I always wanted to be a physician, and specifically a pediatrician. My father is an adult subspecialist, but I was drawn to the care of medically complex children. Now, I enjoy being the bridge between basic research and the clinic.
In my clinical practice, I specialize in treating patients with bone marrow failure and hematopoietic stem cell transplant for non-malignant diseases, with a special emphasis on Shwachman Diamond syndrome and dyskeratosis congenita. My research interests focus on translational and clinical studies in leukemogenesis and bone marrow failure related to these two conditions. I also study the complications of stem cell transplants, including bronchiolitis obliterans and fertility preservation.
I decided to pursue my research interests after my experience as a resident physician and fellow at Cincinnati Children’s. I enjoyed getting to know my patients on the bone marrow transplant and hematology/oncology units. Plus, I was mentored by two of the world’s foremost experts in the field, Dr. Stella Davies and Dr. Richard Harris, right here at Cincinnati Children’s.
After I completed my postdoctoral training, I joined the faculty of the Division of Bone Marrow Transplantation and Immune Deficiency at Cincinnati Children’s within the UC Department of Pediatrics. Now, in addition to clinical work and research, I serve as the co-director of the North American Shwachman Diamond Syndrome Registry.
BS: University of Michigan, Ann Arbor, MI, 2000.
MD: Case Western Reserve University, Cleveland, OH, 2004.
Post-Doctoral: Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 2010.
Certification: Pediatrics, 2007.
Cancer and Blood Diseases, Bone Marrow Transplantation BMT, Fanconi Anemia, Fertility Preservation, Rare Lung Diseases
Bone Marrow Transplantation and Immune Deficiency, Cancer and Blood Diseases
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G-CSF resistance of ELANE-mutant neutropenia depends on SERF1-containing truncated-neutrophil elastase aggregates. The Journal of Clinical Investigation. 2025; 135:e177342.
Regulated GATA1 expression as a universal gene therapy for Diamond-Blackfan anemia. Cell Stem Cell. 2025; 32:38-52.e6.
Outcomes of Hematopoietic Stem Cell Transplantation for High-Risk Marrow Features without Malignancy in Shwachman-Diamond Syndrome. Blood. 2024; 144:441.
Incidence of Myeloid Malignancy in Shwachman-Diamond Syndrome: An International Cohort Study. Blood. 2024; 144:2703.
GATA2-TGF-b1-TAL1 Axis Is Essential for Human NK Cell Development and Function. Blood. 2024; 144:5398.
Clinician Adherence to Screening and Preventive Practices for Non-Malignant Late Effects Among Allogeneic Hematopoietic Cell Transplant Survivors in the United States. Blood. 2024; 144:2170.
Lymphoid Malignancies in Shwachman-Diamond Syndrome. Blood. 2024; 144:5707.
Real-World Clinician Adherence to Screening and Preventive Practices Guidelines for Subsequent Neoplasms Among Allogeneic Hematopoietic Cell Transplant Survivors in the United States. Blood. 2024; 144:4921.
Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia. Haematologica: the hematology journal. 2024; 109:3435-3438.
Late effects after allogeneic haematopoietic cell transplantation in children and adolescents with non-malignant disorders: a retrospective cohort study. The Lancet Child and Adolescent Health. 2024; 8:740-750.
Kasiani C. Myers, MD2/25/2025
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