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Journal Articles

Transcriptional Profiling Reveals Strong Impact of Major Molecular Disease Subgroups and Mixed Epistasis in Chronic Lymphocytic Leukemia

Thorsten Zenz, MD, Almut Luetge, Junyan Lu, PhD, Huellein Jennifer, PhD, Sascha Dietrich, MD, Leopold Sellner, MD, Wolfgang Huber, PhD

Blood (2019) 134 (Supplement_1): 1742.

https://doi.org/10.1182/blood-2019-126388

Published: 2019

Journal Articles

Impact of Infrequently Mutated Genes on Prognosis in 531 Untreated CLL Patients

Sabine Jeromin, PhD, Manja Meggendorfer, PhD, Claudia Haferlach, MD, Torsten Haferlach, MD, Wolfgang Kern, MD

Blood (2017) 130 (Supplement 1): 3005.

https://doi.org/10.1182/blood.V130.Suppl_1.3005.3005

Published: 2017

Journal Articles

Clonal Evolution of Molecular and Cytogenetic Aberrations in 80 CLL Patients

Sabine Jeromin, PhD, Manja Meggendorfer, PhD, Claudia Haferlach, MD, Torsten Haferlach, MD, Wolfgang Kern, MD

Blood (2017) 130 (Supplement 1): 1720.

https://doi.org/10.1182/blood.V130.Suppl_1.1720.1720

Published: 2017

Journal Articles

Characterization and Prognostic Impact of Multiple Productive IGHV Rearrangements in CLL

Sabine Jeromin, PhD, Claudia Haferlach, MD, Frank Dicker, PhD, Manja Meggendorfer, PhD, Torsten Haferlach, MD, Wolfgang Kern, MD

Blood (2016) 128 (22): 3207.

https://doi.org/10.1182/blood.V128.22.3207.3207

Published: 2016

Journal Articles

Oncogenomic Screening Strategies to Identify Tumour Suppressor Genes on Chromosome 12 in Acute Myeloid Leukaemia

Jake Clayton, Joanna Cheng, Sarra Ryan, Christine J. Harrison, Paul Sinclair

Blood (2014) 124 (21): 898.

https://doi.org/10.1182/blood.V124.21.898.898

Published: 2014

Journal Articles

Interim Analysis of the Mmrf Commpass Trial: Identification of Novel Rearrangements Potentially Associated with Disease Initiation and Progression

Blood (2014) 124 (21): 722.

https://doi.org/10.1182/blood.V124.21.722.722

Published: 2014

Journal Articles

Karyotypic and Genetic Abnormalities Associated with Clonal Evolution in Paroxysmal Nocturnal Hemoglobinuria.

Hideki Makishima, MD, PhD, Kenichi Yoshida, MD, Michael J. Clemente, Masashi Sanada, MD, Yasunobu Nagata, MD, Manuel G. Afable, II, MD, Andres Jerez, MD, Kenichi Chiba, BA, Yuichi Shiraishi, PhD, Satoru Miyano, PhD, Seishi Ogawa, MD, PhD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2012) 120 (21): 2371.

https://doi.org/10.1182/blood.V120.21.2371.2371

Published: 2012

Journal Articles

Incidence of ETV6 Cryptic Translocations In Myeloid Disorders

Eva Maria Murga Penas, PhD, Marianne Klokow, Petra Behrmann, Snjezana Janjetovic, MD, Georgia Schilling, MD, Carsten Bokemeyer, MD, Judith Dierlamm, MD, PhD

Blood (2010) 116 (21): 2733.

https://doi.org/10.1182/blood.V116.21.2733.2733

Published: 2010

Journal Articles

Inversion of Chromosome 12 and Translocations of 12q13-q15 In Primary Myelofibrosis (PMF) Are Associated with Disease Progression and a Poor Prognosis

Vesna Najfeld, PhD, Joseph Tripodi, Nathaniel Wisch, MD, Amory Novoselac, MD, Heike L. Pahl, PhD, Ronald Hoffman, MD

Blood (2010) 116 (21): 4110.

https://doi.org/10.1182/blood.V116.21.4110.4110

Published: 2010

Journal Articles

Impact of Immunoglobulin Heavy Chain (IGH) Translocations In Chronic Lymphocytic Leukemia (CLL): Negative Effect on Patients with Isolated Deletion 13q Abnormality

Alina S. Gerrie, MD, FRCPC, Tanya L. Gillan, PhD, FCCMG, Helene Bruyere, MD, FCCMG, Mary Joyce Chan, BMLSc, Chinmay B. Dalal, MD, Cynthia L. Toze, MD, FRCPC

Blood (2010) 116 (21): 2434.

https://doi.org/10.1182/blood.V116.21.2434.2434

Published: 2010

Journal Articles

Whole Genome Copy Number Variation Analysis of Chronic Lymphocytic Leukemia (CLL) Cells From Early-Intermediate Stage, High Risk CLL Patients Prior to First Treatment Reveals New Loss of Heterozygosity and Duplication Events in the CLL Genome.

Steven A. Schichman, MD, PhD, Annjanette Stone, BS, Maria Winters, MPH, Weleetka Carter, BS, Lori Frederick, BS, Jeanette Eckel-Passow, Ph.D., Timothy G. Call, MD, Tait D. Shanafelt, M.D., Neil E. Kay, MD, Clive S. Zent, MD, David S. Viswanatha, MD

Blood (2009) 114 (22): 1265.

https://doi.org/10.1182/blood.V114.22.1265.1265

Published: 2009

Journal Articles

Newly acquired chromosome Abnormalities During Course of CLL: a Retrospective Collection Data From 2 Spanish Centers.

Javier Loscertales, MD, Eva Arranz, PhD, Maria-Angeles Sanz, PhD, Carmen Burgaleta, MD, PhD, Juan-José Gil-Fernández, MD, PhD, Juan Luis Steegmann, MD, PhD, Adrian Alegre, MD

Blood (2009) 114 (22): 4384.

https://doi.org/10.1182/blood.V114.22.4384.4384

Published: 2009

Journal Articles

Presence of a Common Haplotype in the Turkish VWD Patients.

Ergul Berber, PhD, Aslihan Dagdemir, Funda Pehlevan, Mehmet Akin, Kaan Kavakli, MD, Hande S Caglayan

Blood (2009) 114 (22): 4435.

https://doi.org/10.1182/blood.V114.22.4435.4435

Published: 2009

Journal Articles

Array CGH Analysis of Chronic Lymphocytic Leukemia Reveals Frequent Cryptic Monoallelic and Biallelic Deletions of Chromosome 22q11.

William D. McClain, Shelly R. Gunn, Aswani R. Bolla, Lynn L. Barron, Mercedes E. Gorre, David W. Bahler, Clemens H. M. Mellink, Marinus H. J. van Oers, Michael J. Keating, Alessandra Ferrajoli, Kevin R. Coombes, Lynne V Abruzzo, MD, PhD, Ryan S. Robetorye

Blood (2008) 112 (11): 1050.

https://doi.org/10.1182/blood.V112.11.1050.1050

Published: 2008

Journal Articles

Gene Expression Signature of B-Cell Chronic Lymphocytic Leukemia with Trisomy 12.

Blood (2007) 110 (11): 2079.

https://doi.org/10.1182/blood.V110.11.2079.2079

Published: 2007

Journal Articles

Two Distinct Subsets of dic(9;12)(p12;p11.2) among Children with B-Cell Precursor Acute Lymphoblastic Leukemia (ALL): PAX5-ETV6 and ETV6-RUNX1 Rearrangements: A Report from the Children’s Oncology Group.

Julie M. Gastier-Foster, PhD, Andrew J. Carroll, PhD, Denise Ell, BS, Richard Harvey, PhD, I-Ming Chen, PhD, Rhett Ketterling, MD, Aurelia Meloni-Ehrig, PhD, Kent E. Opheim, PhD, Shivanand Patil, PhD, Mark Pettenati, PhD, Kathleen Rao, PhD, ShiQi Wu, PhD, Nyla A. Heerema, PhD

Blood (2007) 110 (11): 1439.

https://doi.org/10.1182/blood.V110.11.1439.1439

Published: 2007

Journal Articles

Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH)

Norimitsu Inoue, Tomohisa Izui-Sarumaru, Yoshiko Murakami, Yuichi Endo, Jun-Ichi Nishimura, Ken Kurokawa, Maki Kuwayama, Hiroaki Shime, Takashi Machii, Yuzuru Kanakura, Gabrielle Meyers, Carl Wittwer, Zhong Chen, William Babcock, Debra Frei-Lahr, Charles J. Parker, Taroh Kinoshita

Blood (2006) 108 (13): 4232–4236.

https://doi.org/10.1182/blood-2006-05-025148

Published: 2006

Journal Articles

Sequences in Intron 51 of the VWF Gene Target Promoter Activation to a Subset of Lung Endothelial Cells in Transgenic Mice.

Nadia Jahroudi, PhD, Marjan Nassiri, MD, Molly S. Stitt, BSC, Karla Wasserloos, BSC, Simon C. Watkins, PHD, Bruce R. Pitt, PHD, Ann M. Kleinschmidt, PHD

Blood (2006) 108 (11): 1798.

https://doi.org/10.1182/blood.V108.11.1798.1798

Published: 2006

Journal Articles

FISH Studies Provide Evidence That JAK 2 , Via a Myriad of Mechanisms Not Limited to Point Mutation, Has Gain of Function in Polycythemia Vera (PV), and Myelodysplasia (MDS).

Vesna Najfeld, PhD, Windy Berkofsky-Fessler, M.Sc., Amanda Cozza, B.Sc

Blood (2006) 108 (11): 2697.

https://doi.org/10.1182/blood.V108.11.2697.2697

Published: 2006

Journal Articles

Gene Expression Profiling of Hyperdiploid Multiple Reveal Complex Gene Dosage Effects and an mRNA Translation/Protein Synthesis Signature.

Wee-Joo Chng, MD, Scott Van Wier, Gregory Ahmann, Tammy Price-Troska, Kim Henderson, Marta Chesi, PhD, Tae-Hoon Chung, Seungchan Kim, PhD, John Carpten, PhD, Morie Gertz, MD, S. Vincent Rajkumar, MD, Martha Lacy, MD, Robert Kyle, MD, Philip Greipp, MD, Angela Dispenzieri, MD, Peter Leif Bergsagel, MD, Rafael Fonseca, MD

Blood (2005) 106 (11): 1538.

https://doi.org/10.1182/blood.V106.11.1538.1538

Published: 2005

NARROW

Transcriptional Profiling Reveals Strong Impact of Major Molecular Disease Subgroups and Mixed Epistasis in Chronic Lymphocytic Leukemia

Impact of Infrequently Mutated Genes on Prognosis in 531 Untreated CLL Patients

Clonal Evolution of Molecular and Cytogenetic Aberrations in 80 CLL Patients

Characterization and Prognostic Impact of Multiple Productive IGHV Rearrangements in CLL

Oncogenomic Screening Strategies to Identify Tumour Suppressor Genes on Chromosome 12 in Acute Myeloid Leukaemia

Interim Analysis of the Mmrf Commpass Trial: Identification of Novel Rearrangements Potentially Associated with Disease Initiation and Progression

Karyotypic and Genetic Abnormalities Associated with Clonal Evolution in Paroxysmal Nocturnal Hemoglobinuria.

Incidence of ETV6 Cryptic Translocations In Myeloid Disorders

Inversion of Chromosome 12 and Translocations of 12q13-q15 In Primary Myelofibrosis (PMF) Are Associated with Disease Progression and a Poor Prognosis

Impact of Immunoglobulin Heavy Chain (IGH) Translocations In Chronic Lymphocytic Leukemia (CLL): Negative Effect on Patients with Isolated Deletion 13q Abnormality

Whole Genome Copy Number Variation Analysis of Chronic Lymphocytic Leukemia (CLL) Cells From Early-Intermediate Stage, High Risk CLL Patients Prior to First Treatment Reveals New Loss of Heterozygosity and Duplication Events in the CLL Genome.

Newly acquired chromosome Abnormalities During Course of CLL: a Retrospective Collection Data From 2 Spanish Centers.

Presence of a Common Haplotype in the Turkish VWD Patients.

Array CGH Analysis of Chronic Lymphocytic Leukemia Reveals Frequent Cryptic Monoallelic and Biallelic Deletions of Chromosome 22q11.

Gene Expression Signature of B-Cell Chronic Lymphocytic Leukemia with Trisomy 12.

Two Distinct Subsets of dic(9;12)(p12;p11.2) among Children with B-Cell Precursor Acute Lymphoblastic Leukemia (ALL): PAX5-ETV6 and ETV6-RUNX1 Rearrangements: A Report from the Children’s Oncology Group.

Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH)

Sequences in Intron 51 of the VWF Gene Target Promoter Activation to a Subset of Lung Endothelial Cells in Transgenic Mice.

FISH Studies Provide Evidence That JAK 2 , Via a Myriad of Mechanisms Not Limited to Point Mutation, Has Gain of Function in Polycythemia Vera (PV), and Myelodysplasia (MDS).

Gene Expression Profiling of Hyperdiploid Multiple Reveal Complex Gene Dosage Effects and an mRNA Translation/Protein Synthesis Signature.

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American Society of Hematology

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American Society of Hematology

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