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Journal Articles

SNP-Array Genome Wide Association Study Meta-Analysis Identifies Innate Immune Susceptibility Loci Associated with Non-Del(5q) Myelodysplastic Syndromes Predisposition

Blood (2018) 132 (Supplement 1): 107.

https://doi.org/10.1182/blood-2018-99-118747

Published: 2018

Journal Articles

Novel Findings for the Role of Microenvironment and Heat Shock Proteins (HSP) in B -Cell Recptor (BCR) Activation, Disease Progression and Transformation of Follicular Non-Hodgkin Lymphoma (FL): Gene Expression Profiling (GEP) and Immuno-Histochemical (IH) Studies Reveal New Pathways for Potential Targeted Therapies

Saad M B Rassam, MD FRCP, FRCPath, John Schofield, FRCPath, Farooq Malik, PhD, Azim M Mohamedali, PhD, Bartlomiej Przychodzen, MSc, Gabrielle Elstein, Ghulam J Mufti, FRCP, FRCPath

Blood (2015) 126 (23): 3897.

https://doi.org/10.1182/blood.V126.23.3897.3897

Published: 2015

Journal Articles

Comparison of Peripheral Blood and Bone Marrow Molecular Profiling in Primary Myelodysplastic Syndromes (MDS)

Azim M Mohamedali, PhD, Joop Gaken, PhD, Momin Ahmed, MD PhD, Austin Kulasekararaj, Alexander E Smith, PhD, Farook Malik, PhD, Ghulam Mufti, MD DM, FRCP, FRCPath

Blood (2014) 124 (21): 4655.

https://doi.org/10.1182/blood.V124.21.4655.4655

Published: 2014

Journal Articles

Comprehensive Mutational Screening Of 5-Azacitidne Treated Myelodysplastic Syndrome (MDS) Patients Fails To Identify a Specific Mutational Profile Predicting Response To Therapy

Austin G. Kulasekararaj, Azim M Mohamedali, PhD, Alexander E Smith, PhD, Syed A Mian, Nazia Matto, Terry J Gaymes, DPhil, Nicholas Lea, PhD, Joop Gaken, PhD, Ghulam J. Mufti, DM, FRCP, FRCPath

Blood (2013) 122 (21): 2792.

https://doi.org/10.1182/blood.V122.21.2792.2792

Published: 2013

Journal Articles

Somatic Mutations Implicated In Myeloid Malignancies Are Frequent In Idiopathic Aplastic Anaemia and Its Relevance To Disease Classification and Treatment- a Comprehensive Analysis Of 150 Patients

Jie Jiang, PhD, Austin G Kulasekararaj, Alexander E Smith, PhD, Azim M Mohamedali, PhD, Shreyans A Gandhi, MBBS, MD, Barbara Czepulkowski, BSc, Judith Marsh, Ghulam J. Mufti, DM, FRCP, FRCPath

Blood (2013) 122 (21): 803.

https://doi.org/10.1182/blood.V122.21.803.803

Published: 2013

Journal Articles

SF3B1 Mutant Clones From Patients With Refractory Anaemia With Ringed Sideroblasts (RARS) Originate From The Early Haematopoietic Stem Cells and Maintain Their Engraftment Potential

Syed A Mian, Kevin Rouault-Pierre, PhD, Alexander E Smith, PhD, Thomas Seidl, Austin G Kulasekararaj, MBBS, MD, MRCP, FRCP, Azim M Mohamedali, PhD, Sneha Shinde, Msc., Dominique Bonnet, PhD, Ghulam J. Mufti, MD, PhD

Blood (2013) 122 (21): 262.

https://doi.org/10.1182/blood.V122.21.262.262

Published: 2013

Journal Articles

Utility of Peripheral Blood for Cytogenetic and Mutation Analysis in Myelodysplastic Syndrome

Heba A Alkhatabi, MSc, Azim M Mohamedali, PhD, Austin G Kulasekararaj, Sneha Shinde, Msc., Joop Gaken, PhD, Syed A Mian, MSc, Alexander E Smith, PhD, Ghulam J. Mufti, MD

Blood (2012) 120 (21): 1707.

https://doi.org/10.1182/blood.V120.21.1707.1707

Published: 2012

Journal Articles

Clinical and Genomic Characterization of Chromosome 7 Lesions in Myeloid Malignancies,

Andres Jerez, MD, Yuka Sugimoto, MD, Hideki Makishima, MD, Amit Verma, MD, Christine L O‘Keefe, PhD, Ramon V Tiu, MD, Azim M Mohamedali, PhD, Michael A McDevitt, MD, PhD, Ghulam J. Mufti, MD, Jacqueline Boultwood, PhD, Jaroslaw P Maciejewski, MD, PhD

Blood (2011) 118 (21): 3549.

https://doi.org/10.1182/blood.V118.21.3549.3549

Published: 2011

Journal Articles

Kings Health Partners 17 Gene Amplicon Panel for Next Generation Sequencing One Stop Mutational Assessment In Myeloid Malignancies

Nicholas C Lea, PhD, Atiyeh Abdallah, PhD, Aytug Kizilors, PhD, Alexander E Smith, PhD, Syed A Mian, Azim M Mohamedali, PhD, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath

Blood (2011) 118 (21): 748.

https://doi.org/10.1182/blood.V118.21.748.748

Published: 2011

Journal Articles

TP53 Mutations Are Restricted Predominantly to 5q- Syndrome and Myelodysplastic Syndrome Patients with Complex Cytogenetics, and Correlate with Adverse Prognosis

Austin G Kulasekararaj, Alexander E Smith, PhD, Syed A Mian, Pramila Krishnamurthy, Azim M Mohamedali, PhD, Nicholas C Lea, PhD, Janet Hayden, Joop Gaken, Modupe Elebute, Robin M. Ireland, FRCP, FRCPath, Sabine Pomplun, ZiYi Lim, MD, Judith C. W. Marsh, Prof MD PhD, Ghulam J. Mufti, MD

Blood (2011) 118 (21): 792.

https://doi.org/10.1182/blood.V118.21.792.792

Published: 2011

Journal Articles

Functional Characterization of CD4 + T-Cells in Aplastic Anemia (AA)

Shahram Y Kordasti, MD, PhD, Judith C. W. Marsh, Prof MD PhD, Sufyan Al-Khan, MD, Jie Jiang, PhD, Alexander E Smith, PhD, Azim M Mohamedali, PhD, Pilar Perez Abellan, Caroline Veen, Benedetta Costantini, MD, Nana Benson Quarm, Thomas Seidl, Syed A Mian, Farzin Farzaneh, DPhil, Ghulam J. Mufti, MD

Blood (2011) 118 (21): 1340.

https://doi.org/10.1182/blood.V118.21.1340.1340

Published: 2011

Journal Articles

Single Nucleotide Polymorphism Array (SNP-A) Karyotype Is the Best Predictor of Prognosis In Normal Cytogenetics Acute Myeloid Leukaemia (AML)

Azim M Mohamedali, PhD, Robert K Hills, MA, MSc, DPhil, Erick E Nasser, Msc., Atiyeh Abdallah, PhD, Sneha Shinde, Msc., Austin G Kulasekararaj, Amanda Gilkes, Nicholas Lea, Alan K Burnett, MD, Ghulam J. Mufti, MD

Blood (2011) 118 (21): 411.

https://doi.org/10.1182/blood.V118.21.411.411

Published: 2011

Journal Articles

Whole Exome Sequencing Reveals Acquired SF3B1 Mutations Defining Patients with Acquired Idiopathic Sideroblastic Anaemia

Alexander E Smith, PhD, Syed A Mian, Austin G Kulasekararaj, Azim M Mohamedali, PhD, Ghulam J. Mufti, MD

Blood (2011) 118 (21): 2793.

https://doi.org/10.1182/blood.V118.21.2793.2793

Published: 2011

Journal Articles

Defining the Topography of Deletion 5q Using SNP-A Identifies Patients with More Aggressive Disease and Correlates with Additional Lesions

Andres Jerez, MD, Anna M Jankowska, PhD, Hideki Makishima, MD, Lukasz P Gondek, MD, Ramon V Tiu, MD, Christine L O‘Keefe, PhD, Azim M Mohamedali, PhD, Denise Batista, PhD, Michael A McDevitt, MD, PhD, Mikkael A Sekeres, MD, Ghulam J. Mufti, MD, Jaroslaw P Maciejewski, MD, PhD

Blood (2011) 118 (21): 2795.

https://doi.org/10.1182/blood.V118.21.2795.2795

Published: 2011

Journal Articles

Microsatellite Instability Induced Mutation in DNA Repair Genes, CTiP and Mre11 Confer Hypersensitivity to PARP Inhibitors in Myeloid Malignancies

Terry J Gaymes, DPhil, Rajani Chelliah, BSc, MSc, Austin G Kulasekararaj, Azim M Mohamedali, PhD, Sydney Shall, DPhil, Ghulam J. Mufti, MD

Blood (2011) 118 (21): 276.

https://doi.org/10.1182/blood.V118.21.276.276

Published: 2011

Journal Articles

Inborn Genomic Variation as Predisposing Factors to Myeloid Malignancies.

Christine O'Keefe, PhD, Bartlomiej P Przychodzen, Azim M Mohamedali, PhD, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath, Michael McDevitt, Jaroslaw P. Maciejewski, MD, PhD

Blood (2009) 114 (22): 1590.

https://doi.org/10.1182/blood.V114.22.1590.1590

Published: 2009

Journal Articles

Acquired Somatic Uniparental Disomy is a Chromosomal Defect Important in Predicting Treatment Responses and Survival Outcomes in MDS, MDS/MPN and Secondary AML.

Ramon V. Tiu, MD, Christine O'Keefe, PhD, Lukasz P. Gondek, MD, Azim M. Mohamedali, PhD, Bartlomiej P. Przychodzen, Ghulam J. Mufti, MBBS, DM, FRCP, FRCPath, Mikkael A. Sekeres, MD, MS, Anjali S. Advani, Michael A. McDevitt, MD, PhD, Jaroslaw P. Maciejewski, MD, PhD

Blood (2009) 114 (22): 2630.

https://doi.org/10.1182/blood.V114.22.2630.2630

Published: 2009

Journal Articles

Recurrent Novel Regions of Uniparental Disomy and Homozygous Deletions in Mycosis Fungoides Identified Using High Resolution Single Nucleotide Polymorphism Analysis.

Azim M Mohamedali, PhD, Tracey J Mitchell, PhD, Silvia Ferreira, PhD, Barbara A Guinn, PhD, Robin M. Ireland, FRCP, FRCPath, Sean J Whittaker, MD, FRCP, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath

Blood (2009) 114 (22): 2644.

https://doi.org/10.1182/blood.V114.22.2644.2644

Published: 2009

Journal Articles

Prevalence of 46/1 JAK2 Haplotype in Patients with Budd-Chiari Syndrome with and without JAK2V617F and TET2 Mutations.

Nicholas C Lea, PhD, Lara N Roberts, Raj K Patel, Rachel Westbrook, Michael A Heneghan, Azim M Mohamedali, PhD, Alex E Smith, Atiyeh Abdallah, Nigel Westwood, PhD, CSci, FIBMS, Trisevgeni Kontou, Deborah Yallop, BSc, FRCPath, MB, BS, MRCP, Roopen Arya, Antonio Pagliuca, MBBS, FRCP, FRCPath, MA, Joop Gaken, PhD, Nigel D Heaton, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath

Blood (2009) 114 (22): 434.

https://doi.org/10.1182/blood.V114.22.434.434

Published: 2009

Journal Articles

Deep Sequencing the Tet2 Gene in 360 Patients with Myeloid Neoplasms Provides a Comprehensive and Quantitative Mutation Map and Reveals Low Level Mutant Clones.

Alexander E Smith, Azim M Mohamedali, PhD, Syed a Mian, Technician, Nicholas C Lea, BSc, PhD, Nigel Westwood, PhD, CSci, FIBMS, Austin G Kulasekararaj, Joop Gaken, PhD, Corinna Strupp, Norbert Gattermann, MD, PhD, Ulrich Germing, Ghulam J Mufti, MBBS, DM, FRCP, FRCPath

Blood (2009) 114 (22): 733.

https://doi.org/10.1182/blood.V114.22.733.733

Published: 2009

NARROW

SNP-Array Genome Wide Association Study Meta-Analysis Identifies Innate Immune Susceptibility Loci Associated with Non-Del(5q) Myelodysplastic Syndromes Predisposition

Comparison of Peripheral Blood and Bone Marrow Molecular Profiling in Primary Myelodysplastic Syndromes (MDS)

Comprehensive Mutational Screening Of 5-Azacitidne Treated Myelodysplastic Syndrome (MDS) Patients Fails To Identify a Specific Mutational Profile Predicting Response To Therapy

Somatic Mutations Implicated In Myeloid Malignancies Are Frequent In Idiopathic Aplastic Anaemia and Its Relevance To Disease Classification and Treatment- a Comprehensive Analysis Of 150 Patients

SF3B1 Mutant Clones From Patients With Refractory Anaemia With Ringed Sideroblasts (RARS) Originate From The Early Haematopoietic Stem Cells and Maintain Their Engraftment Potential

Utility of Peripheral Blood for Cytogenetic and Mutation Analysis in Myelodysplastic Syndrome

Clinical and Genomic Characterization of Chromosome 7 Lesions in Myeloid Malignancies,

Kings Health Partners 17 Gene Amplicon Panel for Next Generation Sequencing One Stop Mutational Assessment In Myeloid Malignancies

TP53 Mutations Are Restricted Predominantly to 5q- Syndrome and Myelodysplastic Syndrome Patients with Complex Cytogenetics, and Correlate with Adverse Prognosis

Functional Characterization of CD4 + T-Cells in Aplastic Anemia (AA)

Single Nucleotide Polymorphism Array (SNP-A) Karyotype Is the Best Predictor of Prognosis In Normal Cytogenetics Acute Myeloid Leukaemia (AML)

Whole Exome Sequencing Reveals Acquired SF3B1 Mutations Defining Patients with Acquired Idiopathic Sideroblastic Anaemia

Defining the Topography of Deletion 5q Using SNP-A Identifies Patients with More Aggressive Disease and Correlates with Additional Lesions

Microsatellite Instability Induced Mutation in DNA Repair Genes, CTiP and Mre11 Confer Hypersensitivity to PARP Inhibitors in Myeloid Malignancies

Inborn Genomic Variation as Predisposing Factors to Myeloid Malignancies.

Acquired Somatic Uniparental Disomy is a Chromosomal Defect Important in Predicting Treatment Responses and Survival Outcomes in MDS, MDS/MPN and Secondary AML.

Recurrent Novel Regions of Uniparental Disomy and Homozygous Deletions in Mycosis Fungoides Identified Using High Resolution Single Nucleotide Polymorphism Analysis.

Prevalence of 46/1 JAK2 Haplotype in Patients with Budd-Chiari Syndrome with and without JAK2V617F and TET2 Mutations.

Deep Sequencing the Tet2 Gene in 360 Patients with Myeloid Neoplasms Provides a Comprehensive and Quantitative Mutation Map and Reveals Low Level Mutant Clones.

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American Society of Hematology

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American Society of Hematology

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