Eduardo Bonilla

12.2k total citations · 4 hit papers
127 papers, 9.0k citations indexed

About

Eduardo Bonilla is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, Eduardo Bonilla has authored 127 papers receiving a total of 9.0k indexed citations (citations by other indexed papers that have themselves been cited), including 109 papers in Molecular Biology, 60 papers in Clinical Biochemistry and 18 papers in Cell Biology. Recurrent topics in Eduardo Bonilla's work include Mitochondrial Function and Pathology (71 papers), Metabolism and Genetic Disorders (60 papers) and ATP Synthase and ATPases Research (35 papers). Eduardo Bonilla is often cited by papers focused on Mitochondrial Function and Pathology (71 papers), Metabolism and Genetic Disorders (60 papers) and ATP Synthase and ATPases Research (35 papers). Eduardo Bonilla collaborates with scholars based in United States, Italy and Spain. Eduardo Bonilla's co-authors include Salvatore DiMauro, Eric A. Schon, Kurenai Tanji, Sara Shanske, Massimo Zeviani, Darryl C. DeVivo, Michio Hirano, András Perl, Lewis P. Rowland and Armand F. Miranda and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Eduardo Bonilla

126 papers receiving 8.8k citations

Hit 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 DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

1989 746 citations Carlos T. Moraes, Salvatore DiMauro et al. New England Journal of Medicine profile →
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)

2000 702 citations Kurenai Tanji, Yasutoshi Koga 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, Armand F. Miranda et al. Cell profile →

Peers

Countries citing papers authored by Eduardo Bonilla

Since Specialization

Citations

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

Fields of papers citing papers by Eduardo Bonilla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eduardo Bonilla

This figure shows the co-authorship network connecting the top 25 collaborators of Eduardo Bonilla. A scholar is included among the top collaborators of Eduardo Bonilla 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 Eduardo Bonilla. Eduardo Bonilla 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	A key role for MAM in mediating mitochondrial dysfunction in Alzheimer disease 2018 ·Cell Death and Disease ·Estela Área-Gómez, Ad de Groof, Eduardo Bonilla, Jorge Montesinos, Kurenai Tanji, István Boldogh, Liza A. Pon, Eric A. Schon	179
2	Activation of Mammalian Target of Rapamycin Controls the Loss of TCRζ in Lupus T Cells through HRES-1/Rab4-Regulated Lysosomal Degradation 2009 ·The Journal of Immunology ·David Fernández, Tiffany Telarico, Eduardo Bonilla, Qing Li, S. K. Banerjee, Frank A. Middleton, Paul E. M. Phillips, Mary K. Crow, Stefanie Oess, Werner Müller‐Esterl, András Perl	198
3	Haplotypes of the HRES‐1 endogenous retrovirus are associated with development and disease manifestations of systemic lupus erythematosus 2008 ·Arthritis & Rheumatism ·R Pullmann, Eduardo Bonilla, Paul E. M. Phillips, Frank A. Middleton, András Perl	44
4	A novel tRNAVal mitochondrial DNA mutation causing MELAS 2008 ·Journal of the Neurological Sciences ·Kurenai Tanji, Petra Kaufmann, Ali Naini, Jiesheng Lu, (unknown), Dong Wang, Joshua Z. Willey, Sara Shanske, Michio Hirano, Eduardo Bonilla, Alexander G. Khandji, Salvatore DiMauro, Lewis P. Rowland	18
5	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
6	A Novel ND3 Mitochondrial DNA Mutation in Three Korean Children With Basal Ganglia Lesions and Complex I Deficiency 2007 ·Pediatric Research ·Jong‐Hee Chae, Jin Sook Lee, Ki Joong Kim, Yong Seung Hwang, Eduardo Bonilla, Kurenai Tanji, Michio Hirano	27
7	Optical Imaging Techniques (Histochemical, Immunohistochemical, and In Situ Hybridization Staining Methods) to Visualize Mitochondria 2007 ·Methods in cell biology ·Kurenai Tanji, Eduardo Bonilla	38
8	Novel Mitochondrial DNA ND5 Mutation in a Patient With Clinical Features of MELAS and MERRF 2005 ·Archives of Neurology ·Ali Naini, Jiesheng Lu, Petra Kaufmann, Richard A. Bernstein, Michelangelo Mancuso, Eduardo Bonilla, Michio Hirano, Salvatore DiMauro	55
9	Unusual Clinical Presentations in Four Cases of Leigh Disease, Cytochrome C Oxidase Deficiency, and SURF1 Gene Mutations 2005 ·Journal of Child Neurology ·S K Tay, Sabrina Sacconi, (unknown), (unknown), Augusto Morales, Darryl C. De Vivo, Sara Shanske, Eduardo Bonilla, Salvatore DiMauro	25
10	A novel mitochondrial tRNALeu(UUR) mutation in a patient with features of MERRF and Kearns–Sayre syndrome 2003 ·Neuromuscular Disorders ·Yutaka Nishigaki, Saba Tadesse, Eduardo Bonilla, Dikoma C. Shungu, Stephen P. Hersh, Bronya J.B. Keats, Charles I. Berlín, Morton F. Goldberg, Jerry Vockley, Salvatore DiMauro, Michio Hirano	50
11	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
12	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
13	Mitochondria in neuromuscular disorders 1998 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Salvatore DiMauro, Eduardo Bonilla, Mercy M. Davidson, Michio Hirano, Eric A. Schon	119
14	A Novel Mitochondrial G8313A Mutation Associated with Prominent Initial Gastrointestinal Symptoms and Progressive Encephaloneuropathy 1997 ·Pediatric Research ·Ashok Verma, David A. Piccoli, Eduardo Bonilla, Gerard T. Berry, Salvatore DiMauro, Carlos T. Moraes	43
15	[43]Cytochemistry and immunocytochemistry of mitochondria in tissue sections 1996 ·Methods in enzymology on CD-ROM/Methods in enzymology ·Monica Sciacco, Eduardo Bonilla	167
16	Carrier detection of duchenne and becker muscular dystrophy using muscle dystrophin immunohistochemistry 1992 ·Arquivos de Neuro-Psiquiatria ·Acary Souza Bullé Oliveira, Alberto Alain Gabbai, Beny Schmidt, (unknown), (unknown), Carlo Minetti, Eduardo Bonilla	4
17	Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: A new approach to the study of mitochondrial myopathies 1991 ·Journal of the Neurological Sciences ·Francesca Andreetta, (unknown), Eric A. Schon, Salvatore DiMauro, Eduardo Bonilla	18
18	Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome breakdown → 1989 ·New England Journal of Medicine ·Carlos T. Moraes, Salvatore DiMauro, Massimo Zeviani, Anne Lombès, Sara Shanske, Armand F. Miranda, Hirofumi Nakase, Eduardo Bonilla, Lineu César Werneck, Serenella Servidei, Ikuya Nonaka, Yasutoshi Koga, Alfred J. Spiro, A. Keith W. Brownell, Beny Schmidt, Donald L. Schotland, Mary L. Zupanc, Darryl C. DeVivo, Eric A. Schon, Lewis P. Rowland	746
19	Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface breakdown → 1988 ·Cell ·Eduardo Bonilla, (unknown), Armand F. Miranda, Arthur P. Hays, G. Salviati, Salvatore DiMauro, Louis M. Kunkel, Eric P. Hoffman, Lewis P. Rowland	528
20	Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32 1988 ·Genomics ·Massimo Zeviani, Basil T. Darras, Rosario Rizzuto, G. Salviati, Romeo Betto, Eduardo Bonilla, Armand F. Miranda, Jing Du, (unknown), George Dickson, Frank S. Walsh, Salvatore DiMauro, Uta Francke, Eric A. Schon	25

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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