Luca Pannone

1.0k total citations
11 papers, 71 citations indexed

About

Luca Pannone is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Luca Pannone has authored 11 papers receiving a total of 71 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Immunology and 2 papers in Genetics. Recurrent topics in Luca Pannone's work include Protein Tyrosine Phosphatases (6 papers), RNA modifications and cancer (3 papers) and Galectins and Cancer Biology (3 papers). Luca Pannone is often cited by papers focused on Protein Tyrosine Phosphatases (6 papers), RNA modifications and cancer (3 papers) and Galectins and Cancer Biology (3 papers). Luca Pannone collaborates with scholars based in Italy, United States and Cyprus. Luca Pannone's co-authors include Simone Martinelli, Marco Tartaglia, Martina Di Rocco, Denise Pires Marafon, Francesca Spadaro, Luca Pasquini, Fabrizio De Benedetti, Simona Coppola, Antonella Insalaco and Eva Trevisson and has published in prestigious journals such as Scientific Reports, Journal of Allergy and Clinical Immunology and The Journal of Physical Chemistry Letters.

In The Last Decade

Luca Pannone

8 papers receiving 67 citations

Peers

Countries citing papers authored by Luca Pannone

Since Specialization

Citations

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

Fields of papers citing papers by Luca Pannone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luca Pannone

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Fluorescent Labeling Can Significantly Perturb Measured Binding Affinity and Selectivity of Peptide–Protein Interactions 2024 ·The Journal of Physical Chemistry Letters ·Sara Bobone, (unknown), (unknown), (unknown), (unknown), (unknown), Paolo Calligari, Luca Pannone, Simone Martinelli, Marco Tartaglia, Gianfranco Bocchinfuso, Fernando Formaggio, Cristina Peggion, Barbara Biondi, Lorenzo Stella	0
2	Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant 2024 ·American Journal of Medical Genetics Part A ·Emilia Stellacci, (unknown), Luca Pannone, David A. Stevenson, (unknown), Serenella Venanzi, (unknown), Jonathan A. Bernstein, Marco Tartaglia, Simone Martinelli	0
3	The recurrent pathogenic Pro890Leu substitution in CLTC causes a generalized defect in synaptic transmission in Caenorhabditis elegans 2023 ·Frontiers in Molecular Neuroscience ·Luca Pannone, Valentina Muto, Francesca Nardecchia, Martina Di Rocco, Emilia Marchei, (unknown), Stefania Petrini, (unknown), (unknown), Lucia Bertuccini, Filippo Manti, Viola Folli, Serena Galosi, Elia Di Schiavi, Vincenzo Leuzzi, Marco Tartaglia, Simone Martinelli	0
4	SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction 2022 ·Clinical Genetics ·Manuela Priolo, (unknown), (unknown), Andrea Ciolfi, Luca Pannone, Valentina Muto, Marialetizia Motta, Cecilia Mancini, Francesca Clementina Radio, Marcello Niceta, Chiara Leoni, (unknown), Rosalba Carrozzo, (unknown), Corrado Mammì, Giuseppe Zampino, Simone Martinelli, Bruno Dallapiccola, Pietro Pichierri, Marco Tartaglia	2
5	Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disorders 2022 ·Journal of Allergy and Clinical Immunology ·Simona Coppola, Antonella Insalaco, (unknown), Martina Di Rocco, Denise Pires Marafon, Francesca Spadaro, Luca Pannone, (unknown), Luca Pasquini, Simone Martinelli, Fabrizio De Benedetti, Marco Tartaglia	22
6	Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings 2021 ·Clinical Genetics ·Alessandra D’Amico, Carmen L. Rosano, Luca Pannone, Valentina Pinna, (unknown), Marialetizia Motta, Lorenzo Ugga, Paola Daniele, (unknown), (unknown), Maria Siano, Claudia Santoro, Giulio Piluso, Simone Martinelli, Pietro Strisciuglio, Alessandro De Luca, Marco Tartaglia, Daniela Melis	5
7	C. elegans-based chemosensation strategy for the early detection of cancer metabolites in urine samples 2021 ·Scientific Reports ·(unknown), Martina Di Rocco, (unknown), (unknown), Edoardo Milanetti, (unknown), (unknown), Luca Pannone, Giancarlo Ruocco, Simone Martinelli, Viola Folli	15
8	Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders 2020 ·Clinical Genetics ·Rebeca Lorca, Luca Pannone, Elías Cuesta‐Llavona, Gianfranco Bocchinfuso, (unknown), Giovanna Carpentieri, (unknown), Elisabetta Flex, Marco Tartaglia, Eliécer Coto, Juan Gómez, Simone Martinelli	3
9	Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation 2020 ·Human Mutation ·Simone Martinelli, Luca Pannone, Christina Lißewski, Julia Brinkmann, Elisabetta Flex, Denny Schanze, Paolo Calligari, Massimiliano Anselmi, Francesca Pantaleoni, (unknown), Francesca Clementina Radio, Adonis S. Ioannides, Nils Rahner, Ina Schanze, Dragana Josifova, Gianfranco Bocchinfuso, Mina Ryten, Lorenzo Stella, Marco Tartaglia, Martin Zenker	1
10	Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy 2020 ·Journal of Medical Genetics ·Valeria Morbidoni, Emanuele Agolini, Kevin C. Slep, Luca Pannone, Daniela Zuccarello, Matteo Cassina, Enrico Grosso, (unknown), Leonardo Salviati, Bruno Dallapiccola, Antonio Novelli, Simone Martinelli, Eva Trevisson	11
11	A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype 2014 ·American Journal of Medical Genetics Part A ·Jonathan J. Edwards, Simone Martinelli, Luca Pannone, Ivan F. M. Lo, Lisong Shi, Lisa Edelmann, Marco Tartaglia, Ho‐Ming Luk, Bruce D. Gelb	12

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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