Stefania Assereto

1.2k citations

24 papers · 791 indexed · h-index 17

Co-authors: Carlo Minetti Federico Zara Claudio Bruno Elisabetta Gazzerro Roberta Biancheri Michael P. Lisanti Federica Sotgia Marina Pedemonte
Topics: Muscle Physiology and Disorders (6 papers)Glycogen Storage Diseases and Myoclonus (4 papers)Mitochondrial Function and Pathology (4 papers)
Cited by: Clinical Biochemistry Physiology Cell Biology
Journals: Nature Genetics Nature Cell Biology Biochemical and Biophysical Research Communications
Partner nations: Italy United States Switzerland

In The Last Decade

Stefania Assereto

24 papers receiving 780 citations

Peers

Countries citing papers authored by Stefania Assereto

Since Specialization

Citations

This map shows the geographic impact of Stefania Assereto'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 Stefania Assereto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stefania Assereto more than expected).

Fields of papers citing papers by Stefania Assereto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefania Assereto. 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 Stefania Assereto. The network helps show where Stefania Assereto may publish in the future.

Co-authorship network of co-authors of Stefania Assereto

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Assereto. A scholar is included among the top collaborators of Stefania Assereto 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 Stefania Assereto. Stefania Assereto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan–Deficient Muscular Dystrophy 2018 ·American Journal Of Pathology ·Elisabetta Gazzerro,(unknown),Stefania Assereto,Sımona Baldassari,Chiara Panicucci,Lizzia Raffaghello,Paolo Scudieri,(unknown),Chiara Fiorillo,Stefano Volpi,Linda Chaabane,Mauro Malnati,Graziella Messina,Santina Bruzzone,Elisabetta Traggiai,Fabio Grassi,Carlo Minetti,Claudio Bruno	10
2	Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene 2018 ·DNA and Cell Biology ·Chiara Fiorillo,Maria Rosaria D’Apice,Federica Trucco,Michela Murdocca,Paola Spitalieri,Stefania Assereto,(unknown),Guido Morcaldi,Carlo Minetti,Federica Sangiuolo,Giuseppe Novelli	19
3	Clinical and molecular consequences of exon 78 deletion in DMD gene 2018 ·Journal of Human Genetics ·Monica Traverso,Stefania Assereto,(unknown),Michele Iacomino,Marina Pedemonte,(unknown),(unknown),Paolo Broda,Carlo Minetti,Elisabetta Gazzerro,Francesca Madia,Claudio Bruno,Federico Zara,Chiara Fiorillo	7
4	The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy 2016 ·Laboratory Investigation ·Stefania Assereto,Rosanna Piccirillo,(unknown),Paolo Scudieri,Chiara Fiorillo,(unknown),Monica Traverso,Luis J. V. Galietta,Claudio Bruno,Carlo Minetti,Federico Zara,Elisabetta Gazzerro	16
5	The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane 2015 ·Nature Cell Biology ·Jeremy M. Baskin,Xudong Wu,Romain Christiano,Michael S. Oh,Curtis Schauder,Elisabetta Gazzerro,Mirko Messa,Sımona Baldassari,Stefania Assereto,Roberta Biancheri,Federico Zara,Carlo Minetti,Andrea Raimondi,Mikael Simons,Tobias C. Walther,Karin M. Reinisch,Pietro De Camilli	85
6	Early onset cardiomyopathy associated with the mitochondrial tRNALeu(UUR) 3271T>C MELAS mutation 2015 ·Biochemical and Biophysical Research Communications ·Giacomo Brisca,Chiara Fiorillo,Claudia Nesti,Federica Trucco,(unknown),(unknown),Stefania Assereto,Guido Morcaldi,Marina Pedemonte,Carlo Minetti,Filippo M. Santorelli,Claudio Bruno	15
7	Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis 2015 ·American Journal Of Pathology ·Elisabetta Gazzerro,Sımona Baldassari,Stefania Assereto,Floriana Fruscione,Angela Pistorio,Chiara Panicucci,Stefano Volpi,Lisa Perruzza,Chiara Fiorillo,Carlo Minetti,Elisabetta Traggiai,Fabio Grassi,Claudio Bruno	44
8	Novel Compound Heterozygous Mutations inTBC1D24Cause Familial Malignant Migrating Partial Seizures of Infancy 2013 ·Human Mutation ·Mathieu Milh,Antonio Falace,Nathalie Villeneuve,Nicola Vanni,Pierre Cacciagli,Stefania Assereto,Rima Nabbout,Fabio Benfenati,Federico Zara,B. Chabrol,Laurent Villard,Anna Fassio	69
9	Novel FAM126A mutations in hypomyelination and congenital cataract disease 2013 ·Biochemical and Biophysical Research Communications ·Monica Traverso,Stefania Assereto,Elisabetta Gazzerro,Salvatore Savasta,Ebtesam Abdalla,Andrea Rossi,Sımona Baldassari,Floriana Fruscione,(unknown),Mahmoud R. Fassad,(unknown),Carlo Minetti,Federico Zara,Roberta Biancheri	13
10	Electroclinical presentation and genotype–phenotype relationships in patients with Unverricht‐Lundborg disease carrying compound heterozygous CSTB point and indel mutations 2012 ·Epilepsia ·Laura Canafoglia,Elena Di Gennaro,Giuseppe Capovilla,Giuseppe Gobbi,Antonella Boni,Francesca Beccaria,Maurizio Viri,Roberto Michelucci,(unknown),Stefania Assereto,Domenico Coviello,(unknown),Davide Rossi Sebastiano,Silvana Franceschetti,Federico Zara	27
11	Therapeutic Potential of Proteasome Inhibition in Duchenne and Becker Muscular Dystrophies 2010 ·American Journal Of Pathology ·Elisabetta Gazzerro,Stefania Assereto,Andrea Bonetto,Federica Sotgia,Sonia Scarfı̀,Angela Pistorio,Gloria Bonuccelli,Michele Cilli,Claudio Bruno,Federico Zara,Michael P. Lisanti,Carlo Minetti	64
12	Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies 2008 ·Cell Cycle ·Stefania Assereto,(unknown),Silvia Stringara,Elisabetta Gazzerro,Paolo Broda,Grazia Paola Nicchia,Maria Svelto,Claudio Bruno,Vincenzo Nigro,Michael P. Lisanti,Antonio Frigeri,Carlo Minetti	16
13	Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro 2008 ·Laboratory Investigation ·Monica Traverso,Elisabetta Gazzerro,Stefania Assereto,Federica Sotgia,Roberta Biancheri,Silvia Stringara,(unknown),Marina Pedemonte,Xiabo Wang,Sara Scapolan,Elisabetta Pasquini,Maria Alice Donati,Federico Zara,Michael P. Lisanti,Claudio Bruno,Carlo Minetti	32
14	Molecular analysis and characterization of nine novel CTSK mutations in twelve patients affected by pycnodysostosis 2007 ·Human Mutation ·(unknown),Stefano Regis,Barbara Tappino,Camillo Rosano,Stefania Assereto,Fabio Corsolini,Maja Di Rocco,Mirella Filocamo	59
15	Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 2006 ·Nature Genetics ·Federico Zara,Roberta Biancheri,Claudio Bruno,(unknown),Stefania Assereto,Elisabetta Gazzerro,Federica Sotgia,Xiaobo Wang,(unknown),Silvia Stringara,Marina Pedemonte,Graziella Uziel,Andrea Rossi,Angelo Schenone,Paolo Tortori‐Donati,Marjo S. van der Knaap,Michael P. Lisanti,Carlo Minetti	74
16	Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment 2005 ·American Journal of Physiology-Cell Physiology ·Stefania Assereto,Silvia Stringara,Federica Sotgia,Gloria Bonuccelli,Aldobrando Broccolini,Marina Pedemonte,Monica Traverso,Roberta Biancheri,Federico Zara,Claudio Bruno,Michael P. Lisanti,Carlo Minetti	56
17	Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositis 2005 ·Biochemical and Biophysical Research Communications ·Carlo Minetti,Marco Gattorno,Silvia Repetto,Andrea Gregorio,Marina Pedemonte,Stefania Assereto,Federico Zara,Claudio Bruno,Alberto Martini	8
18	Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease 2005 ·Neurogenetics ·Roberta Biancheri,Andrea Rossi,(unknown),Rachel Schot,Fabio Corsolini,Stefania Assereto,Grazia M.S. Mancini,F.W. Verheijen,Carlo Minetti,Mirella Filocamo	13
19	Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene 2003 ·Muscle & Nerve ·Claudio Bruno,Filippo M. Santorelli,Stefania Assereto,E. Tonoli,Alessandra Tessa,Monica Traverso,Sara Scapolan,M. Bado,Silvana Tedeschi,Carlo Minetti	40
20	Activation of PKC-β isoforms mediates HNE-induced MCP-1 release by macrophages 2002 ·Biochemical and Biophysical Research Communications ·Mariapaola Nitti,Cinzia Domenicotti,Cristina d’Abramo,Stefania Assereto,Damiano Cottalasso,E. Melloni,Giuseppe Poli,Fiorella Biasi,(unknown),Maria Adelaide Pronzato	45

About Stefania Assereto

Stefania Assereto is a scholar working on Clinical Biochemistry, Physiology and Rheumatology, having authored 24 papers that have together received 791 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (6 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Clinical Biochemistry (79 citations), Physiology (42 citations) and Cell Biology (138 citations). Stefania Assereto has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Carlo Minetti, Federico Zara, Claudio Bruno, Elisabetta Gazzerro, Roberta Biancheri, Michael P. Lisanti, Federica Sotgia, Claudio Bruno, Marina Pedemonte and Silvia Stringara. Their work appears in journals such as Nature Genetics, Nature Cell Biology and Biochemical and Biophysical Research Communications.

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.

Explore authors with similar magnitude of impact