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Journal Articles

Response of Patients with Transfusion-Dependent β-Thalassemia (TDT) to Betibeglogene Autotemcel (beti-cel; LentiGlobin for β-Thalassemia) Gene Therapy Based on HBB Genotype and Disease Genetic Modifiers

Mark C. Walters, MD, David H.K. Chui, MD FRCPC, John J Farrell, PhD, Ashutosh Lal, MD, Franco Locatelli, MD PhD, Janet L. Kwiatkowski, MD MSCE, John B. Porter, MA, MD, FRCP, FRCPath, Martin G. Sauer, MD, Isabelle Thuret, MD, Suradej Hongeng, MD, Andreas E. Kulozik, MD PhD, Adrian J. Thrasher, MBBS, PhD FMedSci, Evangelia Yannaki, MD, Julia Yang, Dustin Whitney, PhD, Alexandria Petrusich, Richard A. Colvin, MD PhD, Alexis A. Thompson, MD

Blood (2020) 136 (Supplement 1): 1–3.

https://doi.org/10.1182/blood-2020-137642

Published: 2020

Journal Articles

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

Paola Sebastiani, PhD, John J. Farrell, PhD, Shuai Wang, MS, Heather L Edward, BA, Heather M. Shappell, BS, Harold T. Bae, PhD, Clinton T. Baldwin, PhD, A. M. Al-Rubaish, MD, Zaki Naserullah, MD, Ahmed Alsuliman, MD, Pradeep K. Patra, PhD, Lindsay A. Farrer, PhD, David H.K. Chui, MD, Abdulrahman Alsultan, MD, Duyen A. Ngo, MD, Haifa Kathrin Al-Ali, MD, Martin H. Steinberg, MD

Blood (2014) 124 (21): 4066.

https://doi.org/10.1182/blood.V124.21.4066.4066

Published: 2014

Journal Articles

The Evolutionary Impact Of Malaria On The Saudi Arabian Genome

John J. Farrell, Ms, Awatif N. Al-Nafaie, MD, Amein K. Al-Ali, Ph.D., Abdullah M. Al-Rubaish, MD, Zaki Naserullah, MD, Ahmed Alsuliman, MD, Martin H. Steinberg, MD, Clinton T. Baldwin, Ph.D.

Blood (2013) 122 (21): 1001.

https://doi.org/10.1182/blood.V122.21.1001.1001

Published: 2013

Journal Articles

Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype

Abdulrahman Alsultan, MD, Duyen A. Ngo, MD, John J. Farrell, MS, Hazem Ghabbour, Idowu Akinsheye, PhD, Amein Al-Ali, PhD, Ahmed Alsuliman, MD, Muneer Al-Baghshi, MD, Waleed Albuali, MD, Mohammed Alabdulaali, MD, Paola Sebastiani, PhD, Clinton T. Baldwin, PhD, David H.K. Chui, MD, Martin H. Steinberg, MD

Blood (2011) 118 (21): 1056.

https://doi.org/10.1182/blood.V118.21.1056.1056

Published: 2011

Journal Articles

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

Blood (2011) 117 (18): 4935–4945.

https://doi.org/10.1182/blood-2010-11-317081

Published: 2011

Includes: Supplemental data

Journal Articles

A 3-Bp Deletion Between Transcription Factor Binding Motifs In the HBS1L-MYB Intergenic Region on Chromosome 6q23 Is Associated with HbF Expression

John J. Farrell, MS, Richard M. Sherva, PhD, Zhi-yi Chen, PhD, Luo Hong-yuan, MD, PhD, Banjamin F. Chu, MD, Shau Yin Ha, MBBS, Chi Kong Li, MBBS, MD, Anselm C.W. Lee, MBBS, Chi Keung Li, MBBS, Hui Leung Yuen, MBBS, Jason C.C. So, MBBS, Edmond ShiuKwan Ma, MD, FRCP, FRCPath, Li Chong Chan, MD, Vivian Chan, PhD, Paola Sebastiani, PhD, Lindsay A. Farrer, PhD, Clinton T. Baldwin, PhD, Martin H. Steinberg, MD, David H.K. Chui, MD

Blood (2010) 116 (21): 1013.

https://doi.org/10.1182/blood.V116.21.1013.1013

Published: 2010

Journal Articles

Association of Polymorphisms of the Transforming Growth Factor-β/Bone Morphogenetic Protein (TGF-β/BMP) Pathway with Sickle Cell Bacteremia.

Adeboye H. Adewoye, MD, Vikki G. Nolan, MPH, Clinton T. Baldwin, PhD, Diego F. Wyszynski, MD, PhD, Qian-Li Ma, BA, John J. Farrell, MS, Alice Bisbee, MPH, Erica Homan, BA, Paola Sebastiani, PhD, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD

Blood (2005) 106 (11): 3170.

https://doi.org/10.1182/blood.V106.11.3170.3170

Published: 2005

Journal Articles

Gene-Gene Interactions and the Pathophysiology of Sickle Cell Disease: Modeling the Effects of SNPs on Sickle Cell-Associated Vasoocclusive Events Using Classification and Regression Trees and Stochastic Gradient Boosting.

Vikki G. Nolan, MPH, Marsha A. Wilcox, EdD, ScD, Paola Sebastiani, PhD, Clinton T. Baldwin, PhD, Diego F. Wyszynski, MD, PhD, Qianli Ma, BS, Alice Bisbee, MPH, John J. Farrell, BA, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD

Blood (2005) 106 (11): 3183.

https://doi.org/10.1182/blood.V106.11.3183.3183

Published: 2005

Journal Articles

Leg Ulcers in Sickle Cell Anemia Are Associated with Laboratory Markers of Hemolysis and SNPs in KL and Genes of the TGF-β/BMP Pathway.

Vikki G. Nolan, MPH, Adeboye H. Adewoye, MD, Clinton T. Baldwin, PhD, Qian-Li Ma, BA, Diego F. Wyszynski, MD, PhD, John J. Farrell, MS, Alice Bisbee, MPH, Matt Fourcade, BA, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD

Blood (2005) 106 (11): 2317.

https://doi.org/10.1182/blood.V106.11.2317.2317

Published: 2005

Journal Articles

Genetic Polymorphisms Associated with Fetal Hemoglobin Response to Hydroxyurea in Patients with Sickle Cell Anemia.

Diego F. Wyszynski, MD, PhD, Clinton T. Baldwin, PhD, Mario Cleves, PhD, John J. Farrell, BA, Alice Bisbee, MPH, Abdullah Kutlar, MD, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD

Blood (2004) 104 (11): 108.

https://doi.org/10.1182/blood.V104.11.108.108

Published: 2004

Journal Articles

Association of Single Nucleotide Polymorphisms in Klotho with Priapism in Sickle Cell Anemia.

Vikki G. Nolan, MA, Clinton Baldwin, PhD, Qianli Ma, BA, Diego F. Wyszynski, MD, PhD, John J. Farrell, BA, Alice Bisbee, MPH, Lindsay A. Farrer, PhD, Martin H. Steinberg, MD

Blood (2004) 104 (11): 1673.

https://doi.org/10.1182/blood.V104.11.1673.1673

Published: 2004

NARROW

Response of Patients with Transfusion-Dependent β-Thalassemia (TDT) to Betibeglogene Autotemcel (beti-cel; LentiGlobin for β-Thalassemia) Gene Therapy Based on HBB Genotype and Disease Genetic Modifiers

BCL11A enhancer Haplotypes Are Associated with the Distribution of HbF in Arab-Indian and African Haplotype Sickle Cell Anemia but Not the Different Population Levels of HbF

The Evolutionary Impact Of Malaria On The Saudi Arabian Genome

Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression

A 3-Bp Deletion Between Transcription Factor Binding Motifs In the HBS1L-MYB Intergenic Region on Chromosome 6q23 Is Associated with HbF Expression

Association of Polymorphisms of the Transforming Growth Factor-β/Bone Morphogenetic Protein (TGF-β/BMP) Pathway with Sickle Cell Bacteremia.

Gene-Gene Interactions and the Pathophysiology of Sickle Cell Disease: Modeling the Effects of SNPs on Sickle Cell-Associated Vasoocclusive Events Using Classification and Regression Trees and Stochastic Gradient Boosting.

Leg Ulcers in Sickle Cell Anemia Are Associated with Laboratory Markers of Hemolysis and SNPs in KL and Genes of the TGF-β/BMP Pathway.

Genetic Polymorphisms Associated with Fetal Hemoglobin Response to Hydroxyurea in Patients with Sickle Cell Anemia.

Association of Single Nucleotide Polymorphisms in Klotho with Priapism in Sickle Cell Anemia.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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