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Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome

Nature communications, 2015-01, Vol.6 (1), p.6042-6042, Article 6042

2015

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A novel hierarchical prognostic model of AML solely based on molecular mutations

Blood, 2012-10, Vol.120 (15), p.2963-2972

2012

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Comprehensive mutational profiling in advanced systemic mastocytosis

Blood, 2013-10, Vol.122 (14), p.2460-2466

2013

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Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

Journal of clinical oncology, 2010-08, Vol.28 (24), p.3858-3865

2010

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Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia

Blood, 2012-03, Vol.119 (13), p.3151-3154

2012

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High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms

Haematologica (Roma), 2013-02, Vol.98 (2), p.e15-e17

2013

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Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2011-12, Vol.96 (12), p.1874-1877

2011

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The corepressors BCOR and BCORL1: two novel players in acute myeloid leukemia

Haematologica (Roma), 2012-01, Vol.97 (1), p.3-5

2012

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Frequency and prognostic impact of CEBPA proximal, distal and core promoter methylation in normal karyotype AML: a study on 623 cases

PloS one, 2013-02, Vol.8 (2), p.e54365-e54365

2013

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Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements

Haematologica (Roma), 2013-03, Vol.98 (3), p.404-408

2013

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Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases

Haematologica (Roma), 2012-12, Vol.97 (12), p.1890-1894

2012

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Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow

Haematologica (Roma), 2012-10, Vol.97 (10), p.1582-1585

2012

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Next‐generation sequencing – feasibility and practicality in haematology

British journal of haematology, 2013-03, Vol.160 (6), p.736-753

2013

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Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes

Diabetes care, 2015-07, Vol.38 (7), p.1356-1364

2015

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SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

Blood, 2012-10, Vol.120 (15), p.3080-3088

2012

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Antitumor Activity of Larotrectinib in Esophageal Carcinoma with NTRK Gene Amplification

The oncologist (Dayton, Ohio), 2020-06, Vol.25 (6), p.e881-e886

2020

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Integration of Next-Generation Sequencing Into Clinical Practice: Are We There Yet?

Seminars in oncology, 2012-02, Vol.39 (1), p.26-36

2012

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The molecular profile of adult T-cell acute lymphoblastic leukemia: Mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL

Genes chromosomes & cancer, 2013-04, Vol.52 (4), p.410-422

2013

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CEBPA double‐mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis

British journal of haematology, 2013-06, Vol.161 (5), p.649-658

2013

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Sex-specific differences in genetic and nongenetic determinants of mean platelet volume: results from the Gutenberg Health Study

Blood, 2016-01, Vol.127 (2), p.251-259

2016

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Investigation of 305 patients with myelodysplastic syndromes and 20q deletion for associated cytogenetic and molecular genetic lesions and their prognostic impact

British journal of haematology, 2014-03, Vol.164 (6), p.822-833

2014

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Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity

Blood, 2012-05, Vol.119 (20), p.4719-4722

2012

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Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases

Genes chromosomes & cancer, 2012-12, Vol.51 (12), p.1079-1085

2012

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Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome

A novel hierarchical prognostic model of AML solely based on molecular mutations

Comprehensive mutational profiling in advanced systemic mastocytosis

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

Development and validation of a real-time quantification assay to detect and monitor BRAFV600E mutations in hairy cell leukemia

High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms

Prognostic relevance of RUNX1 mutations in T-cell acute lymphoblastic leukemia

The corepressors BCOR and BCORL1: two novel players in acute myeloid leukemia

Frequency and prognostic impact of CEBPA proximal, distal and core promoter methylation in normal karyotype AML: a study on 623 cases

Ruxolitinib as potential targeted therapy for patients with JAK2 rearrangements

Use of CBL exon 8 and 9 mutations in diagnosis of myeloproliferative neoplasms and myelodysplastic/myeloproliferative disorders: an analysis of 636 cases

Molecular analyses of 15,542 patients with suspected BCR-ABL1-negative myeloproliferative disorders allow to develop a stepwise diagnostic workflow

Next‐generation sequencing – feasibility and practicality in haematology

Profile of the Immune and Inflammatory Response in Individuals With Prediabetes and Type 2 Diabetes

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

Antitumor Activity of Larotrectinib in Esophageal Carcinoma with NTRK Gene Amplification

Integration of Next-Generation Sequencing Into Clinical Practice: Are We There Yet?

The molecular profile of adult T-cell acute lymphoblastic leukemia: Mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL

EZH2 mutations are frequent and represent an early event in follicular lymphoma

Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

CEBPA double‐mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis

Sex-specific differences in genetic and nongenetic determinants of mean platelet volume: results from the Gutenberg Health Study

Investigation of 305 patients with myelodysplastic syndromes and 20q deletion for associated cytogenetic and molecular genetic lesions and their prognostic impact

Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity

Three novel cytogenetically cryptic EVI1 rearrangements associated with increased EVI1 expression and poor prognosis identified in 27 acute myeloid leukemia cases

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