Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Blood - 28 Apr 2011

Tiu Ramon V, Gondek Lukasz P, O'Keefe Christine L, Elson Paul, Huh Jungwon, Mohamedali Azim, Kulasekararaj Austin, Advani Anjali S, Paquette Ronald, List Alan F, Sekeres Mikkael A, McDevitt Michael A, Mufti Ghulam J, Maciejewski Jaroslaw P

Abstract excerpt

Single nucleotide polymorphism arrays (SNP-As) have emerged as an important tool in the identification of chromosomal defects undetected by metaphase cytogenetics (MC) in hematologic cancers, offering superior resolution of unbalanced chromosomal defects and acquired copy-neutral loss of heterozygosity. Myelodysplastic syndromes (MDSs) and related cancers share recurrent chromosomal defects and molecular lesions...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Aberrations
Share to Genome-Wide Association Study

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Karyotyping

Share to Leukemia, Myeloid, Acute

Share to Myelodysplastic Syndromes

Share to Oligonucleotide Array Sequence Analysis

Share to Predictive Value of Tests

Share to Prognosis

Source

Open in PubMed Open full text

Identifiers

PMID: 21285439
DOI: 10.1182/blood-2010-07-295857
PMCID: PMC3099573

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies.PMID 21285439Read ↗

Combining metaphase cytogenetics with single nucleotide polymorphism arrays can improve the diagnostic yield and identify prognosis more precisely in myelodysplastic syndromes.Semantic proximity Read ↗

The prognostic significance of single-nucleotide polymorphism array-based whole-genome analysis and uniparental disomy in myelodysplastic syndrome.Semantic proximity Read ↗

Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML.Semantic proximity Read ↗

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

SNP array-based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes.Semantic proximity Read ↗

Single-nucleotide polymorphism array (SNP-A) improves the identification of chromosomal abnormalities by metaphase cytogenetics in myelodysplastic syndrome.Semantic proximity Read ↗

Adverse prognostic impact of abnormal lesions detected by genome-wide single nucleotide polymorphism array-based karyotyping analysis in acute myeloid leukemia with normal karyotype.Semantic proximity Read ↗

Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?Semantic proximity Read ↗

SNP Array in Hematopoietic Neoplasms: A ReviewSemantic proximity Read ↗

Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.Semantic proximity Read ↗

The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.Semantic proximity Read ↗

Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.