Simone Martinelli

5.1k total citations
47 papers, 1.3k citations indexed

About

Simone Martinelli is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Simone Martinelli has authored 47 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 14 papers in Immunology and 7 papers in Genetics. Recurrent topics in Simone Martinelli's work include Protein Tyrosine Phosphatases (17 papers), RNA modifications and cancer (12 papers) and Galectins and Cancer Biology (12 papers). Simone Martinelli is often cited by papers focused on Protein Tyrosine Phosphatases (17 papers), RNA modifications and cancer (12 papers) and Galectins and Cancer Biology (12 papers). Simone Martinelli collaborates with scholars based in Italy, United States and Netherlands. Simone Martinelli's co-authors include Marco Tartaglia, Elisabetta Flex, Bruce D. Gelb, Gianfranco Bocchinfuso, M Sorcini, Antonio Palleschi, Lorenzo Stella, Viviana Cordeddu, Gabriele Aquilina and Giuseppe Zampino and has published in prestigious journals such as Journal of Biological Chemistry, Scientific Reports and Journal of Allergy and Clinical Immunology.

In The Last Decade

Simone Martinelli

39 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simone Martinelli Italy	19	1.0k	433	292	175	147	47	1.3k
Martín Bonamino Brazil	20	669 0.7×	195 0.5×	332 1.1×	166 0.9×	102 0.7×	47	1.1k
Joanna Liliental United States	5	1.0k 1.0×	195 0.5×	203 0.7×	150 0.9×	90 0.6×	7	1.3k
Francesca Pantaleoni Italy	19	794 0.8×	603 1.4×	425 1.5×	74 0.4×	41 0.3×	29	1.3k
Luisa Cimmino United States	14	843 0.8×	257 0.6×	182 0.6×	203 1.2×	105 0.7×	18	1.3k
Karoline J. Briegel United States	17	720 0.7×	135 0.3×	242 0.8×	191 1.1×	50 0.3×	28	1.0k
William E. Tidyman United States	15	1.4k 1.4×	414 1.0×	322 1.1×	107 0.6×	61 0.4×	24	1.7k
Steffen Aulwurm Germany	13	599 0.6×	619 1.4×	478 1.6×	118 0.7×	71 0.5×	16	1.3k
Etienne Danis United States	18	1.0k 1.0×	102 0.2×	323 1.1×	232 1.3×	81 0.6×	40	1.4k
Inderpreet Sur Sweden	12	933 0.9×	127 0.3×	163 0.6×	256 1.5×	48 0.3×	17	1.2k
Shinji Mii Japan	23	721 0.7×	218 0.5×	426 1.5×	227 1.3×	58 0.4×	63	1.3k

Countries citing papers authored by Simone Martinelli

Since Specialization

Citations

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

Fields of papers citing papers by Simone Martinelli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Martinelli

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

All Works

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20 of 20 papers shown

Savitsky, Mikhail, Yonika Arum Larasati, Gonzalo P. Solis, et al.. (2025). Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathy. Science Signaling. 18(910). eadu9383–eadu9383.

Martinelli, Simone, Hélène Cavé, Alessandro De Luca, et al.. (2025). Interpreting the functional impact of genetic variants: The need for context qualifiers. The American Journal of Human Genetics. 113(1). 5–15.

Galosi, Serena, Cecilia Mancini, Paolo Calligari, et al.. (2024). Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome. Movement Disorders. 39(7). 1225–1231. 2 indexed citations

Colantoni, Alessio, Д. Н. Силачев, Valeria de Turris, et al.. (2024). Cortical neurons obtained from patient-derived iPSCs with GNAO1 p.G203R variant show altered differentiation and functional properties. Heliyon. 10(5). e26656–e26656. 6 indexed citations

Bobone, Sara, Paolo Calligari, Luca Pannone, et al.. (2024). Fluorescent Labeling Can Significantly Perturb Measured Binding Affinity and Selectivity of Peptide–Protein Interactions. The Journal of Physical Chemistry Letters. 15(40). 10252–10257.

Stellacci, Emilia, Luca Pannone, David A. Stevenson, et al.. (2024). Immunological and hematological findings as major features in a patient with a new germline pathogenic CBL variant. American Journal of Medical Genetics Part A. 194(8). e63627–e63627.

Rocco, Martina Di, Serena Galosi, Viola Folli, et al.. (2023). Phenotypic Assessment of Pathogenic Variants in GNAO1 and Response to Caffeine in C. elegans Models of the Disease. Genes. 14(2). 319–319. 9 indexed citations

Galosi, Serena, Giovanna Zorzi, Simone Martinelli, et al.. (2023). GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments. Parkinsonism & Related Disorders. 111. 105405–105405. 17 indexed citations

Nicita, Francesco, Fabrizia Stregapede, Federica Deodato, et al.. (2022). “Atypical” Krabbe disease in two siblings harboring biallelic GALC mutations including a deep intronic variant. European Journal of Human Genetics. 30(8). 984–988. 4 indexed citations

10.

Priolo, Manuela, Andrea Ciolfi, Luca Pannone, et al.. (2022). SHP2 's gain‐of‐function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics. 102(1). 12–21. 2 indexed citations

11.

D’Amico, Alessandra, Carmen L. Rosano, Luca Pannone, et al.. (2021). Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings. Clinical Genetics. 100(5). 563–572. 5 indexed citations

12.

Rocco, Martina Di, Serena Galosi, Viola Folli, et al.. (2021). Caenorhabditis elegans provides an efficient drug screening platform for GNAO1 -related disorders and highlights the potential role of caffeine in controlling dyskinesia. Human Molecular Genetics. 31(6). 929–941. 26 indexed citations

13.

Rocco, Martina Di, Edoardo Milanetti, Luca Pannone, et al.. (2021). C. elegans-based chemosensation strategy for the early detection of cancer metabolites in urine samples. Scientific Reports. 11(1). 17133–17133. 15 indexed citations

14.

Lorca, Rebeca, Luca Pannone, Elías Cuesta‐Llavona, et al.. (2020). Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders. Clinical Genetics. 99(3). 457–461. 3 indexed citations

15.

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). 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. Human Mutation. 41(6). 1171–1182. 1 indexed citations

16.

Martinelli, Simone, Aurelio Pio Nardozza, Paola Torreri, et al.. (2012). Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome*. Journal of Biological Chemistry. 287(32). 27066–27077. 26 indexed citations

17.

Motta, Marialetizia, Massimo Tatti, Simone Martinelli, et al.. (2011). Efficient one-step chromatographic purification and functional characterization of recombinant human Saposin C. Protein Expression and Purification. 78(2). 209–215. 1 indexed citations

18.

Bartucci, Monica, Susanne Svensson, Paolo Romania, et al.. (2011). Therapeutic targeting of Chk1 in NSCLC stem cells during chemotherapy. Cell Death and Differentiation. 19(5). 768–778. 142 indexed citations

19.

Cappellacci, Sandra, et al.. (2006). De novo pure 12q22q24.33 duplication: First report of a case with mental retardation, ADHD, and Dandy‐Walker malformation. American Journal of Medical Genetics Part A. 140A(11). 1203–1207. 12 indexed citations

20.

Loh, Mignon L., Simone Martinelli, Viviana Cordeddu, et al.. (2004). Acquired PTPN11 mutations occur rarely in adult patients with myelodysplastic syndromes and chronic myelomonocytic leukemia. Leukemia Research. 29(4). 459–462. 49 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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