Edmar Zanoteli

4.1k total citations · 1 hit paper
159 papers, 1.8k citations indexed

About

Edmar Zanoteli is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Edmar Zanoteli has authored 159 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Molecular Biology, 58 papers in Genetics and 29 papers in Surgery. Recurrent topics in Edmar Zanoteli's work include Muscle Physiology and Disorders (57 papers), Neurogenetic and Muscular Disorders Research (57 papers) and RNA modifications and cancer (22 papers). Edmar Zanoteli is often cited by papers focused on Muscle Physiology and Disorders (57 papers), Neurogenetic and Muscular Disorders Research (57 papers) and RNA modifications and cancer (22 papers). Edmar Zanoteli collaborates with scholars based in Brazil, United States and United Kingdom. Edmar Zanoteli's co-authors include Umbertina Conti Reed, Acary Souza Bullé Oliveira, André Macedo Serafim da Silva, Rodrigo de Holanda Mendonça, R. Scalco, Gerson Chadi, Maria Bernadete Dutra de Resende, Osório Lopes Abath Neto, Jocelyn Laporte and Eduardo de Paula Estephan and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Edmar Zanoteli

147 papers receiving 1.8k citations

Hit Papers

Risdiplam-Treated Infants with Type 1 Spinal Muscular Atr... 2021 2026 2022 2024 2021 50 100 150

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Edmar Zanoteli Brazil 22 933 587 413 297 273 159 1.8k
Andrea Klein Switzerland 22 837 0.9× 513 0.9× 301 0.7× 257 0.9× 187 0.7× 70 1.5k
Adnan Y. Manzur United Kingdom 26 1.5k 1.6× 535 0.9× 217 0.5× 283 1.0× 528 1.9× 63 2.1k
S. Pandya United States 12 1.1k 1.2× 312 0.5× 187 0.5× 153 0.5× 231 0.8× 19 1.7k
J. F. Pellissier France 30 1.0k 1.1× 371 0.6× 225 0.5× 456 1.5× 206 0.8× 91 2.2k
Aldobrando Broccolini Italy 26 1.1k 1.1× 249 0.4× 148 0.4× 301 1.0× 273 1.0× 84 1.9k
Maja von der Hagen Germany 22 651 0.7× 196 0.3× 175 0.4× 417 1.4× 154 0.6× 80 1.5k
Anna Kostera‐Pruszczyk Poland 22 613 0.7× 427 0.7× 285 0.7× 446 1.5× 121 0.4× 120 1.4k
Kevin J. Felice United States 23 643 0.7× 501 0.9× 171 0.4× 686 2.3× 177 0.6× 65 1.7k
B. Eymard France 29 1.5k 1.6× 272 0.5× 158 0.4× 478 1.6× 771 2.8× 82 2.6k
Luca Bello Italy 21 1.0k 1.1× 285 0.5× 110 0.3× 221 0.7× 249 0.9× 84 1.4k

Countries citing papers authored by Edmar Zanoteli

Since Specialization
Citations

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

Fields of papers citing papers by Edmar Zanoteli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edmar Zanoteli

This figure shows the co-authorship network connecting the top 25 collaborators of Edmar Zanoteli. A scholar is included among the top collaborators of Edmar Zanoteli 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 Edmar Zanoteli. Edmar Zanoteli 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.
Seaborne, Robert A., Jenni Laitila, Edmar Zanoteli, et al.. (2025). Integrated single‐cell functional‐proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof‐of‐principle study. The Journal of Physiology. 603(10). 3033–3048. 1 indexed citations
2.
Mendonça, Rodrigo de Holanda, et al.. (2025). Brazilian Portuguese version of the revised upper-limb module: cross-cultural adaptation and validation. Arquivos de Neuro-Psiquiatria. 83(3). 1–6.
3.
Seaborne, Robert A., Edmar Zanoteli, Michael W. Lawlor, et al.. (2025). Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy. JCI Insight. 10(24).
4.
Moreno, Cristiane Araújo Martins, Karina Carvalho Donis, Jonas Alex Morales Saute, et al.. (2024). Genetic profile of Brazilian patients with LAMA2 ‐related dystrophies. Clinical Genetics. 106(3). 305–314.
5.
Silva, André Macedo Serafim da, et al.. (2024). Comprehensive analysis of the clinical and genetic features of RYR1-related myopathies. Arquivos de Neuro-Psiquiatria. 128–128.
6.
Laitila, Jenni, Robert A. Seaborne, Justin Kolb, et al.. (2024). Myosin ATPase inhibition fails to rescue the metabolically dysregulated proteome of nebulin‐deficient muscle. The Journal of Physiology. 602(20). 5229–5245. 3 indexed citations
7.
Zanoteli, Edmar, Marcondes C. França, & Wilson Marques. (2024). Gene-based therapies for neuromuscular disorders. Arquivos de Neuro-Psiquiatria. 82(6). 1–10. 2 indexed citations
8.
Andersen, Jesper L., Heinz Jungbluth, Nanna Witting, et al.. (2023). Abnormal myosin post‐translational modifications and ATP turnover time associated with human congenital myopathy‐related RYR1 mutations. Acta Physiologica. 239(2). e14035–e14035. 7 indexed citations
9.
Moreno, Cristiane Araújo Martins, Gisele Chagas de Medeiros, Fernanda Chiarion Sassi, et al.. (2023). Clinical Manifestation of Nebulin-Associated Nemaline Myopathy. Neurology Genetics. 9(1). e200056–e200056. 4 indexed citations
10.
Darras, Basil T., Giovanni Baranello, Odile Boespflug‐Tanguy, et al.. (2023). FIREFISH Parts 1 and 2: 36-month safety and efficacy of risdiplam in Type 1 spinal muscular atrophy (SMA) (P7-9.009). Neurology. 100(17_supplement_2). 1 indexed citations
11.
Mendonça, Rodrigo de Holanda, et al.. (2023). Muscle Ultrasound Changes Correlate With Functional Impairment in Spinal Muscular Atrophy. Ultrasound in Medicine & Biology. 49(7). 1569–1574. 5 indexed citations
12.
Miossi, Renata, et al.. (2021). Brachio-cervical inflammatory myopathy associated with systemic sclerosis. Case series and review of literature. SHILAP Revista de lepidopterología. 73(2). 122–130. 3 indexed citations
13.
Lima, Giscard, Sérgio Rabello Alves, Edmar Zanoteli, et al.. (2021). Risk factors and future directions for preventing and diagnosing exertional rhabdomyolysis. Neuromuscular Disorders. 31(7). 583–595. 13 indexed citations
14.
Chadi, Gerson, et al.. (2019). Skeletal Muscle Response to Deflazacort, Dexamethasone and Methylprednisolone. Cells. 8(5). 406–406. 37 indexed citations
15.
Guimarães, Júlio Brandão, et al.. (2019). Diagnostic Imaging of Inflammatory Myopathies: New Concepts and a Radiological Approach. Current Rheumatology Reports. 21(3). 8–8. 15 indexed citations
16.
Bortolini, Maria Augusta Tezelli, et al.. (2018). Molecular and histomorphological evaluation of female rats’ urethral tissues after an innovative trauma model of prolonged vaginal distention: immediate, short-term and long-term effects. International Urogynecology Journal. 30(3). 465–476. 8 indexed citations
17.
Chadi, Gerson, et al.. (2015). Neuraminidase-1 mediates skeletal muscle regeneration. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(9). 1755–1764. 9 indexed citations
18.
Zanoteli, Edmar, Yvan Campos, Xiaohui Qiu, et al.. (2007). G.P.19.10 Ozz-E3 ligase expression during muscle regeneration. Neuromuscular Disorders. 17(9-10). 896–897. 1 indexed citations
19.
Vainzof, Mariz, Oscar Suzuki, Georgine Faulkner, et al.. (2002). Telethonin protein expression in neuromuscular disorders. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1588(1). 33–40. 41 indexed citations
20.
Anghinah, Renato, et al.. (1995). Atypical EEG pattern in children with absence seizures. Arquivos de Neuro-Psiquiatria. 53(2). 258–261. 6 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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