Matthew M. Heeney, MD
| Department | Hematology/Oncology |
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| Hospital Title | Director, Clinical Hematology; Director, Sickle Cell Program | |
| Academic Title | Assistant Professor of Pediatrics | |
| Phone | 617-355-7700 | |
| Fax | 617-730-0641 | |
| Matthew Heeney | ||
| Location |
300 Longwood Avenue Boston MA 02115 |
Research Overview
Dr. Heeney conducts clinical research focused on sickle cell disorders and their treatment. He is the Children's Hospital Boston Principal Investigator for several clinical trials, including the Children's Hospital Clinical Core of the Boston Sickle Cell Disease Research Network (SCD-CRN), and for the multicenter SWiTCH and TWiTCH trials which are exploring the use of Hydroxyurea as an alternative to chronic transfusion for stroke prevention.
Dr. Heeney also conducts translational research in inherited disorders of iron homeostasis in humans. In particular he is interested in investigating the genetic basis inherited disorders of iron deficiency, sideroblastic anemia and iron overload.
Goals of Dr. Heeney's work include: to improve the understanding of the pathophysiology and treatment of sickle cell anemia through multicenter clinical trials and to elucidate the genetic basis of iron homeostasis and its role in human disease.
About Matthew Heeney
Dr. Heeney received his MD at the University of Calgary, Alberta, completed his residency at Montreal Children's Hospital, McGill University, and a pediatric hemotology/oncology fellowship at Duke University.
Key Publications
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Heeney MM. Howard TA. Zimmerman SA. Ware RE. UGT1A Promoter Polymorphisms Influence Bilirubin Response Hydroxyurea Therapy in Sickle Cell Anemia. Journal of Laboratory and Clinical Medicine. 141(4): 279-282, 2003.
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Heeney MM. Whorton MR. Howard TA. Johnson CA. Ware RE. Chemical and Functional Analysis of Hydroxyurea Oral Solutions. Journal of Pediatric Hematology/Oncology. 26 (3): 179-184, 2004.
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Heeney MM. Andrews NC. Iron Homeostasis and Inherited Iron Overload Disorders: An overview. Hematology/Oncology Clinics of North America. 18(6): 1379-403, 2004.
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Finberg KE. Heeney MM. Campagna DR. Aydinok Y. Pearson HA. Hartman KR. Mayo MM. Samuel SM. Strouse JJ. Markianos K. Andrews NC. Fleming MD. Mutations in TMPRSS6 cause iron-refractory iron deficiency Anemia (IRIDA). Nature Genetics. 40(5): 485-682. 2008.
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Dover GJ. Heeney MM. Sickle Cell Disease. In Nathan and Oski’s Hematology of Infancy and Childhood, 7th Edition (Nathan DG, Orkin SH, Ginsburg D, Look AT. Editors) Philadelphia: WB Saunders 2008; 949-1014.
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Steinberg MH. Ohene-Frempong K. Heeney MM. Clinical and Pathophysiological Aspects of Sickle Cell Anemia. In: Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management, 2nd Edition (Steinberg MH, Forget BG, Higgs DR, Weatherall DJ. Editors). Cambridge: Cambridge University Press. 2009; 437-496.
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Heeney MM, Ware RE. Hydroxyurea for Children with Sickle Cell Disease. Hematology/Oncology Clinics of North America. 24(1):199-214, 2010.
- Sobota A, Neufeld EJ, Sprinz P, Heeney MM. Transition from pediatric to adult care for sickle cell disease: results of a survey of pediatric providers. American Journal of Hematology. 2011 Jun;86(6):512-5.
