Nicola Vanni

538 total citations
6 papers, 278 citations indexed

About

Nicola Vanni is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Nicola Vanni has authored 6 papers receiving a total of 278 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Rheumatology. Recurrent topics in Nicola Vanni's work include Glycogen Storage Diseases and Myoclonus (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Lysosomal Storage Disorders Research (2 papers). Nicola Vanni is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Lysosomal Storage Disorders Research (2 papers). Nicola Vanni collaborates with scholars based in Italy, United States and France. Nicola Vanni's co-authors include Federico Zara, Antonio Falace, Anna Fassio, Fabio Benfenati, Pasquale Striano, Carlo Minetti, Fabia Filipello, Francesca Madia, F. Dagna Bricarelli and Veronica La Padula and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

Nicola Vanni

5 papers receiving 276 citations

Peers

Nicola Vanni
Berge A. Minassian Canada
Anna-Kaisa Anttonen Finland
Miriam Kolníková Slovakia
Emily Tuttle United States
Philippe Couarch France
Anneke J.A. Kievit Netherlands
Marta A. Bayly Australia
Marina Michelson Israel
Martino Montomoli Italy
Berge A. Minassian Canada
Nicola Vanni
Citations per year, relative to Nicola Vanni Nicola Vanni (= 1×) peers Berge A. Minassian

Countries citing papers authored by Nicola Vanni

Since Specialization
Citations

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

Fields of papers citing papers by Nicola Vanni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicola Vanni

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

All Works

6 of 6 papers shown
1.
Gambelunghe, Cristiana, et al.. (2025). Microbial succession after death: genomic and culture-based insights from external sampling sites in forensic science. Legal Medicine. 78. 102685–102685.
2.
Ferlazzo, Edoardo, Pasquale Striano, Domenico Italiano, et al.. (2016). Autosomal recessive progressive myoclonus epilepsy due to impaired ceramide synthesis. Epileptic Disorders. 18(s2). 120–127. 9 indexed citations
3.
Vanni, Nicola, Floriana Fruscione, Edoardo Ferlazzo, et al.. (2014). Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsy. Annals of Neurology. 76(2). 206–212. 69 indexed citations
4.
Milh, Mathieu, Antonio Falace, Nathalie Villeneuve, et al.. (2013). Novel Compound Heterozygous Mutations inTBC1D24Cause Familial Malignant Migrating Partial Seizures of Infancy. Human Mutation. 34(6). 869–872. 69 indexed citations
5.
Licchetta, Laura, Tommaso Pippucci, Francesca Bisulli, et al.. (2013). A novel pedigree with familial cortical myoclonic tremor and epilepsy (FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype. Epilepsia. 54(7). 1298–1306. 17 indexed citations
6.
Falace, Antonio, Fabia Filipello, Veronica La Padula, et al.. (2010). TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy. The American Journal of Human Genetics. 87(3). 365–370. 114 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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