M. Munaro

697 total citations
6 papers, 536 citations indexed

About

M. Munaro is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, M. Munaro has authored 6 papers receiving a total of 536 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Clinical Biochemistry. Recurrent topics in M. Munaro's work include Mitochondrial Function and Pathology (5 papers), ATP Synthase and ATPases Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). M. Munaro is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), ATP Synthase and ATPases Research (3 papers) and Genetic Neurodegenerative Diseases (3 papers). M. Munaro collaborates with scholars based in Italy, Germany and Spain. M. Munaro's co-authors include Massimo Zeviani, Valeria Tiranti, Graziella Uziel, Leopoldo Zelante, R. Marzella, José Antonio Enrı́quez, Carlo Dionisi‐Vici, Matteo Granatiero, Brunella Franco and Thomas Meitinger and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

M. Munaro

6 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Munaro Italy	5	519	272	60	20	15	6	536
K. Weber Germany	6	379 0.7×	233 0.9×	42 0.7×	20 1.0×	13 0.9×	7	402
I Nonaka Japan	4	477 0.9×	292 1.1×	43 0.7×	28 1.4×	11 0.7×	7	513
Paola Venco Italy	7	209 0.4×	118 0.4×	73 1.2×	15 0.8×	21 1.4×	7	301
India Butler South Africa	3	276 0.5×	211 0.8×	38 0.6×	21 1.1×	19 1.3×	5	320
Ghizlane Elachouri France	5	450 0.9×	160 0.6×	54 0.9×	48 2.4×	18 1.2×	6	474
A. Agostino Italy	6	465 0.9×	193 0.7×	53 0.9×	100 5.0×	12 0.8×	7	529
Marzio Bellan Italy	6	240 0.5×	127 0.5×	36 0.6×	15 0.8×	15 1.0×	6	287
Günther Metz Germany	4	404 0.8×	106 0.4×	69 1.1×	22 1.1×	29 1.9×	6	433
Sarah J. Pickett United Kingdom	8	394 0.8×	234 0.9×	43 0.7×	28 1.4×	23 1.5×	15	442
J.A.M. Smeitink Netherlands	10	276 0.5×	218 0.8×	13 0.2×	31 1.6×	10 0.7×	17	348

Countries citing papers authored by M. Munaro

Since Specialization

Citations

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

Fields of papers citing papers by M. Munaro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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6 of 6 papers shown

1.

Tiranti, Valeria, Konstanze Hoertnagel, Rosalba Carrozzo, et al.. (1998). Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency. The American Journal of Human Genetics. 63(6). 1609–1621. 392 indexed citations

2.

Munaro, M., Valeria Tiranti, Doriana Sandonà, et al.. (1997). A Single Cell Complementation Class is Common to Several Cases of Cytochrome c Oxidase-Defective Leigh's Syndrome. Human Molecular Genetics. 6(2). 221–228. 53 indexed citations

3.

Tiranti, Valeria, M. Munaro, Doriana Sandonà, et al.. (1995). Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho transformants. Human Molecular Genetics. 4(11). 2017–2023. 72 indexed citations

4.

Pandolfo, Massimo, Antonio Pizzuti, M. Munaro, et al.. (1994). Isolation of a New Gene in the Friedreich Ataxia Candidate Region on Human Chromosome 9 by cDNA Direct Selection. Biochemical Medicine and Metabolic Biology. 52(2). 115–119. 6 indexed citations

5.

Pianese, Luigi, Sergio Cocozza, G Campanella, et al.. (1994). Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.. Journal of Medical Genetics. 31(2). 133–135. 4 indexed citations

6.

Pandolfo, Massimo, M. Munaro, Luigi Pianese, et al.. (1993). A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1. Human Molecular Genetics. 2(6). 822–822. 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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