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Gregory M. Rice, MD

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Gregory M. Rice, MD Print Friendly Page

Faculty, University of Wisconsin School of Medicine and Public Health

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.



Aurora Children's Health (Green Bay)
(920) 288-5500 | | Map
Marshfield Clinic
(800) 782-8581 | | Map
Waisman Center
(608) 263-3301 | (800) 323-8942 | Map
Waisman Center
(608) 263-3301 | (800) 323-8942 | Map

UW School of Medicine and Public Health

Department of Pediatrics

Professional Certifications and Education

Board Certification Clinical Biochemical Genetics
Fellowship University of Wisconsin Hospital and Clinics, Madison, WI
Residency University of Wisconsin Hospital and Clinics, Madison, WI
Medical School University of Wisconsin School of Medicine and Public Health (formerly UW Medical School), Madison, WI

Medical interpreters are available to help patients communicate with hospital and clinic staff. For more information, please contact interpreter services at (608) 262-9000.
PubMed Articles
Kellom ER Wolf B Rice GM Stepien KE Reversal of Vision Loss in a 49-Year-Old Man With Progressive Optic Atrophy Due to Profound Biotinidase Deficiency. J Neuroophthalmol . 2021 Mar 1;41(1):e27-e30
[PubMed ID: 32235217]
Kellom E Stepien K Rice G Wolf B Biotinidase deficiency is a rare, potentially treatable cause of peripheral neuropathy with or without optic neuropathy in adults. Mol Genet Metab Rep . 2021 Mar;26:100696
[PubMed ID: 33364171]
Dutta S Lai A Scholz-Romero K Shiddiky MJA Yamauchi Y Mishra JS Rice GE Hyett J Kumar S Salomon C Hypoxia-induced small extracellular vesicle proteins regulate proinflammatory cytokines and systemic blood pressure in pregnant rats. Clin Sci (Lond) . 2020 Mar 27;134(6):593-607
[PubMed ID: 32129439]
Held PK Rice GM Kuhl A Drilias N Baker M Deline J Spicer G Sandrock C Seroogy CM Schwoerer JS Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017. Public Health Rep . 2019 Nov Dec;134(2_suppl):58S-63S
[PubMed ID: 31682555]
Tam A AlDhaheri NS Mysore K Tessier ME Goss J Fernandez LA D'Alessandro AM Schwoerer JS Rice GM Elsea SH Scaglia F Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy. Am J Med Genet A . 2019 Jun;179(6):1015-1019
[PubMed ID: 30864297]
Zepeda-Mendoza C Goodenberger ML Kuhl A Rice GM Hoppman N Familial segregation of a 5q15-q21.2 deletion associated with facial dysmorphism and speech delay. Clin Case Rep . 2019 Jun;7(6):1154-1160
[PubMed ID: 31183085]
Hess AS Rice GM Jochman JD Muldowney BL Volatile anesthesia for a pediatric patient with very long-chain acyl-coenzyme A dehydrogenase deficiency: A case report. Paediatr Anaesth . 2018 Mar;28(3):296-297
[PubMed ID: 29316010]
Hendee K Wang LW Reis LM Rice GM Apte SS Semina EV 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. Hum Mutat . 2017 Nov;38(11):1485-1490
[PubMed ID: 28722276]
Reynolds KK Juusola J Rice GM Giampietro PF Prenatal presentation of Mabry syndrome with congenital diaphragmatic hernia and phenotypic overlap with Fryns syndrome. Am J Med Genet A . 2017 Oct;173(10):2776-2781
[PubMed ID: 28817240]
Kuhl A van Calcar S Baker M Seroogy CM Rice G Scott Schwoerer J Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population. Genet Med . 2017 Mar;19(3):352-356
[PubMed ID: 27513192]
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 Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness. Am J Hum Genet . 2016 Dec 1;99(6):1388-1394
[PubMed ID: 27889061]
Ney DM Stroup BM Clayton MK Murali SG Rice GM Rohr F Levy HL Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial. Am J Clin Nutr . 2016 Aug;104(2):334-45
[PubMed ID: 27413125]
Scott Schwoerer J van Calcar S Rice GM Deline J Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community. Mol Genet Metab Rep . 2016 Sep;8:4-7
[PubMed ID: 28649556]
Stroup BM Held PK Williams P Clayton MK Murali SG Rice GM Ney DM Clinical relevance of the discrepancy in phenylalanine concentrations analyzed using tandem mass spectrometry compared with ion-exchange chromatography in phenylketonuria. Mol Genet Metab Rep . 2016 Mar;6:21-6
[PubMed ID: 27014575]
Rice GM Steiner RD Inborn Errors of Metabolism (Metabolic Disorders). Pediatr Rev . 2016 Jan;37(1):3-15; quiz 16-7, 47
[PubMed ID: 26729777]
Longo N Harding CO Burton BK Grange DK Vockley J Wasserstein M Rice GM Dorenbaum A Neuenburg JK Musson DG Gu Z Sile S Single-dose, subcutaneous recombinant phenylalanine ammonia lyase conjugated with polyethylene glycol in adult patients with phenylketonuria: an open-label, multicentre, phase 1 dose-escalation trial. Lancet . 2014 Jul 5;384(9937):37-44
[PubMed ID: 24743000]
Rice GM Raca G Jakielski KJ Laffin JJ Iyama-Kurtycz CM Hartley SL Sprague RE Heintzelman AT Shriberg LD Phenotype of FOXP2 haploinsufficiency in a mother and son. Am J Med Genet A . 2012 Jan;158A(1):174-81
[PubMed ID: 22106036]
Schwoerer JA Obernolte L Van Calcar S Heighway S Bankowski H Williams P Rice G Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome. JIMD Rep . 2012;6:15-20
[PubMed ID: 23430933]
Johnson MD Gentry LR Rice GM Mount DL A case of congenitally absent left internal carotid artery: vascular malformations in 22q11.2 deletion syndrome. Cleft Palate Craniofac J . 2010 May;47(3):314-7
[PubMed ID: 19860531]
Thorson L Bryke C Rice G Artzer A Schilz C Israel J Huber S Laffin J Raca G Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals. Am J Med Genet A . 2010 Apr;152A(4):904-15
[PubMed ID: 20358600]