Sara Gibertini

964 total citations
25 papers, 460 citations indexed

About

Sara Gibertini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Sara Gibertini has authored 25 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Cell Biology. Recurrent topics in Sara Gibertini's work include Muscle Physiology and Disorders (17 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiomyopathy and Myosin Studies (4 papers). Sara Gibertini is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiomyopathy and Myosin Studies (4 papers). Sara Gibertini collaborates with scholars based in Italy, Australia and United States. Sara Gibertini's co-authors include Marina Mora, Simona Zanotti, Renato Mantegazza, Lucía Morandi, Lorenzo Maggi, Pia Bernasconi, Cinzia Bragato, Paolo Savadori, Flavia Blàsevich and S. Saredi and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Biochemical and Biophysical Research Communications.

In The Last Decade

Sara Gibertini

24 papers receiving 455 citations

Peers

Countries citing papers authored by Sara Gibertini

Since Specialization

Citations

This map shows the geographic impact of Sara Gibertini's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sara Gibertini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Gibertini more than expected).

Fields of papers citing papers by Sara Gibertini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sara Gibertini. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sara Gibertini. The network helps show where Sara Gibertini may publish in the future.

Co-authorship network of co-authors of Sara Gibertini

This figure shows the co-authorship network connecting the top 25 collaborators of Sara Gibertini. A scholar is included among the top collaborators of Sara Gibertini based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sara Gibertini. Sara Gibertini is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy 2024 ·International Journal of Molecular Sciences ·Daniela Piga, Simona Zanotti, Michela Ripolone, Laura Napoli, Patrizia Ciscato, Sara Gibertini, Lorenzo Maggi, Francesco Fortunato, Andrea Rigamonti, Dario Ronchi, Giacomo P. Comi, Stefania Corti, Monica Sciacco	1
2	Identification of a muscle-specific isoform of VMA21 as a potent actor in X-linked myopathy with excessive autophagy pathogenesis 2023 ·Human Molecular Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Anne Bigot, Kamel Mamchaoui, Sara Gibertini, (unknown), Daniel J. Ham, Thomas Laumonier, Alexandre Prola, Perrine Castets	1
3	p.Asn1180Ile mutation of SCN4A gene in an Italian family with myopathy and myotonic syndrome 2021 ·Neurological Sciences ·Andrea Rigamonti, Vittorio Mantero, Lorenzo Peverelli, Serena Pagliarani, Sabrina Lucchiari, Giacomo P. Comi, Sara Gibertini, Andrea Salmaggi	1
4	FKRP-dependent glycosylation of fibronectin regulates muscle pathology in muscular dystrophy 2021 ·Nature Communications ·Alasdair J. Wood, Chi‐Hung Lin, (unknown), (unknown), Sara Alaei, Fernando J. Rossello, C. Sonntag, Lucy Hersey, (unknown), Christoph Krisp, Stefanie Dudczig, Alex J. Fulcher, Sara Gibertini, Paul J. Conroy, (unknown), Marina Mora, Patricia R. Jusuf, Nicolle H. Packer, Peter D. Currie	21
5	Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate Myopathy 2021 ·Frontiers in Cell and Developmental Biology ·Elena Conte, Alessandra Pannunzio, Paola Imbrici, Giulia Maria Camerino, Lorenzo Maggi, Marina Mora, Sara Gibertini, Ornella Cappellari, Annamaria De Luca, Mauro Coluccia, Antonella Liantonio	16
6	Multiomic elucidation of a coding 99-mer repeat-expansion skeletal muscle disease 2020 ·Acta Neuropathologica ·Alessandra Ruggieri, Sergey Naumenko, Martin A. Smith, (unknown), Flavia Blàsevich, Cinzia Bragato, Sara Gibertini, Kirston Barton, Matthias Vorgerd, Katrin Marcus, Peixiang Wang, Lorenzo Maggi, Renato Mantegazza, James J. Dowling, Rudolf A. Kley, Marina Mora, Berge A. Minassian	22
7	Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRI 2019 ·Neuromuscular Disorders ·S. Saredi, Sara Gibertini, Leslie Matalonga, Laura Farina, Anna Ardissone, Isabella Moroni, Marina Mora	8
8	Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients 2018 ·Toxicology in Vitro ·Simona Zanotti, Dimos Kapetis, Sara Gibertini, Franco Salerno, Emilio Ciusani, Chiara Colombo, Alessandro Gronchi, Lucía Morandi, Renato Mantegazza, Franco Molteni, Marina Mora	2
9	Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis 2018 ·Matrix Biology ·Simona Zanotti, Sara Gibertini, Flavia Blàsevich, Cinzia Bragato, Alessandra Ruggieri, S. Saredi, Marco Fabbri, Pia Bernasconi, Lorenzo Maggi, Renato Mantegazza, Marina Mora	69
10	Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement 2017 ·Neuromuscular Disorders ·Sara Missaglia, Lorenzo Maggi, Marina Mora, Sara Gibertini, Flavia Blàsevich, Piergiuseppe Agostoni, Laura Moro, Denise Cassandrini, Filippo M. Santorelli, Simonetta Gerevini, Daniela Tavian	22
11	Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy 2015 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Simona Zanotti, Sara Gibertini, (unknown), Paolo Savadori, (unknown), Lucía Morandi, F. Cornelio, Renato Mantegazza, Marina Mora	72
12	A rare mutation in MYH7 gene occurs with overlapping phenotype 2015 ·Biochemical and Biophysical Research Communications ·Lucia Ruggiero, Chiara Fiorillo, Sara Gibertini, Francesco De Stefano, Fiore Manganelli, Rosa Iodice, (unknown), Simona Zanotti, Maurizio Galderisi, Marina Mora, Lucio Santoro	9
13	Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse 2014 ·Cell and Tissue Research ·Sara Gibertini, Simona Zanotti, Paolo Savadori, (unknown), S. Saredi, Franco Salerno, Francesca Andreetta, Pia Bernasconi, Renato Mantegazza, Marina Mora	20
14	A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation 2013 ·European Journal of Paediatric Neurology ·S. Saredi, Sara Gibertini, Anna Ardissone, (unknown), Simona Zanotti, Flavia Blàsevich, (unknown), Isabella Moroni, Marina Mora	14
15	Duchenne muscular dystrophy fibroblast nodules: a cell-based assay for screening anti-fibrotic agents 2013 ·Cell and Tissue Research ·Simona Zanotti, Sara Gibertini, Paolo Savadori, Renato Mantegazza, Marina Mora	14
16	Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature 2012 ·Neurobiology of Disease ·O Brunetti, Paola Imbrici, Fabio Massimo Botti, Vito Enrico Pettorossi, Maria Cristina D’Adamo, Mario Valentino, Christian Zammit, Marina Mora, Sara Gibertini, Giuseppe Di Giovanni, Richard Muscat, Mauro Pessia	27
17	Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis 2011 ·Histopathology ·Simona Zanotti, Sara Gibertini, Claudia Di Blasi, Cristina Cappelletti, Pia Bernasconi, Renato Mantegazza, Lucía Morandi, Marina Mora	46
18	Fibroblasts from the muscles of Duchenne muscular dystrophy patients are resistant to cell detachment apoptosis 2011 ·Experimental Cell Research ·Simona Zanotti, Sara Gibertini, Cinzia Bragato, Renato Mantegazza, Lucía Morandi, Marina Mora	29
19	Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy 2010 ·Neuromuscular Disorders ·Claudia Di Blasi, Flavia Blàsevich, (unknown), (unknown), Sara Gibertini, Simona Zanotti, S. Saredi, Renato Mantegazza, Lucía Morandi, Marina Mora	0
20	Altered production of extra-cellular matrix components by muscle-derived Duchenne muscular dystrophy fibroblasts before and after TGF-β1 treatment 2009 ·Cell and Tissue Research ·Simona Zanotti, Sara Gibertini, Marina Mora	43

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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