Edoardo Malfatti

3.1k total citations
89 papers, 1.1k citations indexed

About

Edoardo Malfatti is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Edoardo Malfatti has authored 89 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 34 papers in Cardiology and Cardiovascular Medicine and 23 papers in Genetics. Recurrent topics in Edoardo Malfatti's work include Muscle Physiology and Disorders (40 papers), Cardiomyopathy and Myosin Studies (32 papers) and Neurogenetic and Muscular Disorders Research (23 papers). Edoardo Malfatti is often cited by papers focused on Muscle Physiology and Disorders (40 papers), Cardiomyopathy and Myosin Studies (32 papers) and Neurogenetic and Muscular Disorders Research (23 papers). Edoardo Malfatti collaborates with scholars based in France, Italy and United States. Edoardo Malfatti's co-authors include Norma B. Romero, Norma B. Romero, Jocelyn Laporte, Pascal Laforêt, Johann Böhm, Massimo Zeviani, Guy Brochier, Maud Beuvin, Claudio Castellan and Lucia Valente and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Circulation Research.

In The Last Decade

Edoardo Malfatti

81 papers receiving 1.1k citations

Peers

Countries citing papers authored by Edoardo Malfatti

Since Specialization

Citations

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

Fields of papers citing papers by Edoardo Malfatti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edoardo Malfatti

This figure shows the co-authorship network connecting the top 25 collaborators of Edoardo Malfatti. A scholar is included among the top collaborators of Edoardo Malfatti 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 Edoardo Malfatti. Edoardo Malfatti 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	Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy–Associated Myopathies 2025 ·Neurology ·(unknown), (unknown), Margherita Milone, Marcus Vinícius Pinto, Edoardo Malfatti, Eli Muchtar, Teerin Liewluck	0
2	Variants in CAPN3 Causing Autosomal Dominant Limb–Girdle Muscular Dystrophy Combined With Calpain‐3 Deficiency 2025 ·Human Mutation ·Thomas Krag, (unknown), Lauren Brady, (unknown), France Leturcq, Edoardo Malfatti, Morten Dunø, Mark A. Tarnopolsky, John Vissing	1
3	Interferon-γ causes myogenic cell dysfunction and senescence in immune myopathies 2025 ·Brain ·(unknown), (unknown), Marianne Gervais, Ludovic Martin, (unknown), Yasmine Baba‐Amer, (unknown), Emmanuèle Lechapt, Edoardo Malfatti, Romain K. Gherardi, Frédéric Relaix, Maximilien Bencze, François‐Jérôme Authier	2
4	Tenascin-X Deficiency Causing Classical-Like Ehlers-Danlos Syndrome Type 1 in Humans is a Significant Risk Factor of Gastrointestinal and Tracheal Ruptures 2025 ·Clinical and Translational Gastroenterology ·(unknown), (unknown), Dimitra Micha, Alessandra Maugeri, (unknown), (unknown), Dániel Keszthelyi, Edoardo Malfatti, Akiharu Kubo, Nicol C. Voermans, Serwet Demirdas	0
5	The Autophagic Activator GHF-201 Can Alleviate Pathology in a Mouse Model and in Patient Fibroblasts of Type III Glycogenosis 2024 ·Biomolecules ·(unknown), Sahar Sweetat, Saja Baraghithy, (unknown), (unknown), (unknown), Hava Glickstein, Joseph Tam, Hanna Rosenmann, Miguel Weil, Edoardo Malfatti, Or Kakhlon	1
6	An up-to-date myopathologic characterisation of facioscapulohumeral muscular dystrophy type 1 muscle biopsies shows sarcolemmal complement membrane attack complex deposits and increased skeletal muscle regeneration 2024 ·Neuromuscular Disorders ·(unknown), (unknown), (unknown), Saskia Lassche, (unknown), Valentina Taglietti, Benno Küsters, (unknown), Frédéric Relaix, Baziel G.M. van Engelen, François‐Jérôme Authier, Nicol C. Voermans, Edoardo Malfatti	1
7	Clinical and functional characterization of a long survivor congenital titinopathy patient with a novel metatranscript-only titin variant 2023 ·Acta Neuropathologica Communications ·(unknown), (unknown), (unknown), (unknown), Marcello Villanova, Corinne Métay, Chiara Fiorillo, (unknown), Luciano Merlini, Patrizia Sabatelli, Norma B. Romero, Frédéric Relaix, François‐Jérôme Authier, Valentina Taglietti, Marco Savarese, (unknown), Coen A. C. Ottenheijm, Isabelle Richard, Edoardo Malfatti	3
8	A 53‐year‐old man with a 16‐year history of asymmetrical proximal muscle weakness, facial muscle weakness, and scapular winging 2023 ·Brain Pathology ·Jantima Tanboon, Rasha El Sherif, Michio Inoue, Mariko Okubo, Edoardo Malfatti, Ichizo Nishino	1
9	Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy 2023 ·Science Translational Medicine ·Valentina Taglietti, Kaouthar Kefi, (unknown), (unknown), (unknown), Fanny Coulpier, (unknown), (unknown), (unknown), François‐Jérôme Authier, France Piétri‐Rouxel, Matthieu P. Robert, Dominique Brémond‐Gignac, Claudio Bruno, Chiara Fiorillo, Edoardo Malfatti, Peggy Lafuste, Laurent Tiret, Frédéric Relaix	25
10	Deep Characterization of a Greek Patient with Desmin-Related Myofibrillar Myopathy and Cardiomyopathy 2023 ·International Journal of Molecular Sciences ·Constantinos Papadopoulos, Edoardo Malfatti, Corinne Métay, Boris Keren, (unknown), Julien Buratti, Sophia Xirou, (unknown), George K. Papadimas	2
11	Generation of two induced pluripotent stem cell lines from a 33-year-old central core disease patient with a heterozygous dominant c.14145_14156delCTACTGGGACA (p.Asn4715_Asp4718del) deletion in the RYR1 gene 2023 ·Stem Cell Research ·K E Driver, (unknown), Carolin K. Scriba, (unknown), (unknown), Edoardo Malfatti, Norma B. Romero, Gianina Ravenscroft, Nigel G. Laing, Rhonda L. Taylor, Joshua S. Clayton	0
12	A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia—Support for the role of LAP1 in NMJ function and disease 2021 ·Neuropathology and Applied Neurobiology ·Edoardo Malfatti, (unknown), Sonia Nouioua, (unknown), Emmanuel Fournier, Robert Carlier, (unknown), Mark R. Davis, Nigel G. Laing, Damien Sternberg, Gianina Ravenscroft	6
13	Proteomic characterisation of polyglucosan bodies in skeletal muscle in RBCK1 deficiency 2021 ·Neuropathology and Applied Neurobiology ·Christer Thomsen, Edoardo Malfatti, Ana Jovanović, Mark Roberts, Ognian Kalev, Christopher Lindberg, Anders Oldfors	13
14	Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene 2021 ·Stem Cell Research ·Joshua S. Clayton, Carolin K. Scriba, Norma B. Romero, Edoardo Malfatti, (unknown), (unknown), Kristen L. Nowak, Gianina Ravenscroft, Nigel G. Laing, Rhonda L. Taylor	6
15	Un cas de myasthénie congénitale des ceintures résolu grâce à une collaboration tripartite 2021 ·médecine/sciences ·Sonia Nouioua, Edoardo Malfatti, Gianina Ravenscroft, (unknown), Meriem Tazir, Jon Andoni Urtizberea	1
16	Diagnostic des myopathies congénitales 2020 ·Journal de Pédiatrie et de Puériculture ·(unknown), Edoardo Malfatti	0
17	A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency 2020 ·Annals of Clinical and Translational Neurology ·Aurélien Perrin, Corinne Métay, Marcello Villanova, Robert‐Yves Carlier, Elena Pegoraro, Raúl Juntas‐Morales, Tanya Stojkovic, Isabelle Richard, Pascale Richard, Norma B. Romero, Henk Granzier, M. Kœnig, Edoardo Malfatti, Mireille Cossée	9
18	The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathies 2020 ·Neuromuscular Disorders ·Aurélien Perrin, Raúl Juntas‐Morales, François Rivier, Claude Cancés, Ulrike Walther‐Louvier, Charles Van Goethem, (unknown), (unknown), (unknown), (unknown), Emmanuelle Uro‐Coste, Nicolas Leboucq, Edoardo Malfatti, Constance Delaby, Sylvain Lehmann, Valérie Rigau, M. Kœnig, Mireille Cossée	14
19	An Integrated Diagnosis Strategy for Congenital Myopathies 2013 ·PLoS ONE ·Johann Böhm, Nasim Vasli, Edoardo Malfatti, Stéphanie Le Gras, Claire Feger, Bernard Jost, Nicole Monnier, Julie Brocard, Hatice Karasoy, Marion Gérard, Maggie C. Walter, Peter Reilich, Valérie Biancalana, Christine Kretz, Nadia Messaddeq, Isabelle Marty, Joël Lunardi, Norma B. Romero, Jocelyn Laporte	43
20	Juvenile-onset permanent weakness in muscle phosphofructokinase deficiency 2012 ·Journal of the Neurological Sciences ·Edoardo Malfatti, Nazha Birouk, Norma B. Romero, Monique Piraud, François Petit, Jean‐Yves Hogrel, Pascal Laforêt	11

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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