East Building, 12th Floor
2450 Riverside Ave.
Minneapolis, MN 55454
Best Doctors in America®, 2009-2010
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.