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Hoai Viet Tran

Has grant

Head

Hôpital Ophtalmique Jules-Gonin

Switzerland

Research Interests

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Professors in Switzerland Professors in Cell Biology Cell Biology professors in Switzerland

Recent Grants

Grant: Open

A new autosomal dominant syndromic ciliopathy

Open Date: 2025-01-01

Close Date: 2030-01-01

Grant: Close

Plenary meeting of the European Retinal Disease Consortium

Open Date: 2023-01-01

Close Date:

Grant: Close

Genomics of inherited retinal diseases

Open Date: 2021-10-01

Close Date: 2025-09-01

Grant: Close

SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis

Open Date: 2017-01-01

Close Date:

Grant: Close

Non-Mendelian inheritance in retinal degenerations

Open Date: 2017-01-01

Close Date:

Articles (12)

Year:

2026

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2026

Year:

2025

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2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

Collaborators (27)

Bence György

Assistant Professor

University of Basel

SWITZERLAND

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Alexis Ceecee Britten-Jones

Senior Research Fellow

University of Melbourne

AUSTRALIA

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Gaël Manes

Chercheur

INSERM

FRANCE

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Panos Sergouniotis

Senior Lecturer & Honorary Consultant

The University of Manchester

UNITED KINGDOM

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Stefan Barakat

Associate professor

Erasmus MC

NETHERLANDS

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Christopher Inglehearn

University of Leeds

UNITED KINGDOM

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Maximilian Pfau

Full Professor

University Hospital Bonn

GERMANY

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Omar A. Mahroo

University College London

UNITED KINGDOM

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Frauke Coppieters

Associate professor, PI of the TaRGeT lab

Ghent University

BELGIUM

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Carmel Toomes

University of Leeds

UNITED KINGDOM

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Akiko Suga

Project Assistant Professor

Keio University

JAPAN

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Julio C Corral Serrano

Research Associate

University College London

UNITED KINGDOM

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Monika Ołdak

Head of the Department

Institute of Physiology and Pathology of Hearing

POLAND

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Karolina Kaminska

Institute of Molecular and Clinical Ophthalmology Basel

SWITZERLAND

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Regina Schlaeger

currently Co-Head Neuromuscular Competence Center/EMG Unit, Research Group Leader

University Hospital Basel

SWITZERLAND

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Carlo Rivolta

Professor of Ophthalmic Genetics

University of Basel

SWITZERLAND

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Suzanne E. de Bruijn

Radboud University Medical Center

NETHERLANDS

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Marianthi Karali

Telethon Institute of Genetics and Medicine

ITALY

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Pietro De Angeli

Project Lead Senior Scientist

Universitätsklinikum Tübingen

GERMANY

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Dror Sharon

Hebrew University of Jerusalem

ISRAEL

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Abigail Moye

Institute of Molecular and Clinical Ophthalmology Basel

SWITZERLAND

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Kinga Bujakowska

Assistant Professor

Harvard University

UNITED STATES

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S. Amer Riazuddin

Johns Hopkins University

UNITED STATES

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Virginie Verhoeven

Researcher

Erasmus University Rotterdam

NETHERLANDS

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Alison Hardcastle

University College London

UNITED KINGDOM

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Adrien Roux

Full Professor UAS

Haute école du paysage d'ingénierie et d'architecture de Genève

SWITZERLAND

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Lubica Dudakova

Charles University

CZECH REPUBLIC

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ApplyKite TwinLearns as you apply

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Hoai Viet Tran

Research Interests

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Recent Grants

Articles (12)

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Resting-state electroretinography reveals pathological retinal oscillations in retinitis pigmentosa mice and patients

Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy

A novel recurrent ARL3 variant c.209G>A p.(Gly70Glu) causes variable non-syndromic dominant retinal dystrophy with defective lipidated protein transport in human retinal stem cell models

Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction

Detection of elusive DNA copy-number variations in hereditary disease and cancer through the use of noncoding and off-target sequencing reads

Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression.

GNB1-Related Rod-Cone Dystrophy: A Case Report.

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis

Genetics of Retinitis Pigmentosa and Other Hereditary Retinal Disorders in Western Switzerland.

Coats-like Vasculopathy in Inherited Retinal Disease

Collaborators (27)

Bence György

Alexis Ceecee Britten-Jones

Gaël Manes

Panos Sergouniotis

Stefan Barakat

Christopher Inglehearn

Maximilian Pfau

Omar A. Mahroo

Frauke Coppieters

Carmel Toomes

Akiko Suga

Julio C Corral Serrano

Monika Ołdak

Karolina Kaminska

Regina Schlaeger

Carlo Rivolta

Suzanne E. de Bruijn

Marianthi Karali

Pietro De Angeli

Dror Sharon

Abigail Moye

Kinga Bujakowska

S. Amer Riazuddin

Virginie Verhoeven

Alison Hardcastle

Adrien Roux

Lubica Dudakova

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