Kelly Dean Stone, M.D., Ph.D.
Allergy and Immunology Clinical Fellowship Program
10 Center Drive
Bethesda, MD 20892
Dr. Stone is the program director of the Allergy and Immunology Clinical Training Program.
Dr. Stone serves as a principal investigator on two protocols to support laboratory interests in the genetics and mechanisms of allergic inflammation in atopic dermatitis, severe atopic diseases, genetic disorders with features of allergic inflammation, and immunodeficiency diseases. He serves as a staff clinician working closely with Dr. Joshua Milner and the Genetics and Pathophysiology of Allergy Section of the Laboratory of Allergic Diseases, with a major interest in the advancement of research and clinical care for children with atopic dermatitis and other allergic and immunologic diseases.
Dr. Stone received his M.D. and Ph.D. in molecular and cell biology from the University of Maryland; completed residency training in pediatrics at the Children’s National Medical Center in Washington, DC; and completed fellowship training in allergy and immunology at Children’s Hospital Boston. He served on the faculty in the department of pediatrics at Harvard Medical School and Children’s Hospital Boston and at Children’s National Medical Center and George Washington University. He joined the Laboratory of Allergic Diseases in 2007, where he serves as deputy chief; director of the National Institutes of Health (NIH) Clinical Center Allergy and Immunology Clinical Fellowship Program; and director of the NIH Clinical Center Allergy and Immunology Consultation Service.
Dr. Stone is a Fellow of the American Academy of Allergy, Asthma & Immunology and American Academy of Pediatrics and a member of the Clinical Immunology Society.
Jhamnani RD, Levin S, Rasooly M, Stone KD, Milner JD, Nelson C, DiMaggio T, Jones N, Guerrerio AL, Frischmeyer-Guerrerio PA. Impact of food allergy on the growth of children with moderate-severe atopic dermatitis. J Allergy Clin Immunol. 2018;141(4):1526-1529.e4.
Lyons JJ, Stotz SC, Chovanec J, Liu Y, Lewis KL, Nelson C, DiMaggio T, Jones N, Stone KD, Sung H, Biesecker LG, Colicos MA, Milner JD. A common haplotype containing functional CACNA1H variants is frequently coinherited with increased TPSAB1 copy number. Genet Med. 2018;20(5):503-512.
Carlson RJ, Bond MR, Hutchins S, Brown Y, Wolfe LA, Lam C, Nelson C, DiMaggio T, Jones N, Rosenzweig SD, Stone KD, Freeman AF, Holland SM, Hanover JA, Milner JD, Lyons JJ. Detection of phosphoglucomutase-3 deficiency by lectin-based flow cytometry. J Allergy Clin Immunol. 2017;140(1):291-294.e4.
Lyons JJ, Liu Y, Ma CA, Yu X, O'Connell MP, Lawrence MG, Zhang Y, Karpe K, Zhao M, Siegel AM, Stone KD, Nelson C, Jones N, DiMaggio T, Darnell DN, Mendoza-Caamal E, Orozco L, Hughes JD, McElwee J, Hohman RJ, Frischmeyer-Guerrerio PA, Rothenberg ME, Freeman AF, Holland SM, Milner JD. ERBIN deficiency links STAT3 and TGF-β pathway defects with atopy in humans. J Exp Med. 2017;214(3):669-680.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E, Gelfand EW, Snow AL, Milner JD. Germline hypomorphic CARD11 mutations in severe atopic disease. Nat Genet. 2017;49(8):1192-1201.
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This page was last updated on August 24th, 2018