Gregory M. Rice

1.0k total citations
26 papers, 593 citations indexed

About

Gregory M. Rice is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Gregory M. Rice has authored 26 papers receiving a total of 593 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Clinical Biochemistry, 8 papers in Molecular Biology and 8 papers in Rheumatology. Recurrent topics in Gregory M. Rice's work include Metabolism and Genetic Disorders (14 papers), Folate and B Vitamins Research (7 papers) and Diet and metabolism studies (4 papers). Gregory M. Rice is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Folate and B Vitamins Research (7 papers) and Diet and metabolism studies (4 papers). Gregory M. Rice collaborates with scholars based in United States, Hong Kong and China. Gregory M. Rice's co-authors include Denise M. Ney, Murray K. Clayton, Bridget M. Stroup, Robert D. Steiner, Barbara K. Burton, Alejandro Dorenbaum, Jerry Vockley, Jutta K. Neuenburg, Donald G. Musson and Saba Sile and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and American Journal of Clinical Nutrition.

In The Last Decade

Gregory M. Rice

26 papers receiving 576 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gregory M. Rice United States 12 303 271 148 130 68 26 593
Kalliopi Sofou Sweden 15 559 1.8× 351 1.3× 118 0.8× 91 0.7× 39 0.6× 29 780
Jin Sook Lee South Korea 14 323 1.1× 99 0.4× 84 0.6× 90 0.7× 37 0.5× 41 623
Aline Cano France 13 288 1.0× 160 0.6× 79 0.5× 85 0.7× 44 0.6× 27 485
Jessica Cohen‐Pfeffer United States 11 292 1.0× 333 1.2× 284 1.9× 92 0.7× 184 2.7× 18 687
Yunting Lin China 14 290 1.0× 60 0.2× 67 0.5× 127 1.0× 37 0.5× 62 552
Natacha Dreumont France 15 586 1.9× 66 0.2× 108 0.7× 99 0.8× 87 1.3× 30 829
Toshikatsu Shinka Japan 18 505 1.7× 150 0.6× 72 0.5× 419 3.2× 17 0.3× 56 894
W W Grody United States 12 173 0.6× 182 0.7× 164 1.1× 58 0.4× 16 0.2× 25 570
Harold A. Taylor United States 16 324 1.1× 58 0.2× 329 2.2× 158 1.2× 61 0.9× 22 681
Shintaro Okada Japan 12 243 0.8× 48 0.2× 130 0.9× 56 0.4× 50 0.7× 27 582

Countries citing papers authored by Gregory M. Rice

Since Specialization
Citations

This map shows the geographic impact of Gregory M. Rice's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gregory M. Rice with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gregory M. Rice more than expected).

Fields of papers citing papers by Gregory M. Rice

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory M. Rice. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gregory M. Rice. The network helps show where Gregory M. Rice may publish in the future.

Co-authorship network of co-authors of Gregory M. Rice

This figure shows the co-authorship network connecting the top 25 collaborators of Gregory M. Rice. A scholar is included among the top collaborators of Gregory M. Rice based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gregory M. Rice. Gregory M. Rice is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Stepien, Kimberly E., et al.. (2020). Biotinidase deficiency is a rare, potentially treatable cause of peripheral neuropathy with or without optic neuropathy in adults. Molecular Genetics and Metabolism Reports. 26. 100696–100696. 2 indexed citations
2.
Seals, Samantha R., et al.. (2020). Human Papilloma Virus Vaccination Compliance in a Military Aviation Training Community. Military Medicine. 185(7-8). e1155–e1160. 1 indexed citations
3.
Held, Patrice K., et al.. (2019). Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017. Public Health Reports. 134(2_suppl). 58S–63S. 4 indexed citations
4.
Hess, Aaron S., et al.. (2018). Volatile anesthesia for a pediatric patient with very long‐chain acyl‐coenzyme A dehydrogenase deficiency: A case report. Pediatric Anesthesia. 28(3). 296–297. 4 indexed citations
5.
6.
George, Aman, Dina J. Zand, Robert B. Hufnagel, et al.. (2016). Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness. The American Journal of Human Genetics. 99(6). 1388–1394. 70 indexed citations
7.
Baker, Mei, et al.. (2016). Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population. Genetics in Medicine. 19(3). 352–356. 7 indexed citations
8.
Rice, Gregory M. & Robert D. Steiner. (2016). Inborn Errors of Metabolism (Metabolic Disorders). Pediatrics in Review. 37(1). 3–17. 23 indexed citations
9.
Ney, Denise M., Bridget M. Stroup, Murray K. Clayton, et al.. (2016). Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial. American Journal of Clinical Nutrition. 104(2). 334–345. 65 indexed citations
10.
Stroup, Bridget M., Patrice K. Held, Phillip Williams, et al.. (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. 6. 21–26. 28 indexed citations
11.
Rice, Gregory M., et al.. (2016). Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community. Molecular Genetics and Metabolism Reports. 8. 4–7. 9 indexed citations
12.
13.
Rice, Gregory M., et al.. (2013). Urinary Tract Calculi in Military Aviators. Aviation Space and Environmental Medicine. 84(10). 1041–1045. 2 indexed citations
14.
Rice, Gregory M., et al.. (2012). Use of Gastrostomy Tube to Prevent Maternal PKU Syndrome. JIMD Reports. 6. 15–20. 3 indexed citations
15.
Rice, Gregory M., Gordana Raca, Kathy J. Jakielski, et al.. (2011). Phenotype of FOXP2 haploinsufficiency in a mother and son. American Journal of Medical Genetics Part A. 158A(1). 174–181. 49 indexed citations
16.
Bryke, Christine R., et al.. (2010). Clinical and molecular characterization of overlapping interstitial Xp21‐p22 duplications in two unrelated individuals. American Journal of Medical Genetics Part A. 152A(4). 904–915. 12 indexed citations
17.
Rice, Gregory M., et al.. (2009). Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism. American Journal of Medical Genetics Part A. 149A(11). 2588–2592. 15 indexed citations
18.
Dimmock, David, Pamela Trapane, Annette Feigenbaum, et al.. (2008). The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia. American Journal of Medical Genetics Part A. 146A(22). 2885–2890. 24 indexed citations
19.
Ney, Denise M., Sally T. Gleason, Sandra C. Van Calcar, et al.. (2008). Nutritional management of PKU with glycomacropeptide from cheese whey. Journal of Inherited Metabolic Disease. 32(1). 32–39. 69 indexed citations
20.
Rice, Gregory M., et al.. (2006). Microdissection‐based high‐resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes. American Journal of Medical Genetics Part A. 140A(15). 1637–1643. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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