Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing. (Q53101662)

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scientific article published on 7 October 2013

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English	Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing.	scientific article published on 7 October 2013

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scholarly article

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Europe PubMed Central

11 May 2018

http://europepmc.org/abstract/MED/24123380

Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing. (English)

1 reference

Europe PubMed Central

11 May 2018

http://europepmc.org/abstract/MED/24123380

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single-nucleotide polymorphism

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Leonor Arenillas

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1 June 2020

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1 June 2020

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1 June 2020

María Abáigar

10

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1 June 2020

Maria Diez-Campelo

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1 June 2020

Guillermo F Sanz

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Jesus Maria Hernandez Rivas

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1 June 2020

Lourdes Florensa

21

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1 June 2020

author name string

Mar Mallo

2

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1 June 2020

Fernando Ramos

3

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1 June 2020

Kathryn Guinta

4

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1 June 2020

Eva Barragán

5

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1 June 2020

María-José Larráyoz

7

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1 June 2020

Raquel De Paz

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1 June 2020

Carme Pedro

11

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1 June 2020

José Cervera

12

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1 June 2020

Esperanza Such

13

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1 June 2020

María José Calasanz

14

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1 June 2020

Elisa Luño

18

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1 June 2020

Sílvia Saumell

19

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1 June 2020

Jaroslaw Maciejewski

20

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1 June 2020

Francesc Solé

22

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1 June 2020

publication date

7 October 2013

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http://europepmc.org/abstract/MED/24123380

Genes, Chromosomes and Cancer

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1 June 2020

52

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1 June 2020

1167-1177

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1 June 2020

12

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1 June 2020

Clinical effect of point mutations in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Proposals for the classification of the myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Mutation in TET2 in myeloid cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Revised international prognostic scoring system for myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

SNP array analysis in hematologic malignancies: avoiding false discoveries

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

TP53 mutations in myeloid malignancies are either homozygous or hemizygous due to copy number-neutral loss of heterozygosity or deletion of 17p.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

The utility of fluorescence in situ hybridization analysis in diagnosing myelodysplastic syndromes is limited to cases with karyotype failure

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

A gain-of-function mutation of JAK2 in myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Acquired mutations in TET2 are common in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Utility of peripheral blood for cytogenetic and mutation analysis in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

Identification of genomic aberrations associated with disease transformation by means of high-resolution SNP array analysis in patients with myeloproliferative neoplasm.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

P030 Prognostic impact on survival of an unsuccessful conventional cytogenetic study in patients with myelodysplastic syndromes (MDS)

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

21 January 2018

FISH analysis of circulating CD34+ cells as a new tool for genetic monitoring in MDS: verification of the method and application to 27 MDS patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparison of interphase FISH and metaphase cytogenetics to study myelodysplastic syndrome: an Eastern Cooperative Oncology Group (ECOG) study

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

7 January 2021

based on heuristic

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Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

7 January 2021

based on heuristic

inferred from DOI database lookup

New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22112

7 January 2021

based on heuristic

inferred from DOI database lookup

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