Gregory Rice, MD

Clinical Biochemical Geneticist

Profile

Dr. Gregory Rice earned his medical degree from the University of Wisconsin School of Medicine and Public Health (formerly UW Medical School), Madison, WI, and completed his residency and a fellowship at University of Wisconsin Hospital and Clinics.

Clinics

Professional Certifications and Education

Board Certification, Clinical Biochemical Genetics
Board Certification, Clinical Genetics
Board Certification, Pediatrics
MD, University of Wisconsin

Selected Publications

Tam A, AlDhaheri NS, Mysore K, Tessier ME, Goss J, Fernandez LA, D’Alessandro AM, Schwoerer JS, Rice GM, Elsea SH, Scaglia F. (2019). Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy. American Journal of Medical Genetics, Part A, 179(6):1015-1019. doi: 10.1002/ajmg.a.61104
Hess AS, Rice GM, Jochman JD, Muldowney BL. (2018). Volatile anesthesia for a pediatric patient with very long-chain acyl-coenzyme A dehydrogenase deficiency: A case report. Paediatric Anaesthesia, 28(3):296-297. doi: 10.1111/pan.13314.
Kuhl A, van Calcar S, Baker M, Seroogy CM, Rice G, Scott Schwoerer J. (2017). Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population. Genetics in Medicine. 19(3):352-356. doi: 10.1038/gim.2016.104
Hendee K, Wang LW, Reis LM, Rice GM, Apte SS, Semina EV. (2017). Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a three-generation human pedigree. Human Mutation, 38(11):1485-1490. doi: 10.1002/humu.23299.
Reynolds KK, Juusola J, Rice GM, Giampietro PF. (2017). Prenatal presentation of Mabry syndrome with congenital diaphragmatic hernia and phenotypic overlap with Fryns syndrome. American Journal of Medical Genetics Part A, 173(10):2776-2781. doi: 10.1002/ajmg.a.38379.
George A, Zand DJ, Hufnagel RB, Sharma R, Sergeev YV, Legare JM, Rice GM, Scott Schwoerer JA, Rius M, Tetri L, Gamm DM, Bharti K, Brooks BP. (2016) Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness. American Journal of Human Genetics. 1;99(6):1388-1394. doi: 10.1016/j.ajhg.2016.11.004.
Ney DM, Stroup BM, Clayton MK, Murali SG, Rice GM, Rohr F, Levy HL. (2016). Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial. American Journal of Clinical Nutrition, 104(2):334-45
Scott Schwoerer J, van Calcar S, Rice GM, Deline J. (2016). Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community. Molecular Genetics and Metabolism Reports, 8:4-7. doi: 10.1016/j.ymgmr.2016.05.003.
Stroup BM, Held PK, Williams P, Clayton MK, Murali SG, Rice GM, Ney DM. (2016). Clinical relevance of the discrepancy in phenylalanine concentrations analyzed using tandem mass spectrometry compared with ion-exchange chromatography in phenylketonuria. Molecular Genetics and Metabolism Reports, 16;6:21-6. doi: 10.1016/j.ymgmr.2016.01.001.
Rice GM, Steiner RD. (2016). Inborn Errors of Metabolism (Metabolic Disorders). Pediatric Reviews, 37(1):3-15; quiz 16-7, 47. doi: 10.1542/pir.2014-0122.
Schwoerer JA, Obernolte L, Van Calcar S, Heighway S, Bankowski H, Williams P, Rice G. (2012) Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome. JIMD Reports. 6:15-20. doi: 10.1007/8904_2011_95.