E. Bonilla

7.3k citations

76 papers · 5.4k · 1 hit paper · h-index 40

Impact in

Clinical Biochemistry top 0.05%
- Metabolism and Genetic Disorders
Molecular Biology top 1%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- Muscle Physiology and Disorders
- RNA modifications and cancer

Papers in

Molecular Biology 63
- Mitochondrial Function and Pathology 37
- Muscle Physiology and Disorders 23
- ATP Synthase and ATPases Research 10
- Nuclear Structure and Function 5
Clinical Biochemistry 26
- Metabolism and Genetic Disorders 26

Co-authors: S. DiMauro (46 shared papers)Eric A. Schon (14 shared papers)Carlos T. Moraes (12 shared papers)Lewis P. Rowland (9 shared papers)Massimo Zeviani (8 shared papers)Donald L. Schotland (13 shared papers)H Nakase (3 shared papers)Sara Shanske (15 shared papers)
Journals: Neurology (24 papers)Annals of Neurology (11 papers)Proceedings of the National Academy of Sciences (2 papers)Journal of the Neurological Sciences (2 papers)Histochemistry and Cell Biology (2 papers)
Partner nations: United States Italy Spain

In The Last Decade

E. Bonilla

76 papers receiving 5.2k citations

E. Bonilla's Hit Papers

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Deletions of mitochondrial DNA in Kearns‐Sayre syndrome 1988 · 591 citations

Peers

Countries citing papers authored by E. Bonilla

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Citations

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Fields of papers citing papers by E. Bonilla

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Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside E. Bonilla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E. Bonilla Line = papers co-authored together E. Bonilla links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Neurology ·Massimo Zeviani, Carlos T. Moraes, S. DiMauro, H Nakase, E. Bonilla, Eric A. Schon, Lewis P. Rowland Hit paper breakdown →	1988	591
2	MELAS: Clinical features, biochemistry, and molecular genetics Annals of Neurology ·Emma Ciafaloni, Enzo Ricci, Sara Shanske, Carlos T. Moraes, Gabriella Silvestri, Michio Hirano, Simonetta Simonetti, C. Angelini, Maria Alice Donati, C. Bousoño García, Andrea Martinuzzi, Russell K. Mosewich, Serenella Servidei, Enrico Zammarchi, E. Bonilla, D. C. DeVivo, Lewis P. Rowland, Eric A. Schon, S. DiMauro	1992	382
3	Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) Neurology ·Michio Hirano, Gabriella Silvestri, D. M. Blake, Anne Lombès, Carlo Minetti, E. Bonilla, Arthur P. Hays, Robert E. Lovelace, India Butler, T. E. Bertoríni, Anisa B. Threlkeld, Hiroshi Mitsumoto, Larry M. Salberg, Lewis P. Rowland, S. DiMauro	1994	311
4	Deletions of mitochondrial DNA in Kearns‐Sayre syndrome Neurology ·Massimo Zeviani, Carlos T. Moraes, S. DiMauro, H Nakase, E. Bonilla, Eric A. Schon, Lewis P. Rowland	1988	291
5	Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome? Annals of Neurology ·Richard A. Berenberg, John M. Pellock, S. DiMauro, D. L. Schotlan, E. Bonilla, Abraham B. Eastwood, Allison G. Hays, C. T. Vicale, Myles M. Behrens, Abe M. Chutorian, Lewis P. Rowland	1977	251
6	The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle. PubMed ·Carlos T. Moraes, Enzo Ricci, E. Bonilla, S. DiMauro, Eric A. Schon	1992	218
7	Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome. Proceedings of the National Academy of Sciences ·Shuji Mita, Beny Schmidt, Eric A. Schon, S. DiMauro, E. Bonilla	1989	182
8	Mitochondrial encephalomyopathy with coenzyme Q ₁₀ deficiency Neurology ·Cláudia Ferreira da Rosa Sobreira, Michio Hirano, Sara Shanske, Ramsi Keller, Ronald G. Haller, Edgar Davidson, Filippo M. Santorelli, Armand F. Miranda, E. Bonilla, Daniel S. Mojon, Amilton Antunes Barreira, Michael P. King, S. DiMauro	1997	156
9	Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA ^Ser(UCN) gene Neurology ·Carolyn M. Sue, Kurenai Tanji, George Hadjigeorgiou, Antoni L. Andreu, Ichizo Nishino, Sindu Krishna, Claudio Bruno, Michio Hirano, Sara Shanske, E. Bonilla, Nathan Fischel‐Ghodsian, S. DiMauro, Rick A. Friedman	1999	138
10	Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndrome Neurology ·Sara Shanske, Carlos T. Moraes, Anne Lombès, Armand F. Miranda, E. Bonilla, Patricia Lewis, Mary Anne Whelan, C. A. Ellsworth, S. DiMauro	1990	136
11	Mitochondrial DNA depletion Neurology ·Michelangelo Mancuso, Leonardo Salviati, Sabrina Sacconi, David Otaegui, Pilar Camaño, Alberto Marina, Sandra R. Bacman, Carlos T. Moraes, Jose Carlo, María J. García, María García‐Álvarez, Lailani Monzon, Ali Naini, Michio Hirano, E. Bonilla, A.L. Taratuto, S. DiMauro, Tuan Vu	2002	124
12	A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene Neuromuscular Disorders ·Giovanni Manfredi, Eric A. Schon, Carlos T. Moraes, E. Bonilla, Gerard T. Berry, John T. Sladky, S. DiMauro	1995	123
13	Luft's disease Journal of the Neurological Sciences ·S. DiMauro, E. Bonilla, C.P. Lee, Donald L. Schotland, A. Scarpa, Hadley L. Conn, B. Chance	1976	107
14	Duchenne Dystrophy: Alteration in Muscle Plasma Membrane Structure Science ·Donald L. Schotland, E. Bonilla, Michael Van Meter	1977	101
15	Differential features of patients with mutations in two COX assembly genes,SURF-1 andSCO2 Annals of Neurology ·Carolyn M. Sue, Charalampos Karadimas, Nicoletta Checcarelli, Kurenai Tanji, Lefkothea C. Papadopoulou, Francesco Pallotti, Fei Guo, Sara Shanske, Michio Hirano, Darryl C. De Vivo, Rudy Van Coster, Paige Kaplan, E. Bonilla, S. DiMauro	2000	101
16	Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients Annals of Neurology ·Filippo M. Santorelli, Monica Sciacco, Kurenai Tanji, Sara Shanske, Tuan Vu, Valeria Golzi, Robert C. Griggs, Jerry R. Mendell, Arthur P. Hays, T. E. Bertoríni, Alan Pestronk, E. Bonilla, S. DiMauro	1996	97
17	A nonsense mutation (G15059A) in the cytochromeb gene in a patient with exercise intolerance and myoglobinuria Annals of Neurology ·Antoni L. Andreu, Claudio Bruno, Tony Dunne, Kurenai Tanji, Sara Shanske, Carolyn M. Sue, Sindu Krishna, George Hadjigeorgiou, Alexander Shtilbans, E. Bonilla, S. DiMauro	1999	91
18	Clinical manifestations of mitochondria1 DNA depletion Neurology ·Tuan Vu, Monica Sciacco, Kurenai Tanji, C. Nichter, E. Bonilla, Sansnee Chatkupt, Paul Maertens, Sara Shanske, Jerry R. Mendell, M. Richard Koenigsberger, Leroy R. Sharer, Eric A. Schon, S. DiMauro, D. C. DeVivo	1998	91
19	A functionally dominant mitochondrial DNA mutation Human Molecular Genetics ·Sabrina Sacconi, Leonardo Salviati, Y. Nishigaki, Winsome F. Walker, Evelyn Hernandez-Rosa, Eva Trevisson, Séverine Delplace, C Desnuelle, Sara Shanske, Michio Hirano, Eric A. Schon, E. Bonilla, Darryl C. De Vivo, S. DiMauro, Mercy M. Davidson	2008	85
20	Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patients. PubMed ·Armand F. Miranda, E. Bonilla, Giuseppe Martucci, Carlos T. Moraes, Arthur P. Hays, S. DiMauro	1988	84

About E. Bonilla

E. Bonilla is a scholar working on Molecular Biology, Clinical Biochemistry, Cellular and Molecular Neuroscience, Physiology and Biomedical Engineering, having authored 76 papers that have together received 5.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (37 papers), Metabolism and Genetic Disorders (26 papers), Muscle Physiology and Disorders (23 papers), ATP Synthase and ATPases Research (10 papers), Genetic Neurodegenerative Diseases (8 papers), Adipose Tissue and Metabolism (6 papers), Cardiomyopathy and Myosin Studies (6 papers) and Nuclear Structure and Function (5 papers). The work is most often cited by research in Clinical Biochemistry (2.6k citations), Molecular Biology (4.7k citations), Cellular and Molecular Neuroscience (720 citations), Biochemistry (141 citations) and Genetics (182 citations). E. Bonilla has collaborated with scholars based in United States, Italy and Spain. Frequent co-authors include S. DiMauro, Eric A. Schon, Carlos T. Moraes, Lewis P. Rowland, Massimo Zeviani, Donald L. Schotland, H Nakase, Sara Shanske, Michio Hirano and Enzo Ricci. Their work appears in journals such as Neurology, Annals of Neurology, Proceedings of the National Academy of Sciences, Journal of the Neurological Sciences and Histochemistry and Cell Biology.

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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