Carlo Rivolta

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Professor of Ophthalmic Genetics

University of Basel

Switzerland

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About

Carlo Rivolta is a Professor of Ophthalmic Genetics at the University of Basel in Switzerland. His research focuses on inherited retinal diseases and the genetic underpinnings of various maculopathies. Recent publications include works on gene atlases for retinal disorders, genetic testing methodologies, and innovative approaches to gene therapy for retinal function restoration.

Recent Grants

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Plenary meeting of the European Retinal Disease Consortium

Open Date: 2023-09-01

Close Date: 2023-11-30

Grant: Close

Genomics of inherited retinal diseases

Open Date: 2021-10-01

Close Date: 2025-09-30

Grant: Close

Solving missing heritability in inherited retinal diseases using integrated omics and gene editing in human cellular and animal models

Open Date: 2020-09-01

Close Date: 2023-08-31

Grant: Close

Host factors in severe COVID-19: learning from extreme cases

Open Date: 2020-06-01

Close Date: 2023-05-31

Grant: Close

Genetic bases of retinoblastoma from liquid biopsies: towards a personalized treatment of pediatric patients

Open Date: 2020-01-01

Close Date: 2022-01-01

Articles (10)

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2025

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2025

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2025

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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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2024

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2024

Collaborators (20)

Andrea L. Vincent

NEW ZEALAND

Carlo Rivolta

Research Interests

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About

Recent Grants

Articles (10)

RetiGene, a comprehensive gene atlas for inherited retinal diseases

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

Generation of a Double Reporter mES Cell Line to Simultaneously Trace the Generation of Retinal Progenitors and Photoreceptors

Fine-tuning FAM161A gene augmentation therapy to restore retinal function

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

Combining a prioritization strategy and functional studies nominates 5'UTR variants underlying inherited retinal disease

An atypical form of 60S ribosomal subunit in Diamond-Blackfan anemia linked to RPL17 variants.

Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa

Genetic Testing of Patients with Inherited Retinal Diseases in the European Countries. An International Survey by the European Vision Institute.

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.

Collaborators (20)

Andrea L. Vincent

Ana Belen Iglesias Romero

Christopher Inglehearn

Corinne Kostic

Raymond T O'Keefe

Carmen Ayuso

Elfride De Baere

Frauke Coppieters

Tom Fowler

Karolina Kaminska

Joaquim Calado

Katherine Wood

Marianthi Karali

Raffaele Renella

Petra Liskova

Jane Farrar

Michael Gorin

Susan M. Downes

Sandro BANFI

Lubica Dudakova

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