Genome-wide arrays in routine diagnostics of hematological malignancies (Q38001406)

26 August 2017

title

Genome-wide arrays in routine diagnostics of hematological malignancies (English)

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26 August 2017

3

Nicole de Leeuw

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26 August 2017

Annet Simons

1

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26 August 2017

Birgit Sikkema-Raddatz

2

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26 August 2017

Nicole Claudia Konrad

4

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26 August 2017

Rosalind J Hastings

5

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26 August 2017

Jacqueline Schoumans

6

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26 August 2017

publication date

9 April 2012

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26 August 2017

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26 August 2017

volume

33

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26 August 2017

issue

6

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26 August 2017

page(s)

941-948

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A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect

26 August 2017

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Broad copy neutral-loss of heterozygosity regions and rare recurring copy number abnormalities in normal karyotype-acute myeloid leukemia genomes.

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Genomic profiling of high-risk acute lymphoblastic leukemia.

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Diagnostic interpretation of array data using public databases and internet sources

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SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control

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Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies

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250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies

21 January 2018

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Acute myeloid leukemia: 2012 update on diagnosis, risk stratification, and management

21 January 2018

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An accumulation of cytogenetic and molecular genetic events characterizes the progression from MDS to secondary AML: an analysis of 38 paired samples analyzed by cytogenetics, molecular mutation analysis and SNP microarray profiling.

21 January 2018

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Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes

21 January 2018

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Rapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays

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Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.

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Array-based genomic screening at diagnosis and during follow-up in chronic lymphocytic leukemia

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Array-based karyotyping for prognostic assessment in chronic lymphocytic leukemia: performance comparison of Affymetrix 10K2.0, 250K Nsp, and SNP6.0 arrays

21 January 2018

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Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics

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SNP array analysis in hematologic malignancies: avoiding false discoveries

21 January 2018

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Chromosomal minimal critical regions in therapy-related leukemia appear different from those of de novo leukemia by high-resolution aCGH.

21 January 2018

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Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours

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High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.

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Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.

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Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies

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Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

21 January 2018

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Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia

21 January 2018

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Comparison of array comparative genomic hybridization (aCGH) to FISH and cytogenetics in prognostic evaluation of chronic lymphocytic leukemia.

21 January 2018

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Aggressive chronic lymphocytic leukemia with elevated genomic complexity is associated with multiple gene defects in the response to DNA double-strand breaks.

21 January 2018

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13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia.

21 January 2018

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Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia

21 January 2018

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Array Comparative Genomic Hybridization Detects Chromosomal Abnormalities in Hematological Cancers That Are Not Detected by Conventional Cytogenetics

21 January 2018

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Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia

21 January 2018

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Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance

21 January 2018

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New lesions detected by single nucleotide polymorphism array-based chromosomal analysis have important clinical impact in acute myeloid leukemia

21 January 2018

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Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

21 January 2018

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Updates in cytogenetics and molecular markers in MDS.

21 January 2018

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Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.

21 January 2018

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Guidelines for molecular karyotyping in constitutional genetic diagnosis

21 January 2018

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Acquired copy number alterations in adult acute myeloid leukemia genomes

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22057

Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22057

Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22057

Monosomal karyotype in acute myeloid leukemia: a better indicator of poor prognosis than a complex karyotype

21 January 2018

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7 January 2021

The rewards and challenges of array-based karyotyping for clinical oncology applications

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7 January 2021

A cryptic deletion in 5q31.2 provides further evidence for a minimally deleted region in myelodysplastic syndromes

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7 January 2021

Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes

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7 January 2021

A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value

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7 January 2021

Identifiers

DOI

10.1002/HUMU.22057

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26 August 2017

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