Patrizia Pappi

408 total citations
9 papers, 278 citations indexed

About

Patrizia Pappi is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Patrizia Pappi has authored 9 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Patrizia Pappi's work include Mitochondrial Function and Pathology (3 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Patrizia Pappi is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Patrizia Pappi collaborates with scholars based in Italy, United States and France. Patrizia Pappi's co-authors include Alfredo Brusco, Nicola Migone, Alessandro Brussino, Claudia Cagnoli, Flora Tassone, Carlo Arduino, Paul J. Hagerman, Simona Cavalieri, Cecilia Mancini and Emanuela Garelli and has published in prestigious journals such as Human Mutation, Cytogenetic and Genome Research and Annals of Human Genetics.

In The Last Decade

Patrizia Pappi

9 papers receiving 275 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrizia Pappi Italy 8 207 123 88 55 24 9 278
Sébastien Moutton France 12 212 1.0× 211 1.7× 64 0.7× 26 0.5× 16 0.7× 17 367
Sophie F. Hill United States 8 215 1.0× 131 1.1× 90 1.0× 28 0.5× 11 0.5× 14 354
Isabelle Souville France 9 225 1.1× 170 1.4× 110 1.3× 26 0.5× 14 0.6× 11 474
Shino Shimada Japan 15 315 1.5× 318 2.6× 68 0.8× 35 0.6× 19 0.8× 36 545
Naomi Takino Japan 9 196 0.9× 131 1.1× 105 1.2× 25 0.5× 29 1.2× 12 323
Daniëlle G.M. Bosch Netherlands 10 183 0.9× 133 1.1× 47 0.5× 57 1.0× 5 0.2× 12 374
María Isabel Álvarez‐Mora Spain 11 170 0.8× 210 1.7× 32 0.4× 96 1.7× 14 0.6× 34 303
Mafalda Barbosa Portugal 7 166 0.8× 221 1.8× 68 0.8× 46 0.8× 19 0.8× 8 330
Amanda Lindy United States 8 225 1.1× 328 2.7× 65 0.7× 23 0.4× 12 0.5× 13 517
Elizabeth Butler United States 7 208 1.0× 299 2.4× 59 0.7× 21 0.4× 8 0.3× 13 468

Countries citing papers authored by Patrizia Pappi

Since Specialization
Citations

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

Fields of papers citing papers by Patrizia Pappi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrizia Pappi

This figure shows the co-authorship network connecting the top 25 collaborators of Patrizia Pappi. A scholar is included among the top collaborators of Patrizia Pappi 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 Patrizia Pappi. Patrizia Pappi 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.
Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations
2.
Sirchia, Fabio, Eleonora Di Gregorio, Gabriella Restagno, et al.. (2017). A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q. European Journal of Medical Genetics. 60(4). 224–227. 8 indexed citations
3.
Biamino, Elisa, Eleonora Di Gregorio, Elga Fabia Belligni, et al.. (2015). A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(2). 290–299. 25 indexed citations
4.
Gregorio, Eleonora Di, Giovanni Botta, Alessandro Calcia, et al.. (2015). Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications. Cytogenetic and Genome Research. 147(1). 10–16. 2 indexed citations
5.
Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2010). Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. Human Mutation. 31(10). 1117–1124. 53 indexed citations
6.
Ferraris, Silvio, Emanuela Garelli, Adriana Carando, et al.. (2009). HDR syndrome: A novel “de novo” mutation in GATA3 gene. American Journal of Medical Genetics Part A. 149A(4). 770–775. 36 indexed citations
7.
Cavalieri, Simona, Ada Funaro, Patrizia Pappi, et al.. (2007). Large Genomic Mutations within the ATM Gene Detected by MLPA, Including a Duplication of 41 kb from Exon 4 to 20. Annals of Human Genetics. 72(1). 10–18. 24 indexed citations
8.
Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2006). Large Pathogenic Expansions in the SCA2 and SCA7 Genes Can Be Detected by Fluorescent Repeat-Primed Polymerase Chain Reaction Assay. Journal of Molecular Diagnostics. 8(1). 128–132. 26 indexed citations
9.
Brussino, Alessandro, Flora Tassone, Carlo Arduino, et al.. (2005). An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene. Journal of Molecular Diagnostics. 7(5). 605–612. 89 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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