Rita C.M. Pavanello

1.5k total citations
50 papers, 1.0k citations indexed

About

Rita C.M. Pavanello is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Rita C.M. Pavanello has authored 50 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 16 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Rita C.M. Pavanello's work include Muscle Physiology and Disorders (36 papers), Genetic Neurodegenerative Diseases (16 papers) and Cardiomyopathy and Myosin Studies (14 papers). Rita C.M. Pavanello is often cited by papers focused on Muscle Physiology and Disorders (36 papers), Genetic Neurodegenerative Diseases (16 papers) and Cardiomyopathy and Myosin Studies (14 papers). Rita C.M. Pavanello collaborates with scholars based in Brazil, United States and United Kingdom. Rita C.M. Pavanello's co-authors include Mariz Vainzof, Maria Rita Passos‐Bueno, Mayana Zatz, Suely Kazue Nagahashi Marie, Mayana Zatz, Sérgio Russo Matioli, A. H. Cerqueira, Antonia Cerqueira, Reinaldo Issao Takata and Mayana Zatz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Rita C.M. Pavanello

48 papers receiving 982 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita C.M. Pavanello Brazil 18 899 303 254 210 154 50 1.0k
Giuliana Galluzzi Italy 19 1.4k 1.6× 331 1.1× 411 1.6× 306 1.5× 153 1.0× 26 1.6k
Maria Luisa Mostacciuolo Italy 22 764 0.8× 521 1.7× 240 0.9× 184 0.9× 125 0.8× 48 1.2k
Marcella Neri Italy 18 546 0.6× 197 0.7× 144 0.6× 99 0.5× 118 0.8× 37 785
Barbara C. Byth Canada 9 1.1k 1.2× 289 1.0× 167 0.7× 287 1.4× 190 1.2× 14 1.2k
L. Feng United Kingdom 13 674 0.7× 107 0.4× 254 1.0× 187 0.9× 69 0.4× 19 795
Pietro Spitali Netherlands 20 1.0k 1.1× 132 0.4× 191 0.8× 115 0.5× 154 1.0× 55 1.1k
L. Specht United States 7 499 0.6× 168 0.6× 152 0.6× 83 0.4× 82 0.5× 11 613
Pervin Dinçer Türkiye 14 825 0.9× 258 0.9× 176 0.7× 135 0.6× 73 0.5× 45 947
Andrée Rouche France 12 462 0.5× 189 0.6× 128 0.5× 102 0.5× 76 0.5× 18 599
Mayana Zatz Brazil 10 1.0k 1.1× 407 1.3× 268 1.1× 116 0.6× 116 0.8× 19 1.2k

Countries citing papers authored by Rita C.M. Pavanello

Since Specialization
Citations

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

Fields of papers citing papers by Rita C.M. Pavanello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita C.M. Pavanello. 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 Rita C.M. Pavanello. The network helps show where Rita C.M. Pavanello may publish in the future.

Co-authorship network of co-authors of Rita C.M. Pavanello

This figure shows the co-authorship network connecting the top 25 collaborators of Rita C.M. Pavanello. A scholar is included among the top collaborators of Rita C.M. Pavanello 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 Rita C.M. Pavanello. Rita C.M. Pavanello 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.
Fernandes, Stephanie, Camila de Almeida, Monize Lazar, et al.. (2019). Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy. Disease Models & Mechanisms. 13(2). 9 indexed citations
2.
Musso, Camila Manso, Lucas Alvizi, Luciano Abreu Brito, et al.. (2018). Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development. Frontiers in Genetics. 9. 149–149. 6 indexed citations
3.
Vieira, Natássia M., Michel Satya Naslavsky, Fernando Kok, et al.. (2014). A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G). Human Molecular Genetics. 23(15). 4103–4110. 84 indexed citations
4.
Paim, Júlia Filardi, Helga Cristina Almeida da Silva, Rita C.M. Pavanello, et al.. (2007). Central core disease due to recessive mutations in RYR1 gene: Is it more common than described?. Muscle & Nerve. 35(5). 670–674. 36 indexed citations
5.
Paim, Júlia Filardi, et al.. (2006). Sarcoglycanopathies: A Multiplex Molecular Analysis for the Most Common Mutations. Diagnostic Molecular Pathology. 15(2). 95–100. 6 indexed citations
6.
Gollop, Thomaz Rafael, et al.. (2004). Protein and DNA Analysis for the Prenatal Diagnosis of α2-Laminin–Deficient Congenital Muscular Dystrophy. Diagnostic Molecular Pathology. 13(3). 167–171. 4 indexed citations
7.
Lino, Angelina Maria Martins, et al.. (2004). A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. 14(5). 313–320. 9 indexed citations
8.
Passos‐Bueno, Maria Rita, et al.. (2003). Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD). Neuromuscular Disorders. 14(1). 33–38. 102 indexed citations
9.
Vainzof, Mariz, Louise V.B. Anderson, Elizabeth M. McNally, et al.. (2001). Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience. 17(1). 71–80. 53 indexed citations
10.
Sertié, Andréa L., et al.. (1999). Linkage Analysis in a Large Brazilian Family with van der Woude Syndrome Suggests the Existence of a Susceptibility Locus for Cleft Palate at 17p11.2-11.1. The American Journal of Human Genetics. 65(2). 433–440. 23 indexed citations
11.
Vainzof, Mariz, et al.. (1999). Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population. Journal of the Neurological Sciences. 164(1). 44–49. 61 indexed citations
12.
Zatz, Mayana, Suely Kazue Nagahashi Marie, Antonia Cerqueira, et al.. (1998). The facioscapulohumeral muscular dystrophy (FSHD1) gene affects males more severely and more frequently than females. American Journal of Medical Genetics. 77(2). 155–161. 2 indexed citations
13.
Zatz, Mayana, Maria Rita Passos‐Bueno, Antonia Cerqueira, et al.. (1995). Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?. Human Molecular Genetics. 4(3). 401–406. 62 indexed citations
14.
Vainzof, Mariz, Suely Kazue Nagahashi Marie, Joseph D. Schwartzman, et al.. (1995). Deficiency of Merosin (Laminin M or α2) in Congenital Muscular Dystrophy Associated with Cerebral White Matter Alterations. Neuropediatrics. 26(6). 293–297. 34 indexed citations
15.
Zatz, Mayana, Kiichiro Matsumura, Mariz Vainzof, et al.. (1994). Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy. Journal of the Neurological Sciences. 123(1-2). 122–128. 14 indexed citations
16.
Vainzof, Mariz, L. V. B. Nicholson, Dennis E. Bulman, et al.. (1993). Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers. Neuromuscular Disorders. 3(2). 135–140. 3 indexed citations
17.
Passos‐Bueno, Maria Rita, Egbert Bakker, Suely Kazue Nagahashi Marie, et al.. (1993). Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families. Human Molecular Genetics. 2(2). 201–202. 5 indexed citations
18.
Vainzof, Mariz, Reinaldo Issao Takata, Maria Rita Passos‐Bueno, Rita C.M. Pavanello, & Mayana Zatz. (1993). Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?. Human Molecular Genetics. 2(1). 39–42. 28 indexed citations
19.
Vainzof, Mariz, et al.. (1990). Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study. Journal of the Neurological Sciences. 98(2-3). 221–233. 32 indexed citations
20.
Pavanello, Rita C.M., et al.. (1989). Estudo imuno-histoquímico da distrofina em músculo de afetados por distrofias musculares progressivas. 14(3). 799–812. 1 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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