Federica Ricci

Azienda Ospedaliera Citta' della Salute e della Scienza di Torino

ORCID: 0000-0003-2019-612X

Also affiliated with Ospedale Regina Margherita, University of Turin

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 7 papers. Top paper: “Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity”.

Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity

Brain(2025)10.1093/brain/awae358

N/A

0.440DataRank · unranked

13 citations

Daniele Sabbatini, Pietro Riguzzi, Giuliana Capece, Marika Pane, Serenella Servidei +58 more

Titin copy number variations associated with dominant inherited phenotypes

Journal of Medical Genetics(2023)10.1136/jmg-2023-109473

N/A

0.269DataRank · unranked

5 citations

Corinne Métay, Marco Savarese, Rabah Ben Yaou, German Demidov, Isabelle Nelson +28 more

Histone deacetylases in Duchenne muscular dystrophy: a role in the mechanism of disease and a target for inhibition

Clinical Epigenetics(2025)10.1186/s13148-025-02031-7

N/A

0.104DataRank · unranked

1 citations

Emilio Albamonte, Luca Bello, Adele D’amico, Riccardo Masson, Vincenzo Nigro +5 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

Circulating protein biomarkers identified in two independent clinical trial cohorts of glucocorticoid-naive Duchenne muscular dystrophy patients.

Scientific Reports(2025)10.1038/s41598-025-23758-6

N/A

0DataRank · unranked

3 citations

Rebecca Tobin, C. Degan, Ahmed Naveed, Michela Guglieri, Albert Jiménez-Requena +88 more

Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1

Developmental Medicine & Child Neurology(2024)10.1111/dmcn.16079

N/A

0DataRank · unranked

8 citations

Emilio Albamonte, Marika Pane, Federica Ricci, Adele D’Amico, Guja Astrea +8 more

Health related quality of life in young, steroid-naïve boys with Duchenne muscular dystrophy

Neuromuscular Disorders(2021)10.1016/j.nmd.2021.06.001

N/A

0DataRank · unranked

8 citations

Elaine McColl, Michael McDermott, William B. Martens, Michela Guglieri, Robert C. Griggs +42 more