Page 1 | Search Results | Blood | American Society of Hematology

1-16 of 16

Sort by

Sort Order Select

Journal Articles

Performance of a Liquid Biopsy Diagnostic Prediction Model for EBV-Positive Burkitt Lymphoma in Sub-Saharan Africa

Blood (2023) 142 (Supplement 1): 4364.

https://doi.org/10.1182/blood-2023-186131

Published: 2023

Journal Articles

Whole Genome Classification of Pre-Malignant B-Cells Disorder of the Oxplored Study

Pauline Robbe, Kate Ridout, Niamh Appleby, Georgeta Ciuban, Gagandeep Batth, Helene Dreau, Thomas Wenban-Smith, Melinda Kormandy, Grigore-Aristide Gafencu, Piero Carninci, Clare Freestone, Daniel McAleese, Dimitrios Vavoulis, Anna Schuh

Blood (2023) 142 (Supplement 1): 3256.

https://doi.org/10.1182/blood-2023-185268

Published: 2023

Journal Articles

Genomic Landscape of Epstein-Barr Virus in Endemic Burkitt Lymphoma

Blood (2023) 142 (Supplement 1): 2985.

https://doi.org/10.1182/blood-2023-190165

Published: 2023

Journal Articles

Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia

Jenny Klintman, Niamh Appleby, Basile Stamatopoulos, Katie Ridout, Toby A. Eyre, Pauline Robbe, Laura Lopez Pascua, Samantha J. L. Knight, Helene Dreau, Maite Cabes, Niko Popitsch, Mats Ehinger, Jose I. Martín-Subero, Elías Campo, Robert Månsson, Davide Rossi, Jenny C. Taylor, Dimitrios V. Vavoulis, Anna Schuh

Blood (2021) 137 (20): 2800–2816.

https://doi.org/10.1182/blood.2020005650

Published: 2021

Includes: Supplemental data

Journal Articles

The poor outcome in high molecular risk, hydroxycarbamide-resistant/intolerant ET is not ameliorated by ruxolitinib

Jennifer M. O’Sullivan, Angela Hamblin, Christina Yap, Sonia Fox, Rebecca Boucher, Anesh Panchal, Samah Alimam, Helene Dreau, Kieran Howard, Pauline Ware, Nicholas C. P. Cross, Mary Frances McMullin, Claire N. Harrison, Adam J. Mead

Blood (2019) 134 (23): 2107–2111.

https://doi.org/10.1182/blood.2019001861

Published: 2019

Includes: Supplemental data

Journal Articles

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Marion Lenglet, Florence Robriquet, Klaus Schwarz, Carme Camps, Anne Couturier, David Hoogewijs, Alexandre Buffet, Samantha J. L. Knight, Sophie Gad, Sophie Couvé, Franck Chesnel, Mathilde Pacault, Pierre Lindenbaum, Sylvie Job, Solenne Dumont, Thomas Besnard, Marine Cornec, Helene Dreau, Melissa Pentony, Erika Kvikstad, Sophie Deveaux, Nelly Burnichon, Sophie Ferlicot, Mathias Vilaine, Jean-Michaël Mazzella, Fabrice Airaud, Céline Garrec, Laurence Heidet, Sabine Irtan, Elpis Mantadakis, Karim Bouchireb, Klaus-Michael Debatin, Richard Redon, Stéphane Bezieau, Brigitte Bressac-de Paillerets, Bin Tean Teh, François Girodon, Maria-Luigia Randi, Maria Caterina Putti, Vincent Bours, Richard Van Wijk, Joachim R. Göthert, Antonis Kattamis, Nicolas Janin, Celeste Bento, Jenny C. Taylor, Yannick Arlot-Bonnemains, Stéphane Richard, Anne-Paule Gimenez-Roqueplo, Holger Cario, Betty Gardie

Blood (2018) 132 (5): 469–483.

https://doi.org/10.1182/blood-2018-03-838235

Published: 2018

Includes: Supplemental data

Journal Articles

Characterization of Recurrent Mutations in Patient with a Richter Syndrome By Targeted Next Generation Sequencing

Basile Stamatopoulos, PhD, Pavlos Antoniou, Dimitris Vavoulis, Toby A. Eyre, MD, Ruth Clifford, MD, Maité Cabes, Msc, Hélène Dreau, MSc, Anna Schuh, MD PhD

Blood (2016) 128 (22): 3200.

https://doi.org/10.1182/blood.V128.22.3200.3200

Published: 2016

Journal Articles

Light Chain IgLV3-21 Is Associated with Poor Prognosis in Chronic Lymphocytic Leukemia Patients Independently of the Presence of Heavy Chain IgHV3-21

Basile Stamatopoulos, PhD, Thomas Smith, PhD, David Sims, PhD, Andreas Heger, PhD, Hélène Dreau, MSc, Anna Schuh, MD PhD

Blood (2016) 128 (22): 3218.

https://doi.org/10.1182/blood.V128.22.3218.3218

Published: 2016

Journal Articles

Next-Generation Deep Sequencing Reveals Multiple Ighv Clones in One Third of CLL Patients Defining New Prognostic Subgroups and Improving Previous Classification

Basile Stamatopoulos, PhD, Adele Timbs, Msc, Hélène Dreau, MSc, Ruth Clifford, Pauline Robbe, MSc, Adam Burns, BSc, Joanne Mason, PhD, Anna Schuh, MD PhD

Blood (2015) 126 (23): 4127.

https://doi.org/10.1182/blood.V126.23.4127.4127

Published: 2015

Journal Articles

Development and Evaluation of the Clinical Utility of a Next Generation Sequencing (NGS) Tool for Myeloid Disorders

Angela Hamblin, MDPhD, Adam Burns, BSc, Christopher Tham, BA, Ruth Clifford, MD, Pauline Robbe, MSc, Adele Timbs, MSc, Joanne Mason, PhD, Helene Dreau, MSc, Andreas Weller, PhD, Puthen Jithesh, PhD, Olivia Fox, BSc, Melody Tabiner, MA, Adam Mead, MDPhD, Andrew Peniket, MD, Paresh Vyas, MDPhD, Shirley Henderson, PhD, Anna Schuh, MDPhD

Blood (2014) 124 (21): 2373.

https://doi.org/10.1182/blood.V124.21.2373.2373

Published: 2014

Journal Articles

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage

Blood (2014) 123 (7): 1021–1031.

https://doi.org/10.1182/blood-2013-04-490847

Published: 2014

Includes: Supplemental data

Journal Articles

SAMHD1, A Putative Tumour Suppressor, Is Recurrently Mutated in Chronic Lymphocytic Leukaemia, and Is Associated with Poor Risk Features

Ruth Clifford, Sam Ackroyd, Adam Burns, Adele Timbs, Jonathan Maelfait, Helene Dreau, Shirley Henderson, Mark Ross, David Bentley, Peter Hillmen, MBChB, PhD, Samantha Knight, Jenny Taylor, Chris S.R Hatton, Jan Rehwinkel, Yanick Crow, Anna Schuh

Blood (2012) 120 (21): 713.

https://doi.org/10.1182/blood.V120.21.713.713

Published: 2012

Journal Articles

Targeted Gene Profiling Identifies Differential Genetic Make-up Depending On Chronic Lymphocytic Leukaemia Subtype

Adam Burns, Ruth Clifford, MB, MRCP, Helene Dreau, MSc, Chris S.R Hatton, Shirley Henderson, PhD, Jenny Taylor, Anna Schuh, PhD

Blood (2012) 120 (21): 1383.

https://doi.org/10.1182/blood.V120.21.1383.1383

Published: 2012

Journal Articles

Nine Novel Mutations in the Erythroid Transcription Factor KLF1 Gene Associated with Increased Fetal Hemoglobin Levels in Adults,

Alice Gallienne, MSc, Helene Dreau, MSc, Anna Schuh, PhD, Chris S.R Hatton, MD, John Old, PhD, Shirley Henderson, PhD

Blood (2011) 118 (21): 3191.

https://doi.org/10.1182/blood.V118.21.3191.3191

Published: 2011

Journal Articles

Selective Persistence of Distinct Stem/B Leukaemic Stem Cells In Childhood Acute Lymphoblastic Leukaemia In Clinical Remission.

Christoph Lutz, MD, Petter Woll, PhD, Anders Castor, MD, PhD, Helen Ferry, PhD, Christina Jensen, PhD, Joanne Green, Helene Dreau, Michael Lutteropp, Anna Schuh, MD, PhD, Georgina Hall, MD, PhD, Chris Mitchell, MD, PhD, Jan Zuna, MD, PhD, Veronica Buckle, PhD, Sten Eirik W Jacobsen, MD, PhD, Tariq Enver, PhD

Blood (2010) 116 (21): 1585.

https://doi.org/10.1182/blood.V116.21.1585.1585

Published: 2010

Journal Articles

Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors

Adele Timbs, Sam Knight, Elham SadighiAkha, Adam Burns, Helene Dreau, Anne-Marie Hewitt, Chris Hatton, Chris Yau, Chris Holmes, Jenny Taylor, Anna Schuh

Blood (2010) 116 (21): 3590.

https://doi.org/10.1182/blood.V116.21.3590.3590

Published: 2010

NARROW

Performance of a Liquid Biopsy Diagnostic Prediction Model for EBV-Positive Burkitt Lymphoma in Sub-Saharan Africa

Whole Genome Classification of Pre-Malignant B-Cells Disorder of the Oxplored Study

Genomic Landscape of Epstein-Barr Virus in Endemic Burkitt Lymphoma

Genomic and transcriptomic correlates of Richter transformation in chronic lymphocytic leukemia

The poor outcome in high molecular risk, hydroxycarbamide-resistant/intolerant ET is not ameliorated by ruxolitinib

Identification of a new VHL exon and complex splicing alterations in familial erythrocytosis or von Hippel-Lindau disease

Characterization of Recurrent Mutations in Patient with a Richter Syndrome By Targeted Next Generation Sequencing

Light Chain IgLV3-21 Is Associated with Poor Prognosis in Chronic Lymphocytic Leukemia Patients Independently of the Presence of Heavy Chain IgHV3-21

Next-Generation Deep Sequencing Reveals Multiple Ighv Clones in One Third of CLL Patients Defining New Prognostic Subgroups and Improving Previous Classification

Development and Evaluation of the Clinical Utility of a Next Generation Sequencing (NGS) Tool for Myeloid Disorders

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage

SAMHD1, A Putative Tumour Suppressor, Is Recurrently Mutated in Chronic Lymphocytic Leukaemia, and Is Associated with Poor Risk Features

Targeted Gene Profiling Identifies Differential Genetic Make-up Depending On Chronic Lymphocytic Leukaemia Subtype

Nine Novel Mutations in the Erythroid Transcription Factor KLF1 Gene Associated with Increased Fetal Hemoglobin Levels in Adults,

Selective Persistence of Distinct Stem/B Leukaemic Stem Cells In Childhood Acute Lymphoblastic Leukaemia In Clinical Remission.

Quantitative Whole Genome Analysis of Sequential Samples From Patients with B-CLL Identifies Novel Recurrent Copy Number Alterations Involving Critical B-Cell Transcription Factors

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only