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Journal Articles

ETNK1 Mutations in Atypical Chronic Myeloid Leukemia Induce a Mutator Phenotype That Can be Reverted with Phosphoethanolamine

Blood (2020) 136 (Supplement_2): LBA-5.

https://doi.org/10.1182/blood-2020-143852

Published: 2020

Journal Articles

Development of a Data Portal for Aggregation and Analysis of Genomics Data in Familial Platelet Disorder with Predisposition to Myeloid Malignancy - the RUNX1.DB

Anna L. Brown, PhD BSc, Mark Armstrong, MSc, David Lawrence, Paul Wang, Peer Arts, PhD, Nicolas Duployez, PharmD, PhD, Jane Churpek, MD, Kiran Tawana, MD, Erin Degelman, MSc, BSc, Georges Natsoulis, PhD, Monica L. Guzman, PhD, Mrinal M. Patnaik, MD MBBS, Akiko Shimamura, MD PhD, Alan B. Cantor, MD PhD, Tim Ripperger, MD PhD, Brigitte Schlegelberger, MD PhD, Doris Steinemann, PhD, Courtney D. DiNardo, MD MSc, Cristina Mecucci, MD PhD, Elvira DRP Velloso, MD PhD, Fabio PS Santos, MD, Marcela CA Silva, Uma Borate, MD, Shannon K. McWeeney, PhD, Grzegorz Nalepa, MD PhD, Susanne Ragg, MD PhD, Erika Mijin Kwon, PhD, Anupriya Agarwal, PhD, Stephen Langabeer, PhD, Jeffery M. Klco, MD PhD, Jun J. Yang, PhD, Cecily Forsyth, FRACP, FRCPA, MBBS, Sally Mapp, MD PhD, Helen Mar Fan, MD, Lesley Rawlings, PhD, Rachel Susman, Sue Morgan, FRACP, FRCPA, MBBS, Andrew H Wei, MBBS,PhD, Inderjeet Dokal, MD, Tom Vulliamy, Devendra K Hiwase, MBBS, MD FRACP, FRCPA, PhD, Deepak Singhal, MBBS, MD FRACP, FRCPA, Susan Branford, PhD, Elli Papaemmanuil, PhD, Jean Soulier, MDPhD, Stefan Fröhling, MD, Alwin Kramer, MD, Guy Sauvageau, MD PhD, Neil Morgan, Carolyn Owen, Csaba Bödör, PhD, Jude Fitzgibbon, Hugh Y. Rienhoff, Jr., MD, Mineo Kurokawa, MD PhD, Lucy Godley, MD PhD, Claude Preudhomme, Paul P Liu, MD PhD, Nicola Poplawski, MD, Christopher N. Hahn, PhD, Hamish S. Scott, PhD

Blood (2018) 132 (Supplement 1): 5241.

https://doi.org/10.1182/blood-2018-99-118017

Published: 2018

Journal Articles

Haploidentical Transplantation with Regulatory and Conventional T Cells Improves Outcome of Patients Affected By Acute Myeloid Leukemia with Complex Karyotype and/or Monosomy 7/Del(7q)

Blood (2018) 132 (Supplement 1): 2183.

https://doi.org/10.1182/blood-2018-99-116638

Published: 2018

Journal Articles

New Recurrently Mutated Genes in Classical Hodgkin Lymphoma Revealed By Whole-Exome Sequencing of Microdissected Tumor Cells

Enrico Tiacci#, Alexander Penson#, Gianluca Schiavoni#, Erik Ladewig#, Elisabetta Fortini#, Yuchun Wang, Ariele Spanhol-Rosseto, Alessandra Venanzi, Alessandro M. Gianni, Simonetta Viviani, MD, Antonello Cabras, Barbara Crescenzi, Cristina Mecucci, MD PhD, Laura Pasqualucci°, Raul Rabadan°, Brunangelo Falini°

Blood (2016) 128 (22): 1088.

https://doi.org/10.1182/blood.V128.22.1088.1088

Published: 2016

Journal Articles

Use of Lenalidomide in DEL(5q) MDS. a National AIFA (Agenzia Italiana del Farmaco) Registry Study

Francesco Arcioni, MD, Andrea Roncadori, Valeria Di Battista, MD, Giuliana Alimena, MD, Fabrizio Pane, MD, Giuseppe Rossi, Francesco Buccisano, MD, Anna D'Emilio, MD, Nicola Di Renzo, Pietro Leoni, Prof., Giovanni Caocci, Alessandro Rambaldi, MD, Paolo Avanzini, Giuseppe Visani, MD, Sante Tura, MD, Anna Covezzoli, Cristina Mecucci, MD PhD

Blood (2015) 126 (23): 1693.

https://doi.org/10.1182/blood.V126.23.1693.1693

Published: 2015

Journal Articles

Targeted Re-Sequencing Analysis of 31 Genes Commonly Mutated in Myeloid Disorders in Serial Samples from Myelodysplastic Syndrome Patients with Disease Progression

Andrea Pellagatti, Cristina Di Genua, Swagata Roy, Adam Burns, BSc, Kathy L McGraw, PhD, Maria José Larrayoz, Marta Fernandez-Mercado, Simona Valletta, Joanne Mason, PhD, Sally Killick, Cristina Mecucci, MD PhD, Maria José Calasanz, Alan F. List, MD, Anna Schuh, MDPhD, Jacqueline Boultwood, PhD

Blood (2014) 124 (21): 1901.

https://doi.org/10.1182/blood.V124.21.1901.1901

Published: 2014

Journal Articles

NUP98 Fusion Proteins Are Recurrent Aberrancies in Childhood Acute Myeloid Leukemia: A Report from the AIEOP AML-2001-02 Study Group

Valeria Bisio, BS, Martina Pigazzi, PhD, Elena Manara, PhD, Riccardo Masetti, MD, Marco Togni, BS, Annalisa Astolfi, PhD, Cristina Mecucci, MD PhD, Vincenzo Zappavigna, PhD, Valentina Salsi, PhD, Pietro Merli, MD, Carmelo Rizzari, Franca Fagioli, MD, Franco Locatelli, Giuseppe Basso, MD

Blood (2014) 124 (21): 1025.

https://doi.org/10.1182/blood.V124.21.1025.1025

Published: 2014

Journal Articles

Therapy-Related Myeloid Neoplasms: Report Of The Italian Network On Secondary Leukemias

Blood (2013) 122 (21): 2659.

https://doi.org/10.1182/blood.V122.21.2659.2659

Published: 2013

Journal Articles

TERT Gene Promoter Mutations In Myelodysplastic Syndromes (MDS)

Caterina Matteucci, Tamara Iannotti, Lucia Brandimarte, Valeria Nofrini, Gianluca Barba, Antonella Sgura, Francesco Berardinelli, Filomena Nozza, Valeria Di Battista, Cristina Mecucci, MD, PhD

Blood (2013) 122 (21): 1570.

https://doi.org/10.1182/blood.V122.21.1570.1570

Published: 2013

Journal Articles

Chemical Genomic Screen Identifies Ionophores as Modulators of Notch1 in T-ALL

Giovanni Roti, MD, Kenneth N. Ross, PhD, Cristina Mecucci, MD, PhD, Adolfo A. Ferrando, MD, PhD, Jon C. Aster, MD, PhD, Kimberly Stegmaier, MD

Blood (2008) 112 (11): 200.

https://doi.org/10.1182/blood.V112.11.200.200

Published: 2008

Journal Articles

Quantitative Detection of NPM1 Mutations as Marker of Minimal Residual Disease (MRD) in the Large Majority of AML with Normal Karyotype.

Giuseppe Saglio, MD, Paolo Gorello, PhD, Giovanni Cazzaniga, PhD, Enrico Gottardi, Maria Grazia Dell’Oro, MD, Roberto Rosati, PhD, Giovanni Roti, MD, Federica Alberti, PhD, Daniela Diverio, PhD, Massimo Fabrizio Martelli, MD, Francesco Lo Coco, MD, Andrea Biondi, MD, Brunangelo Falini, MD, Cristina Mecucci, MD, PhD

Blood (2005) 106 (11): 225.

https://doi.org/10.1182/blood.V106.11.225.225

Published: 2005

NARROW

ETNK1 Mutations in Atypical Chronic Myeloid Leukemia Induce a Mutator Phenotype That Can be Reverted with Phosphoethanolamine

Development of a Data Portal for Aggregation and Analysis of Genomics Data in Familial Platelet Disorder with Predisposition to Myeloid Malignancy - the RUNX1.DB

Haploidentical Transplantation with Regulatory and Conventional T Cells Improves Outcome of Patients Affected By Acute Myeloid Leukemia with Complex Karyotype and/or Monosomy 7/Del(7q)

New Recurrently Mutated Genes in Classical Hodgkin Lymphoma Revealed By Whole-Exome Sequencing of Microdissected Tumor Cells

Use of Lenalidomide in DEL(5q) MDS. a National AIFA (Agenzia Italiana del Farmaco) Registry Study

Targeted Re-Sequencing Analysis of 31 Genes Commonly Mutated in Myeloid Disorders in Serial Samples from Myelodysplastic Syndrome Patients with Disease Progression

NUP98 Fusion Proteins Are Recurrent Aberrancies in Childhood Acute Myeloid Leukemia: A Report from the AIEOP AML-2001-02 Study Group

Therapy-Related Myeloid Neoplasms: Report Of The Italian Network On Secondary Leukemias

TERT Gene Promoter Mutations In Myelodysplastic Syndromes (MDS)

Chemical Genomic Screen Identifies Ionophores as Modulators of Notch1 in T-ALL

Quantitative Detection of NPM1 Mutations as Marker of Minimal Residual Disease (MRD) in the Large Majority of AML with Normal Karyotype.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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