Tony Rupar

606 total citations
15 papers, 325 citations indexed

About

Tony Rupar is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Tony Rupar has authored 15 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 6 papers in Rheumatology. Recurrent topics in Tony Rupar's work include Metabolism and Genetic Disorders (8 papers), Folate and B Vitamins Research (5 papers) and Mitochondrial Function and Pathology (4 papers). Tony Rupar is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Folate and B Vitamins Research (5 papers) and Mitochondrial Function and Pathology (4 papers). Tony Rupar collaborates with scholars based in Canada, United States and Austria. Tony Rupar's co-authors include Chitra Prasad, Asuri N. Prasad, Brian Fowler, Nongnuj Tanphaichitr, Ebba Nexø, Olaf A. Bodamer, Jozef Hertecant, John A. Phillips, Douglas S. Kerr and Mulchand S. Patel and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Lipid Research and The Journal of Pediatrics.

In The Last Decade

Tony Rupar

14 papers receiving 321 citations

Peers

Tony Rupar

RHEUM

PHYSI

BIOCH

Michal Inbar‐Feigenberg Canada

Anke Schumann Germany

Zhuwen Gong China

Junko Muroi Japan

Nanaka Ichihara Japan

Guangchao Zhuo China

Ryuki Hirano Japan

Ee Shien Tan Singapore

James R. Bonham United Kingdom

Mahuya Bose Canada

Michal Inbar‐Feigenberg Canada

Tony Rupar

191 ×1.1

77 ×0.5

63 ×0.7

RHEUM

111 ×1.2

PHYSI

28 ×0.7

BIOCH

Citations per year, relative to Tony Rupar Tony Rupar (= 1×) peers Michal Inbar‐Feigenberg

Countries citing papers authored by Tony Rupar

Since Specialization

Citations

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

Fields of papers citing papers by Tony Rupar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tony Rupar

This figure shows the co-authorship network connecting the top 25 collaborators of Tony Rupar. A scholar is included among the top collaborators of Tony 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 Tony Rupar. Tony Rupar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Levy, Michael A., Jennifer Kerkhof, Frances Belmonte, et al.. (2020). Validation and clinical performance of a combined nuclear‐mitochondrial next‐generation sequencing and copy number variant analysis panel in a Canadian population. American Journal of Medical Genetics Part A. 185(2). 486–499. 6 indexed citations

McMillan, Hugh J., Tony Rupar, Catherine Brunel‐Guitton, et al.. (2019). Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease). Paediatrics & Child Health. 24(4). 270–271. 1 indexed citations

Pasternak, Stephen, Carolina R. A. Silveira, Zhonghan Li, et al.. (2018). P1‐067: AMBROXOL AS PHARMACOLOGICAL CHAPERONE TARGETING GBA1 AS A DISEASE MODIFYING TREATMENT FOR PARKINSON'S DISEASE DEMENTIA: A PHASE 2 RANDOMIZED, DOUBLE‐BLIND, PLACEBO‐CONTROLLED TRIAL. Alzheimer s & Dementia. 14(7S_Part_5). 2 indexed citations

Yıldırım, Zühal Keskin, Ebba Nexø, Tony Rupar, & Mustafa Büyükavcı. (2016). Seven Patients With Transcobalamin Deficiency Diagnosed Between 2010 and 2014: A Single-Center Experience. Journal of Pediatric Hematology/Oncology. 39(1). 38–41. 12 indexed citations

Ünal, Şule, Tony Rupar, Sevgi Yetgin, et al.. (2015). Transcobalamin II Deficiency in Four Cases with Novel Mutations. SHILAP Revista de lepidopterología. 32(4). 317–322. 16 indexed citations

Xu, Hongbin, Kessiri Kongmanas, Charles E. Smith, et al.. (2011). Arylsulfatase A deficiency causes seminolipid accumulation and a lysosomal storage disorder in Sertoli cells. Journal of Lipid Research. 52(12). 2187–2197. 25 indexed citations

Prasad, Chitra, Tony Rupar, & Asuri N. Prasad. (2011). Pyruvate dehydrogenase deficiency and epilepsy. Brain and Development. 33(10). 856–865. 46 indexed citations

Kölker, Stefan, Lawrence Fisher, Tony Rupar, et al.. (2010). Diagnosis of glutaric aciduria type 1 by measuring 3‐hydroxyglutaric acid in dried urine spots by liquid chromatography tandem mass spectrometry. Journal of Inherited Metabolic Disease. 34(1). 173–180. 32 indexed citations

Ratschmann, Rene, Milen Minkov, Christina Hung, et al.. (2009). Transcobalamin II deficiency at birth. Molecular Genetics and Metabolism. 98(3). 285–288. 20 indexed citations

10.

Dimmock, David, Annette Feigenbaum, Tony Rupar, et al.. (2009). 28. Neurological phenotype is the key predictor of long-term outcome in mitochondrial DNA depletion resulting from deoxyguanosine kinase deficiency. Mitochondrion. 9(1). 68–68.

11.

Korotchkina, Lioubov G., C. Prasad, Tony Rupar, et al.. (2008). Mutations of the E1β subunit gene (PDHB) in four families with pyruvate dehydrogenase deficiency. Molecular Genetics and Metabolism. 93(4). 371–380. 34 indexed citations

12.

Randall, Derrick R., Graham Sinclair, Anita C. Thomas, et al.. (2008). Heparin cofactor II–thrombin complex: A biomarker of MPS disease. Molecular Genetics and Metabolism. 94(4). 456–461. 45 indexed citations

13.

Miousse, Isabelle R., David Watkins, David Coelho, et al.. (2008). Clinical and Molecular Heterogeneity in Patients with the CblD Inborn Error of Cobalamin Metabolism. The Journal of Pediatrics. 154(4). 551–556. 34 indexed citations

14.

Horváth, Gabriella, Sylvia Stöckler‐Ipsiroglu, Ramona Salvarinova, et al.. (2008). Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: Evidence of a phenotypic continuum between dominant and recessive forms. Molecular Genetics and Metabolism. 94(1). 127–131. 30 indexed citations

15.

Wu, Alexander T.H., Sitthichai Iamsaard, Krittalak Chakrabandhu, et al.. (2007). Sperm surface arylsulfatase A can disperse the cumulus matrix of cumulus oocyte complexes. Journal of Cellular Physiology. 213(1). 201–211. 22 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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