This map shows the geographic impact of Á. Várkonyi'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 Á. Várkonyi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Á. Várkonyi more than expected).
This network shows the impact of papers produced by Á. Várkonyi. 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 Á. Várkonyi. The network helps show where Á. Várkonyi may publish in the future.
Co-authorship network of co-authors of Á. Várkonyi
This figure shows the co-authorship network connecting the top 25 collaborators of Á. Várkonyi.
A scholar is included among the top collaborators of Á. Várkonyi 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 Á. Várkonyi. Á. Várkonyi is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
László, Aranka, László Tiszlavicz, Á. Várkonyi, et al.. (2013). The fate of tyrosinaemic Hungarian patients before the NTBC aera.. PubMed. 66(11-12). 415–9.2 indexed citations
Décsi, Támas, András Arató, Márta Balogh, et al.. (2005). [Randomised placebo controlled double blind study on the effect of prebiotic oligosaccharides on intestinal flora in healthy infants].. PubMed. 146(48). 2445–50.22 indexed citations
Várkonyi, Á., et al.. (1992). Determination of hair trace elements in childhood celiac disease and in cystic fibrosis.. PubMed. 32(2). 159–65.4 indexed citations
16.
László, A, et al.. (1991). Congenital hyperammonemia: symptomatic carrier girl patient and her asymptomatic heterozygous mother for ornithine transcarbamylase (OTC) deficiency: specific enzyme diagnostic and kinetic investigations for the detection of heterozygous genostatus.. PubMed. 31(3). 291–7.2 indexed citations
17.
Várkonyi, Á., et al.. (1990). [Simultaneous occurrence of selective ACTH deficiency , achalasia, alacrimia and hyperlipoproteinemia].. PubMed. 131(50). 2763–6.3 indexed citations
18.
Várkonyi, Á., et al.. (1984). [Hyperprolactinemia in children with celiac disease].. PubMed. 132(7). 547–9.1 indexed citations
19.
Várkonyi, Á., et al.. (1983). [Pyoderma gangrenosum--as a possible leading symptom in childhood ulcerative colitis].. PubMed. 124(39). 2381–3.1 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.