Carlo Nobile

2.7k total citations
58 papers, 1.4k citations indexed

About

Carlo Nobile is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Carlo Nobile has authored 58 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 24 papers in Genetics and 21 papers in Cell Biology. Recurrent topics in Carlo Nobile's work include Cellular transport and secretion (20 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Epilepsy research and treatment (15 papers). Carlo Nobile is often cited by papers focused on Cellular transport and secretion (20 papers), Genetics and Neurodevelopmental Disorders (19 papers) and Epilepsy research and treatment (15 papers). Carlo Nobile collaborates with scholars based in Italy, United Kingdom and United States. Carlo Nobile's co-authors include Roberto Michelucci, Pasquale Striano, Elena Pasini, Silvio C. E. Tosatto, Salvatore Striano, Simonetta Andreazza, Nigel K. Spurr, Emanuela Dazzo, Ian C. Gray and Sally E. Ford and has published in prestigious journals such as Nature, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Carlo Nobile

58 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlo Nobile Italy 25 581 550 361 355 325 58 1.4k
Bernd Rautenstrauß Germany 26 747 1.3× 224 0.4× 236 0.7× 42 0.1× 330 1.0× 90 1.8k
John A. Damiano Australia 18 398 0.7× 444 0.8× 262 0.7× 389 1.1× 91 0.3× 32 1.3k
Koen L.I. van Gassen Netherlands 22 564 1.0× 407 0.7× 45 0.1× 133 0.4× 87 0.3× 42 1.3k
Jing‐Quan Lan United States 17 801 1.4× 95 0.2× 60 0.2× 171 0.5× 80 0.2× 20 1.2k
Alexander J. Lakhter United States 15 630 1.1× 216 0.4× 59 0.2× 116 0.3× 70 0.2× 21 1.2k
Laura A. Jansen United States 14 512 0.9× 316 0.6× 51 0.1× 221 0.6× 32 0.1× 18 1.0k
Emilia Bellone Italy 24 681 1.2× 176 0.3× 787 2.2× 60 0.2× 195 0.6× 100 1.8k
Elena Ambrosini Italy 20 603 1.0× 84 0.2× 79 0.2× 53 0.1× 82 0.3× 35 1.5k
Tyler Mark Pierson United States 21 737 1.3× 454 0.8× 70 0.2× 185 0.5× 138 0.4× 42 1.3k
Kazutoshi Nishiyama Japan 14 820 1.4× 91 0.2× 114 0.3× 24 0.1× 440 1.4× 20 1.1k

Countries citing papers authored by Carlo Nobile

Since Specialization
Citations

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

Fields of papers citing papers by Carlo Nobile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlo Nobile

This figure shows the co-authorship network connecting the top 25 collaborators of Carlo Nobile. A scholar is included among the top collaborators of Carlo Nobile 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 Carlo Nobile. Carlo Nobile 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.
Bonanni, Paolo, Roberto Giorda, Roberto Michelucci, Carlo Nobile, & Emanuela Dazzo. (2024). A de novo pathogenic variant in MICAL‐1 causes epilepsy with auditory features. Epilepsia Open. 9(3). 1083–1087. 2 indexed citations
2.
Dazzo, Emanuela, Elena Pasini, Sandra Furlan, et al.. (2018). LGI1 tumor tissue expression and serum autoantibodies in patients with primary malignant glioma. Clinical Neurology and Neurosurgery. 170. 27–33. 5 indexed citations
3.
Striano, Pasquale & Carlo Nobile. (2018). The genetic basis of juvenile myoclonic epilepsy. The Lancet Neurology. 17(6). 493–495. 5 indexed citations
4.
Michelucci, Roberto, Patrizia Pulitano, Carlo Di Bonaventura, et al.. (2017). The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations. Epilepsy & Behavior. 68. 103–107. 25 indexed citations
5.
Dazzo, Emanuela, Emanuela Leonardi, Elisa Belluzzi, et al.. (2016). Secretion-Positive LGI1 Mutations Linked to Lateral Temporal Epilepsy Impair Binding to ADAM22 and ADAM23 Receptors. PLoS Genetics. 12(10). e1006376–e1006376. 20 indexed citations
6.
Nobile, Carlo & Pasquale Striano. (2014). PRRT2: A major cause of infantile epilepsy and other paroxysmal disorders of childhood. Progress in brain research. 213. 141–158. 23 indexed citations
7.
Fanciulli, Manuela, Lia Santulli, Chiara Barozzi, et al.. (2012). LGI1 microdeletion in autosomal dominant lateral temporal epilepsy. Neurology. 78(17). 1299–1303. 24 indexed citations
8.
Leonardi, Emanuela, et al.. (2011). A Computational Model of the LGI1 Protein Suggests a Common Binding Site for ADAM Proteins. PLoS ONE. 6(3). e18142–e18142. 31 indexed citations
9.
Striano, Pasquale, Antonio Gambardella, Antonietta Coppola, et al.. (2007). Familial mesial temporal lobe epilepsy (FMTLE). Journal of Neurology. 255(1). 16–23. 44 indexed citations
10.
Furlan, Sandra, Federico Roncaroli, Francesca Forner, et al.. (2006). The LGI1/Epitempin gene encodes two protein isoforms differentially expressed in human brain. Journal of Neurochemistry. 98(3). 985–991. 21 indexed citations
11.
Bisulli, Francesca, Paolo Tinuper, Carla Marini, et al.. (2002). Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q. Epileptic Disorders. 4(3). 183–188. 10 indexed citations
12.
Staub, Eike, Jordi Pérez‐Tur, Reiner Siebert, et al.. (2002). The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. Trends in Biochemical Sciences. 27(9). 441–444. 90 indexed citations
13.
Michelucci, Roberto, D. Passarelli, Sabrina Pitzalis, et al.. (2000). Autosomal Dominant Partial Epilepsy with Auditory Features: Description of a New Family. Epilepsia. 41(8). 967–970. 30 indexed citations
14.
Nobile, Carlo, et al.. (1997). Exon–Intron Organization of the Human Dystrophin Gene. Genomics. 45(2). 421–424. 29 indexed citations
15.
Gray, Ian C., Joanne L. Fallowfield, Sally E. Ford, et al.. (1997). An Integrated Physical and Genetic Map Spanning Chromosome Band 10q24. Genomics. 43(1). 85–88. 18 indexed citations
16.
Nobile, Carlo, et al.. (1995). Genomic Organization of the Human Dystrophin Gene across the Major Deletion Hot Spot and the 3′ Region. Genomics. 28(1). 97–100. 25 indexed citations
17.
Nobile, Carlo, et al.. (1994). A refined restriction map of YAC clones spanning the entire human dystrophin gene. Mammalian Genome. 5(9). 566–571. 15 indexed citations
18.
19.
Nobile, Carlo, et al.. (1986). Nucleosome phasing on a DNA fragment from the replication origin of simian virus 40 and rephasing upon cruciform formation of the DNA.. Molecular and Cellular Biology. 6(8). 2916–2922. 22 indexed citations
20.
Persico, M. Graziella, Daniela Toniolo, Carlo Nobile, Michele D’Urso, & Lucio Luzzatto. (1981). cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322. Nature. 294(5843). 778–780. 37 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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