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Journal Articles

Genomic Profiling Reveals Spatial Intra-Tumor Heterogeneity in Follicular Lymphoma

Blood (2017) 130 (Supplement 1): 2730.

https://doi.org/10.1182/blood.V130.Suppl_1.2730.2730

Published: 2017

Journal Articles

Alloresponses of Human T-Cells from Adult Peripheral Blood and Umbilical Cord Blood Are Differentially Impacted By Lenalidomide

Caroline Besley, MBBChir, FRCPath, MRCP, Eleni Kotsiou, PhD, Robert Petty, PhD, Sangaralingam Ajanthah, PhD, Claude Chelala, BSc, MSc, DEA, PhD, Essam Ghazaly, PhD, Rifca Le Dieu, MBBS, PhD, Jeff Davies, MBBS, PhD, John Gribben

Blood (2016) 128 (22): 5714.

https://doi.org/10.1182/blood.V128.22.5714.5714

Published: 2016

Journal Articles

Genomic Disruption of the Histone Methyltransferase SETD2 in Chronic Lymphocytic Leukemia

Blood (2015) 126 (23): 365.

https://doi.org/10.1182/blood.V126.23.365.365

Published: 2015

Journal Articles

Disease evolution and outcomes in familial AML with germline CEBPA mutations

Blood (2015) 126 (10): 1214–1223.

https://doi.org/10.1182/blood-2015-05-647172

Published: 2015

Includes: Supplemental data

Journal Articles

Familial AML With Germline CEBPA Mutations: Extended Clinical Outcomes and Analysis Of Secondary Mutations Using Whole Exome Sequencing

Kiran Tawana, MD, Aline Renneville, Jun Wang, PhD, Panayiotis Georgiades, Xavier Thomas, MD, Valerie Mialou, MD, Aleksander Savic, MD, Frederik W Van Delft, MD PhD, Jennifer G. Treleaven, MD, Sameena Iqbal, Norio Asou, MD, PhD, Naokuni Uike, MD, Konstanze Döhner, MD, Lars Bullinger, MD, PhD, Matthias Stelljes, MD, Csaba Bödör, PhD, James D. Cavenagh, MD, Doris Steinemann, PhD, Tim Ripperger, MD, Brigitte Schlegelberger, MD, PhD, Peter Vandenberghe, MD, PhD, Anne Uyttebroeck, MD, Josep F. Nomdedeu, MD, Henrik Hjorth-Hansen, MD, PhD, Rosemary E Gale, PhD, Cynthia L. Toze, MD, FRCP(C), Michael J. Barnett, BMBS, FRCPC, FRCP, FRCPath, Marianna Zombori, MD, Krisztian Kallay, MD, Jiri Pavlu, MD, Pim Mutsaers, MD, Fred H Menko, MD, Angela Thomas, PhD, FRCPath, FRCP, MB, BS, Christine Wright, MD, Jessica Okosun, MD, Chey Loveday, PhD, Pierre Fenaux, MD, PhD, Hamish Scott, PhD, Claude Preudhomme, Claude Chelala, PhD, Alison Male, MD, Carolyn J. Owen, MD, FRCPC, Matthew Smith, MD, PhD, Jude Fitzgibbon, PhD

Blood (2013) 122 (21): 740.

https://doi.org/10.1182/blood.V122.21.740.740

Published: 2013

Journal Articles

Investigating The Role Of MLL2 ( Mll4 ) In B Cell Development

Nikolay Popov, PhD, Eleni Maniati, PhD, Jacek Marzec, Jessica Okosun, MD, Richard Scott, MD, Andrea Kranz, PhD, Francis Stewart, PhD, Claude Chelala, PhD, Thorsten Hagemann, MD, PhD, Jude Fitzgibbon, PhD

Blood (2013) 122 (21): 343.

https://doi.org/10.1182/blood.V122.21.343.343

Published: 2013

Journal Articles

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

Blood (2013) 122 (18): 3165–3168.

https://doi.org/10.1182/blood-2013-04-496893

Published: 2013

Includes: Supplemental data

Journal Articles

Whole Genome Sequencing in Sequential Biopsies Reveals the Genetic Evolution of Follicular Lymphoma to Transformed Follicular Lymphoma

Jessica Okosun, MD, Csaba Bödör, PhD, Jun Wang, PhD, Shamzah Araf, MD, Jacek Marzec, PhD, Sameena Iqbal, Janet Matthews, Maria Calaminici, MD, Ciaran O'Riain, MD, PhD, Derville O'Shea, MD, PhD, Emanuela Carlotti, PhD, Andrew Davies, MD, David Wrench, MD, PhD, András Matolcsy, MD, PhD, T. Andrew Lister, MD, John G Gribben, Silvia Montoto, MD, Claude Chelala, PhD, Jude Fitzgibbon, PhD

Blood (2012) 120 (21): 145.

https://doi.org/10.1182/blood.V120.21.145.145

Published: 2012

Journal Articles

Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia

Manoj Raghavan, Lan-Lan Smith, Debra M. Lillington, Tracy Chaplin, Ioannis Kakkas, Gael Molloy, Claude Chelala, Jean-Baptiste Cazier, James D. Cavenagh, Jude Fitzgibbon, T. Andrew Lister, Bryan D. Young

Blood (2008) 112 (3): 814–821.

https://doi.org/10.1182/blood-2008-01-132431

Published: 2008

Journal Articles

A Genome-Wide Map of Acquired Uniparental Disomy in Acute Myeloid Leukemia.

Manu Gupta, Manoj Raghavan, Rosemary E. Gale, Claude Chelala, Christopher Allen, Gael Molloy, Tracy Chaplin, David C. Linch, Jean-Baptiste Cazier, Bryan Young

Blood (2007) 110 (11): 996.

https://doi.org/10.1182/blood.V110.11.996.996

Published: 2007

NARROW

Genomic Profiling Reveals Spatial Intra-Tumor Heterogeneity in Follicular Lymphoma

Alloresponses of Human T-Cells from Adult Peripheral Blood and Umbilical Cord Blood Are Differentially Impacted By Lenalidomide

Genomic Disruption of the Histone Methyltransferase SETD2 in Chronic Lymphocytic Leukemia

Disease evolution and outcomes in familial AML with germline CEBPA mutations

Familial AML With Germline CEBPA Mutations: Extended Clinical Outcomes and Analysis Of Secondary Mutations Using Whole Exome Sequencing

Investigating The Role Of MLL2 ( Mll4 ) In B Cell Development

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

Whole Genome Sequencing in Sequential Biopsies Reveals the Genetic Evolution of Follicular Lymphoma to Transformed Follicular Lymphoma

Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia

A Genome-Wide Map of Acquired Uniparental Disomy in Acute Myeloid Leukemia.

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American Society of Hematology

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American Society of Hematology

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