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Journal Articles

Less-deformable erythrocyte subpopulations biomechanically induce endothelial inflammation in sickle cell disease

Christina Caruso, Xiaopo Cheng, Marina E. Michaud, Hannah M. Szafraniec, Beena E. Thomas, Meredith E. Fay, Robert G. Mannino, Xiao Zhang, Yumiko Sakurai, Wei Li, David R. Myers, Clinton H. Joiner, David K. Wood, Manoj Bhasin, Michael D. Graham, Wilbur A. Lam

Blood (2024) 144 (19): 2050–2062.

https://doi.org/10.1182/blood.2024024608

Published: 2024

Includes: Supplemental data

Journal Articles

Complement Drives Acute Chest Syndrome in a Model of Sickle Cell Disease

Satheesh Chonat, Jayre A Jones, Seema R Patel, Patricia E Zerra, Lauren A Jeffers, Ryan Philip Jajosky, Connie M. Arthur, Michael Koval, Clinton H. Joiner, David R. Archer, Sean R. Stowell

Blood (2022) 140 (Supplement 1): 8221–8222.

https://doi.org/10.1182/blood-2022-170830

Published: 2022

Journal Articles

Complement Activation during Vaso-Occlusive Pain Crisis in Pediatric Sickle Cell Disease

Justin J Yoo, Sara H Graciaa, Jayre A Jones, Zoey Zuo, Connie M Arthur, Traci Leong, Clinton H. Joiner, Sean R Stowell, Satheesh Chonat

Blood (2021) 138 (Supplement 1): 858.

https://doi.org/10.1182/blood-2021-154132

Published: 2021

Journal Articles

Assessment of Cerebral Blood Flow and Oxygen Extraction in Pediatric Sickle Cell Disease with Non-Invasive Diffuse Optical Spectroscopies

Seung Yup Lee, PhD, Eashani Sathilingam, BS, Kyle R. Cowdrick, MS, Rowan O. Brothers, BS, Wilbur A. Lam, MDPhD, R. Clark Brown, MD PhD, Clinton H. Joiner, MD PhD, Claudia R. Morris, MD, Erin M. Buckley, PhD

Blood (2020) 136 (Supplement 1): 7–8.

https://doi.org/10.1182/blood-2020-142029

Published: 2020

Journal Articles

Stiff Erythrocyte Subpopulations Biomechanically Induce Endothelial Inflammation in Sickle Cell Disease

Christina Caruso, MD, Xiao Zhang, BS, Yumiko Sakurai, MSc, Wei Li, MD, Meredith E. Fay, BS, Marcus A. Carden, MD, David R. Myers, PhD, Robert G. Mannino, PhD, Clinton H. Joiner, MD PhD, Michael D. Graham, PhD, Wilbur A. Lam, MD PhD

Blood (2019) 134 (Supplement_1): 3560.

https://doi.org/10.1182/blood-2019-125408

Published: 2019

Journal Articles

Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion

Marcus A. Carden, Meredith E. Fay, Xinran Lu, Robert G. Mannino, Yumiko Sakurai, Jordan C. Ciciliano, Caroline E. Hansen, Satheesh Chonat, Clinton H. Joiner, David K. Wood, Wilbur A. Lam

Blood (2017) 130 (24): 2654–2663.

https://doi.org/10.1182/blood-2017-04-780635

Published: 2017

Includes: Multimedia, Supplemental data

Journal Articles

Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease

Maa-Ohui Quarmyne, MBChB, Janet Figueroa, MPH, Courtney McCracken, PhD, Charles T. Quinn, MD MS, Clark Brown, MD PhD, Clinton H. Joiner, MD PhD

Blood (2017) 130 (Supplement 1): 988.

https://doi.org/10.1182/blood.V130.Suppl_1.988.988

Published: 2017

Journal Articles

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Mary A Risinger, PhD, Neha Dagaonkar, Georgios E Christakopoulos, MD, Jie Liu, PhD, Katie Giger Seu, PhD, Diamantis G Konstantinidis, BSc, PhD, Charles T Quinn, MD, Satheesh Chonat, MD, Clinton H Joiner, MD PhD, Kejian Zhang, MD, Theodosia A Kalfa, MD PhD

Blood (2016) 128 (22): 2446.

https://doi.org/10.1182/blood.V128.22.2446.2446

Published: 2016

Journal Articles

Biochemical Surrogate Markers of Hemolysis Do Not Correlate with Directly Measured Erythrocyte Survival in Sickle Cell Anemia

Charles T. Quinn, MD MS, Eric P. Smith, MD, Shahriar Arbabi, Paramjit Khera, PhD, Christopher J. Lindsell, PhD, Omar Niss, MD, Clinton H Joiner, MD PhD, Robert S. Franco, PhD, Robert M. Cohen, MD

Blood (2016) 128 (22): 2484.

https://doi.org/10.1182/blood.V128.22.2484.2484

Published: 2016

Journal Articles

Engineering a "Self-Healing" Hydrogel-Based Microvasculature-on-a-Chip for Investigating the Effects of Cellular and Biomolecular Interactions on Endothelial Permeability in Sickle Cell Disease

Yongzhi Qiu, PhD, Byungwook Ahn, PhD, Yumiko Sakurai, MSc, Caroline Hansen, BS, Clinton H. Joiner, MD PhD, Solomon Fiifi Ofori-Acquah, PhD, Wilbur A Lam, MD PhD

Blood (2015) 126 (23): 240.

https://doi.org/10.1182/blood.V126.23.240.240

Published: 2015

Journal Articles

Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort Study

Maa-Ohui Quarmyne, MBChB MS, Wei Dong, MS MPH, Vaughn Barry, PhD MPH, Rodney Theodore, MPH, Olufolake A. Adisa, MD, Iris Buchanan, MD MSC, James Bost, PhD, Robert Clark Brown, MD PhD, Clinton H. Joiner, MD PhD, Peter A. Lane, MD

Blood (2015) 126 (23): 2179.

https://doi.org/10.1182/blood.V126.23.2179.2179

Published: 2015

Journal Articles

Vessel Geometry Interacts with Red Blood Cell Stiffness to Promote Endothelial Dysfunction in Sickle Cell Disease

Yichen Wang, Robert G Mannino, BS, David R Myers, PhD, Wei Li, Clinton H. Joiner, MD PhD, Wilbur A Lam, MD PhD

Blood (2015) 126 (23): 965.

https://doi.org/10.1182/blood.V126.23.965.965

Published: 2015

Journal Articles

The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype

Mary A Risinger, PhD, Edyta Glogowska, PhD, Amber Hogart Begtrup, PhD, Neha Dagaonkar, Satheesh Chonat, MD, Clinton H Joiner, MD PhD, Charles T. Quinn, MD, Theodosia A. Kalfa, MD PhD, Patrick G Gallagher, MD

Blood (2014) 124 (21): 741.

https://doi.org/10.1182/blood.V124.21.741.741

Published: 2014

Journal Articles

Impact Of Use Of a Disease-Specific Patient Portal On Transition Readiness and Quality Of Life In Adolescents With Sickle Cell Disease

Lori E Crosby, PsyD, Margaret Hudepohl, PhD, Karen Kalinyak, MD, Maria Britto, MD, MPH, Alana Goldstein, MA, Kara Brown, BA, Aubrey Culp, MS, Clinton H Joiner, MD, PhD

Blood (2013) 122 (21): 2982.

https://doi.org/10.1182/blood.V122.21.2982.2982

Published: 2013

Journal Articles

Six-Month Data From a Pilot Self-Management Intervention ForAdolescents With Sickle Cell Disease

Lori E Crosby, PsyD, Naomi Joffe, PhD, Karen Kalinyak, MD, Alex Bruck, BS, CHES, Clinton H Joiner, MD, PhD

Blood (2013) 122 (21): 1675.

https://doi.org/10.1182/blood.V122.21.1675.1675

Published: 2013

Journal Articles

Measurement Of Erythrocyte Survival In Vivo using a Stable Isotope Label In Sickle Cell Anemia

Charles T. Quinn, MD, MS, Paramjit K Khera, PhD, Christopher J Lindsell, Ph.D., Clinton H Joiner, MD, PhD, Robert M Cohen, MD, Robert S. Franco, PhD

Blood (2013) 122 (21): 2223.

https://doi.org/10.1182/blood.V122.21.2223.2223

Published: 2013

Journal Articles

A Phase I Trial Of Zileuton In Sickle Cell Disease

Marthe-Sandrine Eiymo Mwa Mpollo, M.Sc., Maa-Ohui Quarmyne, MBChB, Omar Rayes, MD, Caryn S. Gonsalves, PhD, Laurie Vanderah, RN, Christina Canter, Johnson Haynes, Jr., MD, Claudia Fernanda Clavijio, MD, Christians Uwe, MD, PhD, Karen Kalinyak, MD, Clinton H. Joiner, MD, PhD, Alexander A. Vinks, PharmD, PhD, FCP, Punam Malik, MD

Blood (2013) 122 (21): 993.

https://doi.org/10.1182/blood.V122.21.993.993

Published: 2013

Journal Articles

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Amber Hogart Begtrup, PhD, Neha Dagaonkar, Suvarnamala Pushkaran, M.Sc., Katie M. Giger, PhD, Ammar Husami, Diane Kissell, Clinton H. Joiner, MD, PhD, Mehdi Keddache, Ph.D., Kejian Zhang, M.D., M.B.A., Theodosia A. Kalfa, M.D., Ph.D.

Blood (2013) 122 (21): 949.

https://doi.org/10.1182/blood.V122.21.949.949

Published: 2013

Journal Articles

Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease

Alex George, Suvarnamala Pushkaran, Diamantis G. Konstantinidis, Sebastian Koochaki, Punam Malik, Narla Mohandas, Yi Zheng, Clinton H. Joiner, Theodosia A. Kalfa

Blood (2013) 121 (11): 2099–2107.

https://doi.org/10.1182/blood-2012-07-441188

Published: 2013

Includes: Supplemental data

Journal Articles

Next Generation Sequencing for Diagnostic Testing of Erythrocyte Cytoskeleton Disorders

Theodosia A Kalfa, M.D., Ph.D., Mary A. Risinger, Ph.D., Suvarnamala Pushkaran, M.Sc., Phillip Dexheimer, Ammar Husami, Diane Kissell, Clinton H. Joiner, MD, PhD, Mehdi Keddache, Ph.D., Kejian Zhang, M.D., M.B.A.

Blood (2012) 120 (21): 976.

https://doi.org/10.1182/blood.V120.21.976.976

Published: 2012

NARROW

Less-deformable erythrocyte subpopulations biomechanically induce endothelial inflammation in sickle cell disease

Complement Drives Acute Chest Syndrome in a Model of Sickle Cell Disease

Complement Activation during Vaso-Occlusive Pain Crisis in Pediatric Sickle Cell Disease

Assessment of Cerebral Blood Flow and Oxygen Extraction in Pediatric Sickle Cell Disease with Non-Invasive Diffuse Optical Spectroscopies

Stiff Erythrocyte Subpopulations Biomechanically Induce Endothelial Inflammation in Sickle Cell Disease

Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion

Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease

Cellular Hydration and Oxidation As Phenotype Modifiers in Sickle Cell Anemia

Biochemical Surrogate Markers of Hemolysis Do Not Correlate with Directly Measured Erythrocyte Survival in Sickle Cell Anemia

Engineering a "Self-Healing" Hydrogel-Based Microvasculature-on-a-Chip for Investigating the Effects of Cellular and Biomolecular Interactions on Endothelial Permeability in Sickle Cell Disease

Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort Study

Vessel Geometry Interacts with Red Blood Cell Stiffness to Promote Endothelial Dysfunction in Sickle Cell Disease

The Novel PIEZO1 Mutation p.L2023V Is Causal for Hereditary Xerocytosis Resulting in Delayed Channel Inactivation and a Dehydrated Red Blood Cell Phenotype

Impact Of Use Of a Disease-Specific Patient Portal On Transition Readiness and Quality Of Life In Adolescents With Sickle Cell Disease

Six-Month Data From a Pilot Self-Management Intervention ForAdolescents With Sickle Cell Disease

Measurement Of Erythrocyte Survival In Vivo using a Stable Isotope Label In Sickle Cell Anemia

A Phase I Trial Of Zileuton In Sickle Cell Disease

Development Of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia

Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease

Next Generation Sequencing for Diagnostic Testing of Erythrocyte Cytoskeleton Disorders

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American Society of Hematology

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American Society of Hematology

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