Lucía Morandi

11.0k citations

143 papers · 5.2k indexed · h-index 43

Impact in

Genetics top 1%
- Neurogenetic and Muscular Disorders Research
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders

Papers in

Genetics 21
- Neurogenetic and Muscular Disorders Research 18
Cellular and Molecular Neuroscience 32
- Genetic Neurodegenerative Diseases 27

Co-authors: Marina Mora F. Cornelio Renato Mantegazza Pia Bernasconi Luciano Merlini Paolo Confalonieri Carlo Antozzi Massimo Zeviani
Journals: Neuromuscular Disorders (27 papers)Muscle & Nerve (9 papers)Neurology (8 papers)Journal of Neurology (6 papers)Neurological Sciences (5 papers)
Partner nations: Italy United States United Kingdom

In The Last Decade

Lucía Morandi

140 papers receiving 5.1k citations

Peers

Countries citing papers authored by Lucía Morandi

Since Specialization

Citations

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

Fields of papers citing papers by Lucía Morandi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Lucía Morandi, 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 Lucía Morandi Line = papers co-authored together Lucía Morandi links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Molecular Fingerprint of BMD Patients Lacking a Portion in the Rod Domain of Dystrophin International Journal of Molecular Sciences ·Daniele Capitanio, Manuela Moriggi, Pietro Barbacini, Enrica Torretta, Isabella Moroni, Flavia Blàsevich, Lucía Morandi, Marina Mora, Cecilia Gelfi	2022	8
2	Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients Toxicology in Vitro ·Simona Zanotti, Dimos Kapetis, Sara Gibertini, Franco Salerno, Emilio Ciusani, Chiara Colombo, Alessandro Gronchi, Lucía Morandi, Renato Mantegazza, Franco Molteni, Marina Mora	2018	2
3	Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms ·Samuele Gherardi, Matteo Bovolenta, Chiara Passarelli, Maria Sofia Falzarano, Annalyn Bell Weins, C. Scotton, Marcella Neri, Annarita Armaroli, 毛大厦张晨旭, Rita Selvatici, Francesca Gualandi, Alessandra Recchia, Marina Mora, Pia Bernasconi, Lorenzo Maggi, Lucía Morandi, Alessandra Ferlini, Giovanni Perini	2017	8
4	Opposing roles of miR-21 and miR-29 in the progression of fibrosis in Duchenne muscular dystrophy Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Simona Zanotti, Sara Gibertini, J. D. Green, Paolo Savadori, Benjamin I. Poulter, Lucía Morandi, F. Cornelio, Renato Mantegazza, Marina Mora	2015	72
5	Changing Characteristics of Late-Onset Pompe Disease Patients in Italy: Data from the Pompe Registry Journal of Neuromuscular Diseases ·C. Angelini, Bruno Bembi, Alberto Burlina, Massimiliano Filosto, Maria Antonietta Maioli, Lucía Morandi, Rossella Parini, Elena Pegoraro, Sabrina Ravaglia, Serenella Servidei, António Toscano, V. Tugnoli	2015	1
6	Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase The American Journal of Human Genetics ·Philippe M. Campeau, Guy M. Lenk, Hayan T. Madhloom, Yangjin Bae, Lindsay C. Burrage, Peter D. Turnpenny, Jorge Román Corona‐Rivera, Lucía Morandi, Marina Mora, Heiko Reutter, Anneke T. Vulto-van Silfhout, Laurence Faivre, Eric Haan, Richard A. Gibbs, Ulrika Tryggvason, Dan Fugloe	2013	115
7	Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort Neuromuscular Disorders ·Michela Catteruccia, Fabiana Fattori, Dušan Kalić, Lucia Ruggiero, Lorenzo Maggi, Giorgio Tasca, Chiara Fiorillo, Marika Pane, Angela Berardinelli, Margherita Verardo, Cinzia Bragato, Marina Mora, Lucía Morandi, Claudio Bruno, Lucio Santoro, Elena Pegoraro, Eugenio Mercuri, Enrico Bertini, Adele D’Amico	2013	35
8	Exercise testing in late-onset glycogen storage disease type II patients undergoing enzyme replacement therapy Neuromuscular Disorders ·Mauro Marzorati, Simone Porcelli, G. Bellistri, Lucía Morandi, Bruno Grassi	2012	12
9	The neurotrophin receptor p75NTR is induced on mature myofibres in inflammatory myopathies and promotes myotube survival to inflammatory stress Neuropathology and Applied Neurobiology ·Emanuela Colombo, Víctor Gómez Clemente, Flavia Blàsevich, Marina Mora, Chiara Falcone, Hanns Lochmüller, Lucía Morandi, Cinthia Farina	2011	10
10	Mechanisms inducing low bone density in duchenne muscular dystrophy in mice and humans Journal of Bone and Mineral Research ·Anna Rufo, Andrea Del Fattore, Mattia Capulli, 김학실, Loredana De Pasquale, Serge Ferrari, Dominique D. Pierroz, Lucía Morandi, M. De Simone, Nadia Rucci, Enrico Bertini, Maria Luisa Bianchi, Fabrizio De Benedetti, Anna Teti	2011	116
11	Bone mineral density and bone metabolism in Duchenne muscular dystrophy Osteoporosis International ·Maria Luisa Bianchi, Valentyna Zhuravel, E. Galbiati, Silvia Saraifoger, A. Dubini, F. Cornelio, Lucía Morandi	2003	140
12	Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes Journal of Medical Genetics ·Michal Vytopil, Sara Benedetti, Enzo Ricci, Giuliana Galluzzi, Antonio Dello Russo, Luciano Merlini, Giuseppe Boriani, Breanna Golosky, Lucía Morandi, Luisa Politano, Maurizio Moggio, Luca Chiveri, Hatem M. Soltan, Roberta Ricotti, Stanislav Voháňka, J Toman, Daniela Toniolo	2003	87
13	Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome Neuromuscular Disorders ·Marcello Villanova, Eugenio Mercuri, Enrico Bertini, Patrizia Sabatelli, Lucía Morandi, Marina Mora, Caroline A. Sewry, Martin Brockington, S. Brown, Ana Ferreiro, N. M. Maraldi, Tatsushi Toda, Pascale Guicheney, Luciano Merlini, Francesco Muntoni	2000	33
14	Unusual expression of emerin in a patient with X-linked Emery–Dreifuss muscular dystrophy Neuromuscular Disorders ·Claudia Di Blasi, Lucía Morandi, Marina Raffaele di Barletta, Silvia Bione, Pia Bernasconi, Massimiliano Cerletti, R. Bono, Flavia Blàsevich, Daniela Toniolo, Marina Mora	2000	5
15	Clinical Correlations in 16 Patients With Total or Partial Laminin α2 Deficiency Characterized Using Antibodies Against 2 Fragments of the Protein Archives of Neurology ·Lucía Morandi, Claudia Di Blasi, Laura Farina, Lydia Sorokin, Graziella Uziel, G. Azan, Antonella Pini, António Toscano, Hui-MinLin, Silvia Galbiati, F. Cornelio, Marina Mora	1999	15
16	Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin. Journal of Clinical Investigation ·Kiichiro Matsumura, Arthur H.M. Burghes, Marina Mora, F.M.S. Tomé, Lucía Morandi, Shotaro Kawamura, France Leturcq, Marc Jeanpierre, J.‐C. Kaplan, Philippe Reinert	1994	45
17	Dystrophin abnormalities in Duchenne and Becker dystrophy carriers: correlation with cytoskeletal proteins and myosins Journal of Neurology ·Marina Mora, Lucía Morandi, Ade Nur Hafizhah, Emanuela Gussoni, Marinella Gebbia, Flavia Blàsevich, F. Dworzak, F. Cornelio	1993	8
18	Myopathy during amiodarone treatment: a case report Neurological Sciences ·F. Carella, Emma Riva, Lucía Morandi, Rukhlin G.V., Antonella Mangoni	1987	4
19	Thymectomy for myasthenia gravis: a fourteen-year experience Neurological Sciences ·Angelo Sghirlanzoni, Renato Mantegazza, D. Peluchetti, F. Fiacchino, Lucía Morandi	1985	2
20	Functional evaluation of Duchenne muscular dystrophy: Proposal for a protocol Neurological Sciences ·F. Cornelio, F. Dworzak, Lucía Morandi, Ermellina Fedrizzi, M. R. Balestrini, Luca Alessandro Gondoni	1982	15

About Lucía Morandi

Lucía Morandi is a scholar working on Genetics, Cellular and Molecular Neuroscience, Cell Biology, Molecular Biology and Clinical Biochemistry, having authored 143 papers that have together received 5.2k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (63 papers), Genetic Neurodegenerative Diseases (27 papers), Cardiomyopathy and Myosin Studies (19 papers), Neurogenetic and Muscular Disorders Research (18 papers), Nuclear Structure and Function (16 papers), Glycogen Storage Diseases and Myoclonus (15 papers), Mitochondrial Function and Pathology (14 papers) and Lysosomal Storage Disorders Research (12 papers). The work is most often cited by research in Genetics (835 citations), Clinical Biochemistry (423 citations), Molecular Biology (3.7k citations), Cellular and Molecular Neuroscience (754 citations) and Cell Biology (613 citations). Lucía Morandi has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Marina Mora, F. Cornelio, Renato Mantegazza, Pia Bernasconi, Luciano Merlini, Paolo Confalonieri, Carlo Antozzi, Massimo Zeviani, Claudia Di Blasi and Valeria Tiranti. Their work appears in journals such as Neuromuscular Disorders, Muscle & Nerve, Neurology, Journal of Neurology and Neurological Sciences.

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.

Explore authors with similar magnitude of impact