litlas
Log inCreate account

C. Angelini

Active 1972–2025

Also published as
C Angelini
151
Papers
20,156
Citations
90
h-index
150
i10-index

Citations

Citations per year for C. Angelini1973: 1 citations1974: 2 citations1975: 3 citations1976: 4 citations1977: 4 citations1978: 2 citations1979: 3 citations1980: 7 citations1981: 4 citations1982: 7 citations1983: 11 citations1984: 7 citations1985: 6 citations1986: 2 citations1987: 12 citations1988: 8 citations1989: 9 citations1990: 16 citations1991: 16 citations1992: 22 citations1993: 47 citations1994: 41 citations1995: 53 citations1996: 83 citations1997: 87 citations1998: 72 citations1999: 105 citations2000: 120 citations2001: 84 citations2002: 79 citations2003: 72 citations2004: 90 citations2005: 95 citations2006: 127 citations2007: 114 citations2008: 126 citations2009: 125 citations2010: 156 citations2011: 150 citations2012: 121 citations2013: 130 citations2014: 154 citations2015: 141 citations2016: 158 citations2017: 102 citations2018: 106 citations2019: 469 citations2020: 596 citations2021: 508 citations2022: 339 citations2023: 256 citations2024: 390 citations2025: 128 citations2026: 2 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,815 citing papers, 25.9% of this breakdownItaly: 767 citing papers, 10.9% of this breakdownUnited Kingdom: 688 citing papers, 9.8% of this breakdownFrance: 383 citing papers, 5.5% of this breakdownGermany: 334 citing papers, 4.8% of this breakdownCanada: 315 citing papers, 4.5% of this breakdownChina: 268 citing papers, 3.8% of this breakdownNetherlands: 249 citing papers, 3.5% of this breakdownJapan: 232 citing papers, 3.3% of this breakdownSpain: 230 citing papers, 3.3% of this breakdownAustralia: 189 citing papers, 2.7% of this breakdownSwitzerland: 105 citing papers, 1.5% of this breakdown
0%25.9%Other 20.5%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology62.4%
  • Medicine27.8%
  • Neuroscience6.9%
  • Agricultural and Biological Sciences0.4%
  • Environmental Science0.4%
  • Nursing0.4%
  • Other1.7%

Topics

  • Muscle Physiology and Disorders12.2%
  • Mitochondrial Function and Pathology8.2%
  • Genetic Neurodegenerative Diseases5.2%
  • Neurogenetic and Muscular Disorders Research4.8%
  • Cardiomyopathy and Myosin Studies4.3%
  • Metabolism and Genetic Disorders3.7%
  • Other61.6%

Coauthors

All papers

Open in search
  1. Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells

    Authors: Marco Spinazzi, Alberto Casarin, Vanessa Pertegato, Leonardo Salviati, C. Angelini - Nature Protocols 2012 cited by 1,006

  2. Regulation of ER-mitochondria contacts by Parkin via Mfn2

    Authors: Valentina Basso, Elena Marchesan, Caterina Peggion, Joy Chakraborty, Sophia von Stockum, Marta Giacomello, Denis Ottolini, Valentina Debattisti, Federico Caicci, Elisabetta Tasca, Valentina Pegoraro, C. Angelini, Angelo Antonini, Alessandro Bertoli, Marisa Brini, Elena Ziviani - Pharmacological Research 2018 cited by 211

  3. 229th ENMC international workshop: Limb girdle muscular dystrophies – Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017

    Authors: Volker Straub, Alexander P. Murphy, Bjarne Udd, C. Angelini, Ségolène Aymé, Carsten Bönneman, Marianne de Visser, Ada Hamosh, Laura Jacobs, Nina Khizanishvili, Madelon Kroneman, Pascal Laflorêt, A. St. J. Murphy, Vincenzo Nigro, Laura Rufibach, Anna Sárközy, Shaun Swanepoel, Ivan Torrente, Bjarne Udd, Andoni Urtizberea, John Vissing, Maggie C. Walter - Neuromuscular Disorders 2018 cited by 384

  4. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

    Authors: Jing Liu, Masashi Aoki, Isabel Illa, Chenyan Wu, Michel Fardeau, C. Angelini, Carmen Serrano, J. Andoni Urtizberea, Fayçal Hentati, Mongi Ben Hamida, Saeed Bohlega, Edward J. Culper, Anthony A. Amato, Karen Bossie, Joshua Oeltjen, Khemissa Bejaoui, Diane McKenna‐Yasek, Betsy A. Hosler, Erwin Schurr, Kiichi Arahata, Pieter J. de Jong, Robert H. Brown - Nature Genetics 1998 cited by 919

  5. Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis

    Authors: Aaron P. Russell, Shogo Wada, Lodovica Vergani, M. Benjamin Hock, Séverine Lamon, Bertrand Léger, Takashi Ushida, Romain Cartoni, Glenn D. Wadley, Peter Hespel, Anastasia Kralli, Gianni Sorarú, C. Angelini, Takayuki Akimoto - Neurobiology of Disease 2012 cited by 221

  6. Redefining phenotypes associated with mitochondrial DNA single deletion

    Authors: Michelangelo Mancuso, Daniele Orsucci, C. Angelini, Enrico Bertini, Valério Carelli, Giacomo P. Comi, Maria Alice Donati, Antonio Federico, Carlo Minetti, Maurizio Moggio, Tiziana Mongini, Filippo M. Santorelli, Serenella Servidei, Paola Tonin, António Toscano, Claudio Bruno, Luca Bello, Elena Caldarazzo Ienco, Elena Cardaioli, Michela Catteruccia, Paola Da Pozzo, Massimiliano Filosto, Costanza Lamperti, Isabella Moroni, Olimpia Musumeci, Elena Pegoraro, Dario Ronchi, Donato Sauchelli, Mauro Scarpelli, Monica Sciacco, Maria Lucia Valentino, Liliana Vercelli, Massimo Zeviani, Gabriele Siciliano - Journal of Neurology 2015 cited by 106

  7. Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample

    Authors: ML Mostacciuolo, Ebe Pastorello, Giovanni Vazza, Marta Miorin, C. Angelini, Giuliano Tomelleri, Giuliana Galluzzi, CP Trevisan - Clinical Genetics 2009 cited by 167

  8. European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience

    Authors: Ans T. van der Ploeg, Michelle E. Kruijshaar, António Toscano, Pascal Laforêt, C. Angelini, Robin Lachmann, Samuel Ignacio Pascual Pascual, Mark Roberts, Kai M. Rösler, Thomas M. Stulnig, Pieter A. van Doorn, Peter Van den Bergh, John Vissing, Benedikt Schoser - European Journal of Neurology 2017 cited by 173

  9. A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

    Authors: Costanza Lamperti, Greta Fabbri, Liliana Vercelli, Roberto D’Amico, Roberto Frusciante, E. Bonifazi, Chiara Fiorillo, C. Borsato, Michelangelo Cao, Maura Servida, Francesca Gabriella Greco, Rita Di Leo, L. Volpi, Claudia Manzoli, Paola Cudia, Ebe Pastorello, Leopoldo Ricciardi, Gabriele Siciliano, Giuliana Galluzzi, Carmelo Rodolico, Lucio Santoro, Giuliano Tomelleri, C. Angelini, Enzo Ricci, L. Palmucci, Maurizio Moggio, Rossella Tupler - Muscle & Nerve 2010 cited by 157

  10. A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes

    Authors: Giulia Ricci, Lucia Ruggiero, Liliana Vercelli, Francesco Sera, Ana Nikolić, Monica Govi, Fabiano Mele, Jessica Daolio, C. Angelini, Giovanni Antonini, Angela Berardinelli, Elisabetta Bucci, Michelangelo Cao, Maria Chiara D’Amico, Maria Grazia D’Angelo, Antonio Di Muzio, Massimiliano Filosto, Lorenzo Maggi, Maurizio Moggio, Tiziana Mongini, Lucía Morandi, Elena Pegoraro, Carmelo Rodolico, Lucio Santoro, Gabriele Siciliano, Giuliano Tomelleri, Luísa Villa, Rossella Tupler - Journal of Neurology 2016 cited by 99

  11. Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb–MyoD pathways in muscle regeneration

    Authors: Marina Bakay, Zuyi Wang, Gisela Melcon, Louis Schiltz, Jianhua Xuan, Po Zhao, Vittorio Sartorelli, Jinwook Seo, Elena Pegoraro, C. Angelini, Ben Shneiderman, Diana M. Escolar, Yi-Wen Chen, Sara T. Winokur, Lauren M. Pachman, Chenguang Fan, Raúl N. Mandler, Yoram Nevo, Erynn S. Gordon, Yitan Zhu, Yibin Dong, Yue Wang, Eric P. Hoffman - Brain 2006 cited by 328

  12. Reliability of the North Star Ambulatory Assessment in a multicentric setting

    Authors: Elena Mazzone, Sonia Messina, Gessica Vasco, Marion Main, Michelle Eagle, Adele D’Amico, Luca Doglio, Luisa Politano, Filippo Cavallaro, Silvia Frosini, Luca Bello, Francesca Magri, Alice Corlatti, E. Zucchini, B. Brancalion, Francesca Rossi, M. Ferretti, M.G. Motta, M.R. Cecio, Angela Berardinelli, Paolo Alfieri, Tiziana Mongini, Antonella Pini, Guja Astrea, Roberta Battini, Giacomo P. Comi, Elena Pegoraro, Lucía Morandi, Marika Pane, C. Angelini, Claudio Bruno, Marcello Villanova, Giuseppe Vita, Maria Alice Donati, Enrico Bertini, Eugenio Mercuri - Neuromuscular Disorders 2009 cited by 229

  13. SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

    Authors: Elena Pegoraro, Eric P. Hoffman, Luisa Piva, Bruno F. Gavassini, Stefano Cagnin, Mario Ermani, Luca Bello, Gianni Sorarú, Beniamina Pacchioni, Marco Domenico Bonifati, G. Lanfranchi, C. Angelini, Akanchha Kesari, I. Lee, Heather Gordish‐Dressman, Joseph M. Devaney, Craig M. McDonald - Neurology 2010 cited by 217

  14. Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

    Authors: Giulia Ricci, Isabella Scionti, Francesco Sera, Monica Govi, Roberto D’Amico, Ilaria Frambolli, Fabiano Mele, Massimiliano Filosto, Liliana Vercelli, Lucia Ruggiero, Angela Berardinelli, C. Angelini, Giovanni Antonini, Elisabetta Bucci, Michelangelo Cao, Jessica Daolio, Antonio Di Muzio, Rita Di Leo, Giuliana Galluzzi, Elisabetta Iannaccone, Lorenzo Maggi, Valerio Maruotti, Maurizio Moggio, Tiziana Mongini, Lucía Morandi, Ana Nikolić, Ebe Pastorello, Enzo Ricci, Carmelo Rodolico, Lucio Santoro, Maura Servida, Gabriele Siciliano, Giuliano Tomelleri, Rossella Tupler - Brain 2013 cited by 126

  15. Circulating microRNAs as biomarkers of muscle differentiation and atrophy in ALS

    Authors: Elisabetta Tasca, Valentina Pegoraro, Antonio Merico, C. Angelini - Clinical Neuropathology 2015 cited by 81

  16. Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy

    Authors: Lucia Ruggiero, Fabiano Mele, Fiore Manganelli, Dario Bruzzese, Giulia Ricci, Liliana Vercelli, Monica Govi, Antonio Vallarola, Silvia Tripodi, Luísa Villa, Antonio Di Muzio, Marina Scarlato, Elisabetta Bucci, Giovanni Antonini, Lorenzo Maggi, Carmelo Rodolico, Giuliano Tomelleri, Massimiliano Filosto, Stefano C. Previtali, C. Angelini, Angela Berardinelli, Elena Pegoraro, Maurizio Moggio, Tiziana Mongini, Gabriele Siciliano, Lucio Santoro, Rossella Tupler - JAMA Network Open 2020 cited by 62

  17. LGMD. Identification, description and classification.

    Authors: C. Angelini - 2020 cited by 55

  18. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

    Authors: Judith Melki, Sonia Abdelhak, P. Sheth, M.F. Bachelot, P Burlet, Alun Marcadet, Jean Aicardi, A Barois, Jessica Carrière, Michel Fardeau, D Fontan, G Ponsot, T. Billette, C. Angelini, C. Barbosa, G. Ferrière, G. Lanzi, Alun Ottolini, Marie‐Claude Babron, Daniel Cohen, A. Hanauer, Françoise Clerget‐Darpoux, Mark Lathrop, Alun Munnich, J Frézal - Nature 1990 cited by 399

  19. Improved diagnosis of Becker muscular dystrophy by dystrophin testing

    Authors: Eric P. Hoffman, Louis M. Kunkel, C. Angelini, Angus Clarke, Mark Johnson, J.B. Harris - Neurology 1989 cited by 292

  20. Interpreting Genetic Variants in Titin in Patients With Muscle Disorders

    Authors: Marco Savarese, Lorenzo Maggi, Anna Vihola, Per Harald Jonson, Giorgio Tasca, Lucia Ruggiero, Luca Bello, Francesca Magri, Teresa Giugliano, Annalaura Torella, Anni Evilä, Giuseppina Di Fruscio, Olivier Vanakker, Sara Gibertini, Liliana Vercelli, Alessandra Ruggieri, Carlo Antozzi, H. Luque, Sandra Janssens, Maria Barbara Pasanisi, Chiara Fiorillo, Monika Raimondi, Manuela Ergoli, Luisa Politano, Claudio Bruno, Anna Rubegni, Marika Pane, Filippo M. Santorelli, Carlo Minetti, C. Angelini, Jan De Bleecker, Maurizio Moggio, Tiziana Mongini, Giacomo P. Comi, Lucio Santoro, Eugenio Mercuri, Elena Pegoraro, Marina Mora, Peter Hackman, Bjarne Udd, Vincenzo Nigro - JAMA Neurology 2018 cited by 93

  21. Autophagy dysregulation in Danon disease

    Authors: Anna Chiara Nascimbeni, Marina Fanin, C. Angelini, Marco Sandri - Cell Death and Disease 2017 cited by 78

  22. Advances in Dystrophinopathy Diagnosis and Therapy

    Authors: Fawzy A. Saad, Gabriele Siciliano, C. Angelini - Biomolecules 2023 cited by 26

  23. Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

    Authors: Alan H. Beggs, Eric P. Hoffman, J R Snyder, Kiichi Arahata, L. Specht, Frederic Shapiro, C. Angelini, Hideo Sugita, Louis M. Kunkel - 1991 cited by 401

  24. Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition

    Authors: Leonardo Salviati, Sabrina Sacconi, Luisa Murer, G Zacchello, Lorenzo Franceschini, Anna Maria Laverda, Giuseppe Basso, Catarina M. Quinzii, C. Angelini, Michio Hirano, Ali Naini, Plácido Navas, S. DiMauro, Giovanni Montini - Neurology 2005 cited by 192