M.P. Freda

860 citations

11 papers · 616 indexed · h-index 10

Impact in

Cardiology and Cardiovascular Medicine top 10%
- Cardiomyopathy and Myosin Studies
Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases

Papers in ⓘ

Molecular Biology 11
- Muscle Physiology and Disorders 10
- Mitochondrial Function and Pathology 2
- Ion channel regulation and function 1
Cellular and Molecular Neuroscience 9
- Genetic Neurodegenerative Diseases 9

Co-authors: C. Angelini (10 shared papers)Eric P. Hoffman (4 shared papers)David Duggan (4 shared papers)Flávia Martinello (4 shared papers)Paola Melacini (3 shared papers)Sergio Dalla Volta (2 shared papers)Marta Miorin (3 shared papers)Elena Pegoraro (3 shared papers)
Journals: Muscle & Nerve (3 papers)Neuromuscular Disorders (2 papers)Brain (1 paper)Neurology (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: Italy United States Netherlands

In The Last Decade

M.P. Freda

11 papers receiving 600 citations

Peers

Countries citing papers authored by M.P. Freda

Since Specialization

Citations

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

Fields of papers citing papers by M.P. Freda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.P. Freda. 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 M.P. Freda. The network helps show where M.P. Freda may publish in the future.

Co-authors

The 25 scholars most cited alongside M.P. Freda, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M.P. Freda Line = papers co-authored together M.P. Freda links everyone, so they are left out of the graph.

All Works

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11 of 11 papers shown

#	Work
1	Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy Circulation ·Paola Melacini, (unknown), G Danieli, C Villanova, Flávia Martinello, Marta Miorin, M.P. Freda, Manuela Miorelli, M.L. Mostacciuolo, G Fasoli, C. Angelini, Sergio Dalla Volta	1996	139
2	Heart involvement in muscular dystrophies due to sarcoglycan gene mutations Muscle & Nerve ·Paola Melacini, (unknown), David Duggan, M.P. Freda, Angela Berardinelli, G. A. Danieli, Agata Barchitta, Eric P. Hoffman, Sergio Dalla Volta, C. Angelini	1999	94
3	Riboflavin therapy Brain ·Lodovica Vergani, Maria Barile, C. Angelini, Alberto Burlina, Leo Nijtmans, M.P. Freda, Carmen Brizio, Elisabetta Zerbetto, Federica Dabbeni‐Sala	1999	69
4	The clinical spectrum of sarcoglycanopathies Neurology ·C. Angelini, (unknown), M.P. Freda, David Duggan, Gabriele Siciliano, Eric P. Hoffman	1999	67
5	Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations. Journal of Medical Genetics ·(unknown), David Duggan, Maria Luisa Mostacciuolo, Flávia Martinello, M.P. Freda, Gianni Sorarú, Carlo P. Trevisan, Eric P. Hoffman, C. Angelini	1997	66
6	Homozygous ?-sarcoglycan mutation in two siblings: One asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient Muscle & Nerve ·C. Angelini, Francesco Mari, E. Menegazzo, M.P. Freda, David Duggan, Eric P. Hoffman	1998	51
7	Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: Characterization of sub-clinical phenotypes Neuromuscular Disorders ·C. Angelini, (unknown), Elena Pegoraro, M.P. Freda, Morena Cadaldini, Flávia Martinello	1994	40
8	Prognostic factors in mild dystrophinopathies Journal of the Neurological Sciences ·C. Angelini, (unknown), M.P. Freda, Flávia Martinello, Marta Miorin, Paola Melacini, Gabriele Siciliano, Elena Pegoraro, M Rosa, G. A. Danieli	1996	38
9	Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: Threshold effect for deletion size? Muscle & Nerve ·Francesco Mari, M.P. Freda, Libero Vitiello, Gian Antonio Danieli, Elena Pegoraro, C. Angelini	1996	36
10	Prevalent cardiac involvement in dystrophin Becker type mutation Neuromuscular Disorders ·Gabriele Siciliano, (unknown), C. Angelini, Le Pollina, Marta Miorin, Fawzy A. Saad, M.P. Freda, A Muratorio	1994	12
11	Ataxia and Congenital Muscular Dystrophy: the follow-up of a new specific phenotype Brain and Development ·Carlo P. Trevisan, Ebe Pastorello, Simone Tonello, Mario Armani, Maria Teresa Rigoni, A Tormene, M.P. Freda, M. Zortea, Stefania Lombardi	2001	4

About M.P. Freda

M.P. Freda is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Physiology and Surgery, having authored 11 papers that have together received 616 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Genetic Neurodegenerative Diseases (9 papers), Cardiomyopathy and Myosin Studies (3 papers), Mitochondrial Function and Pathology (2 papers), Metabolism and Genetic Disorders (1 paper), Ion channel regulation and function (1 paper), Muscle metabolism and nutrition (1 paper) and Neurogenetic and Muscular Disorders Research (1 paper). The work is most often cited by research in Cardiology and Cardiovascular Medicine (280 citations), Cellular and Molecular Neuroscience (157 citations), Genetics (87 citations), Molecular Biology (559 citations) and Clinical Biochemistry (48 citations). M.P. Freda has collaborated with scholars based in Italy, United States and Netherlands. Frequent co-authors include C. Angelini, Eric P. Hoffman, David Duggan, Flávia Martinello, Paola Melacini, Sergio Dalla Volta, Marta Miorin, Elena Pegoraro, Gabriele Siciliano and Francesco Mari. Their work appears in journals such as Muscle & Nerve, Neuromuscular Disorders, Brain, Neurology and Journal of Medical Genetics.

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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