Marco Savarese

3.2k total citations
72 papers, 1.3k citations indexed

About

Marco Savarese is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Marco Savarese has authored 72 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 39 papers in Cardiology and Cardiovascular Medicine and 22 papers in Genetics. Recurrent topics in Marco Savarese's work include Muscle Physiology and Disorders (39 papers), Cardiomyopathy and Myosin Studies (36 papers) and Neurogenetic and Muscular Disorders Research (17 papers). Marco Savarese is often cited by papers focused on Muscle Physiology and Disorders (39 papers), Cardiomyopathy and Myosin Studies (36 papers) and Neurogenetic and Muscular Disorders Research (17 papers). Marco Savarese collaborates with scholars based in Finland, Italy and France. Marco Savarese's co-authors include Vincenzo Nigro, Bjarne Udd, Peter Hackman, Anna Vihola, J. Sarparanta, Annalaura Torella, Giuseppina Di Fruscio, Per Harald Jonson, Margherita Mutarelli and Arcomaria Garofalo and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Neurology.

In The Last Decade

Marco Savarese

68 papers receiving 1.2k citations

Peers

Countries citing papers authored by Marco Savarese

Since Specialization

Citations

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

Fields of papers citing papers by Marco Savarese

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Savarese

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Savarese. A scholar is included among the top collaborators of Marco Savarese 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 Marco Savarese. Marco Savarese 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	Gene prioritisation for enhancing molecular diagnosis in rare skeletal muscle disease cohort 2025 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Ivana Babič Božović, Annalaura Torella, Mridul Johari, Aleš Maver, Katarina Pelin, Filippo M. Santorelli, Vincenzo Nigro, Peter Hackman, (unknown), Bjarne Udd, Marco Savarese	1
2	Myotilin gene duplication causing late‐onset myotilinopathy 2025 ·European Journal of Neurology ·Marco Spinazzi, Marco Savarese, Franck Letournel, (unknown), Florence Manero, (unknown), (unknown), Corinne Métay, (unknown), Bjarne Udd	1
3	Different Lower Limb Muscle MRI Patterns in Autosomal Dominant Titinopathies 2025 ·European Journal of Neurology ·David Gómez‐Andrés, (unknown), Jordi Díaz‐Manera, Katrin Õunap, (unknown), (unknown), Marco Savarese, Francina Munell, Bjarne Udd	0
4	Protein‐extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregation 2024 ·Annals of Clinical and Translational Neurology ·(unknown), Kevin J. Felice, Per Harald Jonson, J. Sarparanta, (unknown), Inès Harzallah, Renaud Touraine, Lynn Pais, Christina Austin‐Tse, Vijay Ganesh, (unknown), Heidi L. Rehm, Michael K. Hehir, S. H. Subramony, Qian Wu, Bjarne Udd, Marco Savarese	1
5	A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family 2024 ·Neurology Genetics ·Kristl G. Claeys, Marco Savarese, Per Harald Jonson, (unknown), Ana Töpf, Anna Vihola, Volker Straub, Bjarne Udd	0
6	Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions 2024 ·Communications Biology ·Huahua Zhong, (unknown), Mridul Johari, Shintaro Katayama, Ali Oghabian, Per Harald Jonson, Peter Hackman, Marco Savarese, Bjarne Udd	2
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	The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum 2023 ·Journal of Medical Genetics ·(unknown), (unknown), Manu Jokela, Meriel McEntagart, Tessa Homfray, Elisa Giorgio, (unknown), Alfredo Brusco, Maria Iascone, Luigina Spaccini, (unknown), Marco Savarese, Bjarne Udd	8
9	Long‐term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophy 2023 ·European Journal of Neurology ·(unknown), Marco Savarese, Niina Sandholm, Peter Hackman, Bjarne Udd	2
10	Differential effects of mutations of POPDC proteins on heteromeric interaction and membrane trafficking 2023 ·Acta Neuropathologica Communications ·(unknown), (unknown), Marco Savarese, (unknown), Susanne Rinné, (unknown), Anne Schänzer, Andreas Hahn, Mario Sabatelli, Francesco Perna, Kathryn Chapman, Mark Pfuhl, Alan C. Spivey, Niels Decher, Bjarne Udd, Giorgio Tasca, Thomas Brand	4
11	Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function 2022 ·International Journal of Molecular Sciences ·(unknown), Marco Savarese, Esther Picillo, Luigia Passamano, Vincenzo Nigro, Luisa Politano	6
12	Comprehensive transcriptomic analysis shows disturbed calcium homeostasis and deregulation of T lymphocyte apoptosis in inclusion body myositis 2022 ·Journal of Neurology ·Mridul Johari, Anna Vihola, Johanna Palmio, Manu Jokela, Per Harald Jonson, J. Sarparanta, Sanna Huovinen, Marco Savarese, Peter Hackman, Bjarne Udd	14
13	Mutation update for the ACTN2 gene 2022 ·Human Mutation ·(unknown), Montse Olivé, (unknown), (unknown), Cristina Domínguez‐González, Mridul Johari, Annalaura Torella, Johann Böhm, (unknown), Vincenzo Nigro, Peter Hackman, Jocelyn Laporte, Bjarne Udd, Marco Savarese	15
14	Adult‐onset dominant muscular dystrophy in Greek families caused by Annexin A11 2022 ·Annals of Clinical and Translational Neurology ·Mridul Johari, George K. Papadimas, Constantinos Papadopoulos, Sophia Xirou, (unknown), (unknown), (unknown), Marco Savarese, Peter Hackman, Bjarne Udd	12
15	Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness 2021 ·Neurology Genetics ·Marco Savarese, Anna Vihola, Manu Jokela, Sanna Huovinen, Simonetta Gerevini, Annalaura Torella, Mridul Johari, Marina Scarlato, Per Harald Jonson, (unknown), Peter Hackman, Mathias Gautel, Vincenzo Nigro, Stefano C. Previtali, Bjarne Udd	7
16	An unusual ryanodine receptor 1 (RYR1) phenotype 2019 ·Neurology ·Manu Jokela, Giorgio Tasca, Anna Vihola, Eugenio Mercuri, Per Harald Jonson, Sara Lehtinen, (unknown), Marika Pane, Maria Alice Donati, Mridul Johari, Marco Savarese, Sanna Huovinen, Pirjo Isohanni, Johanna Palmio, Päivi Hartikainen, Bjarne Udd	12
17	Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations 2019 ·Annals of Neurology ·Marco Savarese, Johanna Palmio, Juan José Poza, Jan Weinberg, Montse Olivé, Ana María Cobo, Anna Vihola, Per Harald Jonson, J. Sarparanta, F. García-Bragado, Jon Andoni Urtizberea, Peter Hackman, Bjarne Udd	26
18	The complexity of titin splicing pattern in human adult skeletal muscles 2018 ·Skeletal Muscle ·Marco Savarese, Per Harald Jonson, Sanna Huovinen, Lars Paulín, Petri Auvinen, Bjarne Udd, Peter Hackman	46
19	Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report 2018 ·Neuromuscular Disorders ·Simona Fecarotta, Vincenza Gragnaniello, Roberto Della Casa, Alessandro Romano, (unknown), Annalaura Torella, Marco Savarese, Vincenzo Nigro, Pietro Strisciuglio, Generoso Andria, Giancarlo Parenti	4
20	Association study reveals novel risk loci for sporadic inclusion body myositis 2017 ·European Journal of Neurology ·Mridul Johari, Meharji Arumilli, Johanna Palmio, Marco Savarese, Giorgio Tasca, Massimiliano Mirabella, Niina Sandholm, Hannes Lohi, Peter Hackman, Bjarne Udd	9

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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