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

Tiziana Mongini

Neuroscience Institute

ORCID: 0000-0003-4061-4261
Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicineImmunology and Microbiology

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 11 papers. Top paper: “Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial”.

Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

The Lancet Neurology(2021)10.1016/s1474-4422(21)00241-6
N/A
2.9DataRank · unranked
185 citations

Priya S. Kishnani, Hani Kushlaf, Shafeeq Ladha, Tahseen Mozaffar, Volker Straub +95 more

Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies

International Journal of Molecular Sciences(2020)10.3390/ijms21072635
N/A
0DataRank · unranked
29 citations

Takako I. Jones, Monica Govi, Fabiano Mele, Louise Maranda, Francesco Sera +30 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

Digenic Inheritance Involving a Muscle Specific Protein Kinase and the Giant Titin Protein Causes a Skeletal Muscle Myopathy

SSRN Electronic Journal(2021)10.2139/ssrn.3801723
N/A
0DataRank · unranked
2 citations

Irina Zaharieva, Valeria Di Leo, Anna Vihola, Neha Wali, Marco Savarese +60 more

Genetic modifiers of upper limb function in Duchenne muscular dystrophy

Journal of Neurology(2022)10.1007/s00415-022-11133-8
N/A
0DataRank · unranked
7 citations

Aurora Fusto, Sara Vianello, Matteo Villa, J.A. Janik, Grazia D’Angelo +28 more

Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy

Nature Genetics(2024)10.1038/s41588-023-01651-0
N/A
0DataRank · unranked
33 citations

Dan Cox, Irina Zaharieva, Valeria Di Leo, J. Sarparanta, Per Harald Jonson +80 more

A novel family of lncRNAs relate facioscapulohumeral muscular dystrophy to nucleolar architecture and protein synthesis

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.06.29.600824
N/A
0DataRank · unranked
0 citations

Francesca Losi, Bruno Fosso, Marco Ferrarini, Sara Pini, Marcello Manfredi +9 more

Nucleolar FRG2 lncRNAs inhibit rRNA transcription and cytoplasmic translation, linking FSHD to dysregulation of muscle-specific protein synthesis

Nucleic Acids Research(2025)10.1093/nar/gkaf643
N/A
0DataRank · unranked
6 citations

Francesca Losi, Bruno Fosso, Marco Ferrarini, Sara Pini, Marcello Manfredi +9 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

Genetic modifiers of respiratory function in Duchenne muscular dystrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51046
N/A
0DataRank · unranked
45 citations

Maria Grazia D’Angelo, Matteo Villa, Aurora Fusto, Sara Vianello, Beatrice Merlo +36 more

Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability

medRxiv(2025)10.1101/2025.10.01.25336578
N/A
0DataRank · unranked
0 citations

Stefano Facchini, Arianna Manini, Ricardo Parolin Schnekenberg, Chiara Pisciotta, Stefania Magri +37 more