Marco Rimoldi

1.2k citations

17 papers · 908 indexed · h-index 13

Co-authors: Massimo Zeviani A. Prelle Valeria Tiranti Ivano Di Meo Michael D. Levitt Rossana Mineri Gigliola Fagiolari Carlo Viscomi
Topics: Metabolism and Genetic Disorders (10 papers)Mitochondrial Function and Pathology (7 papers)Biochemical and Molecular Research (4 papers)
Cited by: Clinical Biochemistry Biochemistry Neurology
Journals: Nature Medicine Neurology Annals of Neurology
Partner nations: Italy United States Ireland

In The Last Decade

Marco Rimoldi

17 papers receiving 888 citations

Peers

Countries citing papers authored by Marco Rimoldi

Since Specialization

Citations

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

Fields of papers citing papers by Marco Rimoldi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Rimoldi

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Mesenchymal Stromal Cells Uptake and Release Paclitaxel without Reducing its Anticancer Activity 2015 ·Anti-Cancer Agents in Medicinal Chemistry ·Massimo Mariotti,Renato Colognato,Marco Rimoldi,(unknown),Francesca Sisto,Valentina Coccè,Arianna Bonomi,Eugenio Parati,Giulio Alessandri,Renzo Bagnati,Augusto Pessina	7
2	Human CD14+ cells loaded with Paclitaxel inhibit in vitro cell proliferation of glioblastoma 2014 ·Cytotherapy ·Arianna Bonomi,Daniela Lisini,Stefania Elena Navone,Simona Frigerio,Marta Dossena,Emilio Ciusani,Paolo Rampini,Giovanni Marfia,Valentina Coccè,Loredana Cavicchini,Francesca Sisto,Eugenio Parati,Renato Mantegazza,Marco Rimoldi,(unknown),Giulio Alessandri,Augusto Pessina	12
3	Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms 2012 ·Orphanet Journal of Rare Diseases ·Ettore Salsano,Silvia Tabano,Silvia Maria Sirchia,Patrizia Colapietro,Barbara Castellotti,Cinzia Gellera,Marco Rimoldi,Viviana Pensato,Caterina Mariotti,Davide Pareyson,Monica Miozzo,Graziella Uziel	27
4	Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect 2011 ·Neurological Sciences ·Maria Sofia Cotelli,Valentina Vielmi,Marco Rimoldi,(unknown),Barbara Castellotti,Valeria Bertasi,Alice Todeschini,(unknown),Carla Baronchelli,Cinzia Gellera,Alessandro Padovani,Massimiliano Filosto	11
5	Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients 2011 ·Neurogenetics ·Barbara Castellotti,Caterina Mariotti,Marco Rimoldi,Roberto Fancellu,Massimo Plumari,(unknown),Graziella Uziel,Nardo Nardocci,Isabella Moroni,Giovanna Zorzi,Davide Pareyson,Daniela Di Bella,Stefano Di Donato,Franco Taroni,Cinzia Gellera	33
6	Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations 2011 ·Molecular Genetics and Metabolism ·Valerio Leoni,Laura Strittmatter,Giovanna Zorzi,Federica Zibordi,Sabrina Dusi,Barbara Garavaglia,Paola Venco,Claudio Caccia,Amanda L. Souza,Amy Deik,Clary B. Clish,Marco Rimoldi,Emilio Ciusani,Enrico Bertini,Nardo Nardocci,Vamsi K. Mootha,Valeria Tiranti	98
7	Preparation of yeast mitochondria and in vitro assay of respiratory chain complex activities 2010 ·Protocol Exchange ·Stefania Magri,(unknown),Marco Rimoldi,Franco Taroni	8
8	Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy 2009 ·Nature Medicine ·Valeria Tiranti,Carlo Viscomi,Tatjana M. Hildebrandt,Ivano Di Meo,Rossana Mineri,Cecilia Tiveron,Michael D. Levitt,A. Prelle,Gigliola Fagiolari,Marco Rimoldi,Massimo Zeviani	318
9	Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defect 1996 ·Journal of the Neurological Sciences ·Gian Maria Fabrizi,Raffaele Lodi,(unknown),Alessandro Malandrini,Tiziana Cavallaro,Marco Rimoldi,P. Zaniol,Bruno Barbiroli,(unknown)	9
10	Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiency 1995 ·Journal of the Neurological Sciences ·Carlo Antozzi,Silvana Franceschetti,Graziella Filippini,Bruno Barbiroli,M. Savoiardo,F. Fiacchino,Marco Rimoldi,Raffaele Lodi,P. Zaniol,Massimo Zeviani	19
11	Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA 1995 ·Journal of Neurology ·Caterina Mariotti,(unknown),Anu Suomalainen,Marco Rimoldi,Giacomo P. Comi,A. Prelle,Carlo Antozzi,Serenella Servidei,Laura Jarre,Stefano DiDonato,Massimo Zeviani	80
12	Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy 1995 ·Pediatric Neurology ·Graziella Uziel,Barbara Garavaglia,Elisa Ciceri,Isabella Moroni,Marco Rimoldi	22
13	Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments 1994 ·Neuromuscular Disorders ·Francesco Muntoni,Gualtiero Catani,Anna Mateddu,Marco Rimoldi,Terenzio Congiu,Gavino Faa,Maria Giovanna Marrosu,Carlo Cianchetti,Maurizio Porcu	44
14	Experience on Therapy of Adrenoleukodystrophy and Adrenomyeloneuropathy 1991 ·Developmental Neuroscience ·Graziella Uziel,Enrico Bertini,(unknown),Marco Rimoldi,(unknown)	44
15	Normalization of short‐chain acylcoenzyme a dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme a dehydrogenase—deficient myopathy 1989 ·Annals of Neurology ·Stefano DiDonato,Cinzia Gellera,D. Peluchetti,Graziella Uziel,A. Antonelli,Giacomo Lus,Marco Rimoldi	38
16	Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities 1988 ·Pediatric Research ·France Demaugre,Jean‐Paul Bonnefont,Grant Mitchell,(unknown),Anna Pelet,Marco Rimoldi,Stefano Di Donato,Jean-Marie Saudubray	105
17	Systemic carnitine deficiency 1984 ·Neurology ·Stefano Di Donato,(unknown),Marco Rimoldi,Marina Mora,Barbara Garavaglia,Gaetano Finocchiaro	33

About Marco Rimoldi

Marco Rimoldi is a scholar working on Clinical Biochemistry, Biochemistry and Molecular Medicine, having authored 17 papers that have together received 908 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (10 papers), Mitochondrial Function and Pathology (7 papers) and Biochemical and Molecular Research (4 papers). The work is most often cited by research in Clinical Biochemistry (436 citations), Biochemistry (206 citations) and Neurology (79 citations). Marco Rimoldi has collaborated with scholars based in Italy, United States and Ireland. Frequent co-authors include Massimo Zeviani, A. Prelle, Valeria Tiranti, Ivano Di Meo, Michael D. Levitt, Rossana Mineri, Gigliola Fagiolari, Carlo Viscomi, Tatjana M. Hildebrandt and Cecilia Tiveron. Their work appears in journals such as Nature Medicine, Neurology and Annals of Neurology.

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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