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, Ferruccio Galbiati and Daniela Volonté 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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Phenotypic characterization of hypomyelination and congenital cataract 2007 ·Annals of Neurology ·Roberta Biancheri, Federico Zara, Claudio Bruno, Andrea Rossi, (unknown), Elisabetta Gazzerro, Federica Sotgia, Marina Pedemonte, Sara Scapolan, M. Bado, Graziella Uziel, Marianna Bugiani, (unknown), (unknown), Angelo Schenone, Annemieke J.M. Rozemüller, Paolo Tortori‐Donati, Michael P. Lisanti, Marjo S. van der Knaap, Carlo Minetti	33
2	Long‐term survival in Stuve‐Wiedemann syndrome: A neuro‐myo‐skeletal disorder with manifestations of dysautonomia 2003 ·American Journal of Medical Genetics Part A ·Maja Di Rocco, (unknown), Claudio Bruno, (unknown), M. Bado, Andrea Superti‐Furga	34
3	Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene 2003 ·Muscle & Nerve ·Claudio Bruno, Filippo M. Santorelli, Stefania Assereto, E. Tonoli, Alessandra Tessa, Monica Traverso, Sara Scapolan, M. Bado, Silvana Tedeschi, Carlo Minetti	40
4	Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency 2002 ·American Journal Of Pathology ·Carlo Minetti, M. Bado, Paolo Broda, Federica Sotgia, Claudio Bruno, Ferruccio Galbiati, Daniela Volonté, Giuseppe Lucania, Antonio Pavan, Eduardo Bonilla, Michael P. Lisanti, G Cordone	92
5	A Novel Mutation in the SURF1 Gene in a Child With Leigh Disease, Peripheral Neuropathy, and Cytochrome-c Oxidase Deficiency 2002 ·Journal of Child Neurology ·Claudio Bruno, Roberta Biancheri, Barbara Garavaglia, (unknown), Andrea Rossi, (unknown), M. Bado, M. Gréco, Massimo Zeviani, Carlo Minetti	25
6	Novel Mutation in the CPT II Gene in a Child With Periodic Febrile Myalgia and Myoglobinuria 2000 ·Journal of Child Neurology ·Claudio Bruno, M. Bado, Carlo Minetti, G Cordone, Salvatore DiMauro	12
7	Congenital hypomyelination due to myelin protein zero Q215X mutation 1999 ·Annals of Neurology ·Paola Mandich, Gianluigi Mancardi, (unknown), (unknown), Emilio Di Maria, Emilia Bellone, M. Bado, (unknown), Anthony J. Windebank, F. Ajmar, Angelo Schenone	35
8	Increased Number of Caveolae and Caveolin-3 Overexpression in Duchenne Muscular Dystrophy 1999 ·Biochemical and Biophysical Research Communications ·Silvia Repetto, M. Bado, Paolo Broda, Giuseppe Lucania, (unknown), Federica Sotgia, Ilaria Carbone, Antonio Pavan, Eduardo Bonilla, G Cordone, Michael P. Lisanti, Carlo Minetti	84
9	A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy 1999 ·Neuromuscular Disorders ·Claudio Bruno, M. DiRocco, (unknown), M. Bado, C Marino, Seiichi Tsujino, Sara Shanske, Giulia Maria Stella, Carlo Minetti, O. P. van Diggelen, S. DiMauro	22
10	Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria 1998 ·Neuromuscular Disorders ·Carlo Minetti, Barbara Garavaglia, M. Bado, Federica Invernizzi, Claudio Bruno, M. Rimoldi, Roser Pons, Franco Taroni, G Cordone	20
11	Mitochondrial Activity of Orbicularis Oris Muscle in Unilateral Cleft Lip Patients 1998 ·Plastic & Reconstructive Surgery ·Edoardo Raposio, M. Bado, (unknown), Pierluigi Santi	14
12	Primary adrenal insufficiency in a child with a mitochondrial DNA deletion 1998 ·Journal of Inherited Metabolic Disease ·Claudio Bruno, Carlo Minetti, Yingying Tang, Paulo Magalhães, Filippo M. Santorelli, Sara Shanske, M. Bado, G Cordone, R. Gatti, S. DiMauro	16
13	Mitochondrial Activity of Orbicularis Oris Muscle in Unilateral Cleft Lip Patients 1998 ·Plastic & Reconstructive Surgery ·Edoardo Raposio, M. Bado, (unknown), Pierluigi Santi	11
14	Disorganization of dystrophin costameric lattice in Becker muscular dystrophy 1998 ·Muscle & Nerve ·Carlo Minetti, G Cordone, Francesco Beltrame, M. Bado, E. Bonilla	11
15	Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy 1998 ·Nature Genetics ·Carlo Minetti, Federica Sotgia, Claudio Bruno, Paolo Scartezzini, Paolo Broda, M. Bado, (unknown), Michela Mazzocco, Aliana Egeo, Maria Alice Donati, Daniela Volonté, Ferruccio Galbiati, G Cordone, F. Dagna Bricarelli, Michael P. Lisanti, Federico Zara	456
16	Apoptosis of Human Neuroblastoma Cells Induced by Liposome-Encapsulated Fenretinide 1998 ·Journal of Liposome Research ·Gabriella Pagnan, Gianluca Caridi, Paolo G. Montaldo, M. Bado, (unknown), Theresa M. Allen, Mirco Ponzoni	13
17	Induction of differentiation and apoptosis by interferon-γ in human neuroblastoma cells in vitro as a dual and alternative early biological response 1997 ·Cell Death and Differentiation ·Paolo G. Montaldo, (unknown), M. Bado, Lizzia Raffaghello, Carla Rozzo, Mirco Ponzoni	10
18	Severe dystrophinopathy in a patient with congenital hypotonia 1996 ·Child s Nervous System ·G Cordone, M. Bado, Giuseppe Morreale, Marina Pedemonte, Carlo Minetti	2
19	[Early myoclonic encephalopathy and spinal muscular atrophy type I]. 1995 ·PubMed ·M. Bado, Cristina Bruno, Giuseppe Morreale, Francesca Parisi, Carlo Minetti, G Cordone	0
20	[The myopathy of congenital fiber type disproportion]. 1984 ·PubMed ·Carlo Minetti, G. Meola, Elio Scarpini, G Cordone, M. Bado, G. Scarlato	2

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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