Lubica Dudakova

Charles University

Czech Republic

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Articles (15)

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2024

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2024

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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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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

Collaborators (17)

Andrea L. Vincent

NEW ZEALAND

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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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Elfride De Baere

BELGIUM

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Lenka Noskova

Charles University

CZECH REPUBLIC

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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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Petra Liskova

Charles University in Prague

CZECH REPUBLIC

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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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Michael Cheetham

University College London

UNITED KINGDOM

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Susan M. Downes

Oxford University Hospitals NHS Foundation Trust

UNITED KINGDOM

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Hana Hartmannova

Charles University

CZECH REPUBLIC

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Sandro BANFI

University of Campania “Luigi Vanvitelli”

ITALY

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Pavlína Skalická

Charles University

CZECH REPUBLIC

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Lubica Dudakova

Research Interests

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Articles (15)

Deciphering novel TCF4-driven mechanisms underlying a common triplet repeat expansion-mediated disease.

Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy

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

Novel disease‐causing variants and phenotypic features of X‐linked megalocornea

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

Axenfeld-Rieger syndrome: more than meets the eye.

PRIMARY OPEN-ANGLE GLAUCOMA DUE TO MUTATIONS IN THE MYOC GENE.

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

Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.

Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles.

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

Collaborators (17)

Andrea L. Vincent

Stephen Tuft

Christopher Inglehearn

Carmen Ayuso

Elfride De Baere

Lenka Noskova

Alice Davidson

Carlo Rivolta

Marianthi Karali

Petra Liskova

Jane Farrar

Michael Gorin

Michael Cheetham

Susan M. Downes

Hana Hartmannova

Sandro BANFI

Pavlína Skalická

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