Salvatore DiMauro

42.2k citations

408 papers · 29.6k indexed · 11 hit papers · h-index 87

Molecular Biology top 0.05%
Clinical Biochemistry top 0.01%
Physiology top 0.5%
Rheumatology top 0.1%
Cellular and Molecular Neuroscience top 0.5%

Co-authors: Eric A. Schon Michio Hirano Eduardo Bonilla Sara Shanske Massimo Zeviani Lewis P. Rowland Ali Naini Darryl C. De Vivo
Topics: Mitochondrial Function and Pathology (261 papers)Metabolism and Genetic Disorders (223 papers)ATP Synthase and ATPases Research (123 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: Nature Science New England Journal of Medicine
Partner nations: United States Italy Canada

In The Last Decade

Salvatore DiMauro

407 papers receiving 28.7k citations

Hit Papers

5 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.

Mitochondrial Respiratory-Chain Diseases

2003 1.2k citations Salvatore DiMauro, Eric A. Schon profile →
Mitochondrial diseases

2016 1.0k citations Salvatore DiMauro, Michio Hirano et al. profile →
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1984 888 citations Salvatore DiMauro, Darryl C. De Vivo et al. profile →
Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

1989 746 citations Salvatore DiMauro, Massimo Zeviani et al. profile →
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

2000 702 citations Yasutoshi Koga, Sara Shanske et al. profile →
Inclusion body myositis and myopathies

1995 604 citations Salvatore DiMauro et al. profile →
Human mitochondrial DNA: roles of inherited and somatic mutations

2012 552 citations Eric A. Schon, Salvatore DiMauro et al. profile →
Mitochondrial myopathies

1985 531 citations Salvatore DiMauro, Eduardo Bonilla et al. profile →
Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface

1988 528 citations Eduardo Bonilla, Salvatore DiMauro et al. profile →
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

1989 483 citations Massimo Zeviani, Serenella Servidei et al. profile →
Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society

2014 372 citations Sumit Parikh, Amy Goldstein et al. Genetics in Medicine profile →

Peers

Countries citing papers authored by Salvatore DiMauro

Since Specialization

Citations

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

Fields of papers citing papers by Salvatore DiMauro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Salvatore DiMauro

This figure shows the co-authorship network connecting the top 25 collaborators of Salvatore DiMauro. A scholar is included among the top collaborators of Salvatore DiMauro 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 Salvatore DiMauro. Salvatore DiMauro 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	Cytochrome c Oxidase Activity Is a Metabolic Checkpoint that Regulates Cell Fate Decisions During T Cell Activation and Differentiation 2017 ·Cell Metabolism ·Т. Н. Тарасенко,Susan E. Pacheco,Mary Kay Koenig,Julio Gómez‐Rodríguez,Senta M. Kapnick,Francisca Díaz,Patricia M. Zerfas,Emanuele Barca,Jessica Sudderth,Ralph J. DeBerardinis,Raúl Covián,Robert S. Balaban,Salvatore DiMauro,Peter J. McGuire	132
2	An exon trap with proper poly-A site in the GBE1 is the common missing cause in Adult Polyglucosan Body Disease (S42.006) 2015 ·Neurology ·(unknown),Or Kakhlon,Jorida Çoku,Lorenzo Peverelli,Hanna Rosenmann,(unknown),Julie Turnbull,Vardiella Meiner,(unknown),Israela Lerer,Shoshi Shpitzen,Eran Leitersdorf,(unknown),Mary Wallace,Raphael Schiffmann,Salvatore DiMauro,Alexander Lossos,Berge A. Minassian	1
3	Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Societybreakdown → 2014 ·Genetics in Medicine ·Sumit Parikh,Amy Goldstein,Mary Kay Koenig,Fernando Scaglia,Gregory M. Enns,Russell P. Saneto,Irina Anselm,Bruce H. Cohen,Marni J. Falk,Carol L. Greene,Andrea Gropman,Richard Haas,Michio Hirano,Philip G. Morgan,Katherine B. Sims,Mark A. Tarnopolsky,Johan L.K. Van Hove,Lynne A. Wolfe,Salvatore DiMauro	372
4	Survival transcriptome in the coenzyme Q ₁₀ deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q ₁₀ deficiencies 2013 ·BMJ Open ·Daniel J.M. Fernández‐Ayala,(unknown),Sandra Jiménez-Gancedo,María V. Cascajo,(unknown),Salvatore DiMauro,Michio Hirano,Paz Briones,Rafael Artuch,Rafael de Cabo,Leonardo Salviati,Plácido Navas	16
5	Coenzyme Q deficiency in muscle 2011 ·Current Opinion in Neurology ·Eva Trevisson,Salvatore DiMauro,Plácido Navas,Leonardo Salviati	62
6	Short Communication: Transplacental Nucleoside Analogue Exposure and Mitochondrial Parameters in HIV-Uninfected Children 2010 ·AIDS Research and Human Retroviruses ·Susan B. Brogly,Salvatore DiMauro,Russell B. Van Dyke,Paige L. Williams,Ali Naini,Daniel Libutti,(unknown),Michelle Chung,Mariana Gerschenson	30
7	Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations 2010 ·Mitochondrion ·Yutaka Nishigaki,Hitomi Ueno,Jorida Çoku,Yasutoshi Koga,Tatsuya Fujii,Ko Sahashi,Kazutoshi Nakano,Makoto Yoneda,Michiko Nonaka,Lin-ya Tang,Chia‐Wei Liou,Véronique Paquis‐Flucklinger,Yasuo Harigaya,Tohru Ibi,Yu‐ichi Goto,Hiroko Hosoya,Salvatore DiMauro,Michio Hirano,Masashi Tanaka	24
8	Autonomic Symptoms in Carriers of the m.3243A>G Mitochondrial DNA Mutation 2010 ·Archives of Neurology ·(unknown),Louis H. Weimer,Kristin Engelstad,(unknown),Vanessa Battista,Ying Wei,Michio Hirano,Salvatore DiMauro,Darryl C. De Vivo,Petra Kaufmann	18
9	Caveolin-1(−/−)- and Caveolin-2(−/−)-Deficient Mice Both Display Numerous Skeletal Muscle Abnormalities, with Tubular Aggregate Formation 2007 ·American Journal Of Pathology ·William Schubert,Federica Sotgia,Alex W. Cohen,Franco Capozza,Gloria Bonuccelli,Claudio Bruno,Carlo Minetti,Eduardo Bonilla,Salvatore DiMauro,Michael P. Lisanti	52
10	Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: Report of a family 2007 ·Journal of Affective Disorders ·Michelangelo Mancuso,Giulia Ricci,Anna Choub,Massimiliano Filosto,Salvatore DiMauro,Guido Davidzon,Alessandra Tessa,Filippo M. Santorelli,Luigi Murri,Gabriele Siciliano	21
11	A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency 2006 ·The American Journal of Human Genetics ·Catarina M. Quinzii,Ali Naini,Leonardo Salviati,Eva Trevisson,Plácido Navas,Salvatore DiMauro,Michio Hirano	263
12	Mitochondrial encephalomyopathies: an update 2005 ·Neuromuscular Disorders ·Salvatore DiMauro,Michio Hirano	109
13	Clinical and Biochemical Heterogeneity in an Italian Family with CPT II Deficiency due to Ser 113 Leu Mutation 2005 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Mubeen F. Rafay,E. Gordon Murphy,Julie McGarry,Petra Kaufmann,Salvatore DiMauro,Ingrid Tein	5
14	Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene 2003 ·Journal of the Neurological Sciences ·Michelangelo Mancuso,Massimiliano Filosto,J. Clarke Stevens,Marc C. Patterson,Sara Shanske,Sindu Krishna,Salvatore DiMauro	33
15	Mitochondrial myopathy and myoclonic epilepsy 1990 ·Arquivos de Neuro-Psiquiatria ·Walter O. Arruda,Luíz Fernando Bleggi Torres,Anne Lombès,Salvatore DiMauro,(unknown),Hélio Afonso Ghizoni Teive,(unknown),(unknown)	3
16	Subunit Va of human and bovine cytochrome c oxidase is highly conserved 1988 ·Gene ·Rosario Rizzuto,Hirofumi Nakase,Massimo Zeviani,Salvatore DiMauro,Eric A. Schon	38
17	Severe cardiopathy in branching enzyme deficiency 1987 ·The Journal of Pediatrics ·Serenella Servidei,(unknown),Claire Langston,Lloyd Y. Tani,J. Timothy Bricker,(unknown),Henry Travers,Dawna Armstrong,Salvatore DiMauro	71
18	Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain 1984 ·Pediatric Research ·Nancy G. Kennaway,Neil R.M. Buist,Victor Darley‐Usmar,(unknown),Salvatore DiMauro,Richard I. Kelley,Roderick Capaldi,Nathan K. Blank,Anthony N. D’Agostino	2
19	Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain 1984 ·Pediatric Research ·Nancy G. Kennaway,Neil R.M. Buist,Victor Darley‐Usmar,(unknown),Salvatore DiMauro,Richard I. Kelley,Roderick Capaldi,Nathan K. Blank,Anthony N. D’Agostino	68
20	Carnitine deficiency presenting as familial cardiomyopathy: A treatable defect in carnitine transport 1982 ·The Journal of Pediatrics ·Lewis Waber,David Valle,Catherine A. Neill,Salvatore DiMauro,Austin L. Shug	191

About Salvatore DiMauro

Salvatore DiMauro is a scholar working on Clinical Biochemistry, Rheumatology and Molecular Biology, having authored 408 papers that have together received 29.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (261 papers), Metabolism and Genetic Disorders (223 papers) and ATP Synthase and ATPases Research (123 papers). The work is most often cited by research in Clinical Biochemistry (12.6k citations), Molecular Biology (23.0k citations) and Biochemistry (1.6k citations). Salvatore DiMauro has collaborated with scholars based in United States, Italy and Canada. Frequent co-authors include Eric A. Schon, Michio Hirano, Eduardo Bonilla, Sara Shanske, Massimo Zeviani, Lewis P. Rowland, Ali Naini, Darryl C. De Vivo, Armand F. Miranda and Carlos T. Moraes. Their work appears in journals such as Nature, Science and New England Journal of Medicine.

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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