Giacomo Calzetti

Also affiliated with Institute of Molecular and Clinical Ophthalmology Basel

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration”.

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

Genetics in Medicine(2024)10.1016/j.gim.2024.101106

N/A

0.416DataRank · unranked

15 citations

Kim Rodenburg, Tamar Hayman, Giacomo Calzetti, Karolina Kamińska, Mathieu Quinodoz +20 more

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

Nature Genetics(2026)10.1038/s41588-025-02451-4

N/A

0.370DataRank · unranked

8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

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

medRxiv(2025)10.1101/2025.01.06.24317169

N/A

0DataRank · unranked

15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more