🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Simona Orcesi

University of Pavia

ORCID: 0000-0001-8947-9342

Also affiliated with Foundation Center, Fondazione Istituto Neurologico Nazionale Casimiro Mondino, Urology Foundation

Immunology and MicrobiologyMedicineBiochemistry, 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 13 papers. Top paper: “Early Parenting Intervention – Biobehavioral Outcomes in infants with Neurodevelopmental Disabilities (EPI-BOND): study protocol for an Italian multicentre randomised controlled trial”.

Early Parenting Intervention – Biobehavioral Outcomes in infants with Neurodevelopmental Disabilities (EPI-BOND): study protocol for an Italian multicentre randomised controlled trial

BMJ Open(2020)10.1136/bmjopen-2019-035249
N/A
0.837DataRank · unranked
30 citations

Elisa Rosa, Roberto Giorda, Elisa Fazzi, Simona Orcesi, Anna Cavallini +2 more

Development of a neurologic severity scale for Aicardi Goutières Syndrome

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.03.008
N/A
0DataRank · unranked
49 citations

Francesco Gavazzi, Abbas F. Jawad, Stacy V. Cusack, Kimberly Kopin, Kyle Peer +9 more

Case Report: The JAK-Inhibitor Ruxolitinib Use in Aicardi-Goutieres Syndrome Due to ADAR1 Mutation

Frontiers in Pediatrics(2021)10.3389/fped.2021.725868
N/A
0DataRank · unranked
24 citations

Jessica Galli, Fiammetta Zunica, Rosalba Monica Ferraro, Marialuisa Carpanelli, Simona Orcesi +6 more

Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome

Frontiers in Immunology(2021)10.3389/fimmu.2021.672952
N/A
0DataRank · unranked
4 citations

Silvia Masnada, Francesca Dragoni, Daisy Sproviero, Federico Fogolari, Stella Gagliardi +9 more

The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS

Arthritis & Rheumatology(2022)10.1002/art.42087
N/A
0DataRank · unranked
47 citations

Lovro Lamot, Micol Romano, Erkan Demirkaya, David Piskin, Sofia Torreggiani +27 more

Characterization of Mitochondrial Alterations in Aicardi–Goutières Patients Mutated in RNASEH2A and RNASEH2B Genes

International Journal of Molecular Sciences(2022)10.3390/ijms232214482
N/A
0DataRank · unranked
14 citations

Jessica Garau, Daisy Sproviero, Simona Orcesi, Costanza Varesio, Silvia De Siervi +4 more

Characterization of mitochondrial alterations in Aicardi-Goutières patients mutated in RNASEH2A and RNASEH2B genes

Research Square(2022)10.21203/rs.3.rs-1816035/v1
N/A
0DataRank · unranked
1 citations

Jessica Garau, Daisy Sproviero, Simona Orcesi, Costanza Varesio, Silvia De Siervi +4 more

Altered DNA methylation and gene expression predict disease severity in patients with Aicardi-Goutières syndrome

Clinical Immunology(2023)10.1016/j.clim.2023.109299
N/A
0DataRank · unranked
18 citations

Amandine Charras, Costanza Varesio, Simona Orcesi, Francesca Dragoni, Jessica Galli +6 more

Comparison between D-loop methylation and mtDNA copy number in patients with Aicardi-Goutières Syndrome

Frontiers in Endocrinology(2023)10.3389/fendo.2023.1152237
N/A
0DataRank · unranked
6 citations

Jessica Garau, Simona Orcesi, Costanza Varesio, Matteo Bordoni, Eveljn Scarian +8 more

Metformin reduces oxidative damage in RNASEH2-mutant Aicardi-Goutières cells

(2024)10.22541/au.172114231.10387344/v1
N/A
0DataRank · unranked
0 citations

Jessica Garau, Bartolo Rizzo, Simona Orcesi, Costanza Varesio, Rosalinda Di Gerlando +6 more

Clinical Characterization of a Multicenter International Cohort of Patients With Aicardi-Goutières Syndrome Homozygous for the RNASEH2B:p.Ala177Thr Variant: Early Clinical Markers of Disease Severity

Pediatric Neurology(2025)10.1016/j.pediatrneurol.2025.07.011
N/A
0DataRank · unranked
1 citations

Davide Politano, Laura Adang, Elena Ballante, Roberta Battini, Enrico Bertini +20 more

Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function

Human Mutation(2020)10.1002/humu.23975
N/A
0DataRank · unranked
113 citations

Sehoon Park, Francesco Gavazzi, Laura Adang, Loveline A. Ayuk, Lien Van Eyck +58 more

Metformin Reduces Oxidative Damage in RNASEH2-Mutant Aicardi-Goutières Cells

Genes(2025)10.3390/genes16080922
N/A
0DataRank · unranked
0 citations

Jessica Garau, Bartolo Rizzo, Simona Orcesi, Costanza Varesio, Rosalinda Di Gerlando +6 more