Certification: American Board of Medical Genetics

Professional School: Virginia Commonwealth University Medical School

Residency: Massachusetts General Hospital

Fellowship: Harvard Medical School / Children's Hospital of Boston

Internship: Massachusetts General Hospital

Special Interests: Pediatric Medical Genetics

Simon J, Stoll K, Fick R, Mott J, Lawson-Yuen A. Homozygous 15q13.3 microdeletion in a child with hypotonia and impaired vision: A new report and review of the literature. Clinical case reports. 2019;7(12):2311-5. 

Mitchell E, Douglas A, Kjaegaard S, Callewaert B, Vanlander A, Janssens S, Yuen AL, Skinner C, Failla P, Alberti A, Avola E, Fichera M, Kibaek M, Digilio MC, Hannibal MC, den Hollander NS, Bizzarri V, Renieri A, Mencarelli MA, Fitzgerald T, Piazzolla S, van Oudenhove E, Romano C, Schwartz C, Eichler EE, Slavotinek A, Escobar L, Rajan D, Crolla J, Carter N, Hodge JC, Mefford HC. Recurrent duplications of 17q12 associated with variable phenotypes. Am J Med Genet A. 2015 Dec;167A(12):3038-45. doi: 10.1002/ajmg.a.37351. Epub 2015 Sep 30.

Learn more about ongoing studies and medical research at the MultiCare Institute for Research & Innovation.