Štěpánka Průhová

1.9k total citations
66 papers, 1.4k citations indexed

About

Štěpánka Průhová is a scholar working on Genetics, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Štěpánka Průhová has authored 66 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 41 papers in Surgery and 36 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Štěpánka Průhová's work include Pancreatic function and diabetes (39 papers), Diabetes and associated disorders (36 papers) and Diabetes Management and Research (21 papers). Štěpánka Průhová is often cited by papers focused on Pancreatic function and diabetes (39 papers), Diabetes and associated disorders (36 papers) and Diabetes Management and Research (21 papers). Štěpánka Průhová collaborates with scholars based in Czechia, Denmark and United Kingdom. Štěpánka Průhová's co-authors include Jan Lebl, Ondřej Cinek, Oluf Pedersen, Torben Hansen, Petra Dušátková, Zdenĕk Šumnı́k, Stanislava Koloušková, Barbora Obermannová, Jakob Ek and Anders Johansen and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Immunology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Štěpánka Průhová

64 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Štěpánka Průhová Czechia 21 984 918 652 483 74 66 1.4k
Amanda L. Posgai United States 21 645 0.7× 792 0.9× 506 0.8× 171 0.4× 474 6.4× 60 1.3k
Fredrik Lindgren Sweden 16 497 0.5× 608 0.7× 506 0.8× 71 0.1× 102 1.4× 22 817
Travis Monchamp United States 6 752 0.8× 420 0.5× 418 0.6× 201 0.4× 20 0.3× 8 915
Pál Pánczél Hungary 12 295 0.3× 367 0.4× 307 0.5× 116 0.2× 92 1.2× 26 580
Daizhi Yang China 14 224 0.2× 339 0.4× 502 0.8× 294 0.6× 20 0.3× 66 823
Hisafumi Yasuda Japan 17 313 0.3× 374 0.4× 203 0.3× 188 0.4× 243 3.3× 49 764
Maria Giulia Santaguida Italy 16 185 0.2× 169 0.2× 474 0.7× 98 0.2× 64 0.9× 30 777
José Luis Santiago Spain 17 187 0.2× 214 0.2× 73 0.1× 148 0.3× 236 3.2× 40 717
Noritaka Onoda Japan 17 153 0.2× 160 0.2× 232 0.4× 211 0.4× 19 0.3× 29 734
Naotake Akutsu Japan 13 211 0.2× 162 0.2× 76 0.1× 166 0.3× 36 0.5× 49 695

Countries citing papers authored by Štěpánka Průhová

Since Specialization
Citations

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

Fields of papers citing papers by Štěpánka Průhová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Štěpánka Průhová

This figure shows the co-authorship network connecting the top 25 collaborators of Štěpánka Průhová. A scholar is included among the top collaborators of Štěpánka Průhová 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 Štěpánka Průhová. Štěpánka Průhová 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.
Plachý, Lukáš, Petra Dušátková, Vít Neuman, et al.. (2024). Monogenic causes of familial short stature. Frontiers in Endocrinology. 15. 1506323–1506323. 1 indexed citations
2.
Molnes, Janne, Erling Tjora, Arne Raasakka, et al.. (2024). Molecular mechanism of HNF-1A–mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes. JCI Insight. 9(11). 2 indexed citations
3.
Plachý, Lukáš, Vít Neuman, Barbora Obermannová, et al.. (2024). Telemedicine maintains good glucose control in children with type 1 diabetes but is not time saving for healthcare professionals: KITES randomized study. Diabetes Research and Clinical Practice. 209. 111602–111602. 2 indexed citations
4.
Průhová, Štěpánka & Petra Dušátková. (2023). Monogenic diabetes mellitus hidden in autoantibody-negative diabetes mellitus. Nature Reviews Endocrinology. 19(3). 132–133. 2 indexed citations
5.
Plachý, Lukáš, Petra Dušátková, Lenka Elblová, et al.. (2023). The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature. Hormone Research in Paediatrics. 97(1). 40–52. 14 indexed citations
6.
Dušátková, Petra, Markéta Pavlı́ková, Lenka Elblová, et al.. (2022). Search for a time- and cost-saving genetic testing strategy for maturity-onset diabetes of the young. Acta Diabetologica. 59(9). 1169–1178. 1 indexed citations
7.
Cinek, Ondřej, Renata Pomahačová, Lenka Petruželková, et al.. (2022). Type 1 diabetes incidence increased during the COVID ‐19 pandemic years 2020–2021 in Czechia: Results from a large population‐based pediatric register. Pediatric Diabetes. 23(7). 956–960. 10 indexed citations
8.
Petruželková, Lenka, Jan Šoupal, Lukáš Plachý, et al.. (2021). Pre‐school and school‐aged children benefit from the switch from a sensor‐augmented pump to an AndroidAPS hybrid closed loop: A retrospective analysis. Pediatric Diabetes. 22(4). 594–604. 31 indexed citations
9.
Šumnı́k, Zdenĕk, Markéta Pavlı́ková, Renata Pomahačová, et al.. (2021). Use of continuous glucose monitoring and its association with type 1 diabetes control in children over the first 3 years of reimbursement approval: Population data from the ČENDA registry. Pediatric Diabetes. 22(3). 439–447. 15 indexed citations
10.
11.
Neuman, Vít, Ondřej Cinek, David P. Funda, et al.. (2019). Human gut microbiota transferred to germ-free NOD mice modulate the progression towards type 1 diabetes regardless of the pace of beta cell function loss in the donor. Diabetologia. 62(7). 1291–1296. 21 indexed citations
12.
Paračková, Zuzana, Adam Klocperk, Jana Kayserová, et al.. (2017). Alteration of B cell subsets and the receptor for B cell activating factor (BAFF) in paediatric patients with type 1 diabetes. Immunology Letters. 189. 94–100. 11 indexed citations
13.
Kočova, Mirjana, Lenka Elblová, Štěpánka Průhová, Jan Lebl, & Petra Dušátková. (2017). Novel glucokinase gene mutation in the first Macedonian family tested for MODY. Diabetes Research and Clinical Practice. 130. 86–89. 1 indexed citations
14.
Kotalová, Radana, Petra Dušátková, Lenka Elblová, et al.. (2017). Choledochal Cyst with 17q12 Chromosomal Duplication. Annals of Human Genetics. 82(1). 48–51. 4 indexed citations
15.
Borowiec, Maciej, Wojciech Fendler, Petra Dušátková, et al.. (2012). HbA1c‐based diabetes diagnosis among patients with glucokinase mutation (GCK‐MODY) is affected by a genetic variant of glucose‐6‐phosphatase (G6PC2). Diabetic Medicine. 29(11). 1465–1469. 4 indexed citations
16.
Dušátková, Petra, Štěpánka Průhová, Maciej Borowiec, et al.. (2012). Ancestral mutations may cause a significant proportion of GCK-MODY. Pediatric Diabetes. 13(6). 489–498. 4 indexed citations
17.
Průhová, Štěpánka, Ondřej Cinek, Jakob Ek, et al.. (2008). Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation inNEUROD1. Pediatric Diabetes. 9(4pt2). 367–372. 37 indexed citations
18.
Průhová, Štěpánka, et al.. (2003). [Normal course of autoimmune thyroid disease in diabetic children].. PubMed. 142(4). 235–9. 1 indexed citations
19.
Hansen, Sara K., Marcelina Párrizas, Štěpánka Průhová, et al.. (2002). Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function. Journal of Clinical Investigation. 110(6). 827–833. 77 indexed citations
20.
Hansen, Sara K., Marcelina Párrizas, Štěpánka Průhová, et al.. (2002). Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function. Journal of Clinical Investigation. 110(6). 827–833. 4 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Amanda L. Posgai Breakdown of academic impact, for papers by Fredrik Lindgren Breakdown of academic impact, for papers by Travis Monchamp Breakdown of academic impact, for papers by Pál Pánczél Breakdown of academic impact, for papers by Daizhi Yang Breakdown of academic impact, for papers by Hisafumi Yasuda Breakdown of academic impact, for papers by Maria Giulia Santaguida Breakdown of academic impact, for papers by José Luis Santiago Breakdown of academic impact, for papers by Noritaka Onoda Breakdown of academic impact, for papers by Naotake Akutsu
Rankless by CCL
2026