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Journal Articles

Cohort Analysis of FISH Testing of CD138+ Cells in Relapsed Multiple Myeloma: Implications for Prognosis and Choice of Therapy

Dean Smith, MBBS, Clemency Stephenson, Anna Lach, Steve Chatters, Helena Kempski, Kwee L Yong, MBChB, PhD

Blood (2014) 124 (21): 3399.

https://doi.org/10.1182/blood.V124.21.3399.3399

Published: 2014

Journal Articles

Distinctive Genotypes In Infants With T-Cell Acute Lymphoblastic Leukemia (T-ALL)

Marcela B Mansur, PhD, Frederik W Van Delft, MD PhD, Caroline L Furness, MD, Mariana Emerenciano, PhD, Susan M Colman, Emma Butcher, Helena Kempski, Emmanuelle Clappier, Hélène Cave, PhD, Jean Soulier, MD, PhD, Maria S. Pombo-de-Oliveira, MD, PhD, Mel Greaves, PhD, FRS, Anthony M Ford, PhD

Blood (2013) 122 (21): 1377.

https://doi.org/10.1182/blood.V122.21.1377.1377

Published: 2013

Journal Articles

RAG-Mediated Recombination Is The Predominant Driver Of Oncogenic Rearrangement In ETV6-RUNX1 Acute Lymphoblastic Leukemia

Elli Papaemmanuil, PhD, Yilong Li, Nicola E. Potter, PhD, David Wedge, Giovanni Cazzaniga, PhD, Andrea Biondi, MD, Jan Zuna, Peter Van Loo, PhD, Helena Kempski, Anthony M. Ford, PhD, Mel Greaves, PhD, FRS, Peter J. Campbell, PhD

Blood (2013) 122 (21): 807.

https://doi.org/10.1182/blood.V122.21.807.807

Published: 2013

Journal Articles

The Genomic Landscape of TEL-AML1 + ( ETV6-RUNX1 ) Acute Lymphoblastic Leukaemia

Elli Papaemmanuil, Inmaculada Rapado, Anthony M Ford, Keiran Raine, Jonathan Hinton, David Jones, John Marshall, Laura J Mudie, Jan Zuna, Giovanni Cazzaniga, Helena Kempski, Maria S Pombo de Oliveira, Mike R Stratton, P Andrew Futreal, Peter Campbell, Mel Greaves

Blood (2011) 118 (21): 403.

https://doi.org/10.1182/blood.V118.21.403.403

Published: 2011

Journal Articles

PAX5 Is a Frequently Altered Transcription Factor In Genetically Unclassified Childhood Common/B-Cell Precursor Acute Lymphoblastic Leukemia

Iryna Stasevich, Sarah Inglott, Philip Ancliff, Owen Williams, Helena Kempski

Blood (2011) 118 (21): 1458.

https://doi.org/10.1182/blood.V118.21.1458.1458

Published: 2011

Journal Articles

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia

Frederik W. van Delft, Sharon Horsley, Sue Colman, Kristina Anderson, Caroline Bateman, Helena Kempski, Jan Zuna, Cornelia Eckert, Vaskar Saha, Lyndal Kearney, Anthony Ford, Mel Greaves

Blood (2011) 117 (23): 6247–6254.

https://doi.org/10.1182/blood-2010-10-314674

Published: 2011

Includes: Supplemental data

Journal Articles

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2 : a report from the International BFM Study Group

Blood (2010) 115 (5): 1006–1017.

https://doi.org/10.1182/blood-2009-08-235408

Published: 2010

Includes: Supplemental data

Journal Articles

DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.

Blood (2009) 114 (22): 11.

https://doi.org/10.1182/blood.V114.22.11.11

Published: 2009

Journal Articles

Clonal Origins of 'late' Relapses in ETV6-RUNX1 Acute Lymphoblastic Leukemia..

Frederik W van Delft, Sharon W Horsley, Kristina Anderson, Caroline M Bateman, MBBS, MRCP, Susan Colman, Jan Zuna, MD, PhD, Cornelia Eckert, PhD, MSc, Helena Kempski, Vaskar Saha, PhD, FRCP, FRCPath, Lyndal Kearney, Anthony Ford, Mel Greaves

Blood (2009) 114 (22): 1583.

https://doi.org/10.1182/blood.V114.22.1583.1583

Published: 2009

Journal Articles

Complexity of Clonal Architecture in Childhood Acute Lymphoblastic Leukaemia

Kristina Anderson, Christoph Lutz, Frederik W. van Delft, Sue Colman, Yanping Guo, Helena Kempski, Anthony . Moorman, V, Tariq Enver, John Swansbury, Lyndal Kearney, Mel Greaves

Blood (2009) 114 (22): LBA-5.

https://doi.org/10.1182/blood.V114.22.LBA-5.LBA-5

Published: 2009

Journal Articles

Specific JAK2 mutation ( JAK2 R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia

Lyndal Kearney, David Gonzalez De Castro, Jenny Yeung, Julia Procter, Sharon W. Horsley, Minenori Eguchi-Ishimae, Caroline M. Bateman, Kristina Anderson, Tracy Chaplin, Bryan D. Young, Christine J. Harrison, Helena Kempski, Chi Wai E. So, Anthony M. Ford, Mel Greaves

Blood (2009) 113 (3): 646–648.

https://doi.org/10.1182/blood-2008-08-170928

Published: 2009

Includes: Supplemental data

Journal Articles

NOTCH 1 mutation can be an early, prenatal genetic event in T-ALL

Minenori Eguchi-Ishimae, Mariko Eguchi, Helena Kempski, Mel Greaves

Blood (2008) 111 (1): 376–378.

https://doi.org/10.1182/blood-2007-02-074690

Published: 2008

Journal Articles

Collaboration between Activating Mutations in JAK2 and Trisomy 21 in the Acute Lymphoblastic Leukemias of Down Syndrome (DS).

Blood (2007) 110 (11): LB6.

https://doi.org/10.1182/blood.V110.11.LB6.lb6

Published: 2007

Journal Articles

Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)

Blood (2006) 109 (8): 3451–3461.

https://doi.org/10.1182/blood-2006-08-041012

Published: 2006

Includes: Supplemental data

Journal Articles

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

Phil J. Ancliff, Michael P. Blundell, Giles O. Cory, Yolanda Calle, Austen Worth, Helena Kempski, Siobhan Burns, Gareth E. Jones, Jo Sinclair, Christine Kinnon, Ian M. Hann, Rosemary E. Gale, David C. Linch, Adrian J. Thrasher

Blood (2006) 108 (7): 2182–2189.

https://doi.org/10.1182/blood-2006-01-010249

Published: 2006

Includes: Multimedia, Supplemental data

Journal Articles

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

Liat Rainis, Dan Bercovich, Sabine Strehl, Andrea Teigler-Schlegel, Batia Stark, Jan Trka, Ninette Amariglio, Andrea Biondi, Inna Muler, Gideon Rechavi, Helena Kempski, Oskar A. Haas, Shai Izraeli

Blood (2003) 102 (3): 981–986.

https://doi.org/10.1182/blood-2002-11-3599

Published: 2003

Journal Articles

In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia

Joseph L. Wiemels, Zhijian Xiao, Patricia A. Buffler, Ana T. Maia, Xiaomei Ma, Brian M. Dicks, Martyn T. Smith, Luoping Zhang, James Feusner, John Wiencke, Kathy Pritchard-Jones, Helena Kempski, Mel Greaves

Blood (2002) 99 (10): 3801–3805.

https://doi.org/10.1182/blood.V99.10.3801.h81002003801_3801_3805

Published: 2002

Journal Articles

Loss of Heterozygosity and Microsatellite Instability at the MLL Locus Are Common in Childhood Acute Leukemia, but not in Infant Acute Leukemia

Julie C. Webb, Irina Golovleva, Alan H. Simpkins, Helena Kempski, Brian Reeves, Natalie Sturt, Judith M. Chessells, Paul M. Brickell

Blood (1999) 94 (1): 283–290.

https://doi.org/10.1182/blood.V94.1.283.413k23_283_290

Published: 1999

NARROW

Cohort Analysis of FISH Testing of CD138+ Cells in Relapsed Multiple Myeloma: Implications for Prognosis and Choice of Therapy

Distinctive Genotypes In Infants With T-Cell Acute Lymphoblastic Leukemia (T-ALL)

RAG-Mediated Recombination Is The Predominant Driver Of Oncogenic Rearrangement In ETV6-RUNX1 Acute Lymphoblastic Leukemia

The Genomic Landscape of TEL-AML1 + ( ETV6-RUNX1 ) Acute Lymphoblastic Leukaemia

PAX5 Is a Frequently Altered Transcription Factor In Genetically Unclassified Childhood Common/B-Cell Precursor Acute Lymphoblastic Leukemia

Clonal origins of relapse in ETV6-RUNX1 acute lymphoblastic leukemia

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2 : a report from the International BFM Study Group

DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.

Clonal Origins of 'late' Relapses in ETV6-RUNX1 Acute Lymphoblastic Leukemia..

Complexity of Clonal Architecture in Childhood Acute Lymphoblastic Leukaemia

Specific JAK2 mutation ( JAK2 R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia

NOTCH 1 mutation can be an early, prenatal genetic event in T-ALL

Collaboration between Activating Mutations in JAK2 and Trisomy 21 in the Acute Lymphoblastic Leukemias of Down Syndrome (DS).

Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)

Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia

Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21

In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia

Loss of Heterozygosity and Microsatellite Instability at the MLL Locus Are Common in Childhood Acute Leukemia, but not in Infant Acute Leukemia

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American Society of Hematology

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American Society of Hematology

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