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

1-20 of 21

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

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

Evaluation of Newborns Screening Laboratory Tests for Sickle Cell Disease and Other Haemoglobinopathies in Tanzania

Heavenlight Hebron Christopher, BSc, Adam Burns, BSc, PhD, Emmanuel Josephat, BSc, Sephord Saul, BSc, Josephine Mgaya, BSc, Julie Makani, MD PhD FRCP, Siana Watoky Nkya, PhD MSc, BSc, Anna Schuh, PhD

Blood (2019) 134 (Supplement_1): 4817.

https://doi.org/10.1182/blood-2019-129900

Published: 2019

Journal Articles

Highly Comprehensive Genomic Testing for CLL: WGS, One Key to CLL Patient Stratification

Blood (2018) 132 (Supplement 1): 3115.

https://doi.org/10.1182/blood-2018-99-115935

Published: 2018

Journal Articles

Detection of Clinically Relevant Molecular Alterations in Chronic Lymphocytic Leukemia (CLL) By Nanopore Sequencing

Adam Burns, BSc, PhD, David Robert Bruce, MRCP, Pauline Robbe, MSc, PhD, Adele Timbs, Basile Stamatopoulos, PhD, Ruth Clifford, FRCPath, PhD, Maria Lopopolo, Duncan Parkes, Kate E Ridout, PhD, Anna Schuh, MD PhD

Blood (2018) 132 (Supplement 1): 1847.

https://doi.org/10.1182/blood-2018-99-110948

Published: 2018

Journal Articles

Identifying High-Risk CLL to Predict Early Relapse after FCR Based Treatment Using Whole Genome Sequencing: First Results from the Genomics England CLL Pilot

Pauline Robbe, Kate Ridout, Jennifer Becq, Miao He, Ruth Clifford, MD, Reem Alsolami, Adam Burns, Samantha JL Knight, Melanie Oates, Dena Howard, Andrew R. Pettitt, Augusto Rendon, Niko Popitsch, Peter Hillmen, Jenny C Taylor, Mark Caulfield, David Bentley, Clare Turnbull, Anna Schuh, MD PhD

Blood (2016) 128 (22): 2022.

https://doi.org/10.1182/blood.V128.22.2022.2022

Published: 2016

Journal Articles

Differing Mutational Profiles of IgHV + and IgHV - Patients Revealed By Whole Genome Sequencing in Chronic Lymphocytic Leukaemia (CLL)

Kate Ridout, Reem Alsolami, Adam Burns, Dimitris Vavoulis, Pavlos Antoniou, Peter Hillmen, Samantha JL Knight, Anna Schuh

Blood (2016) 128 (22): 5590.

https://doi.org/10.1182/blood.V128.22.5590.5590

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

Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL

Blood (2015) 126 (18): 2110–2117.

https://doi.org/10.1182/blood-2015-05-647578

Published: 2015

Includes: Supplemental data

Journal Articles

Mutational Landscape of 118 Relapsed Chronic Lymphocytic Leukemia Clinical Trial Samples; Evidence for a Multiple-Hit Profile Using Targeted Next Generation Sequencing

Blood (2014) 124 (21): 1974.

https://doi.org/10.1182/blood.V124.21.1974.1974

Published: 2014

Journal Articles

Targeted Re-Sequencing Analysis of 31 Genes Commonly Mutated in Myeloid Disorders in Serial Samples from Myelodysplastic Syndrome Patients with Disease Progression

Andrea Pellagatti, Cristina Di Genua, Swagata Roy, Adam Burns, BSc, Kathy L McGraw, PhD, Maria José Larrayoz, Marta Fernandez-Mercado, Simona Valletta, Joanne Mason, PhD, Sally Killick, Cristina Mecucci, MD PhD, Maria José Calasanz, Alan F. List, MD, Anna Schuh, MDPhD, Jacqueline Boultwood, PhD

Blood (2014) 124 (21): 1901.

https://doi.org/10.1182/blood.V124.21.1901.1901

Published: 2014

Journal Articles

Whole Genome Sequencing, Targeted Deep Sequencing and Copy-Number Analysis Provide a Comprehensive Picture of the Mutational Landscape of 41 Clinically Annotated CLL Cases

Adam Burns, BSc, Susanne Weller, PhD, Sean Humphray, PhD, Jennifer Becq, PhD, Reem Alsolami, MSc, Angela Hamblin, MDPhD, Ruth M Clifford, MD, Samantha JL Knight, PhD CBiol, MSB, FRCPath, Pauline Robbe, MSc, Maite Cabes, BSc, Joanne Mason, PhD, Chris S.R Hatton, MD, Jenny Taylor, DPhil, David Bentley, DPhil, Anna Schuh, MDPhD

Blood (2014) 124 (21): 1958.

https://doi.org/10.1182/blood.V124.21.1958.1958

Published: 2014

Journal Articles

The Identification of Further Minimal Regions of Overlap in Chronic Lymphocytic Leukemia Using High-Resolution SNP Arrays

Samantha JL Knight, PhD CBiol, MSB, FRCPath, Ruth Clifford, MD, Pauline Robbe, MSc, Sara DC Ramos, MSc, Adam Burns, BSc, Adele T Timbs, MSc, Reem Alsolami, BSc, Susanne Weller, PhD, Angela Hamblin, MDPhD, Joanne Mason, PhD, Melanie Oates, PhD, Michalis Titsias, PhD, Christopher Yau, DPhil, Chris C Holmes, PhD, Andrew R Pettitt, FRCP, PhD, Peter Hillmen, MB, ChB, PhD, Jenny Taylor, DPhil, Anna Shuh, MD PhD FRCP, FRCPath

Blood (2014) 124 (21): 3315.

https://doi.org/10.1182/blood.V124.21.3315.3315

Published: 2014

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

Towards Response Prediction Using Integrated Genomics in Chronic Lymphocytic Leukaemia: Results on 250 First-Line FCR Treated Patients from UK Clinical Trials

Ruth M Clifford, MD, Pauline Robbe, MSc, Susanne Weller, PhD, Adele T Timbs, MSc, Michalis Titsias, PhD, Adam Burns, BSc, Maite Cabes, BSc, Reem Alsolami, MSc, Christopher Yau, DPhil, Angela Hamblin, MDPhD, Joanne Mason, PhD, Melanie Oates, PhD, Andrew Pettitt, MD PhD, Chris Holmes, PhD, Peter Hillmen, MB, ChB, PhD, Jenny Taylor, DPhil, Samantha JL Knight, PhD CBiol, MSB, FRCPath, Anna Schuh, MDPhD

Blood (2014) 124 (21): 1942.

https://doi.org/10.1182/blood.V124.21.1942.1942

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

Impact of isolated germline JAK2V617I mutation on human hematopoiesis

Adam J. Mead, Onima Chowdhury, Christian Pecquet, Alexandra Dusa, Petter Woll, Deborah Atkinson, Adam Burns, Joannah Score, Michelle Rugless, Ruth Clifford, Simon Moule, Nicola Bienz, Paresh Vyas, Nick Cross, Rosemary E. Gale, Shirley Henderson, Stefan N. Constantinescu, Anna Schuh, Sten Eirik W. Jacobsen

Blood (2013) 121 (20): 4156–4165.

https://doi.org/10.1182/blood-2012-05-430926

Published: 2013

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

Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns

Anna Schuh, Jennifer Becq, Sean Humphray, Adrian Alexa, Adam Burns, Ruth Clifford, Stephan M. Feller, Russell Grocock, Shirley Henderson, Irina Khrebtukova, Zoya Kingsbury, Shujun Luo, David McBride, Lisa Murray, Toshi Menju, Adele Timbs, Mark Ross, Jenny Taylor, David Bentley

Blood (2012) 120 (20): 4191–4196.

https://doi.org/10.1182/blood-2012-05-433540

Published: 2012

Includes: Supplemental data

NARROW

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

Genomic Landscape of Epstein-Barr Virus in Endemic Burkitt Lymphoma

Evaluation of Newborns Screening Laboratory Tests for Sickle Cell Disease and Other Haemoglobinopathies in Tanzania

Highly Comprehensive Genomic Testing for CLL: WGS, One Key to CLL Patient Stratification

Detection of Clinically Relevant Molecular Alterations in Chronic Lymphocytic Leukemia (CLL) By Nanopore Sequencing

Identifying High-Risk CLL to Predict Early Relapse after FCR Based Treatment Using Whole Genome Sequencing: First Results from the Genomics England CLL Pilot

Differing Mutational Profiles of IgHV + and IgHV - Patients Revealed By Whole Genome Sequencing in Chronic Lymphocytic Leukaemia (CLL)

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

Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL

Mutational Landscape of 118 Relapsed Chronic Lymphocytic Leukemia Clinical Trial Samples; Evidence for a Multiple-Hit Profile Using Targeted Next Generation Sequencing

Targeted Re-Sequencing Analysis of 31 Genes Commonly Mutated in Myeloid Disorders in Serial Samples from Myelodysplastic Syndrome Patients with Disease Progression

Whole Genome Sequencing, Targeted Deep Sequencing and Copy-Number Analysis Provide a Comprehensive Picture of the Mutational Landscape of 41 Clinically Annotated CLL Cases

The Identification of Further Minimal Regions of Overlap in Chronic Lymphocytic Leukemia Using High-Resolution SNP Arrays

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

Towards Response Prediction Using Integrated Genomics in Chronic Lymphocytic Leukaemia: Results on 250 First-Line FCR Treated Patients from UK Clinical Trials

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

Impact of isolated germline JAK2V617I mutation on human hematopoiesis

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

Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only