Guidelines for genomic array analysis in acquired haematological neoplastic disorders-Reference-Cited by-同舟云学术

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Guidelines for genomic array analysis in acquired haematological neoplastic disorders

Published:2016-02-23 Issue:5 Volume:55 Page:480-491
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Schoumans Jacqueline¹,Suela Javier²,Hastings Ros³,Muehlematter Dominique¹,Rack Katrina⁴⁵,van den Berg Eva⁶,Berna Beverloo H.⁷,Stevens-Kroef Marian⁸

Affiliation:

1. Unité De Génétique Du Cancer, Service De Génétique Médicale; Centre Hospitalier Universitaire Vaudois; Lausanne CH-1011 Switzerland

2. Cytogenomics Laboratory, NIMGenetics; Madrid Spain

3. Cytogenetic External Quality Assessment, Women's Centre, John Radcliffe Hospital; Oxford University Hospitals NHS Trust; Oxford UK

4. Institut De Pathologie Et De Génétique; Gosselies Belgium

5. West Midland Regional Genetic Laboratory; Birmingham Womens Hospital; Birmingham UK

6. Dept Genet; University Groningen, University Medical Centre Groningen; Groningen the Netherlands

7. Department of Clinical Genetics; Erasmus Medical Centre; Rotterdam the Netherlands

8. Department of Human Genetics; Radboud University Medical Centre; Nijmegen the Netherlands

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gcc.22350/fullpdf

Reference61 articles.

1. Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myeloma;Affer;Leukemia,2014

2. Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing;Arenillas;Genes Chromosomes Cancer,2013

3. Prognostic significance of copy-number alterations in multiple myeloma;Avet-Loiseau;J Clin Oncol,2009

4. Clonal selection of 11q CN-LOH and CBL gene mutation in a serially studied patient during MDS progression to AML;Barresi;Leuk Res,2010

5. Mapping of chromosome 1p deletions in myeloma identifies FAM46C at 1p12 and CDKN2C at 1p32.3 as being genes in regions associated with adverse survival;Boyd;Clin Cancer Res,2011

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