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Personal History
1996 - 1997: George Washington University1997 - 2000: B.S., Biology, Magna Cum Laude, University of Maryland Baltimore County
2000 - 2004: M.D., University of Maryland School of Medicine
Post-Graduate Education and Training
2004 - 2007: Intern/Resident in Pediatrics, St. Louis Children's Hospital, Washington University, St. Louis, Missouri
2007 - 2009: Resident in Medical Genetics, Stanford University, Stanford, California
Research Interests
Newborn screening educationClinical Speciality
General genetics and dysmorphologyPublications
Shieh JTC, Swidler P, Martignetti JA, Ramirez MCM, Balboni I, Kaplan J, Kennedy J, Abdul-Rahman O, Enns GM, Sandborg C, Slavotinek A, Hoyme HE. Systemic Hyalinosis: A Distinctive Early Childhood-Onset Disorder Characterized by Mutations in the Anthrax Toxin Receptor 2 Gene (ANTRX2). Pediatrics 118(5):e1485-92, 2006.Kaplan, JD, Kwan A, Bernstein JA, Hudgins L. Clues to an Early Diagnosis of Kallmann Syndrome. Am J Med Genet. 2010 Nov;152A(11):2796-801.
Kaplan J and Hudgins L. Neonatal Presentations of CHARGE syndrome and VATER/VACTERL Association. NeoReviews 9:7, e299, 2008.
Faculty members:
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