Petra Dušátková

1.2k total citations
60 papers, 817 citations indexed

About

Petra Dušátková is a scholar working on Genetics, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Petra Dušátková has authored 60 papers receiving a total of 817 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 30 papers in Surgery and 29 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Petra Dušátková's work include Pancreatic function and diabetes (24 papers), Diabetes and associated disorders (19 papers) and Growth Hormone and Insulin-like Growth Factors (14 papers). Petra Dušátková is often cited by papers focused on Pancreatic function and diabetes (24 papers), Diabetes and associated disorders (19 papers) and Growth Hormone and Insulin-like Growth Factors (14 papers). Petra Dušátková collaborates with scholars based in Czechia, United Kingdom and Denmark. Petra Dušátková's co-authors include Jan Lebl, Štěpánka Průhová, Ondřej Cinek, Zdenĕk Šumnı́k, Stanislava Koloušková, Barbora Obermannová, Lenka Elblová, Lukáš Plachý, Štěpánka Průhová and Lenka Dušátková and has published in prestigious journals such as Bioinformatics, The Journal of Clinical Endocrinology & Metabolism and Diabetes Care.

In The Last Decade

Petra Dušátková

55 papers receiving 800 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Petra Dušátková Czechia 17 509 430 384 314 69 60 817
Doris Taha United States 13 378 0.7× 331 0.8× 266 0.7× 238 0.8× 18 0.3× 27 655
S. Lesage France 4 313 0.6× 385 0.9× 166 0.4× 263 0.8× 57 0.8× 7 595
Sandrine Beaufils France 7 560 1.1× 430 1.0× 139 0.4× 478 1.5× 90 1.3× 8 865
Travis Monchamp United States 6 420 0.8× 752 1.7× 418 1.1× 201 0.6× 20 0.3× 8 915
Guan-Qi Gao China 12 135 0.3× 95 0.2× 216 0.6× 159 0.5× 85 1.2× 26 448
Erin E. Baschal United States 17 410 0.8× 290 0.7× 229 0.6× 130 0.4× 146 2.1× 30 607
Suk Kyeong Kim South Korea 13 122 0.2× 240 0.6× 663 1.7× 176 0.6× 30 0.4× 22 769
Cora Groffen Netherlands 13 138 0.3× 80 0.2× 484 1.3× 357 1.1× 51 0.7× 16 766
Daniela Liberati Italy 12 191 0.4× 238 0.6× 163 0.4× 206 0.7× 73 1.1× 16 551
Mario Andreoli Italy 11 135 0.3× 386 0.9× 565 1.5× 117 0.4× 32 0.5× 17 799

Countries citing papers authored by Petra Dušátková

Since Specialization
Citations

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

Fields of papers citing papers by Petra Dušátková

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petra Dušátková

This figure shows the co-authorship network connecting the top 25 collaborators of Petra Dušátková. A scholar is included among the top collaborators of Petra Dušátková 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 Petra Dušátková. Petra Dušátková 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.
Dušátková, Petra, et al.. (2023). Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq. Diabetologia. 67(1). 113–123. 1 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.
Plachý, Lukáš, Lenka Petruželková, Petra Dušátková, et al.. (2023). Analysis of children with familial short stature: who should be indicated for genetic testing?. Endocrine Connections. 12(10). 6 indexed citations
7.
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
8.
Plachý, Lukáš, Petra Dušátková, Lenka Petruželková, et al.. (2021). Familial Short Stature—A Novel Phenotype of Growth Plate Collagenopathies. The Journal of Clinical Endocrinology & Metabolism. 106(6). 1742–1749. 21 indexed citations
9.
Plachý, Lukáš, Petra Dušátková, Lenka Petruželková, et al.. (2020). NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy. The Journal of Clinical Endocrinology & Metabolism. 105(3). e746–e752. 30 indexed citations
10.
Malíková, Jana, Petra Dušátková, Ingvild Aukrust, et al.. (2020). Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants. The Journal of Clinical Endocrinology & Metabolism. 105(4). e1377–e1386. 15 indexed citations
11.
Plachý, Lukáš, Petra Dušátková, Lenka Petruželková, et al.. (2020). NPR2 Variants are frequent among children with familial short stature and respond well to growth hormone therapy. Yearbook of pediatric endocrinology. 1 indexed citations
12.
Elblová, Lenka, Matthew B. Johnson, Petra Dušátková, et al.. (2019). Screening of monogenic autoimmune diabetes among children with type 1 diabetes and multiple autoimmune diseases: is it worth doing?. Journal of Pediatric Endocrinology and Metabolism. 32(10). 1147–1153. 6 indexed citations
13.
Plachý, Lukáš, Lenka Elblová, Barbora Obermannová, et al.. (2019). High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH. The Journal of Clinical Endocrinology & Metabolism. 104(10). 4273–4281. 49 indexed citations
14.
Průhová, Štěpánka, Lenka Elblová, Matthew B. Johnson, et al.. (2018). Significant Prevalence of Severe Monogenic Immune Defects Among Children with Type 1 Diabetes and Low T1D-Genetic Risk Score. 1 indexed citations
15.
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
16.
Klammt, Jürgen, Petra Dušátková, Mithat Bahçeci, et al.. (2017). Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes. Journal of Human Genetics. 62(8). 755–762. 19 indexed citations
17.
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
18.
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
19.
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
20.
Vaxillaire, Martine, Štěpánka Průhová, Aurélie Dechaume, et al.. (2011). Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations. Pediatric Diabetes. 12(3pt2). 266–269. 13 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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