Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

Topography, Clinical, and Genomic Correlates of 5q Myeloid Malignancies Revisited

(2012) Andres Jerez et al.   JOURNAL OF CLINICAL ONCOLOGY

Marked down-regulation of nucleophosmin-1 is associated with advanced del(5q) myelodysplastic syndrome

(2011) Andrea Pellagatti et al.   BRITISH JOURNAL OF HAEMATOLOGY

Better prognosis for patients with del(7q) than for patients with monosomy 7 in myelodysplastic syndrome

(2011) Iris Cordoba et al.   CANCER

Disruption of the ASXL1 gene is frequent in primary, post-essential thrombocytosis and post-polycythemia vera myelofibrosis, but not essential thrombocytosis or polycythemia vera: analysis of molecular genetics and clinical phenotypes

(2011) B. L. Stein et al.   HAEMATOLOGICA

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

(2010) D. Grimwade et al.   BLOOD

Cytogenetic risk stratification in chronic myelomonocytic leukemia

(2010) E. Such et al.   HAEMATOLOGICA

Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies

(2010) H Makishima et al.   LEUKEMIA

Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

(2010) A Pellagatti et al.   LEUKEMIA

Does monosomy 5 really exist in myelodysplastic syndromes and acute myeloid leukemia?

(2010) Ana Belén Galván et al.   LEUKEMIA RESEARCH

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

(2010) Thomas Ernst et al.   NATURE GENETICS

New Lesions Detected by Single Nucleotide Polymorphism Array–Based Chromosomal Analysis Have Important Clinical Impact in Acute Myeloid Leukemia

(2009) Ramon V. Tiu et al.   JOURNAL OF CLINICAL ONCOLOGY

Mutation inTET2in Myeloid Cancers

(2009) François Delhommeau et al.   NEW ENGLAND JOURNAL OF MEDICINE

250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of c-Cbl, in Myeloid Malignancies

(2008) A. J. Dunbar et al.   CANCER RESEARCH

High frequency of copy-neutral LOH inMUTYH-associated polyposis carcinomas

(2008) A Middeldorp et al.   JOURNAL OF PATHOLOGY

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

(2008) Benjamin L. Ebert et al.   NATURE

Hypocellularity in myelodysplastic syndrome is an independent factor which predicts a favorable outcome

(2007) Gang Yue et al.   LEUKEMIA RESEARCH