Mario Ćuk

841 total citations
24 papers, 575 citations indexed

About

Mario Ćuk is a scholar working on Molecular Biology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, Mario Ćuk has authored 24 papers receiving a total of 575 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Rheumatology and 8 papers in Clinical Biochemistry. Recurrent topics in Mario Ćuk's work include Metabolism and Genetic Disorders (8 papers), Folate and B Vitamins Research (8 papers) and Biochemical and Molecular Research (5 papers). Mario Ćuk is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Folate and B Vitamins Research (8 papers) and Biochemical and Molecular Research (5 papers). Mario Ćuk collaborates with scholars based in Croatia, United States and Germany. Mario Ćuk's co-authors include Ivo Barić, Stefan Feske, Ksenija Fumić, Oliver Vugrek, S. Harvey Mudd, Rita Horváth, Vladimir Sarnavka, Jun J. Yang, Mireille Ouimet and Zofia M. Chrzanowska‐Lightowlers and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Cell Metabolism.

In The Last Decade

Mario Ćuk

20 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mario Ćuk Croatia 10 315 153 116 84 78 24 575
Pim Suwannarat United States 13 314 1.0× 38 0.2× 50 0.4× 421 5.0× 158 2.0× 21 664
Gillian P. Smith United Kingdom 16 227 0.7× 53 0.3× 22 0.2× 40 0.5× 130 1.7× 43 745
Célia Harumi Tengan Brazil 13 391 1.2× 14 0.1× 21 0.2× 136 1.6× 119 1.5× 36 551
Marsha F. Browning United States 13 221 0.7× 26 0.2× 110 0.9× 86 1.0× 122 1.6× 15 704
Eleni Beli United States 18 297 0.9× 20 0.1× 16 0.1× 35 0.4× 126 1.6× 27 808
Satoshi Akahane Japan 14 149 0.5× 82 0.5× 27 0.2× 6 0.1× 143 1.8× 21 563
Naomi Cook Australia 14 217 0.7× 13 0.1× 30 0.3× 40 0.5× 105 1.3× 19 524
Yuki Nakamura Japan 16 294 0.9× 26 0.2× 26 0.2× 8 0.1× 211 2.7× 32 856
A. Stefanutti France 13 240 0.8× 131 0.9× 7 0.1× 16 0.2× 232 3.0× 15 646

Countries citing papers authored by Mario Ćuk

Since Specialization
Citations

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

Fields of papers citing papers by Mario Ćuk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Ćuk

This figure shows the co-authorship network connecting the top 25 collaborators of Mario Ćuk. A scholar is included among the top collaborators of Mario Ćuk 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 Mario Ćuk. Mario Ćuk 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
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Ćuk, Mario, et al.. (2024). Novel RAI1:c.2736delC Variant in Smith–Magenis Syndrome: Identification by Whole Genome Sequencing and Joint Analysis. Journal of Personalized Medicine. 14(9). 901–901. 1 indexed citations
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Pušeljić, Silvija, et al.. (2023). First Reported Case of Gabriele-de Vries Syndrome with Spinal Dysraphism. Children. 10(4). 623–623. 5 indexed citations
7.
Maus, Máté, Mario Ćuk, Bindi Patel, et al.. (2017). Store-Operated Ca 2+ Entry Controls Induction of Lipolysis and the Transcriptional Reprogramming to Lipid Metabolism. Cell Metabolism. 25(3). 698–712. 126 indexed citations
8.
Ćuk, Mario, Sascha Kahlfuß, Lina Kozhaya, et al.. (2017). ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency. Journal of Allergy and Clinical Immunology. 142(4). 1297–1310.e11. 63 indexed citations
9.
Sarnavka, Vladimir, Mario Ćuk, Danijela Petković Ramadža, et al.. (2016). Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature. Journal of Pediatric Endocrinology and Metabolism. 29(9). 1083–8. 9 indexed citations
10.
Concepcion, Axel R., Martin Vaeth, Larry E. Wagner, et al.. (2016). Store-operated Ca2+ entry regulates Ca2+-activated chloride channels and eccrine sweat gland function. Journal of Clinical Investigation. 126(11). 4303–4318. 68 indexed citations
11.
Horn, Denise, Dagmar Wieczorek, Kay Metcalfe, et al.. (2013). Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome. European Journal of Human Genetics. 22(6). 762–767. 31 indexed citations
12.
Sedić, Mirela, Sandra Kraljević Pavelić, Mario Cindrić, et al.. (2011). Plasma biomarker identification in S‐adenosylhomocysteine hydrolase deficiency. Electrophoresis. 32(15). 1970–1975. 4 indexed citations
13.
Gagro, Alenka, Rita Horváth, Mario Ćuk, et al.. (2008). Mitochondriopathy presenting with immune disorder. European Journal of Human Genetics. 116. 1 indexed citations
14.
Ćuk, Mario, et al.. (2008). S-Adenosylhomocysteine hydrolase (AdoHcyase) deficiency: Enzymatic capabilities of human AdoHcyase are highly effected by changes to codon 89 and its surrounding residues. Biochemical and Biophysical Research Communications. 368(1). 30–36. 11 indexed citations
15.
Lovrić, Mila, et al.. (2007). Whole blood S-adenosylhomoysteine - a reliable biomarker of S-adenosylhomocysteine hydrolase deficiency. Journal of Inherited Metabolic Disease. 30. 1 indexed citations
16.
Ćuk, Mario, Mila Lovrić, Ksenija Fumić, et al.. (2007). The fourth S-adenosylhomocysteine hydrolase deficient patient : Further evidence of congenital miopathy. Clinical Chemistry and Laboratory Medicine (CCLM). 43. 8 indexed citations
17.
Fumić, Ksenija, Mario Ćuk, Tea Pavkov‐Keller, et al.. (2006). Functional analysis of human S-adenosylhomocysteine hydrolase isoforms SAHH-2 and SAHH-3. European Journal of Human Genetics. 15(3). 347–351. 10 indexed citations
18.
Fumić, Ksenija, Oliver Vugrek, Mario Ćuk, et al.. (2005). S-Adenosylhomocysteine (AdoHcy) hydrolase deficiency: myopathy seems to be congenital. 1 indexed citations
19.
Barić, Ivo, Ksenija Fumić, Mario Ćuk, et al.. (2004). S -adenosylhomocysteine hydrolase deficiency in a human: A genetic disorder of methionine metabolism. Proceedings of the National Academy of Sciences. 101(12). 4234–4239. 162 indexed citations
20.
Trkulja, Vladimir, et al.. (2003). Use of psychoactive substances among Zagreb University medical students: follow-up study.. PubMed. 44(1). 50–8. 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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