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Sandro Banfi

17PUBLICATIONS

202CO-AUTHORS

Sensory systemsMicrobial geneticsNeurology and neuromuscular diseasesGene mappingCell and nuclear division

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Publications (17)

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|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 <i>ABCA4</i>-Associated Retinopathy.

Zelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald

|Mar 28, 2024

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

Rebekkah J Hitti-Malin, Daan M Panneman, Zelia Corradi

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Frequent Collaborators

7 joint publications

Marianthi Karali

4 joint publications

Carlo Rivolta

3 joint publications

Lubica Dudakova

3 joint publications

Petra Liskova

3 joint publications

Zelia Corradi

3 joint publications

Marie Vajter

3 joint publications

Carmen Ayuso

3 joint publications

Dror Sharon

3 joint publications

Chris F Inglehearn

3 joint publications

Monika Ołdak

Frequent Collaborators

7 joint publications

Marianthi Karali

4 joint publications

Carlo Rivolta

3 joint publications

Lubica Dudakova

3 joint publications

Petra Liskova

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