Francesco Fortunato

Also affiliated with Magna Graecia University, Ferrari (Italy)

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 9 papers. Top paper: “Event‐based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross‐sectional data”.

Event‐based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross‐sectional data

Epilepsia(2022)10.1111/epi.17316

N/A

0DataRank · unranked

27 citations

Leon Aksman, Neil P. Oxtoby, Sjoerd B. Vos, Jun Rao, Erik Kaestner +72 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

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.21.562994

N/A

0DataRank · unranked

4 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +60 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

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study

Epilepsia(2024)10.1111/epi.17881

N/A

0DataRank · unranked

23 citations

Andrew Perry, Lucy Vivash, Terence J. O’Brien, Marina K. M. Alvim, Donatello Arienzo +59 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675

N/A

0DataRank · unranked

12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more