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RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Leukemia, 2016-11, Vol.30 (11), p.2160-2168

2016

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Activation of Evi1 inhibits cell cycle progression and differentiation of hematopoietic progenitor cells

Leukemia, 2013-05, Vol.27 (5), p.1127-1138

2013

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Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential

Leukemia, 2021-07, Vol.35 (7), p.2139-2139

2021

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Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing

Clinical genetics, 2018-03, Vol.93 (3), p.665-670

2018

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SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications

Leukemia, 2012-05, Vol.26 (5), p.1137-1140

2012

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Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential

Leukemia, 2021-03, Vol.35 (3), p.933-933

2021

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Acute myeloid leukemia derived from lympho-myeloid clonal hematopoiesis

Leukemia, 2017-06, Vol.31 (6), p.1286-1295

2017

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DNMT3A mutant transcript levels persist in remission and do not predict outcome in patients with acute myeloid leukemia

Leukemia, 2018-01, Vol.32 (1), p.30-37

2018

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Genomic profiling of Acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsis

Leukemia, 2017-10, Vol.31 (10), p.2048-2056

2017

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31 Cytogenetics – for how much longer?

Leukemia research, 2011, Vol.35, p.S11-S11

Schlegelberger, B

2011

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Leukemia induction after a single retroviral vector insertion in Evi1 or Prdm16

Leukemia, 2008-08, Vol.22 (8), p.1519-1528

2008

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RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Leukemia, 2016-11, Vol.30 (11), p.2282

2016

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Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression

Haematologica (Roma), 2009-12, Vol.94 (12), p.1762-1766

2009

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Clinical impact of GATA2 mutations in acute myeloid leukemia patients harboring CEBPA mutations: a study of the AML study group

Leukemia, 2016-11, Vol.30 (11), p.2248-2250

2016

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Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma

Clinical genetics, 2018-07, Vol.94 (1), p.185-186

2018

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Prognostic effect of calreticulin mutations in patients with myelofibrosis after allogeneic hematopoietic stem cell transplantation

Leukemia, 2014-07, Vol.28 (7), p.1552-1555

2014

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Hyperactivation of mTORC1 and mTORC2 by multiple oncogenic events causes addiction to eIF4E-dependent mRNA translation in T-cell leukemia

Oncogene, 2015-07, Vol.34 (27), p.3593-3604

2015

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TEGDMA Causes Apoptosis in Primary Human Gingival Fibroblasts

Journal of dental research, 2003-10, Vol.82 (10), p.814-818

2003

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Prognostic implications and molecular associations of NADH dehydrogenase subunit 4 (ND4) mutations in acute myeloid leukemia

Leukemia, 2012-02, Vol.26 (2), p.289-295

2012

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Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes

Leukemia, 2008-02, Vol.22 (2), p.313-322

2008

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Analysis of NUP98/NSD1 translocations in adult AML and MDS patients

Leukemia, 2013-03, Vol.27 (3), p.750-754

2013

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Altered miRNA and gene expression in acute myeloid leukemia with complex karyotype identify networks of prognostic relevance

Leukemia, 2013-02, Vol.27 (2), p.353-361

2013

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Frequency and prognostic impact of casein kinase 1A1 mutations in MDS patients with deletion of chromosome 5q

Leukemia, 2015-09, Vol.29 (9), p.1942-1945

2015

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Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31

Leukemia, 2004-01, Vol.18 (1), p.113-119

2004

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A critical appraisal of tools available for monitoring epigenetic changes in clinical samples from patients with myeloid malignancies

Haematologica (Roma), 2012-09, Vol.97 (9), p.1380-1388

2012

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RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Activation of Evi1 inhibits cell cycle progression and differentiation of hematopoietic progenitor cells

Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential

Diagnosis of monogenic liver diseases in childhood by next‐generation sequencing

SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications

Correction: Generation and characterization of a novel hematopoietic progenitor cell line with DC differentiation potential

Acute myeloid leukemia derived from lympho-myeloid clonal hematopoiesis

DNMT3A mutant transcript levels persist in remission and do not predict outcome in patients with acute myeloid leukemia

Genomic profiling of Acute lymphoblastic leukemia in ataxia telangiectasia patients reveals tight link between ATM mutations and chromothripsis

31 Cytogenetics – for how much longer?

Leukemia induction after a single retroviral vector insertion in Evi1 or Prdm16

RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Clonal heterogeneity in the 5q- syndrome: p53 expressing progenitors prevail during lenalidomide treatment and expand at disease progression

Clinical impact of GATA2 mutations in acute myeloid leukemia patients harboring CEBPA mutations: a study of the AML study group

Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma

Prognostic effect of calreticulin mutations in patients with myelofibrosis after allogeneic hematopoietic stem cell transplantation

Hyperactivation of mTORC1 and mTORC2 by multiple oncogenic events causes addiction to eIF4E-dependent mRNA translation in T-cell leukemia

TEGDMA Causes Apoptosis in Primary Human Gingival Fibroblasts

Prognostic implications and molecular associations of NADH dehydrogenase subunit 4 (ND4) mutations in acute myeloid leukemia

Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes

Analysis of NUP98/NSD1 translocations in adult AML and MDS patients

Altered miRNA and gene expression in acute myeloid leukemia with complex karyotype identify networks of prognostic relevance

Frequency and prognostic impact of casein kinase 1A1 mutations in MDS patients with deletion of chromosome 5q

Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31

A critical appraisal of tools available for monitoring epigenetic changes in clinical samples from patients with myeloid malignancies

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