C. Anthony Rupar

2.6k total citations
80 papers, 1.6k citations indexed

About

C. Anthony Rupar is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, C. Anthony Rupar has authored 80 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 23 papers in Clinical Biochemistry and 20 papers in Physiology. Recurrent topics in C. Anthony Rupar's work include Metabolism and Genetic Disorders (23 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (13 papers). C. Anthony Rupar is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (13 papers). C. Anthony Rupar collaborates with scholars based in Canada, United States and United Kingdom. C. Anthony Rupar's co-authors include K. K. Carroll, Jack W. Rip, Chitra Prasad, Asuri N. Prasad, Ravi Kothapalli, Kenneth K. Carroll, Robert A. Hegele, Victoria Mok Siu, Nilabh Chaudhary and Gregory S. Zaric and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

C. Anthony Rupar

75 papers receiving 1.5k citations

Peers

C. Anthony Rupar
Monique Piraud France
Mariarita Bertoldi Italy
Barbara Cellini Italy
Kirk Beebe United States
Tomoji Maeda Japan
Frank Gaunitz Germany
Kondala R. Atkuri United States
Bruno Casetta Italy
Jing Xie China
Andrea E. DeBarber United States
Monique Piraud France
C. Anthony Rupar
Citations per year, relative to C. Anthony Rupar C. Anthony Rupar (= 1×) peers Monique Piraud

Countries citing papers authored by C. Anthony Rupar

Since Specialization
Citations

This map shows the geographic impact of C. Anthony Rupar'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 C. Anthony Rupar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Anthony Rupar more than expected).

Fields of papers citing papers by C. Anthony Rupar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Anthony Rupar. 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 C. Anthony Rupar. The network helps show where C. Anthony Rupar may publish in the future.

Co-authorship network of co-authors of C. Anthony Rupar

This figure shows the co-authorship network connecting the top 25 collaborators of C. Anthony Rupar. A scholar is included among the top collaborators of C. Anthony Rupar 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 C. Anthony Rupar. C. Anthony Rupar 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.
Khan, Anzalee, Dwayne L. Barber, William M. McKillop, et al.. (2025). Lentivirus‐mediated gene therapy for Fabry disease: 5‐year End‐of‐Study results from the Canadian FACTs trial. Clinical and Translational Medicine. 15(1). e70073–e70073. 4 indexed citations
2.
Spagnolo, P., Enis Cela, Cheril Clarson, et al.. (2024). Metabolomic signature of pediatric diabetic ketoacidosis: key metabolites, pathways, and panels linked to clinical variables. Molecular Medicine. 30(1). 250–250. 3 indexed citations
3.
Prasad, Chitra, et al.. (2024). Long-term follow-up of an attenuated presentation of NAXE-related disease, a potentially actionable neurometabolic disease: a case report. Frontiers in Neurology. 15. 1204848–1204848. 3 indexed citations
4.
5.
Gratton, Robert, Kevin Coughlin, Victoria Mok Siu, et al.. (2023). Dual diagnosis of trisomy 21 and lethal perinatal Gaucher disease as a cause of non‐immune hydrops fetalis in a twin pregnancy for a consanguineous couple. SHILAP Revista de lepidopterología. 11(8). e7827–e7827.
6.
Felizardo, Tania C., C. Anthony Rupar, S.R. Foley, et al.. (2022). Autologous, lentivirus‐modified, T‐rapa cell “micropharmacies” for lysosomal storage disorders. EMBO Molecular Medicine. 14(4). e14297–e14297. 9 indexed citations
7.
Rupar, C. Anthony, et al.. (2019). Use of complementary and alternative medicine in patients with inborn errors of metabolism: A single‐center study. JIMD Reports. 51(1). 105–112. 3 indexed citations
8.
Silveira, Carolina R. A., Julia MacKinley, Kristy Coleman, et al.. (2019). Ambroxol as a novel disease-modifying treatment for Parkinson’s disease dementia: protocol for a single-centre, randomized, double-blind, placebo-controlled trial. BMC Neurology. 19(1). 20–20. 102 indexed citations
9.
Farhan, Sali M.K., Kevin C. Nixon, Tara N. Edwards, et al.. (2017). Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy. Human Molecular Genetics. 26(21). 4278–4289. 32 indexed citations
10.
Kerkhof, Jennifer, Laila C. Schenkel, Jack Reilly, et al.. (2017). Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels. Journal of Molecular Diagnostics. 19(6). 905–920. 94 indexed citations
11.
Rupar, C. Anthony, et al.. (2016). The expanding phenotype of MELAS caused by the m.3291T > C mutation in the MT-TL1 gene. Molecular Genetics and Metabolism Reports. 6. 64–69. 10 indexed citations
12.
Prasad, Chitra, Kathy N. Speechley, Sarah Dyack, et al.. (2012). Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening. Paediatrics & Child Health. 17(4). 185–189. 6 indexed citations
13.
Loucks, Catrina M., Jillian S. Parboosingh, Jessica X. Chong, et al.. (2012). A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America. American Journal of Medical Genetics Part A. 158A(5). 1229–1232. 8 indexed citations
14.
Prasad, C. Venkata Siva Rama & C. Anthony Rupar. (2010). Inborn errors of metabolism in infancy and childhood presenting with metabolic acidosis.. 12(2). 155–164.
15.
Lahiry, Piya, Jian Wang, J. F. Robinson, et al.. (2009). A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems. The American Journal of Human Genetics. 84(6). 822–822. 5 indexed citations
16.
Lahiry, Piya, Jian Wang, John F. Robinson, et al.. (2009). A Multiplex Human Syndrome Implicates a Key Role for Intestinal Cell Kinase in Development of Central Nervous, Skeletal, and Endocrine Systems. The American Journal of Human Genetics. 84(2). 134–147. 53 indexed citations
17.
18.
Sharma, Pushpa, C. Anthony Rupar, & Jack W. Rip. (1998). Consequences of Aging on Mitochondrial Respiratory Chain Enzymes in Cultured Human Fibroblasts Treated with Ascorbate. Gerontology. 44(2). 78–84. 12 indexed citations
19.
Rupar, C. Anthony, et al.. (1992). Rat liver lysosome membranes are enriched in α-tocopherol. Biochemistry and Cell Biology. 70(6). 486–488. 18 indexed citations
20.
Harvey, P.Robert C., C. Anthony Rupar, Steven Gallinger, C N Petrunka, & Steven M. Strasberg. (1986). Quantitative and qualitative comparison of gall bladder mucus glycoprotein from patients with and without gall stones.. Gut. 27(4). 374–381. 52 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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