Marina Mora

11.5k total citations · 2 hit papers
159 papers, 6.7k citations indexed

About

Marina Mora is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marina Mora has authored 159 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Molecular Biology, 36 papers in Cell Biology and 28 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marina Mora's work include Muscle Physiology and Disorders (83 papers), Cardiomyopathy and Myosin Studies (20 papers) and Genetic Neurodegenerative Diseases (19 papers). Marina Mora is often cited by papers focused on Muscle Physiology and Disorders (83 papers), Cardiomyopathy and Myosin Studies (20 papers) and Genetic Neurodegenerative Diseases (19 papers). Marina Mora collaborates with scholars based in Italy, United States and France. Marina Mora's co-authors include Lucía Morandi, F. Cornelio, Renato Mantegazza, Pia Bernasconi, Massimo Zeviani, Simona Zanotti, Claudia Di Blasi, Paolo Confalonieri, Sara Gibertini and Rita Barresi and has published in prestigious journals such as Nature, Cell and Journal of Clinical Investigation.

In The Last Decade

Marina Mora

154 papers receiving 6.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

2000 702 citations Marina Mora et al. profile →
Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease

1998 586 citations Marina Mora et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marina Mora Italy	41	4.7k	1.1k	1.0k	954	903	159	6.7k
Lucía Morandi Italy	43	3.7k 0.8×	754 0.7×	613 0.6×	786 0.8×	365 0.4×	143	5.2k
Haluk Topaloğlu Türkiye	49	5.5k 1.2×	1.8k 1.7×	1.5k 1.5×	753 0.8×	353 0.4×	261	8.2k
Zarife Sahenk United States	49	4.6k 1.0×	1.9k 1.7×	784 0.8×	778 0.8×	492 0.5×	145	7.7k
Patrizia Sabatelli Italy	39	4.3k 0.9×	478 0.4×	912 0.9×	553 0.6×	569 0.6×	147	5.6k
John S. Rudge United States	38	6.4k 1.3×	1.7k 1.6×	630 0.6×	879 0.9×	344 0.4×	57	10.9k
Francesco Muntoni United Kingdom	50	6.6k 1.4×	1.2k 1.1×	947 0.9×	1.9k 2.0×	194 0.2×	158	7.7k
Alessandra Ferlini Italy	43	5.9k 1.2×	835 0.8×	629 0.6×	1.4k 1.5×	258 0.3×	233	7.1k
Andrew H. Crosby United Kingdom	36	3.9k 0.8×	1.7k 1.6×	1.0k 1.0×	1.0k 1.1×	229 0.3×	125	7.1k
Annika Armulik Sweden	19	3.9k 0.8×	871 0.8×	919 0.9×	323 0.3×	444 0.5×	20	8.7k
Alberto Auricchio Italy	54	6.3k 1.3×	1.2k 1.1×	586 0.6×	500 0.5×	782 0.9×	154	8.3k

Countries citing papers authored by Marina Mora

Since Specialization

Citations

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

Fields of papers citing papers by Marina Mora

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Mora

This figure shows the co-authorship network connecting the top 25 collaborators of Marina Mora. A scholar is included among the top collaborators of Marina Mora 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 Marina Mora. Marina Mora 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

Mora, Marina, et al.. (2023). Management of hypocalcemia following thyroid surgery in children. Frontiers in Pediatrics. 11. 1151537–1151537.

Capitanio, Daniele, Manuela Moriggi, Pietro Barbacini, et al.. (2022). Molecular Fingerprint of BMD Patients Lacking a Portion in the Rod Domain of Dystrophin. International Journal of Molecular Sciences. 23(5). 2624–2624. 8 indexed citations

Moriggi, Manuela, Daniele Capitanio, Enrica Torretta, et al.. (2021). Muscle Proteomic Profile before and after Enzyme Replacement Therapy in Late-Onset Pompe Disease. International Journal of Molecular Sciences. 22(6). 2850–2850. 27 indexed citations

Cafora, Marco, Cinzia Bragato, Daniele Capitanio, et al.. (2021). Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophy. Pharmacological Research. 170. 105750–105750. 27 indexed citations

Capitanio, Daniele, Manuela Moriggi, Enrica Torretta, et al.. (2020). Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients. Journal of Cachexia Sarcopenia and Muscle. 11(2). 547–563. 66 indexed citations

Marchet, Silvia, Federica Invernizzi, Flavia Blàsevich, et al.. (2019). Alteration of mitochondrial membrane inner potential in three Italian patients with megaconial congenital muscular dystrophy carrying new mutations in CHKB gene. Mitochondrion. 47. 24–29. 10 indexed citations

Bersini, Simone, Mara Gilardi, Giovanni Stefano Ugolini, et al.. (2019). Engineering an environment for the study of fibrosis: A 3D human muscle model with endothelium-specificity and endomysium. 790–790. 1 indexed citations

Zanotti, Simona, Dimos Kapetis, Sara Gibertini, et al.. (2018). Botulinum toxin type A affects the transcriptome of cell cultures derived from muscle biopsies of controls and spastic patients. Toxicology in Vitro. 50. 124–136. 2 indexed citations

Gherardi, Samuele, Matteo Bovolenta, Chiara Passarelli, et al.. (2017). 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. 1860(11). 1138–1147. 8 indexed citations

10.

Zanotti, Simona, Sara Gibertini, Paolo Savadori, et al.. (2015). 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. 1852(7). 1451–1464. 72 indexed citations

11.

Maggi, Lorenzo, Franco Salerno, Cinzia Bragato, et al.. (2013). Familial adult-onset Pompe disease associated with unusual clinical and histological features.. PubMed Central. 6 indexed citations

12.

Filocamo, Mirella, Chiara Baldo, Stefano Goldwurm, et al.. (2013). Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases. Orphanet Journal of Rare Diseases. 8(1). 129–129. 36 indexed citations

13.

Blasi, Claudia Di, et al.. (2008). Danon disease: A novel LAMP2 mutation affecting the pre-mRNA splicing and causing aberrant transcripts and partial protein expression. Neuromuscular Disorders. 18(12). 962–966. 13 indexed citations

14.

Zanotti, Simona & Marina Mora. (2006). Proteoglycans are Differentially Altered in Muscular Dystrophies. The Scientific World JOURNAL. 6. 446–448. 2 indexed citations

15.

Villanova, Marcello, Eugenio Mercuri, Enrico Bertini, et al.. (2000). Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome. Neuromuscular Disorders. 10(8). 541–547. 33 indexed citations

16.

Morandi, Luca, et al.. (1996). An unusual association: celiac disease and Becker muscular dystrophy.. PubMed. 91(7). 1459–60.

17.

Dworzak, F., Marina Mora, F. Cornelio, et al.. (1995). Generalized lysosomal storage in Yunis Varón syndrome. Neuromuscular Disorders. 5(5). 423–428. 12 indexed citations

18.

Matsumura, Kiichiro, Arthur H.M. Burghes, Marina Mora, et al.. (1994). 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. 93(1). 99–105. 45 indexed citations

19.

Mora, Marina. (1989). Fibrous-adipose replacement in skeletal muscle biopsy. European Heart Journal. 10(suppl D). 103–104. 13 indexed citations

20.

Cornelio, F., Stefano Di Donato, D. Testa, et al.. (1979). “Carnitine deficient” myopathy and cardiomyopathy with fatal outcome. The Italian Journal of Neurological Sciences. 1(1). 95–100. 9 indexed citations

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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