Ramona Salvarinova

1.6k total citations
18 papers, 202 citations indexed

About

Ramona Salvarinova is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Ramona Salvarinova has authored 18 papers receiving a total of 202 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Clinical Biochemistry, 8 papers in Physiology and 6 papers in Molecular Biology. Recurrent topics in Ramona Salvarinova's work include Metabolism and Genetic Disorders (10 papers), Diet and metabolism studies (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Ramona Salvarinova is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Diet and metabolism studies (4 papers) and Amino Acid Enzymes and Metabolism (3 papers). Ramona Salvarinova collaborates with scholars based in Canada, United States and Netherlands. Ramona Salvarinova's co-authors include Gabriella Horváth, Sylvia Stöckler‐Ipsiroglu, Yolanda Lillquist, Paula J. Waters, Mari Mori, George Hoganson, Andrew C. Edmondson, Jolanta Sykut‐Cegielska, Katrin Õunap and Peter Witters and has published in prestigious journals such as Annals of Neurology, Journal of Nutrition and Gene.

In The Last Decade

Ramona Salvarinova

16 papers receiving 200 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ramona Salvarinova Canada 8 109 80 46 40 24 18 202
Mara Lúcia Schmitz Ferreira Santos Brazil 8 101 0.9× 57 0.7× 68 1.5× 23 0.6× 28 1.2× 37 276
Kristin Lindstrom United States 9 126 1.2× 64 0.8× 86 1.9× 35 0.9× 31 1.3× 19 241
Elisenda Cortès‐Saladelafont Spain 9 99 0.9× 111 1.4× 47 1.0× 47 1.2× 15 0.6× 21 231
Sharita Timal Netherlands 3 167 1.5× 52 0.7× 27 0.6× 53 1.3× 26 1.1× 4 213
Germaine Pierre United Kingdom 8 108 1.0× 52 0.7× 18 0.4× 37 0.9× 22 0.9× 16 187
Tony Rupar Canada 11 168 1.5× 141 1.8× 91 2.0× 29 0.7× 96 4.0× 15 325
Vladimı́r Bzdúch Slovakia 8 103 0.9× 65 0.8× 83 1.8× 39 1.0× 42 1.8× 28 259
Loreta Cimbalistienė Lithuania 11 121 1.1× 60 0.8× 79 1.7× 53 1.3× 40 1.7× 22 233
Makiko Tajika Japan 8 217 2.0× 144 1.8× 39 0.8× 19 0.5× 24 1.0× 15 283
Melis Köse Türkiye 8 74 0.7× 71 0.9× 59 1.3× 22 0.6× 13 0.5× 42 195

Countries citing papers authored by Ramona Salvarinova

Since Specialization
Citations

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

Fields of papers citing papers by Ramona Salvarinova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ramona Salvarinova

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

All Works

18 of 18 papers shown
1.
Boutin, Rozlyn C. T., et al.. (2024). Immune Dysregulation in a Child With SOD1 ‐Related Neurological Disease. American Journal of Medical Genetics Part A. 197(4). e63949–e63949.
2.
Yeganeh, Mehdi, Catherine Jones, Gloria Y. F. Ho, et al.. (2023). Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency. Molecular Genetics and Metabolism Reports. 35. 100961–100961. 1 indexed citations
3.
4.
Stöckler, Sylvia, et al.. (2021). Long term follow-up of the dietary intake in propionic acidemia. Molecular Genetics and Metabolism Reports. 27. 100757–100757. 6 indexed citations
5.
Prada, Carlos E., Shailly Jain‐Ghai, Natalya Karp, et al.. (2021). Hyperleucinosis during infections in maple syrup urine disease post liver transplantation. Molecular Genetics and Metabolism Reports. 27. 100763–100763. 7 indexed citations
6.
Witters, Peter, Rita Barone, Katrin Õunap, et al.. (2020). Clinical and biochemical improvement with galactose supplementation in SLC35A2-CDG. Genetics in Medicine. 22(6). 1102–1107. 56 indexed citations
7.
Micallef, Johann, Sylvia Stöckler‐Ipsiroglu, Clara D.M. van Karnebeek, Ramona Salvarinova, & Gabriella Horváth. (2020). Recurrent Dystonic Crisis and Rhabdomyolysis Treated with Dantrolene in Two Patients with Aromatic L-Amino Acid Decarboxylase Deficiency. Neuropediatrics. 51(3). 229–232. 2 indexed citations
8.
9.
Datta, Anita, et al.. (2017). Case Report. Journal of Child Neurology. 32(4). 403–407. 4 indexed citations
10.
Kevelam, Sietske H., Jörgen Bierau, Ramona Salvarinova, et al.. (2015). Recessive ITPA mutations cause an early infantile encephalopathy. Annals of Neurology. 78(4). 649–658. 37 indexed citations
11.
Salvarinova, Ramona, Andrea Rossi, Roberta Biancheri, et al.. (2014). Expansion of the QARS deficiency phenotype with report of a family with isolated supratentorial brain abnormalities. Neurogenetics. 16(2). 145–149. 10 indexed citations
12.
Stöckler‐Ipsiroglu, Sylvia, Nataliya Yuskiv, Ramona Salvarinova, et al.. (2014). Individualized long-term outcomes in blood phenylalanine concentrations and dietary phenylalanine tolerance in 11 patients with primary phenylalanine hydroxylase (PAH) deficiency treated with Sapropterin-dihydrochloride. Molecular Genetics and Metabolism. 114(3). 409–414. 6 indexed citations
13.
Horváth, Gabriella, Sandra Sirrs, Sylvia Stöckler, et al.. (2013). Three years experience with dried blood spot α-glucosidase screening for Pompe disease in British Columbia, Canada. BMC Musculoskeletal Disorders. 14(S2). 5 indexed citations
14.
Dias, Cristina, Murat Sincan, Rosemarie Rupps, et al.. (2013). Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation. European Journal of Human Genetics. 21(11). 1232–1239. 11 indexed citations
15.
Salvarinova, Ramona, et al.. (2013). Long-term outcomes of blood phenylalanine concentrations in children with classical phenylketonuria. Molecular Genetics and Metabolism. 108(4). 255–258. 10 indexed citations
16.
Al‐Thihli, Khalid, Derralynn Hughes, Millan S. Patel, et al.. (2012). A variant of unknown significance in the GLA gene causing diagnostic uncertainty in a young female with isolated hypertrophic cardiomyopathy. Gene. 497(2). 320–322. 4 indexed citations
17.
Salvarinova, Ramona, Graham Sinclair, David Dix, et al.. (2012). The use of parenteral nutrition for the management of PKU patient undergoing chemotherapy for lymphoma: A case report. Molecular Genetics and Metabolism. 105(4). 571–574. 6 indexed citations
18.
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

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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