Clinton H Joiner MD PhD

PubMed

• Red blood cell transfusion survival in sickle cell disease is reduced by donor characteristics and recipient spleen activity.
  Marianne E M Yee, Patricia E Zerra, Richard O Francis, Kirk A Easley, Christopher M Lough
  Blood Advances. 2026-07-14
• 9 citations
  Complement is activated in patients with acute chest syndrome caused by sickle cell disease and represents a therapeutic target.
  Satheesh Chonat, Jayre A Jones, Seema R Patel, William M Briones, Michelle L Schoettler
  Science Translational Medicine. 2025-07-16
• 12 citations
  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
  Blood. 2024-11-07

Journal Articles

• Clinical Outcomes Associated with Sickle Cell Trait: A Systematic Review  
  Kathryn L Hassell, Rakhi P Naik, Puneet Sahota, Gregory J Kato, Clinton H Joiner, Annals of Internal Medicine
• Activationof Protein Kinase C by Phorbol Ester Increases Red Blood Cell Scramblase Activity and External Phosphatidylserine  
  Barber LA1, Palascak MB, Qi X, Joiner CH, Franco RS, Eur J Haematol, 1/1/2015
• Use of an oral stable isotope label to confirm variation in red blood cell mean age that influences HbA1c interpretation  
  Khera PK1, Smith EP, Lindsell CJ, Rogge MC, Haggerty S, Wagner DA, Palascak MB, Mehta S, Hibbert JM, Joiner CH, Franco RS, Cohen RM, Am J Hematol, 1/1/2015

Books/Book Chapters

• Disorders of Hemoglobin. 
  Chapter: Red Cell Membrane in Sickle Cell Disease. 
  Page 158 - 184Gallagher PG and Joiner CHEditors: M.H. Steinberg, B.G. Forget, D.R. Higgs, and R.L. Nagel.Cambridge University Press, United Kingdom2009
• The Renaissance of Sickle Cell Disease in the Human Genome Era 
  Chapter: Damage to the RBC Membrane in Sickle Cell Disease. 
  Goodman SR and Joiner CHEditors: B Pace.Imperial College Press, United Kingdom2007
• Pediatrics and Perinatology: The Scientific Basis. 
  Chapter: Membrane function, Ion Transport and Cellular Ion Regulation 
  Page 40 - 53Joiner CHEditors: P.D. Gluckman and M. Heyman.Edward Arnold Ltd, London, United Kingdom1996

Abstracts/Posters

• Stiff Erythrocyte Subpopulations Biomechanically Induce Endothelial Inflammation in Sickle Cell Disease
  Clinton H. Joiner, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/9/2019
• 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, Edyta Glogowska, Amber Ht Begtrup, Neha Dagaonkar, Satheesh Chonat, Clinton H Joiner, Charles T. Quinn, Theodosia A. Kalfa, and Patrick G Gallagher, Blood; ASH, San Francisco, CA, 1/1/2014
• Development of a Comprehensive Rapid Next-Generation Sequencing Assay For The Diagnosis Of Inherited Hemolytic Anemia.
  Amber Hogart Begtrup, Neha Dagaonkar, Suvarnamala Pushkaran, Katie M. Giger, Ammar Husami, Diane Kissell, Clinton H. Joiner, Mehdi Keddache, Kejian Zhang, Theodosia A...., Blood; ASH, New Orleans, LA, 1/1/2013

Lectures

• Moving the Clinical Research Agenda Forward 
  Baltimore, MD - 1/1/2013
• Regulation of Erythroid Expression of KCl Cotransporter Genes 
  Bethesda, MD - 1/1/2013
• Sickle Cell Disease Pathophysiology 
  1/1/2012

Other

• Global Burden of Sickle Cell Disease. Commentary 
  Joiner CH, and Frederickson, ME, HemeOnc Today
  1/1/2013
• Genetic screening in NCAA has the potential to be discriminatory. Guest editorial. 
  Joiner CH, and Frederickson, ME, Cincinnati Enquirer
  1/9/2010
• What is Sickle Cell Trait? 
  Joiner CH, Sickle Cell News and Views, Sickle Cell Disease Association of America
  1/1/2008