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Petra Lišková

First Faculty of Medicine

34H-index
229Paper Count
4.7KCitation Count
Published Papers 78
Publication Date
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The AP5B1 p.Leu785Pro variant is a frequent cause of late-onset macular dystrophy with variable extraocular manifestations
errHuman Genetics and Genomics Advances
IF3.6
err2026-08-07
err0
errOAAI
errPetra Liskova; Lubica Dudakova; Karolina Kaminska; Laura Kühlewein; Stefanida Shliaga; Rina Leibu; Miriam Ehrenberg; Dinah Zur; Jana Zernant; Miriam Bauwens; Gavin Arno; Isabelle Müller; Focke Ziemssen; Viktoria Bothe; Francesca Cancellieri; Julie De Zaeytijd; Pascale Mazzola; Winston Lee; Bohdan Kousal; Marie Vajter
errShare
errSave
Paediatric Keratoconus: An ERN-EYE Clinical Consensus Statement on Diagnosis, Treatment and Follow-Up Care
errOphthalmology and Therapy
IF3.2
err2026-07-31
err0
errOAAI
errLuca Buzzonetti; Cosimo Mazzotta; Michele Iester; Mikk Pauklin; Daniel Boehringer; Reda Zemaitiene; Martino Vannucchi; Lidia Cocho; Pavel Studeny; Amélie Gavard; Cristina Monterosso; Dominique Bremond-Gignac; Manca Tekavcic Pompe; Jean-Louis Bourges; Petra Liskova
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errSave
Influence of inflammatory and metabolic factors on keratoconus risk: a causal inference analysis
errEye
IF3.2
err2026-02-19
err0
errOAAI
errPirro G. Hysi; Alison J. Hardcastle; Alice E. Davidson; Loretta Szczotka-Flynn; Anthony P. Khawaja; Petra Liskova; Sudha Iyengar; Chris J. Hammond; Stephen J. Tuft
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errSave
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
errNature Genetics
IF29
err2026-01-09
err0
errOAAI
errMathieu Quinodoz; Kim Rodenburg; Zuzana Cvackova; Karolina Kaminska; Suzanne E. de Bruijn; Ana Belén Iglesias-Romero; Erica G. M. Boonen; Mukhtar Ullah; Nick Zomer; Marc Folcher; Jacques Bijon; Lara K. Holtes; Stephen H. Tsang; Zelia Corradi; K. Bailey Freund; Stefanida Shliaga; Daan M. Panneman; Rebekkah J. Hitti-Malin; Manir Ali; Ala’a AlTalbishi; Sten Andréasson; Georg Ansari; Gavin Arno; Galuh D. N. Astuti; Carmen Ayuso; Radha Ayyagari; Sandro Banfi; Eyal Banin; Tahsin Stefan Barakat; Mirella T. S. Barboni; Miriam Bauwens; Tamar Ben-Yosef; Virginie Bernard; David G. Birch; Pooja Biswas; Fiona Blanco-Kelly; Beatrice Bocquet; Camiel J. F. Boon; Kari Branham; Dominique Bremond-Gignac; Alexis Ceecee Britten-Jones; Kinga M. Bujakowska; Cyril Burin des Roziers; Elizabeth L. Cadena; Giacomo Calzetti; Francesca Cancellieri; Luca Cattaneo; Naomi Chadderton; Peter Charbel Issa; Luísa Coutinho-Santos; Stephen P. Daiger; Elfride De Baere; Marieke De Bruyne; Berta de la Cerda; John N. De Roach; Julie De Zaeytijd; Ronny Derks; Claire-Marie Dhaenens; Lubica Dudakova; Jacque L. Duncan; G. Jane Farrar; Nicolas Feltgen; Beau J. Fenner; Lidia Fernández-Caballero; Juliana M. Ferraz Sallum; Simone Gana; Alejandro Garanto; Jessica C. Gardner; Christian Gilissen; Roser Gonzàlez-Duarte; Kensuke Goto; Sam Griffiths-Jones; Tobias B. Haack; Lonneke Haer-Wigman; Alison J. Hardcastle; Takaaki Hayashi; Elise Héon; Lies H. Hoefsloot; Alexander Hoischen; Josephine P. Holtan; Carel B. Hoyng; Manuel Benjamin B. Ibanez; Chris F. Inglehearn; Takeshi Iwata; Brynjar O. Jensson; Kaylie Jones; Vasiliki Kalatzis; Smaragda Kamakari; Marianthi Karali; Ulrich Kellner; Caroline C. W. Klaver; Krisztina Knézy; Robert K. Koenekoop; Susanne Kohl; Taro Kominami; Laura Kühlewein; Tina M. Lamey; Rina Leibu; Bart P. Leroy; Petra Liskova; Irma Lopez; Victor R. de J. López-Rodríguez; Quinten Mahieu; Omar A. Mahroo; Gaël Manes; Luke Mansard; M. Pilar Martín-Gutiérrez; Nelson Martins; Laura Mauring; Martin McKibbin; Terri L. McLaren; Isabelle Meunier; Michel Michaelides; José M. Millán; Kei Mizobuchi; Rajarshi Mukherjee; Zoltán Zsolt Nagy; Kornelia Neveling; Monika Ołdak; Michiel Oorsprong; Yang Pan; Anastasia Papachristou; Antonio Percesepe; Maximilian Pfau; Eric A. Pierce; Emily Place; Raj Ramesar; Francis Ramond; Florence Andrée Rasquin; Gillian I. Rice; Lisa Roberts; María Rodríguez-Hidalgo; Javier Ruiz-Ederra; Ataf H. Sabir; Ai Fujita Sajiki; Ana Isabel Sánchez-Barbero; Asodu Sandeep Sarma; Riccardo Sangermano; Cristina M. Santos; Margherita Scarpato; Hendrik P. N. Scholl; Dror Sharon; Sabrina G. Signorini; Francesca Simonelli; Ana Berta Sousa; Maria Stefaniotou; Kari Stefansson; Katarina Stingl; Akiko Suga; Patrick Sulem; Lori S. Sullivan; Viktória Szabó; Jacek P. Szaflik; Gita Taurina; Alberta A. H. J. Thiadens; Carmel Toomes; Viet H. Tran; Miltiadis K. Tsilimbaris; Pavlina Tsoka; Veronika Vaclavik; Marie Vajter; Sandra Valeina; Enza Maria Valente; Casey Valentine; Rebeca Valero; Sophie Valleix; Joseph van Aerschot; L. Ingeborgh van den Born; Mattias Van Heetvelde; Virginie J. M. Verhoeven; Andrea L. Vincent; Andrew R. Webster; Laura Whelan; Bernd Wissinger; Georgia G. Yioti; Kazutoshi Yoshitake; Juan C. Zenteno; Roberta Zeuli; Theresia Zuleger; Chaim Landau; Allan I. Jacob; Siying Lin; Frans P. M. Cremers; Winston Lee; Jamie M. Ellingford; David Stanek; Susanne Roosing; Carlo Rivolta
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errSave
Molecular characterization of CHST6 in Egyptian families with macular corneal dystrophy reveals recurrent and novel variants
errOphthalmic Genetics
IF1
err2026-01-01
err0
PREAI
errKenawy Amin, Asmaa; Mahmoud, Shahira; Goweida, Mohamed Bahgat; Ghazy, Asmaa Eisa; Jedlickova, Jana; Dudakova, Lubica; Liskova, Petra
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errSave
Rare variants in MIR184 are a novel genetic cause of Fuchs endothelial corneal dystrophy.
errGenetics in Medicine
IF6.2
err2025-08-21
err0
errOAAI
errMarcos Abreu Costa; Amanda N. Sadan; Nihar Bhattacharyya; Niuzheng Chai; Christina Zarouchlioti; Siyin Liu; Anita Szabo; Cian Murphy; Lubica Dudakova; Kirithika Muthusamy; Pavlina Skalicka; Ismail Moghul; Nikolas Pontikos; Petra Liskova; Stephen J. Tuft; Alice E. Davidson
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errSave
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity
errJAMA OPHTHALMOLOGY
IF9.2
err2025-04-01
err0
errOAAI
errLiu, Siyin; Sadan, Amanda N.; Bhattacharyya, Nihar; Zarouchlioti, Christina; Szabo, Anita; Abreu Costa, Marcos; Hafford-Tear, Nathaniel J.; Kladny, Anne-Marie S.; Dudakova, Lubica; Ciosi, Marc; Moghul, Ismail; Wilkins, Mark R.; Allan, Bruce; Skalicka, Pavlina; Hardcastle, Alison J.; Pontikos, Nikolas; Bunce, Catey; Monckton, Darren G.; Muthusamy, Kirithika; Liskova, Petra; Tuft, Stephen J.; Davidson, Alice E.
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errSave
Genotype-Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights
errCLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
IF5.6
err2025-03-01
err0
errOAAI
errLiskova, Petra; Skalicka, Pavlina; Dudakova, Lubica; Vincent, Andrea L.
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errSave
Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease ( vol 18 , e0288907 , 2023)
errPLOS ONE
IF2.6
err2025-01-30
err0
errOAAI
errNeroldova, Magdalena; Ciara, Elzbieta; Slatinska, Janka; Frankova, Sona; Liskova, Petra; Kotalova, Radana; Globinovska, Janka; Safarikova, Marketa; Pfeiferova, Lucie; Zunova, Hana; Mrazova, Lenka; Stranecky, Viktor; Vrbacka, Alena; Fabian, Ondrej; Sticova, Eva; Skanderova, Daniela; Sperl, Jan; Kalousova, Marta; Zima, Tomas; Macek, Milan; Pawlowska, Joanna; Knisely, A. S.; Kmoch, Stanislav; Jirsa, Milan
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errSave
Tissue-specific TCF4 triplet repeat instability revealed by optical genome mapping
errEBIOMEDICINE
IF10.8
err2024-10-01
err1
errOAAI
errZarouchlioti, Christina; Efthymiou, Stephanie; Facchini, Stefano; Dominik, Natalia; Bhattacharyya, Nihar; Liu, Siyin; Costa, Marcos Abreu; Szabo, Anita; Sadan, Amanda N.; Jun, Albert S.; Bugiardini, Enrico; Houlden, Henry; Cortese, Andrea; Skalicka, Pavlina; Dudakova, Lubica; Muthusamy, Kirithika; Cheetham, Michael E.; Hardcastle, Alison J.; Liskova, Petra; Tuft, Stephen J.; Davidson, Alice E.
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errSave
Autosomal dominant stromal corneal dystrophy associated with a SPARCL1 missense variant
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-08-21
err3
errOAAI
errBraddock, Freddie L.; Gardner, Jessica C.; Bhattacharyya, Nihar; Sanchez-Pintado, Beatriz; Costa, Marcos; Zarouchlioti, Christina; Szabo, Anita; Liskova, Petra; Cheetham, Michael E.; Young, Robert D.; Thaung, Caroline; Davidson, Alice E.; Tuft, Stephen J.; Hardcastle, Alison J.
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errSave
Leber hereditary optic neuropathy in Czechia and Slovakia: Quality of life and costs from patient perspective
errHELIYON
IF3.6
err2024-06-01
err0
errOAAI
errBusanyova, Beata; Vajter, Marie; Kelifova, Silvie; Liskova, Petra; Mikova, Hedviga; Brecikova, Katarina; Zigmond, Jan; Rogalewicz, Vladimir; Tichopad, Ales; Visnansky, Martin; Sarkanova, Ivana
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errSave
Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease
errPLOS GENETICS
IF3.7
err2024-05-07
err5
errOAAI
errBhattacharyya, Nihar; Chai, Niuzheng; Hafford-Tear, Nathaniel J.; Sadan, Amanda N.; Szabo, Anita; Zarouchlioti, Christina; Jedlickova, Jana; Leung, Szi Kay; Liao, Tianyi; Dudakova, Lubica; Skalicka, Pavlina; Parekh, Mohit; Moghul, Ismail; Jeffries, Aaron R.; Cheetham, Michael E.; Muthusamy, Kirithika; Hardcastle, Alison J.; Pontikos, Nikolas; Liskova, Petra; Tuft, Stephen J.; Davidson, Alice E.
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errSave
Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1
errAMERICAN JOURNAL OF OPHTHALMOLOGY
IF4.2
err2024-02-01
err2
errOAAI
errPatterson, Karynne; Chong, Jessica x.; Chung, Doug d.; Lisch, Walter; Karp, Carol l.; Dreisler, Erling; Lockington, David; Rohrbach, Jens m.; Garczarczyk-asim, Dorota; Mueller, Thomas; Tuft, Stephen j.; Skalicka, Pavlina; Wilnai, Yael; Samra, Nadra naser; Ibrahim, Ali; Mandel, Hanna; Davidson, Alice e.; Liskova, Petra; Aldave, Anthony j.; Bamshad, Michael j.; Janecke, Andreas r.
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errSave
Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy
errHUMAN MUTATION
IF3.7
err2024-01-04
err0
errOAAI
errDudakova, Lubica; Noskova, Lenka; Kmoch, Stanislav; Filipec, Martin; Filous, Ales; Davidson, Alice E.; Toulis, Vasileios; Jedlickova, Jana; Skalicka, Pavlina; Hartmannova, Hana; Stranecky, Viktor; Drabova, Jana; Novotna, Drahuse; Havlovicova, Marketa; Sedlacek, Zdenek; Liskova, Petra
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errSave
Ovol2 promoter mutations in mice and human illuminate species-specific phenotypic divergence
errHUMAN MOLECULAR GENETICS
IF3.2
err2023-11-16
err1
PREAI
errSunny, Sweetu Susan; Lachova, Jitka; Kasparek, Petr; Palkova, Marcela; Spoutil, Frantisek; Prochazka, Jan; Sedlacek, Radislav; Liskova, Petra; Kozmik, Zbynek
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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
errPLOS ONE
IF2.6
err2023-11-15
err0
errOAAI
errWasserbauer, Martin; Mala, Sarka; Stechova, Katerina; Hlava, Stepan; Cernikova, Pavlina; Stovicek, Jan; Drabek, Jiri; Broz, Jan; Pichlerova, Dita; Kucerova, Barbora; Liskova, Petra; Kral, Jan; Bartuskova, Lucia; Keil, Radan
errShare
errSave
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability
errHUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
err2023-10-01
err7
errOAAI
errCorradi, Zelia; Khan, Mubeen; Hitti-Malin, Rebekkah; Mishra, Ketan; Whelan, Laura; Cornelis, Stephanie S.; Hoyng, Carel B.; Kampjarvi, Kati; Klaver, Caroline C. W.; Liskova, Petra; Stoehr, Heidi; Weber, Bernhard H. F.; Banfi, Sandro; Farrar, G. Jane; Sharon, Dror; Zernant, Jana; Allikmets, Rando; Dhaenens, Claire-Marie; Cremers, Frans P. M.
errShare
errSave
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
errHUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
err2023-04-01
err14
errOAAI
errReurink, Janine; Weisschuh, Nicole; Garanto, Alejandro; Dockery, Adrian; van den Born, L. Ingeborgh; Fajardy, Isabelle; Haer-Wigman, Lonneke; Kohl, Susanne; Wissinger, Bernd; Farrar, G. Jane; Ben-Yosef, Tamar; Pfiffner, Fatma Kivrak; Berger, Wolfgang; Weener, Marianna E.; Dudakova, Lubica; Liskova, Petra; Sharon, Dror; Salameh, Manar; Offenheim, Ashley; Heon, Elise; Girotto, Giorgia; Gasparini, Paolo; Morgan, Anna; Bergen, Arthur A.; ten Brink, Jacoline B.; Klaver, Caroline C. W.; Tranebjaerg, Lisbeth; Rendtorff, Nanna D.; Vermeer, Sascha; Smits, Jeroen J.; Pennings, Ronald J. E.; Aben, Marco; Oostrik, Jaap; Astuti, Galuh D. N.; Galbany, Jordi Corominas; Kroes, Hester Y.; Phan, Milan; Zelst-Stams, Wendy A. G. van; Thiadens, Alberta A. H. J.; Verheij, Joke B. G. M.; Schooneveld, Mary J. van; Bruijn, Suzanne E. de; Li, Catherina H. Z.; Hoyng, Carel B.; Gilissen, Christian; Vissers, Lisenka E. L. M.; Cremers, Frans P. M.; Kremer, Hannie; van Wijk, Erwin; Roosing, Susanne
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errSave
Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy
errACTA OPHTHALMOLOGICA
IF2.8
err2023-03-07
err0
errOAAI
errLiu, Siyin; Sadan, Amanda N.; Muthusamy, Kirithika; Zarouchlioti, Christina; Jedlickova, Jana; Pontikos, Nikolas; Thaung, Caroline; Hardcastle, Alison J.; Netukova, Magdalena; Skalicka, Pavlina; Dudakova, Lubica; Bunce, Catey; Tuft, Stephen J.; Davidson, Alice E.; Liskova, Petra
errShare
errSave

Research Directions

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Co-authors
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