Petra Lišková

4.7k total citations
115 papers, 1.7k citations indexed

About

Petra Lišková is a scholar working on Radiology, Nuclear Medicine and Imaging, Molecular Biology and Ophthalmology. According to data from OpenAlex, Petra Lišková has authored 115 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Radiology, Nuclear Medicine and Imaging, 52 papers in Molecular Biology and 36 papers in Ophthalmology. Recurrent topics in Petra Lišková's work include Corneal surgery and disorders (52 papers), Corneal Surgery and Treatments (43 papers) and Retinal Development and Disorders (27 papers). Petra Lišková is often cited by papers focused on Corneal surgery and disorders (52 papers), Corneal Surgery and Treatments (43 papers) and Retinal Development and Disorders (27 papers). Petra Lišková collaborates with scholars based in Czechia, United Kingdom and United States. Petra Lišková's co-authors include Kateřina Jirsová, Stephen J. Tuft, Ľubica Ďuďáková, Alison J. Hardcastle, Martin Filipec, Neil D. Ebenezer, Shomi S. Bhattacharya, Pirro G. Hysi, Alice E. Davidson and Rhian Gwilliam and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Petra Lišková

107 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Petra Lišková Czechia	27	1.1k	684	487	364	176	115	1.7k
Magda A. Meester‐Smoor Netherlands	20	423 0.4×	637 0.9×	589 1.2×	51 0.1×	141 0.8×	49	1.2k
Ramesh C. Tripathi United States	9	462 0.4×	858 1.3×	337 0.7×	97 0.3×	91 0.5×	9	1.1k
Akito Hirakata Japan	27	1.7k 1.5×	2.1k 3.1×	419 0.9×	63 0.2×	51 0.3×	140	2.4k
Kimberly C. Sippel United States	16	451 0.4×	305 0.4×	276 0.6×	322 0.9×	75 0.4×	31	960
Arif O. Khan Saudi Arabia	24	396 0.4×	669 1.0×	845 1.7×	47 0.1×	610 3.5×	131	1.8k
Toru Noda Japan	14	513 0.5×	681 1.0×	363 0.7×	35 0.1×	36 0.2×	46	987
Sachiko Nishina Japan	20	455 0.4×	481 0.7×	533 1.1×	48 0.1×	230 1.3×	82	1.2k
Shivakumar Vasanth United States	17	354 0.3×	196 0.3×	611 1.3×	49 0.1×	486 2.8×	28	1.1k
Henrik Forsius Finland	16	383 0.3×	512 0.7×	316 0.6×	109 0.3×	136 0.8×	45	927
Enrique Rodríguez-de-la-Rúa-Franch Spain	16	637 0.6×	736 1.1×	414 0.9×	53 0.1×	91 0.5×	80	1.1k

Countries citing papers authored by Petra Lišková

Since Specialization

Citations

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

Fields of papers citing papers by Petra Lišková

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petra Lišková

This figure shows the co-authorship network connecting the top 25 collaborators of Petra Lišková. A scholar is included among the top collaborators of Petra Lišková 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 Lišková. Petra Lišková is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lišková, Petra, Pavlína Skalická, Ľubica Ďuďáková, & Andrea L. Vincent. (2025). Genotype–Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights. Clinical and Experimental Ophthalmology. 53(3). 232–245. 1 indexed citations

Gardner, Jessica C., Nihar Bhattacharyya, Petra Lišková, et al.. (2024). Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant. European Journal of Human Genetics. 32(12). 1583–1589. 1 indexed citations

Khan, Mubeen, Ketan Mishra, Laura Whelan, et al.. (2023). Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability. Human Genetics and Genomics Advances. 4(4). 100237–100237. 7 indexed citations

Bárta, Tomáš, Graeme C. Black, Rahat Perveen, et al.. (2023). MIR204 n. 37C >T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early‐onset cataracts and congenital glaucoma. Clinical Genetics. 104(4). 418–426. 4 indexed citations

Černá, Kateřina Amruz, Jan Oppelt, Birthe Dorgau, et al.. (2023). Light-responsive microRNA molecules in human retinal organoids are differentially regulated by distinct wavelengths of light. iScience. 26(7). 107237–107237. 7 indexed citations

Štechová, Kateřina, Štěpán Hlava, Jir̆ı́ Drábek, et al.. (2023). Dysfunction of peripheral somatic and autonomic nervous system in patients with severe forms of Crohn’s disease on biological therapy with TNFα inhibitors–A single center study. PLoS ONE. 18(11). e0294441–e0294441. 1 indexed citations

Paděrová, Jana, Markéta Havlovičová, M. Balaščaková, et al.. (2020). Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes. Annals of Human Genetics. 84(5). 380–392. 11 indexed citations

Ďuďáková, Ľubica, Pavlína Skalická, Olga Ulmanová, et al.. (2020). Pseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant. Journal of Ophthalmology. 2020. 1–9. 1 indexed citations

Kozmík, Zbyněk, et al.. (2020). Phenotype Variability in Czech Patients Carrying PAX6 Disease-Causing Variants. Folia Biologica. 66(4). 123–132. 2 indexed citations

10.

Lišková, Petra, Martin Magner, Josef Zámečnı́k, et al.. (2020). The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions. Brain Sciences. 10(11). 766–766. 13 indexed citations

11.

Kousal, Bohdan, Tomáš Honzík, Hana Hansíková, et al.. (2019). Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case. Folia Biologica. 65(3). 134–141. 10 indexed citations

12.

Gardner, Jessica C., Petra Lišková, Jonathan B. Ruddle, et al.. (2018). X-linked cone dystrophy and Blue Cone Monochromacy caused by novel and rare L/M opsin interchange haplotypes.. Investigative Ophthalmology & Visual Science. 59(9). 2325–2325. 1 indexed citations

13.

Lišková, Petra, Ľubica Ďuďáková, Karla E. Rojas López, et al.. (2018). Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4. The American Journal of Human Genetics. 102(3). 447–459. 40 indexed citations

14.

Szabó, Dóra, Zoltán Veréb, Agate Noer, et al.. (2017). Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution. SZTE Publicatio Repozitórium (University of Szeged). 3 indexed citations

15.

Trková, Marie, et al.. (2016). Early detection of bilateral cataracts in utero may represent a manifestation of severe congenital disease. American Journal of Medical Genetics Part A. 170(7). 1843–1848. 4 indexed citations

16.

Lišková, Petra, Ľubica Ďuďáková, Vladimı́r Tesař, et al.. (2014). Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous <b><i>SLC4A11 </i></b>Nonsense Mutation. Ophthalmic Research. 53(1). 30–35. 7 indexed citations

17.

Lišková, Petra, et al.. (2013). Crohn's disease: Is there a place for neurological screening?. Scandinavian Journal of Gastroenterology. 49(2). 173–176. 11 indexed citations

18.

Tuft, Stephen J., et al.. (2012). Keratoconus in 18 pairs of twins. Acta Ophthalmologica. 90(6). e482–6. 93 indexed citations

19.

Lišková, Petra, et al.. (2011). Phenotype and Hereditability of Keratoconus in Twins. 52(14). 1094–1094. 1 indexed citations

20.

Lišková, Petra, et al.. (2010). Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in theZEB1gene. Ophthalmic Genetics. 31(4). 230–234. 28 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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