M. Bado

1.7k total citations
29 papers, 1.2k citations indexed

About

M. Bado is a scholar working on Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, M. Bado has authored 29 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in M. Bado's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and RNA Research and Splicing (6 papers). M. Bado is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and RNA Research and Splicing (6 papers). M. Bado collaborates with scholars based in Italy, United States and Netherlands. M. Bado's co-authors include Carlo Minetti, G Cordone, Michael P. Lisanti, Federica Sotgia, Paolo Broda, Claudio Bruno, Federico Zara, F. Dagna Bricarelli, Daniela Volonté and Ferruccio Galbiati and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

M. Bado

28 papers receiving 1.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
M. Bado 956 520 221 176 154 29 1.2k
G Cordone 907 0.9× 534 1.0× 238 1.1× 212 1.2× 131 0.9× 38 1.2k
Tania Tiepolo 840 0.9× 158 0.3× 84 0.4× 185 1.1× 131 0.9× 9 1.1k
Beate Schlotter‐Weigel 779 0.8× 240 0.5× 112 0.5× 348 2.0× 338 2.2× 24 1.3k
Martin Krahn 1.1k 1.1× 175 0.3× 245 1.1× 201 1.1× 289 1.9× 64 1.4k
Helen Griffin 1.0k 1.1× 160 0.3× 101 0.5× 92 0.5× 374 2.4× 49 1.5k
Edoardo Malfatti 867 0.9× 94 0.2× 370 1.7× 134 0.8× 164 1.1× 89 1.1k
Paolo Broda 1.0k 1.1× 503 1.0× 273 1.2× 166 0.9× 113 0.7× 17 1.2k
Roberto Cotrufo 603 0.6× 129 0.2× 70 0.3× 119 0.7× 198 1.3× 39 988
Stefania Assereto 563 0.6× 138 0.3× 53 0.2× 105 0.6× 71 0.5× 24 791
Sebahattin Çırak 538 0.6× 142 0.3× 83 0.4× 157 0.9× 106 0.7× 62 943

Countries citing papers authored by M. Bado

Since Specialization
Citations

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

Fields of papers citing papers by M. Bado

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Bado

This figure shows the co-authorship network connecting the top 25 collaborators of M. Bado. A scholar is included among the top collaborators of M. Bado 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 M. Bado. M. Bado is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Biancheri, Roberta, Federico Zara, Claudio Bruno, et al.. (2007). Phenotypic characterization of hypomyelination and congenital cataract. Annals of Neurology. 62(2). 121–127. 33 indexed citations
2.
Bruno, Claudio, Filippo M. Santorelli, Stefania Assereto, et al.. (2003). Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene. Muscle & Nerve. 28(4). 508–511. 40 indexed citations
3.
Rocco, Maja Di, et al.. (2003). Long‐term survival in Stuve‐Wiedemann syndrome: A neuro‐myo‐skeletal disorder with manifestations of dysautonomia. American Journal of Medical Genetics Part A. 118A(4). 362–368. 34 indexed citations
4.
Minetti, Carlo, M. Bado, Paolo Broda, et al.. (2002). Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency. American Journal Of Pathology. 160(1). 265–270. 92 indexed citations
5.
Frigeri, Antonio, Grazia Paola Nicchia, Silvia Repetto, et al.. (2002). Altered aquaporin‐4 expression in human muscular dystrophies: a common feature?. The FASEB Journal. 16(9). 1120–1122. 55 indexed citations
6.
Bruno, Claudio, M. Bado, Carlo Minetti, G Cordone, & Salvatore DiMauro. (2000). Novel Mutation in the CPT II Gene in a Child With Periodic Febrile Myalgia and Myoglobinuria. Journal of Child Neurology. 15(6). 390–393. 12 indexed citations
7.
Carbone, Ilma Floriana, Claudio Bruno, Federica Sotgia, et al.. (2000). Mutation in the CAV3 gene causes partial caveolin-3 deficiency and persistent elevated levels of serum creatine kinase. Neurology. 54(6). 1373–1376. 113 indexed citations
8.
Repetto, Silvia, M. Bado, Paolo Broda, et al.. (1999). Increased Number of Caveolae and Caveolin-3 Overexpression in Duchenne Muscular Dystrophy. Biochemical and Biophysical Research Communications. 261(3). 547–550. 84 indexed citations
9.
Mandich, Paola, Gianluigi Mancardi, Emilio Di Maria, et al.. (1999). Congenital hypomyelination due to myelin protein zero Q215X mutation. Annals of Neurology. 45(5). 676–678. 35 indexed citations
10.
Bruno, Claudio, M. DiRocco, M. Bado, et al.. (1999). A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy. Neuromuscular Disorders. 9(6-7). 403–407. 22 indexed citations
11.
Minetti, Carlo, G Cordone, Francesco Beltrame, M. Bado, & E. Bonilla. (1998). Disorganization of dystrophin costameric lattice in Becker muscular dystrophy. Muscle & Nerve. 21(2). 211–216. 11 indexed citations
12.
Minetti, Carlo, Barbara Garavaglia, M. Bado, et al.. (1998). Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria. Neuromuscular Disorders. 8(1). 3–6. 20 indexed citations
13.
Minetti, Carlo, Federica Sotgia, Claudio Bruno, et al.. (1998). Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nature Genetics. 18(4). 365–368. 456 indexed citations
14.
Raposio, Edoardo, et al.. (1998). Mitochondrial Activity of Orbicularis Oris Muscle in Unilateral Cleft Lip Patients. Plastic & Reconstructive Surgery. 102(4). 968–971. 14 indexed citations
15.
Bruno, Claudio, Carlo Minetti, Yingying Tang, et al.. (1998). Primary adrenal insufficiency in a child with a mitochondrial DNA deletion. Journal of Inherited Metabolic Disease. 21(2). 155–161. 16 indexed citations
16.
Raposio, Edoardo, et al.. (1998). Mitochondrial Activity of Orbicularis Oris Muscle in Unilateral Cleft Lip Patients. Plastic & Reconstructive Surgery. 102(4). 968–971. 11 indexed citations
17.
Montaldo, Paolo G., et al.. (1997). Induction of differentiation and apoptosis by interferon-γ in human neuroblastoma cells in vitro as a dual and alternative early biological response. Cell Death and Differentiation. 4(2). 150–158. 10 indexed citations
18.
Cordone, G, M. Bado, Giuseppe Morreale, Marina Pedemonte, & Carlo Minetti. (1996). Severe dystrophinopathy in a patient with congenital hypotonia. Child s Nervous System. 12(8). 466–9. 2 indexed citations
19.
Bruno, Claudio, M. Bado, Giuseppe Morreale, et al.. (1994). [Muscle phosphorylase deficiency in childhood. A case report].. PubMed. 46(10). 459–62. 3 indexed citations
20.
Minetti, Carlo, G. Meola, Elio Scarpini, et al.. (1984). [The myopathy of congenital fiber type disproportion].. PubMed. 36(4). 181–7. 2 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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