E. Bonilla

7.3k total citations · 1 hit paper
76 papers, 5.4k citations indexed

About

E. Bonilla is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, E. Bonilla has authored 76 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 29 papers in Clinical Biochemistry and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in E. Bonilla's work include Mitochondrial Function and Pathology (38 papers), Metabolism and Genetic Disorders (29 papers) and Muscle Physiology and Disorders (23 papers). E. Bonilla is often cited by papers focused on Mitochondrial Function and Pathology (38 papers), Metabolism and Genetic Disorders (29 papers) and Muscle Physiology and Disorders (23 papers). E. Bonilla collaborates with scholars based in United States, Italy and Spain. E. Bonilla's 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 and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

E. Bonilla

76 papers receiving 5.2k citations

Hit Papers

Deletions of mitochondria... 1988 2026 2000 2013 1988 100 200 300 400 500
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.

  1. Deletions of mitochondrial DNA in Kearns‐Sayre syndrome
    1988 590 citations Carlos T. Moraes, S. DiMauro et al. Neurology profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
E. Bonilla 4.8k 2.8k 771 393 325 76 5.4k
Mary G. Sweeney 2.8k 0.6× 1.1k 0.4× 1.0k 1.3× 192 0.5× 154 0.5× 71 4.0k
Morten Dunø 2.6k 0.5× 777 0.3× 745 1.0× 443 1.1× 481 1.5× 184 3.8k
Lucía Morandi 3.7k 0.8× 423 0.1× 754 1.0× 744 1.9× 786 2.4× 143 5.2k
Marina Mora 4.7k 1.0× 500 0.2× 1.1k 1.4× 798 2.0× 954 2.9× 159 6.7k
Beril Talim 3.0k 0.6× 210 0.1× 580 0.8× 416 1.1× 492 1.5× 138 4.0k
Victor Ionâşescu 2.2k 0.5× 256 0.1× 1.7k 2.2× 356 0.9× 219 0.7× 107 3.9k
Reginald E. Bittner 2.1k 0.4× 175 0.1× 417 0.5× 348 0.9× 509 1.6× 82 3.5k
Roberta Biancheri 1.3k 0.3× 264 0.1× 350 0.5× 453 1.2× 72 0.2× 100 2.5k
Arnold Munnich 1.6k 0.3× 365 0.1× 341 0.4× 96 0.2× 53 0.2× 55 2.3k
Bjarne Udd 3.8k 0.8× 312 0.1× 1.2k 1.6× 304 0.8× 2.1k 6.3× 158 5.2k

Countries citing papers authored by E. Bonilla

Since Specialization
Citations

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

Fields of papers citing papers by E. Bonilla

Since Specialization
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-authorship network of co-authors of E. Bonilla

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

All Works

20 of 20 papers shown
1.
Bonilla, E., et al.. (2023). Survey of COVID-19 Vaccine Attitudes in Predominately Minority Pregnant Women. Southern Medical Journal. 116(8). 677–682. 2 indexed citations
2.
Cutler, Sally J., et al.. (2010). Does RecA have a role in Borrelia recurrentis?. Clinical Microbiology and Infection. 17(2). 195–197. 1 indexed citations
3.
Cutler, Sally J., et al.. (2010). Population Structure of East African Relapsing FeverBorreliaspp.. Emerging infectious diseases. 16(7). 1076–1080. 42 indexed citations
4.
Sacconi, Sabrina, Leonardo Salviati, Y. Nishigaki, et al.. (2008). A functionally dominant mitochondrial DNA mutation. Human Molecular Genetics. 17(12). 1814–1820. 84 indexed citations
5.
Szigeti, Kinga, Adekunle M. Adesina, Don Armstrong, et al.. (2004). Increased blood–brain barrier permeability with thymidine phosphorylase deficiency. Annals of Neurology. 56(6). 881–886. 23 indexed citations
6.
Andreu, Antoni L., Claudio Bruno, Kurenai Tanji, et al.. (1999). A nonsense mutation (G15059A) in the cytochromeb gene in a patient with exercise intolerance and myoglobinuria. Annals of Neurology. 45(1). 127–130. 91 indexed citations
7.
Andreu, Antoni L., Kurenai Tanji, Claudio Bruno, et al.. (1999). Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene. Annals of Neurology. 45(6). 820–823. 63 indexed citations
8.
Hadjigeorgiou, George, K. H. Fischbeck, Antoni L. Andreu, et al.. (1999). A new mitochondrial DNA mutation (A3288G) in the tRNALeu(UUR) gene associated with familial myopathy. Journal of the Neurological Sciences. 164(2). 153–157. 26 indexed citations
9.
Minetti, Carlo, G Cordone, Francesco Beltrame, M. Bado, & E. Bonilla. (1998). Disorganization of dystrophin costameric lattice in Becker muscular dystrophy. Muscle & Nerve. 21(2). 211–216. 11 indexed citations
10.
Wilhelmsen, Kirk C., Timothy Lynch, Mildred Vera, et al.. (1996). Chromosome 12‐linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39(4). 507–520. 63 indexed citations
11.
Santorelli, Filippo M., Monica Sciacco, Kurenai Tanji, et al.. (1996). Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients. Annals of Neurology. 39(6). 789–795. 97 indexed citations
12.
Manfredi, Giovanni, Eric A. Schon, Carlos T. Moraes, et al.. (1995). A new mutation associated with MELAS is located in a mitochondrial DNA polypeptide-coding gene. Neuromuscular Disorders. 5(5). 391–398. 123 indexed citations
13.
Moraes, Carlos T., Monica Sciacco, Enzo Ricci, et al.. (1995). Phenotype-genotype correlations in skeletal muscle of patients with mtDNA deletions. Muscle & Nerve. 18(S14). S150–S153. 27 indexed citations
14.
Hirano, Michio, Gabriella Silvestri, Anne Lombès, et al.. (1994). Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE). Neurology. 44(4). 721–721. 310 indexed citations
15.
Minetti, Carlo, Kurenai Tanji, Hai Won Chang, et al.. (1993). Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria. European Journal of Pediatrics. 152(10). 848–851. 23 indexed citations
16.
Prelle, A., R. Medori, Maurizio Moggio, et al.. (1992). Dystrophin deficiency in a case of congenital myopathy. Journal of Neurology. 239(2). 76–78. 13 indexed citations
17.
Ciafaloni, Emma, Enzo Ricci, Sara Shanske, et al.. (1992). MELAS: Clinical features, biochemistry, and molecular genetics. Annals of Neurology. 31(4). 391–398. 381 indexed citations
18.
Miranda, Armand F., Tiziana Mongini, E. Bonilla, A. Dusty Miller, & Woodring E. Wright. (1990). Myogenic Conversion of Human Non-Muscle Cells for the Diagnosis and Therapy of Neuromuscular Diseases. Advances in experimental medicine and biology. 280. 205–210. 4 indexed citations
19.
Francke, Uta, et al.. (1989). Dystrophin immunocytochemistry in muscle culture: Detection of a carrier of Duchenne muscular dystrophy. American Journal of Medical Genetics. 32(2). 268–273. 24 indexed citations
20.
Bonilla, E., et al.. (1979). Lamellar bodies at the cell periphery of human muscle fibers.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 20(2). 159–67. 3 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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