University of Minnesota Amplatz Children’s Hospital Position
Pediatric Genetics and Metabolics Physician

Other Related Positions Currently Held
Division Director, Division of Genetics and Metabolism, University of Minnesota Department of Pediatrics

Professor, Departments of Pediatrics, Ophthalmology and Genetics, Cell Biology and Development, University of Minnesota

Specialty
Genetics and Metabolism

Board Certifications
Pediatrics
Medical Genetics

Sees Patients At
University of Minnesota Amplatz Children’s Hospital (Genetics & Metabolism)
Pediatric Specialty Clinic (Minneapolis)
St. Mary's-Duluth Clinic

Clinical Interests
Genetic Diagnosis and Consultation
Inborn Errors of Metabolism
Birth Defects
Dysmorphology

Research Interests
Long-term follow-up after newborn screening 

Education
Medical School
University of Kansas School of Medicine

Site of Residency
University of Minnesota (Pediatrics)

Site of Fellowship
University of Minnesota (Medical Genetics)

Awards and Honors
Mpls.St.Paul Magazine Top Doctors 2010
Best Doctors in America^®, 2009-2010
Mpls.St.Paul Magazine Top Doctors 2009
Best Doctors in America^®, 2007-2008
Mpls.St.Paul Magazine Top Doctors 2008
Mpls.St.Paul Magazine Top Doctors 2007

Selected Recent Publications
Foker JE, Berry JM, Pyles LA, Treatment Algorithm for PAIVS. Progress in Pediatric Cardiology 2010; 29(1):61-63.

Foker JE, Berry JM, Setty SP, Harvey BA, Rivard AL, Gittenberger-de Groot AC, Pyles LA. Growth and Function of Hypoplastic Right Ventricles and Tricuspid Valves in Infants with Pulmonary Atresia and Intact Ventricular Septum. Progress in Pediatric Cardiology 2010; 29(1):49-54.

Pyles LA, Berry JM, Steinberger JS, Foker JE. Initial, Intra-Operative, and Post-Operative Evaluation of Children with Pulmonary Atresia with Intact Ventricular Septum with Emphasis on Evaluation of Coronary Connections to the Right Ventricle. Progress in Pediatric Cardiology 2010; 29(1):25-34.

Bishop L, Kanoff R, Charnas L, Krenzel C, Berry SA, Schimmenti LA: Severe methylenetetrahydrofolate reductase deficiency: a case report of nonclassical homocystinuria, J Child Neurol 23:823-8, 2008.

Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A: Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.  New Engl J Med 356(12): 2282-2292, 2007.

Schimmenti LA, Crombez EA, Schwahn BC, Heese BA, Wood TC, Schroer RJ, Bentler K, Cederbaum S, Sarafoglou K, McCann M, Rinaldo P, Matern D, di San Filippo CA, Pasquali M, Berry SA*, Longo N*:  Expanded newborn screening identifies maternal primary carnitine deficiency. Mol Genet Metab 90:441-445, 2007 *shared senior authorship.

del Gaudio D, Fang P, Scaglia F, Ward PA, Craigen WJ, Glaze DG, Neul JL, Patel A, Lee JA, Irons M, Berry SA, Pursley AA, Grebe TA, Freedenberg D, Martin RA, Hsich GE, Khera JR, Friedman NR, Zoghbi HY, Eng CM, Lupski JR, Beaudet AL, Cheung SW, Roa BB: Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males. Genet Med 8:784-92, 2006.

Thompson DB, Ahrens MJ, LeRoy BS, Brown D, Berry SA: Newborn blood spot screening and genetic services: a survey of Minnesota primary care physicians. Genet Med 7(8): 564-70, 2005.

Ensenauer R, Vockley J, Willard JM, Huey JC, Sass JO, Edland SD, Burton BK, Berry SA, Santer R, Grünert S, Koch HG, Marquardt I, Rinaldo P, Hahn S, Matern D:  A common mutation is associated with a mild, potentially asymptomatic phenotype in patients with isovaleric acidemia diagnosed by newborn screening. Amer J Hum Genet 75(6): 1136-42, 2004.

Wu-Chen WY, Christiansen SP, Berry SA, Engel WK Fray KJ, and Summers CG: Ophthalmic manifestations of Wolf–Hirschhorn syndrome J AAPOS 8:345-348, 2004.