Paula Iughetti

467 total citations
9 papers, 297 citations indexed

About

Paula Iughetti is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Paula Iughetti has authored 9 papers receiving a total of 297 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 2 papers in Neurology and 2 papers in Genetics. Recurrent topics in Paula Iughetti's work include Prion Diseases and Protein Misfolding (3 papers), Neurological diseases and metabolism (2 papers) and Muscle Physiology and Disorders (2 papers). Paula Iughetti is often cited by papers focused on Prion Diseases and Protein Misfolding (3 papers), Neurological diseases and metabolism (2 papers) and Muscle Physiology and Disorders (2 papers). Paula Iughetti collaborates with scholars based in Brazil, Netherlands and Canada. Paula Iughetti's co-authors include Maria Rita Passos‐Bueno, Mayana Zatz, Andréa C. LeBlanc, Paulo Caramelli, Ricardo Nitríni, Sérgio Rosemberg, Eloísa S. Moreira, Steffen Albrecht, Maria Papadopoulos and Luís Garcia Alonso and has published in prestigious journals such as Annals of Neurology, Neurobiology of Aging and Genomics.

In The Last Decade

Paula Iughetti

9 papers receiving 285 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paula Iughetti Brazil 7 244 71 51 45 42 9 297
Hartmut Engel Germany 9 380 1.6× 30 0.4× 69 1.4× 18 0.4× 40 1.0× 15 518
Saïd Ghandour France 9 264 1.1× 58 0.8× 52 1.0× 10 0.2× 114 2.7× 12 420
Jacomijn P. Dijksterhuis Sweden 8 438 1.8× 37 0.5× 57 1.1× 10 0.2× 94 2.2× 10 574
Corine Gartioux France 10 321 1.3× 14 0.2× 55 1.1× 68 1.5× 31 0.7× 23 419
Thuyen Nguyen United States 8 254 1.0× 14 0.2× 120 2.4× 48 1.1× 61 1.5× 9 375
Lauren Brady Canada 17 360 1.5× 33 0.5× 57 1.1× 10 0.2× 102 2.4× 40 558
Sietske H. Kevelam Netherlands 10 283 1.2× 56 0.8× 43 0.8× 7 0.2× 32 0.8× 11 473
Pavan K. Kommareddi United States 8 114 0.5× 74 1.0× 23 0.5× 9 0.2× 85 2.0× 12 330
Fariba Sedehizade Germany 10 164 0.7× 25 0.4× 37 0.7× 4 0.1× 50 1.2× 12 376
Stephen J. A. Shemilt United Kingdom 6 220 0.9× 58 0.8× 181 3.5× 8 0.2× 72 1.7× 9 425

Countries citing papers authored by Paula Iughetti

Since Specialization
Citations

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

Fields of papers citing papers by Paula Iughetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paula Iughetti

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

All Works

9 of 9 papers shown
1.
Mazzeu, Juliana F., et al.. (2006). Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant. Genetics and Molecular Biology. 29(4). 601–604. 2 indexed citations
2.
Bever, Yolande van, Jenneke van den Ende, Paula Iughetti, et al.. (2003). Waardenburg syndrome: Clinical differentiation between types I and II. American Journal of Medical Genetics Part A. 117A(3). 223–235. 41 indexed citations
3.
Nitríni, Ricardo, Sérgio Rosemberg, Paulo Caramelli, et al.. (2001). Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17. Arquivos de Neuro-Psiquiatria. 59(2A). 161–164. 16 indexed citations
4.
Iughetti, Paula, Oscar Suzuki, Paulo H. Godoi, et al.. (2001). A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma.. PubMed. 61(20). 7375–8. 62 indexed citations
5.
Iughetti, Paula, Luís Garcia Alonso, William R. Wilcox, Nivaldo Alonso, & Maria Rita Passos‐Bueno. (2000). Mapping of the autosomal recessive (AR) craniometaphyseal dysplasia locus to chromosome region 6q21-22 and confirmation of genetic heterogeneity for mild AR spondylocostal dysplasia. American Journal of Medical Genetics. 95(5). 482–491. 28 indexed citations
6.
Nitríni, Ricardo, Sérgio Rosemberg, Maria Rita Passos‐Bueno, et al.. (1997). Familial spongiform encephalopathy associated with a novel prion protein gene mutation. Annals of Neurology. 42(2). 138–146. 78 indexed citations
7.
Nitríni, Ricardo, Sérgio Rosemberg, Maria Rita Passos‐Bueno, et al.. (1996). 643 Familial spongiform encephalopathy with distinct clinico-pathological features associated with a novel mutation of the prion protein gene. Neurobiology of Aging. 17(4). S160–S160. 1 indexed citations
8.
Passos‐Bueno, Maria Rita, Eloísa S. Moreira, Suely Kazue Nagahashi Marie, et al.. (1996). Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.. Journal of Medical Genetics. 33(2). 97–102. 38 indexed citations
9.
Passos-Bueno, Maria-Rita, Eloísa S. Moreira, Mariz Vainzof, et al.. (1995). Confirmation of the 2p Locus for the Mild Autosomal Recessive Limb-Girdle Muscular Dystrophy Gene (LGMD2B) in Three Families Allows Refinement of the Candidate Region. Genomics. 27(1). 192–195. 31 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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