Stefano Paolacci

591 total citations
4 papers, 54 citations indexed

About

Stefano Paolacci is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Stefano Paolacci has authored 4 papers receiving a total of 54 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Stefano Paolacci's work include Genetic Syndromes and Imprinting (1 paper), Protein Tyrosine Phosphatases (1 paper) and Cellular transport and secretion (1 paper). Stefano Paolacci is often cited by papers focused on Genetic Syndromes and Imprinting (1 paper), Protein Tyrosine Phosphatases (1 paper) and Cellular transport and secretion (1 paper). Stefano Paolacci collaborates with scholars based in Italy, Germany and Netherlands. Stefano Paolacci's co-authors include Marco Tartaglia, Raoul C. M. Hennekam, Bernd Wollnik, Shehla Mohammed, José Francisco da Silva Franco, Débora Romeo Bertola, Francesca Romana Lepri, Francesca Pantaleoni, Marialetizia Motta and Ersilia Barbato and has published in prestigious journals such as Human Mutation, Archives of Oral Biology and American Journal of Medical Genetics Part A.

In The Last Decade

Stefano Paolacci

4 papers receiving 54 citations

Peers

Stefano Paolacci
Xia Zhong China
Stuart Ingram United Kingdom
Chris Eijsbouts United Kingdom
Ebba Alkhunaizi Canada
Jack Huey United States
Mariana Aracena Chile
Precilla D’Souza United States
Narges Rezaie United States
Abolfazl Heidari Iran
Tanja Nielsen United States
Xia Zhong China
Stefano Paolacci
Citations per year, relative to Stefano Paolacci Stefano Paolacci (= 1×) peers Xia Zhong

Countries citing papers authored by Stefano Paolacci

Since Specialization
Citations

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

Fields of papers citing papers by Stefano Paolacci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Paolacci

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

All Works

4 of 4 papers shown
1.
Traversa, Alice, Silvia Bernardo, Alessandro Paiardini, et al.. (2019). Prenatal whole exome sequencing detects a new homozygous fukutin (FKTN) mutation in a fetus with an ultrasound suspicion of familial Dandy–Walker malformation. Molecular Genetics & Genomic Medicine. 8(1). e1054–e1054. 4 indexed citations
2.
Barbato, Ersilia, Alice Traversa, Stefano Paolacci, et al.. (2018). Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies. Archives of Oral Biology. 91. 96–102. 10 indexed citations
3.
Paolacci, Stefano, Débora Romeo Bertola, José Francisco da Silva Franco, et al.. (2017). Wiedemann–Rautenstrauch syndrome: A phenotype analysis. American Journal of Medical Genetics Part A. 173(7). 1763–1772. 27 indexed citations
4.
Pantaleoni, Francesca, Dorit Lev, Ion Cristian Cirstea, et al.. (2017). AberrantHRAStranscript processing underlies a distinctive phenotype within the RASopathy clinical spectrum. Human Mutation. 38(7). 798–804. 13 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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2026