Denise Cassandrini

2.9k total citations
62 papers, 1.3k citations indexed

About

Denise Cassandrini is a scholar working on Molecular Biology, Rheumatology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Denise Cassandrini has authored 62 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 12 papers in Rheumatology and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Denise Cassandrini's work include Metabolism and Genetic Disorders (10 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Muscle Physiology and Disorders (9 papers). Denise Cassandrini is often cited by papers focused on Metabolism and Genetic Disorders (10 papers), Glycogen Storage Diseases and Myoclonus (10 papers) and Muscle Physiology and Disorders (9 papers). Denise Cassandrini collaborates with scholars based in Italy, United States and United Kingdom. Denise Cassandrini's co-authors include Filippo M. Santorelli, Claudio Bruno, Carlo Minetti, Federico Zara, Enrico Bertini, Chiara Fiorillo, Roberta Biancheri, C. Angelini, Marina Pedemonte and Andrea Rossi and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Denise Cassandrini

61 papers receiving 1.3k citations

Peers

Countries citing papers authored by Denise Cassandrini

Since Specialization

Citations

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

Fields of papers citing papers by Denise Cassandrini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denise Cassandrini

This figure shows the co-authorship network connecting the top 25 collaborators of Denise Cassandrini. A scholar is included among the top collaborators of Denise Cassandrini 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 Denise Cassandrini. Denise Cassandrini 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	CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy 2024 ·Cells ·Diego Lopergolo, Gian Nicola Gallus, Giuseppe Pieraccini, Francesca Boscaro, Gianna Berti, (unknown), Nila Volpi, Patrizia Formichi, Silvia Bianchi, Denise Cassandrini, Vincenzo Sorrentino, Daniela Rossi, Filippo M. Santorelli, Nicola De Stefano, Alessandro Malandrini	1
2	MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form 2020 ·Molecular Genetics & Genomic Medicine ·(unknown), Serena Pagliarani, (unknown), Patrizia Ciscato, Gigliola Fagiolari, Denise Cassandrini, N. Grimoldi, Giorgio Conte, Claudia Cinnante, Filippo M. Santorelli, Giacomo P. Comi, Monica Sciacco, Lorenzo Peverelli	11
3	Protein aggregates and autophagy involvement in a family with a mutation in Z-band alternatively spliced PDZ-motif protein 2020 ·Neuromuscular Disorders ·Denise Cassandrini, Luciano Merlini, Federico Pilla, Vittoria Cenni, Spartaco Santi, (unknown), Filippo M. Santorelli, Patrizia Sabatelli	4
4	Complex multisystem phenotype associated with the mitochondrial DNA m.5522G>A mutation 2019 ·Neurological Sciences ·Claudia Nesti, Anna Rubegni, (unknown), (unknown), Denise Cassandrini, (unknown), Filippo M. Santorelli	4
5	Congenital myopathies: clinical phenotypes and new diagnostic tools 2017 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·(unknown), Denise Cassandrini, Rosanna Trovato, Anna Rubegni, (unknown), Chiara Fiorillo, (unknown), Carlo Minetti, Guja Astrea, Claudio Bruno, Filippo M. Santorelli	70
6	Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report 2016 ·BMC Medical Genetics ·Guja Astrea, Antonio Petrucci, Denise Cassandrini, Marco Savarese, Rosanna Trovato, (unknown), Anna Rubegni, Manlio Giacanelli, Roberto Massa, Vincenzo Nigro, Filippo M. Santorelli	5
7	Dolichol-phosphate mannose synthase depletion in zebrafish leads to dystrophic muscle with hypoglycosylated α-dystroglycan 2016 ·Biochemical and Biophysical Research Communications ·Maria Marchese, Andrea A. Pappalardo, (unknown), Tiziano Verri, Stefano Doccini, Denise Cassandrini, Claudio Bruno, Chiara Fiorillo, Mercedes Garcia‐Gil, Enrico Bertini, Letizia Pitto, Filippo M. Santorelli	13
8	A Diagnostic Dilemma in a Family With Cystinuria Type B Resolved by Muscle Magnetic Resonance 2015 ·Pediatric Neurology ·Guja Astrea, Iulia Munteanu, Denise Cassandrini, Suzanne Lillis, Rosanna Trovato, Elena Pegoraro, Giovanni Cioni, Eugenio Mercuri, Francesco Muntoni, Roberta Battini	4
9	Common and Novel TMEM70 Mutations in a Cohort of Italian Patients with Mitochondrial Encephalocardiomyopathy 2014 ·JIMD Reports ·Daria Diodato, Federica Invernizzi, Eleonora Lamantea, Gigliola Fagiolari, Rossella Parini, Francesca Menni, Giancarlo Parenti, Lina Bollani, Elisabetta Pasquini, Maria Alice Donati, Denise Cassandrini, Filippo M. Santorelli, Tobias B. Haack, Holger Prokisch, Daniele Ghezzi, Costanza Lamperti, Massimo Zeviani	23
10	EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement 2013 ·Journal of Neurology ·Roberta Biancheri, Denise Cassandrini, (unknown), Rosanna Trovato, Maja Di Rocco, Marisol Mirabelli-Badenier, Marina Pedemonte, Chiara Panicucci, Holger Trucks, Thomas Sander, Federico Zara, Andrea Rossi, Pasquale Striano, Carlo Minetti, Filippo M. Santorelli	19
11	Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII) 2011 ·Neuromuscular Disorders ·Olimpia Musumeci, Claudio Bruno, Tiziana Mongini, Carmelo Rodolico, M. Aguennouz, Emanuele Barca, (unknown), Denise Cassandrini, Luigi Serlenga, Giuseppe Vita, António Toscano	36
12	Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT‐II deficiency 2011 ·Clinical Genetics ·(unknown), (unknown), Denise Cassandrini, Chiara Fiorillo, Sara Scapolan, Carlo Minetti, Michela Cassanello, (unknown), Gabriele Siciliano, Adele D’Amico, Franco Lilliu, Claudio Bruno, C. Angelini	34
13	The spectrum of GNE mutations: allelic heterogeneity for a common phenotype 2010 ·Neurological Sciences ·Marina Grandis, Rossella Gulli, Denise Cassandrini, Elisabetta Gazzerro, Luana Benedetti, (unknown), Lucilla Nobbio, Claudio Bruno, Carlo Minetti, Emilia Bellone, Lizia Reni, Gianluigi Mancardi, Paola Mandich, Angelo Schenone	14
14	White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1 2009 ·Neuromuscular Disorders ·Roberta Biancheri, (unknown), Andrea Rossi, Alessandra Tessa, Denise Cassandrini, Carlo Minetti, Filippo M. Santorelli	34
15	Unusual presentation of phosphoglycerate mutase deficiency due to two different mutations in PGAM-M gene 2009 ·Neuromuscular Disorders ·Paola Tonin, Claudio Bruno, Denise Cassandrini, (unknown), Eleonora Tavazzi, Giuliano Tomelleri, G. Piccolo	14
16	Peroxisomal acyl‐CoA‐oxidase deficiency: Two new cases 2008 ·American Journal of Medical Genetics Part A ·Rosalba Carrozzo, Carlo Bellini, S. Lucioli, Federica Deodato, Denise Cassandrini, Michela Cassanello, Ubaldo Caruso, Cristiano Rizzo, Teresa Rizza, (unknown), Ronald J. A. Wanders, Cornelis Jakobs, Claudio Bruno, Filippo M. Santorelli, Carlo Dionisi‐Vici, E Bonioli	27
17	Clinical and genetic characterization of Chanarin–Dorfman syndrome 2008 ·Biochemical and Biophysical Research Communications ·Claudio Bruno, Enrico Bertini, Maja Di Rocco, Denise Cassandrini, (unknown), Teresa De Toni, Marco Seri, Marco Spada, Giovanni Li Volti, Adele D’Amico, Federica Trucco, Marcello Arca, Carlo Casali, C. Angelini, Salvatore DiMauro, Carlo Minetti	49
18	Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations 2006 ·Epilepsy & Behavior ·Pasquale Striano, Nicola Specchio, Roberta Biancheri, (unknown), Alessandro Simonati, Denise Cassandrini, Andrea Rossi, Claudio Bruno, Lucia Fusco, R. Gaggero, Federico Vigevano, Enrico Bertini, Federico Zara, Filippo M. Santorelli, Salvatore Striano	17
19	A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy 2006 ·Biochemical and Biophysical Research Communications ·Denise Cassandrini, Maria Grazia Calevo, Alessandra Tessa, Giovanni Manfredi, Fabiana Fattori, Maria Chiara Meschini, Rosalba Carrozzo, E. Tonoli, Marina Pedemonte, Carlo Minetti, Federico Zara, Filippo M. Santorelli, Claudio Bruno	30
20	Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies 2001 ·Neurogenetics ·Koen J. T. Venken, Emilio Di Maria, Emilia Bellone, (unknown), Denise Cassandrini, Paola Mandich, Peter De Jonghe, Vincent Timmerman, John Svaren	7

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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