Sandro Banfi

18PUBLICATIONS
206CO-AUTHORS
Vision scienceSensory systemsMicrobial geneticsNeurology and neuromuscular diseasesGene mapping
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (18)

|Sep 16, 2026
Biallelic RDH11 variants cause syndromic retinitis pigmentosa with early-onset cataracts and neurodevelopmental delay: a multicenter case series.

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Nov 10, 2025
The Role of miRNAs in Retinal Physiology and in Inherited Retinal Disorders.

Paola Brandi, Maria Zawadzka, Sandro Banfi

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Dec 13, 2024
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss.

Marianthi Karali, Gema García-García, Karolina Kaminska

|Jun 19, 2024
Novel and Recurrent Copy Number Variants in ABCA4-Associated Retinopathy.

Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald

Pageof 3

Frequent Collaborators

8 joint publications

Marianthi Karali

4 joint publications

Carlo Rivolta

3 joint publications

Lubica Dudakova

3 joint publications

Petra Liskova