Amarilis Sanchez-Valle, MD

College Of Medicine Pediatrics

Assistant Professor, Pediatrics, Division of Genetics and Metabolism, University of South Florida

Contact Info 2 Tampa General Circle
Tampa, FL 33606


  • Genetics, Clinical Genetics, Baylor College of Medicine, 2010
  • Pediatrics, Pediatrics Residency, University of Texas, 2008
  • MD, Medicine, University Of Puerto Rico, 2005

Interdisciplinary and Emerging Signature Programs

  • Other


  • Society of Inherited Metabolic Disorders (Member, 2012 - Present)
  • American Medical Association (Member, 2004 - Present)

Recent Publications

  • Toriello, HV.Erick, M.Alessandri, JL.Bailey, D.Brunetti-Pierri, N.Cox, H.Fryer, A.Marty, D.McCurdy, C.Mulliken, JB.Murphy, H.Omlor, J.Pauli, RM.Ranells, JD.Sanchez-Valle, A.Tobiasz, A.Van Maldergem, L.Lin, AE. Maternal vitamin K deficient embryopathy: association with hyperemesis gravidarum and Crohn disease. American journal of medical genetics. Part A. 161(3) : 417-29, 2013.
  • Balasa A, Sanchez-Valle A, Sadikovic B, Sangi-Haghpeykar H, Bravo J, Chen L, Liu W, Wen S, Fiorotto ML, Veyver IB. Chronic maternal protein deprivation in mice is associated with overexpression of the cohesin-mediator complex in liver of their offspring. The Journal of Nutrition. 12(141) : 2106-12, 2011.
  • Sanchez-Valle, A.Pierpont, ME.Potocki, L. The severe end of the spectrum: Hypoplastic left heart in Potocki-Lupski syndrome. American journal of medical genetics. Part A. 155A(2) : 363-6, 2011.
  • Zhang, F.Potocki, L.Sampson, JB.Liu, P.Sanchez-Valle, A.Robbins-Furman, P.Navarro, AD.Wheeler, PG.Spence, JE.Brasington, CK.Withers, MA.Lupski, JR. Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS. American journal of human genetics. 86(3) : 462-70, 2010.
  • Sanchez-Valle, A.Wang, X.Potocki, L.Xia, Z.Kang, SH.Carlin, ME.Michel, D.Williams, P.Cabrera-Meza, G.Brundage, EK.Eifert, AL.Stankiewicz, P.Cheung, SW.Lalani, SR. HERV-mediated genomic rearrangement of EYA1 in an individual with branchio-oto-renal syndrome. American journal of medical genetics. Part A. 152A(11) : 2854-60, 2010.


  • Humanism and Teaching Award (Gold Foundation - 2007)