MD: Jordan University of Science and Technology, 2004.
Residency: Pediatrics, University of Nebraska Medical Center, Omaha, NE, 2010.
Fellowship: Pediatric Hematology Oncology, Cincinnati Children’s Hospital Medical Center, 2013; Sickle Cell Scholar, Cincinnati Children’s Hospital Medical Center, 2014.
Certification: Pediatrics, 2010; Pediatric Hematology/Oncology, 2015.
Pediatric hematology; sickle cell disease; hemoglobinopathies; congenital anemias; immune mediated cytopenia
Cancer and Blood Diseases, Sickle Cell and Hemoglobin Disorders, Cardio-Oncology
Cardiopulmonary complications of sickle cell disease; congenital anemias
Hematology
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Improving Transition of Emerging Adults with Sickle Cell Disease to Adult Care through a Multidisciplinary Process: The Development of a Transition Clinic to Support Transition Success. Blood. 2023; 142:5055.
Genetic Variants in Canonical Wnt Signaling Pathway Associated with Pediatric ITP. Blood. 2023; 142:2593.
Congenital Dyserythropoietic Anemia Type II: An Update from the Congenital Dyseryhtropoietic Anemia Registry of North America (CDAR). Blood. 2023; 142:1079.
Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial. Blood. 2022; 140:5416-5417.
Early hydroxyurea use is neuroprotective in children with sickle cell anemia. American Journal of Hematology. 2022; 97:E368-E370.
Chapter 3 Classification and diagnosis of anemia in children and neonates. Lanzkowsky's Manual of Pediatric Hematology and Oncology. : Elsevier; Elsevier; 2022.
Rapid and automated quantitation of dense red blood cells: A robust biomarker of hydroxyurea treatment response. Blood Cells, Molecules, and Diseases. 2021; 90:102576.
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics-guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia. British Journal of Haematology. 2021; 194:617-625.
Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience. Pediatric Blood and Cancer. 2021; 68:e29008.
Hydroyxurea improves cerebral oxygen saturation in children with sickle cell anemia. American Journal of Hematology. 2021; 96:538-544.
Omar Niss, MD, Punam Malik, MD4/15/2020
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