Lidia Di Vito

Istituto delle Scienze Neurologiche di Bologna

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 5 papers. Top paper: “Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset”.

Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset

Ophthalmology(2021)10.1016/j.ophtha.2020.12.012

N/A

3.6DataRank · unranked

166 citations

Patrick Yu‐Wai‐Man, Valério Carelli, Mark L. Moster, Valérie Biousse, Catherine Vignal +55 more

Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation

Ophthalmology and Therapy(2022)10.1007/s40123-022-00611-x

N/A

0.755DataRank · unranked

30 citations

Nancy J. Newman, Patrick Yu‐Wai‐Man, Valérie Biousse, Mark L. Moster, Prem S. Subramanian +79 more

Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic Neuropathy

JAMA Ophthalmology(2024)10.1001/jamaophthalmol.2024.5375

N/A

0.743DataRank · unranked

24 citations

Nancy J. Newman, Valérie Biousse, Valério Carelli, Mark L. Moster, Catherine Vignal‐Clermont +59 more

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01485-w

N/A

0DataRank · unranked

217 citations

Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi +95 more

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8

N/A

0DataRank · unranked

58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more