCA4

Identifiers

DOI

10.1097/CCO.0B013E328333DCA4

1 reference

21 August 2017

1 reference