Éva Kereszturi

1.3k total citations
35 papers, 913 citations indexed

About

Éva Kereszturi is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Éva Kereszturi has authored 35 papers receiving a total of 913 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Surgery and 10 papers in Genetics. Recurrent topics in Éva Kereszturi's work include Pancreatic function and diabetes (8 papers), Endoplasmic Reticulum Stress and Disease (7 papers) and Lipid metabolism and biosynthesis (5 papers). Éva Kereszturi is often cited by papers focused on Pancreatic function and diabetes (8 papers), Endoplasmic Reticulum Stress and Disease (7 papers) and Lipid metabolism and biosynthesis (5 papers). Éva Kereszturi collaborates with scholars based in Hungary, United States and Netherlands. Éva Kereszturi's co-authors include Miklós Sahin‐Tóth, Miklós Csala, Mária Sasvári‐Székely, Gábor Bánhegyi, Péter Szelényi, Orsolya Király, Veronika Zámbó, Laura Simon‐Szabó, Zsófia Nemoda and Júlia Gádoros and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Clinical Endocrinology & Metabolism and Gut.

In The Last Decade

Éva Kereszturi

34 papers receiving 901 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Éva Kereszturi Hungary 15 252 220 161 135 132 35 913
Joan Rodríguez Spain 16 182 0.7× 588 2.7× 126 0.8× 166 1.2× 102 0.8× 24 1.3k
Thierry Lesté-Lasserre France 24 129 0.5× 387 1.8× 204 1.3× 90 0.7× 140 1.1× 49 1.5k
Séverine Trabado France 21 167 0.7× 424 1.9× 67 0.4× 275 2.0× 79 0.6× 70 1.4k
Susan Terris United States 9 346 1.4× 469 2.1× 58 0.4× 124 0.9× 107 0.8× 13 992
Ambikaipakan Balasubramaniam United States 25 209 0.8× 838 3.8× 123 0.8× 43 0.3× 52 0.4× 73 1.7k
Carla Marinelli Italy 19 164 0.7× 386 1.8× 119 0.7× 187 1.4× 47 0.4× 29 1.2k
Ryszard Wiaderkiewicz Poland 19 104 0.4× 285 1.3× 99 0.6× 77 0.6× 71 0.5× 72 1.1k
Robert A. Furlong United Kingdom 19 120 0.5× 679 3.1× 107 0.7× 309 2.3× 48 0.4× 32 1.5k
Xiangping Zhou China 11 56 0.2× 301 1.4× 75 0.5× 95 0.7× 67 0.5× 35 841
Kazuhiro Nakayama Japan 16 71 0.3× 280 1.3× 163 1.0× 144 1.1× 52 0.4× 47 867

Countries citing papers authored by Éva Kereszturi

Since Specialization
Citations

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

Fields of papers citing papers by Éva Kereszturi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Éva Kereszturi

This figure shows the co-authorship network connecting the top 25 collaborators of Éva Kereszturi. A scholar is included among the top collaborators of Éva Kereszturi 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 Éva Kereszturi. Éva Kereszturi 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.
Zámbó, Veronika, Péter Szelényi, Viola Tamási, et al.. (2024). Allele-specific effect of various dietary fatty acids and ETS1 transcription factor on SCD1 expression. Scientific Reports. 14(1). 24–28. 3 indexed citations
2.
Zámbó, Veronika, et al.. (2023). Molecular Basis of Unequal Alternative Splicing of Human SCD5 and Its Alteration by Natural Genetic Variations. International Journal of Molecular Sciences. 24(7). 6517–6517.
3.
Németh, Krisztína, Blanka Tóth, Éva Kereszturi, et al.. (2023). High fat diet and PCSK9 knockout modulates lipid profile of the liver and changes the expression of lipid homeostasis related genes. Nutrition & Metabolism. 20(1). 19–19. 10 indexed citations
4.
Kereszturi, Éva. (2023). Diversity and Classification of Genetic Variations in Autism Spectrum Disorder. International Journal of Molecular Sciences. 24(23). 16768–16768. 18 indexed citations
5.
Simon‐Szabó, Laura, Veronika Zámbó, Tamás Csizmadia, et al.. (2018). Cellular toxicity of dietary trans fatty acids and its correlation with ceramide and diglyceride accumulation. Food and Chemical Toxicology. 124. 324–335. 20 indexed citations
6.
Zámbó, Veronika, et al.. (2016). Cytosolic localization of NADH cytochrome b5 oxidoreductase (Ncb5or). FEBS Letters. 590(5). 661–671. 3 indexed citations
7.
Geisz, Andrea, et al.. (2015). Functional significance of SPINK1 promoter variants in chronic pancreatitis. American Journal of Physiology-Gastrointestinal and Liver Physiology. 308(9). G779–G784. 11 indexed citations
8.
Lizák, Beáta, Szilvia K. Nagy, Tamás Mészáros, et al.. (2013). Natural mutations lead to enhanced proteasomal degradation of human Ncb5or, a novel flavoheme reductase. Biochimie. 95(7). 1403–1410. 7 indexed citations
9.
Abdul‐Rahman, Omar, Mária Sasvári‐Székely, Ágota Vér, et al.. (2012). Altered gene expression profiles in the hippocampus and prefrontal cortex of type 2 diabetic rats. BMC Genomics. 13(1). 81–81. 46 indexed citations
10.
Senesi, Silvia, Balázs Legeza, Zoltán Balázs, et al.. (2010). Contribution of Fructose-6-Phosphate to Glucocorticoid Activation in the Endoplasmic Reticulum: Possible Implication in the Metabolic Syndrome. Endocrinology. 151(10). 4830–4839. 34 indexed citations
11.
12.
Kereszturi, Éva & Miklós Sahin‐Tóth. (2009). Intracellular Autoactivation of Human Cationic Trypsinogen Mutants Causes Reduced Trypsinogen Secretion and Acinar Cell Death. Journal of Biological Chemistry. 284(48). 33392–33399. 39 indexed citations
13.
Kereszturi, Éva, Richárd Szmola, Zoltán Kukor, et al.. (2009). Hereditary pancreatitis caused by mutation-induced misfolding of human cationic trypsinogen: A novel disease mechanism. Human Mutation. 30(4). 575–582. 112 indexed citations
14.
Héjjas, Krisztina, Enikő Kubinyi, Zsolt Rónai, et al.. (2009). Molecular and behavioral analysis of the intron 2 repeat polymorphism in the canine dopamine D4 receptor gene. Genes Brain & Behavior. 8(3). 330–336. 44 indexed citations
15.
Kereszturi, Éva, Zsanett Tárnok, Krisztina Lakatos, et al.. (2008). Catechol‐O‐methyltransferase Val158Met polymorphism is associated with methylphenidate response in ADHD children. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(8). 1431–1435. 66 indexed citations
16.
Kereszturi, Éva, Orsolya Király, & Miklós Sahin‐Tóth. (2008). Minigene analysis of intronic variants in common SPINK1 haplotypes associated with chronic pancreatitis. Gut. 58(4). 545–549. 55 indexed citations
17.
Tárnok, Zsanett, Zsolt Rónai, Judit Gervai, et al.. (2007). Dopaminergic candidate genes in Tourette syndrome: Association between tic severity and 3′ UTR polymorphism of the dopamine transporter gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 900–905. 46 indexed citations
18.
Kereszturi, Éva, Orsolya Király, Zsolt Csapó, et al.. (2007). [Analysis of the dopamine D4 receptor gene variants in attention deficit hyperactivity disorder].. PubMed. 9(1). 11–8. 3 indexed citations
19.
Kereszturi, Éva, et al.. (2006). No direct effect of the -521 C/T polymorphism in the human dopamine D4 receptor gene promoter on transcriptional activity. BMC Molecular Biology. 7(1). 18–18. 38 indexed citations
20.
Szántai, Eszter, Orsolya Király, Zsófia Nemoda, et al.. (2005). Linkage analysis and molecular haplotyping of the dopamine D4 receptor gene promoter region. Psychiatric Genetics. 15(4). 259–270. 11 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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