Michael Alan Levine

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Professor of Pediatrics at the Children's Hospital of Philadelphia
Department: Pediatrics

Contact information
The Children's Hospital of Philadelphia
34th & Civic Center Blvd.
Philadelphia, PA 19104
Office: 215-590-3618
Fax: 215-590-3053
Rutgers College, New Brunswick, NJ, 1972.
Drexel University (formerly Hahnemann) College of Medicine, Philadelpia, PA, 1976.
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Description of Itmat Expertise

Bone and mineral metabolism; genetic control of parathyroid cell development and growth; imprinting mechanisms and their influence on phenotypic variation.

Selected Publications

Hawkes Colin Patrick, Li Dong, Hakonarson Hakon, Meyers Kevin E, Thummel Kenneth E, Levine Michael A: CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations. The Journal of clinical endocrinology and metabolism 102(5): 1440-1446, May 2017.

Li Dong, Streeten Elizabeth A, Chan Alice, Lwin Wint, Tian Lifeng, Pellegrino da Silva Renata, Kim Cecilia E, Anderson Mark S, Hakonarson Hakon, Levine Michael A: Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism. The Journal of clinical endocrinology and metabolism 102(5): 1726-1733, May 2017.

McCormack Shana E, Li Dong, Kim Yeon Joo, Lee Ji Young, Kim Soo-Hyun, Rapaport Robert, Levine Michael A: Digenic Inheritance of PROKR2 and WDR11 Mutations in Pituitary Stalk Interruption Syndrome. The Journal of clinical endocrinology and metabolism Apr 2017.

Dhir Gauri, Li Dong, Hakonarson Hakon, Levine Michael A: Late-onset hereditary hypophosphatemic rickets with hypercalciuria (HHRH) due to mutation of SLC34A3/NPT2c. Bone 97: 15-19, Apr 2017.

Ackermann Amanda M, Levine Michael A: Compound heterozygous mutations in COL1A1 associated with an atypical form of type I osteogenesis imperfecta. American journal of medical genetics. Part A Apr 2017.

Abraham Mary B, Li Dong, Tang Dave, O'Connell Susan M, McKenzie Fiona, Lim Ee Mun, Hakonarson Hakon, Levine Michael A, Choong Catherine S: Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene. International journal of pediatric endocrinology 2017: 1, 2017.

Chandra Abhishek, Lin Tiao, Young Tiffany, Tong Wei, Ma Xiaoyuan, Tseng Wei-Ju, Kramer Ina, Kneissel Michaela, Levine Michael A, Zhang Yejia, Cengel Keith, Liu X Sherry, Qin Ling: Suppression of Sclerostin Alleviates Radiation-Induced Bone Loss by Protecting Bone Forming Cells and Their Progenitors through Distinct Mechanisms. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 32(2): 360-372, Sep 2016.

Hysinger Erik B, Roizen Jeffrey D, Mentch Frank D, Vazquez Lyam, Connolly John J, Bradfield Jonathan P, Almoguera Berta, Sleiman Patrick M, Allen Julian L, Levine Michael A, Hakonarson Hakon: Mendelian randomization analysis demonstrates that low vitamin D is unlikely causative for pediatric asthma. The Journal of allergy and clinical immunology 138(6): 1747-1749.e4, Aug 2016.

Thacher Tom D, Levine Michael A: CYP2R1 mutations causing vitamin D-deficiency rickets. The Journal of steroid biochemistry and molecular biology Jul 2016.

Li Qiaoli, Kingman Joshua, Sundberg John P, Levine Michael A, Uitto Jouni: Etidronate prevents, but does not reverse, ectopic mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6-/-). Oncotarget Jul 2016.

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Last updated: 09/17/2017
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