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Journal Articles

Whole Exome Sequencing in Children with Sickle Cell Anemia Who Developed Ischemic Stroke Prior to 4 Years of Age Reveals a Strong Association with Inherited Dyslipidemias

John N. Brewin, Riley Cook, MD, Alexander E Smith, PhD, Valentine Brousse, MD PhD, Julie Brent, MD, Sanjay Tewari, FRCPath, MBBS, Baba PD Inusa, MD, Stephan Menzel, MD PhD, David C Rees

Blood (2019) 134 (Supplement_1): 3571.

https://doi.org/10.1182/blood-2019-123764

Published: 2019

Journal Articles

Common Fetal Hemoglobin Variants Modify Hematological Phenotypes in MDS/MPN/Myeloma Patients Receiving Cytotoxic Drugs

Norris E. Igbineweka, MBBS, BSc (Hons), MRCP, Adam Pilarski, MBBS, BA (Hons), MRCS, Helen Rooks, BSc, Amandine Breton, PhD BS, MSc, Hannah Hall, BMBS, Dilan D. Joshi, MSc, BMBS, Daveena Meeks, MBBS BSc, Stephan Menzel, MD PhD, Timothy Chevassut, BMBCh MA, MPH, PhD, Swee Lay Thein, DSc,FRCP,FRCPath,MBBS,MRCPath,MRCP

Blood (2017) 130 (Supplement 1): 1202.

https://doi.org/10.1182/blood.V130.Suppl_1.1202.1202

Published: 2017

Journal Articles

A Multicentre Study of Environmental Factors on the Severity of Sickle Cell Disease

Sanjay Tewari, MBBS DCH MRCPCH, Fred Piel, PhD, Valentine Brousse, MD, Baba PD Inusa, MD FRCPCH, DCP, Paul Telfer, MD, Stephan Menzel, MD, Mariane De Montalembert, Kate Gardner, Gary Fuller, Swee Lay Thein, DSc, FRCP, FMedSci, MB, BS, FRCP, David Rees, FRCPCH

Blood (2014) 124 (21): 4841.

https://doi.org/10.1182/blood.V124.21.4841.4841

Published: 2014

Journal Articles

Haplotype Signatures At HBS1L-MYB In Global Populations

Swee Lay Thein, MBBS, DSc, Helen Rooks, BSc, Emma Drasar, MBBS MRCP, Akshala Gnanakulasekaran, MB., BS, Nicholas Silver, PhD, Tim D Spector, MD, Mark Lathrop, PhD, Stephan Menzel, MD

Blood (2013) 122 (21): 3672.

https://doi.org/10.1182/blood.V122.21.3672.3672

Published: 2013

Journal Articles

HBS1L-MYB intergenic Variants Modulate Fetal Hemoglobin Via Long-Range MYB Enhancers

Ralph Stadhouders, BSc, Suleyman Aktuna, BSc, Supat Thongjuea, PhD, Ali Aghajanirefah, PhD, Farzin Pourfarzad, PhD, Wilfred van Ijcken, PhD, Boris Lenhard, PhD, Helen Rooks, BSc, Steve Best, PhD, Stephan Menzel, MD, Frank Grosveld, PhD, Swee Lay Thein, MBBS, DSc, Eric Soler, PhD

Blood (2013) 122 (21): 43.

https://doi.org/10.1182/blood.V122.21.43.43

Published: 2013

Journal Articles

European Chromosome 6 Haplotypes Significantly Augment Fetal Hemoglobin Levels in Brazilian Sickle Cell Anemia Patients: Influence of Four HBS1L-MYB Intergenic Region SNPs

Flávia Costa Leonardo, Ph.D., Stephan Menzel, MD, Ana Flavia Brugnerotto, Kleber Yotsumoto Fertrin, MD, PhD, Marcos André Cavalcanti Bezerra, MSc, PhD, Aderson S Araujo, MD, PhD, Fernando Ferreira Costa, MD, PhD, Swee Lay Thein, MD, FRCP, FRCPath, DSc, Nicola Conran, Ph.D.

Blood (2012) 120 (21): 1002.

https://doi.org/10.1182/blood.V120.21.1002.1002

Published: 2012

Journal Articles

Stress Erythropoiesis and Genetic Regulation of Fetal Hemoglobin in Inherited Bone Marrow Failure Syndromes

Blanche P Alter, MD, MPH, Philip S. Rosenberg, PhD, Thomas Day, MB ChB MRes, Stephan Menzel, MD, Neelam Giri, MD, Sharon A Savage, MD, Swee Lay Thein, DSc, FRCP, FRCPath, FMedSci

Blood (2011) 118 (21): 2401.

https://doi.org/10.1182/blood.V118.21.2401.2401

Published: 2011

Journal Articles

Two Distinct Genetic Mechanisms Modify the Level of HbA 2 in Peripheral Blood,

Swee Lay Thein, DSc, FRCP, FRCPath, FMedSci, Chad P. Garner, PhD, Tim D Spector, MD, Stephan Menzel, MD

Blood (2011) 118 (21): 3193.

https://doi.org/10.1182/blood.V118.21.3193.3193

Published: 2011

Journal Articles

The Interaction of UGT1A, HO1 and α-Thalassemia Variants with Bilirubin Levels and Gallstones in Sickle Cell Disease.

Nisha Vasavda, PhD, Stephan Menzel, MD, Sheila Kondaveeti, PhD, Emma Maytham, BSc, Moji Awogbade, BMedSc,MRCP, MRCPath, Sybil Bannister, RN, BSN, Juliette Cunningham, Yvonne Daniel, PhD, Iheanyi Okpala, MRCP, MRCPath, Tony Fulford, PhD, Swee Lay Thein, FRCP,FRCPath,DSc

Blood (2006) 108 (11): 1202.

https://doi.org/10.1182/blood.V108.11.1202.1202

Published: 2006

Journal Articles

Circulating DNA as a Prognostic Marker in Sickle Cell Disease.

Pinar Ulug, BSc, MSc, Nisha Vasavda, PhD, Stephan Menzel, MD, Karthik Ramasamy, MD, Taku Sugai, MD, Gordon Cheung, MD, Sheila Kondaveeti, PhD, Moji Awogbade, BMedSc,MRCP, MRCPath, Sybil Bannister, RN, BSN, Juliette Cunningham, David Rees, FRCP, Swee Lay Thein, FRCP, FRCPath, DSc

Blood (2006) 108 (11): 1218.

https://doi.org/10.1182/blood.V108.11.1218.1218

Published: 2006

Journal Articles

Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing HbF Levels in Adults.

Swee Lay Thein, FRCP, DSc, Stephan Menzel, MD, Xu Peng, MD, Steve Best, BSc,PhD, Jie Jiang, BSc,PhD, James Close, BSc,DPhil, Nicholas Silver, BSc,MSc, Ageliki Gerovasilli, BSc, Chen Ping, MD, Masao Yamaguchi, MD, Karin Wahlberg, BSc, Heike Muller, BSc, Tim D. Spector, MD, Chad Garner, BSc,DPhil, Fumihiko Matsuda, MD, Martin Farrall, MD, Mark Lathrop, PhD

Blood (2006) 108 (11): 652.

https://doi.org/10.1182/blood.V108.11.652.652

Published: 2006

Journal Articles

Two Candidate Genes for Low Platelet Count Identified by Genome-Wide Linkage Analysis: Glycoprotein IX and Thrombopoietin.

Swee Lay Thein, MD, DSc, Steve Best, BSc, PhD, Stephan Menzel, MD, Helen Rooks, BSc, Tim D. Spector, MD, Chad Garner, BSc, PhD

Blood (2005) 106 (11): 2160.

https://doi.org/10.1182/blood.V106.11.2160.2160

Published: 2005

Journal Articles

AHSP Is a Quantitative Trait Gene That Modifies the Phenotype of β Thalassemia.

Mei I. Lai, BSc, Jie Jiang, BSc, PhD, Nicholas Silver, BSc, MSc, Steve Best, BSc, PhD, Stephan Menzel, MD, Chad Garner, BSc, PhD, Mitchell J. Weiss, MD, PhD, Swee Lay Thein, MD, DSc

Blood (2005) 106 (11): 3638.

https://doi.org/10.1182/blood.V106.11.3638.3638

Published: 2005

NARROW

Whole Exome Sequencing in Children with Sickle Cell Anemia Who Developed Ischemic Stroke Prior to 4 Years of Age Reveals a Strong Association with Inherited Dyslipidemias

Common Fetal Hemoglobin Variants Modify Hematological Phenotypes in MDS/MPN/Myeloma Patients Receiving Cytotoxic Drugs

A Multicentre Study of Environmental Factors on the Severity of Sickle Cell Disease

Haplotype Signatures At HBS1L-MYB In Global Populations

HBS1L-MYB intergenic Variants Modulate Fetal Hemoglobin Via Long-Range MYB Enhancers

European Chromosome 6 Haplotypes Significantly Augment Fetal Hemoglobin Levels in Brazilian Sickle Cell Anemia Patients: Influence of Four HBS1L-MYB Intergenic Region SNPs

Stress Erythropoiesis and Genetic Regulation of Fetal Hemoglobin in Inherited Bone Marrow Failure Syndromes

Two Distinct Genetic Mechanisms Modify the Level of HbA 2 in Peripheral Blood,

The Interaction of UGT1A, HO1 and α-Thalassemia Variants with Bilirubin Levels and Gallstones in Sickle Cell Disease.

Circulating DNA as a Prognostic Marker in Sickle Cell Disease.

Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing HbF Levels in Adults.

Two Candidate Genes for Low Platelet Count Identified by Genome-Wide Linkage Analysis: Glycoprotein IX and Thrombopoietin.

AHSP Is a Quantitative Trait Gene That Modifies the Phenotype of β Thalassemia.

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American Society of Hematology

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American Society of Hematology

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