Petra Liskova

Charles University in Prague

Czech Republic

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Articles (13)

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2024

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2024

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2024

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2023

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2021

Collaborators (24)

Andrea L. Vincent

NEW ZEALAND

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Isabelle Audo

Professor

Université Pierre et Marie Curie

FRANCE

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Valeria Lo Faro

University Medical Center Groningen

NETHERLANDS

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Stephen Tuft

University College London

UNITED KINGDOM

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Christopher Inglehearn

University of Leeds

UNITED KINGDOM

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Carmen Ayuso

SPAIN

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Thomy de Ravel

Vrije Universiteit Brussel

BELGIUM

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Mark Simcoe

University College London

UNITED KINGDOM

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Elfride De Baere

BELGIUM

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Delphine Blain

National Eye Institute

UNITED STATES

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Ditta Zobor

assistant professor

Semmelweis University

HUNGARY

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Francesco Benedicenti

ITALY

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Alice Davidson

Professor of Molecular Genetics

University College London

UNITED KINGDOM

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Carlo Rivolta

Professor of Ophthalmic Genetics

University of Basel

SWITZERLAND

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Marianthi Karali

Telethon Institute of Genetics and Medicine

ITALY

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Peggy Reuter

institute of biochemistry university of tübingen tübingen germany

GERMANY

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Jane Farrar

Head of School

Trinity College Dublin

IRELAND

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Michael Gorin

Professor

University of California, Los Angeles

UNITED STATES

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Susan M. Downes

Oxford University Hospitals NHS Foundation Trust

UNITED KINGDOM

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Alison Hardcastle

University College London

UNITED KINGDOM

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Sandro BANFI

University of Campania “Luigi Vanvitelli”

ITALY

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Lubica Dudakova

Charles University

CZECH REPUBLIC

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Graeme Black

Professor of Genetics and Ophthalmology

The University of Manchester

UNITED KINGDOM

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Pavlína Skalická

Charles University

CZECH REPUBLIC

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Petra Liskova

Research Interests

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Articles (13)

Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes

Blau Syndrome: Challenging Molecular Genetic Diagnostics of Autoinflammatory Disease

Disease-Causing <i>TIMP3</i> Variants and Deep Phenotyping of Two Czech Families with Sorsby Fundus Dystrophy Associated with Novel p.(Tyr152Cys) Mutation

MIR204 n.37C>T variant as a cause of chorioretinal dystrophy variably associated with iris coloboma, early‐onset cataracts and congenital glaucoma

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy.

Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant

The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement.

Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?

A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.

ALG3-CDG: a patient with novel variants and review of the genetic and ophthalmic findings

Clinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech Population.

Hereditary gelsolin amyloidosis – clinical symptoms and molecular genetic cause

Collaborators (24)

Andrea L. Vincent

Isabelle Audo

Valeria Lo Faro

Stephen Tuft

Christopher Inglehearn

Carmen Ayuso

Thomy de Ravel

Mark Simcoe

Elfride De Baere

Delphine Blain

Ditta Zobor

Francesco Benedicenti

Alice Davidson

Carlo Rivolta

Marianthi Karali

Peggy Reuter

Jane Farrar

Michael Gorin

Susan M. Downes

Alison Hardcastle

Sandro BANFI

Lubica Dudakova

Graeme Black

Pavlína Skalická

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