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Journal Articles

Exon-Level Genomic Abnormalities Are Frequent in Cytogenetically Normal Patients with Philadelphia-Chromosome Negative Myeloproliferative Neoplasms (MPNs)

Joseph Tripodi, Douglas Tremblay, MD, Ronald Hoffman, MD, Umut Ozbek, PhD, John Mascarenhas, MD, Marina Kremyanskaya, Vesna Najfeld, PhD

Blood (2019) 134 (Supplement_1): 1687.

https://doi.org/10.1182/blood-2019-128948

Published: 2019

Journal Articles

Recurrent Copy Number Variants Are Highly Prevalent in Acute Myeloid Leukemia

Katherine Tarlock, MD, Yuting He, James Sun, Rhonda E. Ries, MA, Eric A Severson, MD PhD MMSc, Mark Bailey, MS, Samantha Morley, PhD, Sohail Balasubramanian, Rachel Erlich, PhD, Doron Lipson, PhD, Geoff Otto, PhD, Jo-Anne Vergillo, Jeffrey S Ross, MD, Tariq Mughal, FRCP, Phil Stephens, PhD, Vincent Miller, MD, Soheil Meshinchi, MD PhD, Jie He, PhD

Blood (2017) 130 (Supplement 1): 3800.

https://doi.org/10.1182/blood.V130.Suppl_1.3800.3800

Published: 2017

Journal Articles

Identification of Progression-Associated Mutations in Chronic Myeloid Leukemia (CML) By Comparative Genomic Analysis

Shady Adnan Awad, MD, Matti Kankainen, PhD, Samuli Eldfors, Bhagwan Yadav, PhD, Soili Kytölä, Pekka Ellonen, Mahmoud Kamel, MD PhD, Caroline A Heckman, PhD, Kimmo Porkka, MD PhD, Satu Mustjoki, MDPhD

Blood (2017) 130 (Supplement 1): 250.

https://doi.org/10.1182/blood.V130.Suppl_1.250.250

Published: 2017

Journal Articles

Impact of I(17q) in Myeloproliferative Neoplasms

Zimu Gong, MD, Zi Chen, MD, Srdan Verstovsek, MD PhD, Jorge E. Cortes, MD, Arash Ronaghy, MD, Wei Wang, MD PhD, Carlos E. Bueso-Ramos, MD PhD, L. Jeffrey Medeiros, MD, Shimin Hu, PhD MD

Blood (2017) 130 (Supplement 1): 2911.

https://doi.org/10.1182/blood.V130.Suppl_1.2911.2911

Published: 2017

Journal Articles

Analyzing the Transcriptome Discovers up-Regulation of HOXA Genes in Patients with Myeloid Neoplasms and Isochromosome 17q and Mutations in ASXL1 , SETBP1 and SRSF2

Manja Meggendorfer, PhD, Niroshan Nadarajah, M.Sc., Claudia Haferlach, MD, Wolfgang Kern, MD, Torsten Haferlach, MD

Blood (2016) 128 (22): 2703.

https://doi.org/10.1182/blood.V128.22.2703.2703

Published: 2016

Journal Articles

Experience of Conventional Cytogenetics in Elderly Cytopenic Indian Patients Suspected with Myelodysplastic Syndromes

Bani Bandana Ganguly, PhD, Mandal Shouvik, MD, Nitin N Kadam, MD, Debasis Banerjee, MD, Sharmila Chandra, MD, Tuphan Kanti Dolai, MD, Mohan Agarwal, MDMNAMS

Blood (2016) 128 (22): 5488.

https://doi.org/10.1182/blood.V128.22.5488.5488

Published: 2016

Journal Articles

Whole Genome and Transcriptome Analysis of Waldenstrom's Cell Lines Show Preservation of Many Important Genomic Features of Primary Disease, and Identify a Non-L265P Mutation in MYD88

Zachary Hunter, PhD, Yang Cao, MD, Guang Yang, PhD, Xia Liu, MD, Jie Chen, PhD, Lian Xu, Nicholas Tsakmaklis, Jiaji Chen, Christopher J Patterson, MFA, Jorge J Castillo, MD, Steven P Treon, MD PhD

Blood (2015) 126 (23): 2665.

https://doi.org/10.1182/blood.V126.23.2665.2665

Published: 2015

Journal Articles

The Landscape of Myeloid Neoplasms with Isochromosome 17q Discloses a Specific Mutation Profile and Is Characterized By an Accumulation of Prognostically Adverse Molecular Markers

Manja Meggendorfer, PhD, Claudia Haferlach, MD, Wolfgang Kern, MD, Susanne Schnittger, PhD, Torsten Haferlach

Blood (2015) 126 (23): 1656.

https://doi.org/10.1182/blood.V126.23.1656.1656

Published: 2015

Journal Articles

A Compendium of Cytogenetic Abnormalities in Myelofibrosis: Molecular and Phenotypic Correlates in 826 Patients

Emnet A Wassie, MD, Christy Finke, BS, Naseema Gangat, MD, Terra L Lasho, PhD, Animesh Pardanani, MBBS, PhD, Curtis A. Hanson, MD, Ketterling Rhett, Ayalew Tefferi, MD

Blood (2014) 124 (21): 403.

https://doi.org/10.1182/blood.V124.21.403.403

Published: 2014

Journal Articles

Revised Cytogenetic Risk Stratification in Primary Myelofibrosis: A Mayo Clinic Study of 903 Patients

Ayalew Tefferi, MD, Emnet A Wassie, MD, Kebede Begna, MD, Christy Finke, BS, Alem A Belachew, Naseema Gangat, MD, Terra L Lasho, PhD, Animesh Pardanani, MBBS, PhD, Curtis A. Hanson, MD, Rhett Ketterling, MD

Blood (2014) 124 (21): 631.

https://doi.org/10.1182/blood.V124.21.631.631

Published: 2014

Journal Articles

Population Based Study of Cytogenetic Abnormalities in Addition to Philadelphia (Ph) Chromosome in Patients with Chronic Myeloid Leukaemia (CML) and Impact on Survival

Jo Tomlins, MSc, Nick Telford, PhD, Mike Dennis, FRCPath, Tim Somervaille, FRCPath, Adrian Bloor, PhD FRCPath, Jim Cavet, FRCPath, Mike Green, PhD, Sven Armin Sommerfeld, MRCP, John Murray, RGN, MSc, Samar Kulkarni, FRCPath

Blood (2014) 124 (21): 4567.

https://doi.org/10.1182/blood.V124.21.4567.4567

Published: 2014

Journal Articles

FISH: negative. Morphology: positive.

Armin Rashidi, Stephen I. Fisher

Blood (2014) 124 (23): 3501.

https://doi.org/10.1182/blood-2014-09-597468

Published: 2014

Journal Articles

Molecular Characterization Of Myeloid Neoplasms Harboring Isochromosome 17q Abnormality

Valeria Visconte, PhD, Ali Tabarroki, MD, Li Zhang, Edy Hasrouni, Chris Gerace, Robyn Frum, Anjali S. Advani, MD, Hien K. Duong, MD, Matt Kalaycio, MD, Yogen Saunthararajah, M.D., Mikkael A. Sekeres, MD, MS, Eric D. Hsi, MD, Shashirekha Shetty, PhD, Heesun J. Rogers, MD, PhD, Ramon V. Tiu, MD

Blood (2013) 122 (21): 2596.

https://doi.org/10.1182/blood.V122.21.2596.2596

Published: 2013

Journal Articles

Characterization and Quantification Of Rare BCR-ABL1 Fusion Transcripts

Susanne Schnittger, PhD, Frank Dicker, PhD, Tamara Alpermann, Christiane Eder, PhD, Annette Fasan, PhD, Simone Weber, Sabine Jeromin, PhD, Manja Meggendorfer, PhD, Wolfgang Kern, MD, Torsten Haferlach, MD, Claudia Haferlach, MD

Blood (2013) 122 (21): 4013.

https://doi.org/10.1182/blood.V122.21.4013.4013

Published: 2013

Journal Articles

Myeloid Malignancies With Isochromosome 17q Harbor Frequently Mutations In ASXL1 , SETBP1 , and SRSF2 - This Distinct Genotype Presents With Various Morphological Phenotypes

Manja Meggendorfer, PhD, Tamara Alpermann, Claudia Haferlach, MD, Elisabeth Sirch, Wolfgang Kern, MD, Torsten Haferlach, MD, Susanne Schnittger, PhD

Blood (2013) 122 (21): 1364.

https://doi.org/10.1182/blood.V122.21.1364.1364

Published: 2013

Journal Articles

Molecular Analysis of Primary Cutaneous Aggressive T-Cell Lymphomas: the Epidermotropic CD8+, the Pleomorphic CD8+ and the Gamma Delta Subsets.

Emilio Berti, MD, Daniele Fanoni, MS, Francesco Onida, MD, Valentina Girgenti, MD, Francesca Novara, MS, Laura Corti, MS, PhD, Luigia Venegoni, MS, Francesca Viganò, MD, Giorgia Saporiti, MD, Orsetta Zuffardi, MD, Marco Paulli

Blood (2012) 120 (21): 2713.

https://doi.org/10.1182/blood.V120.21.2713.2713

Published: 2012

Journal Articles

A Reappraisal of the Biological and Clinical Implications of Chromosomal Translocations in Chronic Lymphocytic Leukemia

Panagiotis Baliakas, Michalis Iskas, Anne Gardiner, Zadie Davis, Karla Plevova, Jitka Malcikova, Achilles Anagnostopoulos, Sharron Glide, Sarah Mould, Gabriela Vankova, Sarka Pospisilova, Anastasia Athanasiadou, Kostas Stamatopoulos, David Oscier

Blood (2012) 120 (21): 3915.

https://doi.org/10.1182/blood.V120.21.3915.3915

Published: 2012

Journal Articles

Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms

Joannah Score, Claire Hidalgo-Curtis, Amy V. Jones, Nils Winkelmann, Alison Skinner, Daniel Ward, Katerina Zoi, Thomas Ernst, Frank Stegelmann, Konstanze Döhner, Andrew Chase, Nicholas C. P. Cross

Blood (2012) 119 (5): 1208–1213.

https://doi.org/10.1182/blood-2011-07-367243

Published: 2012

Includes: Supplemental data

Journal Articles

Survival Analysis of Additional Chromosomal Aberrations in Philadelphia Chromosome Positive and Negative Cells: A Single Institutional

William Bulkeley, MD, Bijal D. Shah, MD, Monique A Hartley, MD, John M. Bennett, MD, Rami S. Komrokji, MD, Ling Zhang, MD, Javier Pinilla

Blood (2011) 118 (21): 2523.

https://doi.org/10.1182/blood.V118.21.2523.2523

Published: 2011

Journal Articles

Predictors of greater than 80% 2-year mortality in primary myelofibrosis: a Mayo Clinic study of 884 karyotypically annotated patients

Ayalew Tefferi, Thitina Jimma, Naseema Gangat, Rakhee Vaidya, Kebede H. Begna, Curtis A. Hanson, Daniel L. Van Dyke, Domenica Caramazza, Animesh Pardanani

Blood (2011) 118 (17): 4595–4598.

https://doi.org/10.1182/blood-2011-08-371096

Published: 2011

Includes: Supplemental data

NARROW

Exon-Level Genomic Abnormalities Are Frequent in Cytogenetically Normal Patients with Philadelphia-Chromosome Negative Myeloproliferative Neoplasms (MPNs)

Recurrent Copy Number Variants Are Highly Prevalent in Acute Myeloid Leukemia

Identification of Progression-Associated Mutations in Chronic Myeloid Leukemia (CML) By Comparative Genomic Analysis

Impact of I(17q) in Myeloproliferative Neoplasms

Analyzing the Transcriptome Discovers up-Regulation of HOXA Genes in Patients with Myeloid Neoplasms and Isochromosome 17q and Mutations in ASXL1 , SETBP1 and SRSF2

Experience of Conventional Cytogenetics in Elderly Cytopenic Indian Patients Suspected with Myelodysplastic Syndromes

Whole Genome and Transcriptome Analysis of Waldenstrom's Cell Lines Show Preservation of Many Important Genomic Features of Primary Disease, and Identify a Non-L265P Mutation in MYD88

The Landscape of Myeloid Neoplasms with Isochromosome 17q Discloses a Specific Mutation Profile and Is Characterized By an Accumulation of Prognostically Adverse Molecular Markers

A Compendium of Cytogenetic Abnormalities in Myelofibrosis: Molecular and Phenotypic Correlates in 826 Patients

Revised Cytogenetic Risk Stratification in Primary Myelofibrosis: A Mayo Clinic Study of 903 Patients

Population Based Study of Cytogenetic Abnormalities in Addition to Philadelphia (Ph) Chromosome in Patients with Chronic Myeloid Leukaemia (CML) and Impact on Survival

FISH: negative. Morphology: positive.

Molecular Characterization Of Myeloid Neoplasms Harboring Isochromosome 17q Abnormality

Characterization and Quantification Of Rare BCR-ABL1 Fusion Transcripts

Myeloid Malignancies With Isochromosome 17q Harbor Frequently Mutations In ASXL1 , SETBP1 , and SRSF2 - This Distinct Genotype Presents With Various Morphological Phenotypes

Molecular Analysis of Primary Cutaneous Aggressive T-Cell Lymphomas: the Epidermotropic CD8+, the Pleomorphic CD8+ and the Gamma Delta Subsets.

A Reappraisal of the Biological and Clinical Implications of Chromosomal Translocations in Chronic Lymphocytic Leukemia

Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms

Survival Analysis of Additional Chromosomal Aberrations in Philadelphia Chromosome Positive and Negative Cells: A Single Institutional

Predictors of greater than 80% 2-year mortality in primary myelofibrosis: a Mayo Clinic study of 884 karyotypically annotated patients

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American Society of Hematology

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American Society of Hematology

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