Gregory M. Rice - Concepedia

Author

Gregory M. Rice

University of Wisconsin–Madison

Also Known As

G Merrill Rice, G. M. Rice, G. Merrill Rice, G.M. Rice, Gregory M Rice, Gregory M. Rice, Gregory Rice, Gregory M. Rice

Publications

995

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison Baylor College of Medicine Oregon Health & Science University Medical College of Wisconsin University of California, San Francisco

About

Gregory M. Rice is an author at University of Wisconsin–Madison specializing in medicine, genetics, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	486
2	Health Sciences	1	1	41
3	Public Health	1	1	13
4	Biochemistry	1	1	25
5	Cell Biology	1	1	34

Gregory M. Rice

Publications

831

Citations

H-Index

Page 1

	Year	Citations
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 Nicola Longo, Cary O. Harding, Barbara K. Burton, The Lancet MedicineAdult PatientsPharmacologyDose-escalation TrialChronic Kidney Disease	2014	162
<i>TBC1D24</i> genotype–phenotype correlation Simona Balestrini, Mathieu Milh, Claudia Castiglioni, Neurology	2016	126
Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness Aman George, Dina J. Zand, Robert B. Hufnagel, The American Journal of Human Genetics Biallelic MutationsMendelian DisorderDisease MechanismGenetic DisorderGenetics	2016	88
Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial Denise M. Ney, Bridget M. Stroup, Murray K. Clayton, American Journal of Clinical Nutrition NutritionRenal FunctionMedicineDiabetesClinical Nutrition	2016	83
Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism Chanel T. Tyler, Gregory M. Rice, Margo Grady, American Journal of Medical Genetics Part A	2009	73
Phenotype of <i>FOXP2</i> haploinsufficiency in a mother and son Gregory M. Rice, Gordana Raca, Kathy J. Jakielski, American Journal of Medical Genetics Part A	2011	61
Inborn Errors of Metabolism (Metabolic Disorders) Gregory M. Rice, Robert D. Steiner Pediatrics in Review ObesityMetabolic SyndromeEnergy MetabolismInborn ErrorsHealth Sciences	2016	41
Clinical relevance of the discrepancy in phenylalanine concentrations analyzed using tandem mass spectrometry compared with ion-exchange chromatography in phenylketonuria Bridget M. Stroup, Patrice K. Held, Phillip Williams, Molecular Genetics and Metabolism Reports	2016	36
Identification and functional analysis of an<i>ADAMTSL1</i>variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a three‐generation human pedigree Kathryn Hendee, Lauren Weiping Wang, Linda M. Reis, Human Mutation Family MembersGeneticsMolecular GeneticsDisease Gene IdentificationFunctional Analysis	2017	34
Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy Allison Tam, Noura S. AlDhaheri, Krupa R. Mysore, American Journal of Medical Genetics Part A	2019	32

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