Davide Tonduti

4.3k total citations
64 papers, 1.1k citations indexed

About

Davide Tonduti is a scholar working on Molecular Biology, Immunology and Rheumatology. According to data from OpenAlex, Davide Tonduti has authored 64 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 16 papers in Immunology and 10 papers in Rheumatology. Recurrent topics in Davide Tonduti's work include RNA regulation and disease (29 papers), interferon and immune responses (16 papers) and RNA Research and Splicing (14 papers). Davide Tonduti is often cited by papers focused on RNA regulation and disease (29 papers), interferon and immune responses (16 papers) and RNA Research and Splicing (14 papers). Davide Tonduti collaborates with scholars based in Italy, United States and France. Davide Tonduti's co-authors include Simona Orcesi, Adeline Vanderver, Umberto Balottin, Odile Boespflug‐Tanguy, Raphael Schiffmann, Elisa Fazzi, Roberta La Piana, Diana Rodriguez, Luisa Chiapparini and Geneviève Bernard and has published in prestigious journals such as Neurology, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Davide Tonduti

57 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Davide Tonduti Italy 19 728 198 183 127 106 64 1.1k
Guy Helman United States 19 692 1.0× 156 0.8× 108 0.6× 23 0.2× 113 1.1× 41 1.0k
Boris Keren France 21 649 0.9× 115 0.6× 515 2.8× 41 0.3× 49 0.5× 70 1.1k
Steffen Uebe Germany 22 819 1.1× 138 0.7× 507 2.8× 65 0.5× 69 0.7× 58 1.3k
David Nascene United States 17 583 0.8× 112 0.6× 76 0.4× 39 0.3× 230 2.2× 72 950
Patricia G. Wheeler United States 22 529 0.7× 73 0.4× 400 2.2× 49 0.4× 37 0.3× 41 1.1k
Christel Thauvin‐Robinet France 21 762 1.0× 54 0.3× 532 2.9× 24 0.2× 95 0.9× 80 1.4k
Hanna Mierzewska Poland 15 444 0.6× 37 0.2× 127 0.7× 44 0.3× 126 1.2× 57 728
Haike Reznik‐Wolf Israel 15 554 0.8× 128 0.6× 171 0.9× 16 0.1× 40 0.4× 39 888
Nadia Sakati Saudi Arabia 22 819 1.1× 42 0.2× 546 3.0× 348 2.7× 144 1.4× 78 1.7k
Ahmet Okay Çağlayan Türkiye 18 482 0.7× 41 0.2× 390 2.1× 72 0.6× 36 0.3× 79 1.1k

Countries citing papers authored by Davide Tonduti

Since Specialization
Citations

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

Fields of papers citing papers by Davide Tonduti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davide Tonduti

This figure shows the co-authorship network connecting the top 25 collaborators of Davide Tonduti. A scholar is included among the top collaborators of Davide Tonduti 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 Davide Tonduti. Davide Tonduti 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.
Gavazzi, Francesco, Sarah Woidill, Evangeline Wassmer, et al.. (2025). Critical Functional Domains in Pediatric Onset TUBB4A-Related Leukodystrophy: A Clinical and Caregiver's Perspective. Pediatric Neurology. 173. 156–165.
2.
Whitehead, Matthew T., Davide Tonduti, Laura Farina, et al.. (2024). Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease. American Journal of Neuroradiology. 45(6). 769–772.
3.
4.
Garone, Giacomo, Alessandro Capuano, Flaminia Frascarelli, et al.. (2024). Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology. Parkinsonism & Related Disorders. 126. 107057–107057. 4 indexed citations
5.
Rey, Federica, Silvia Anna Ciafrè, Silvia Galardi, et al.. (2023). Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1. Genes & Diseases. 11(3). 101028–101028. 2 indexed citations
6.
Rey, Federica, Clarissa Berardo, Giovanna Casili, et al.. (2023). Redox Imbalance in Neurological Disorders in Adults and Children. Antioxidants. 12(4). 965–965. 8 indexed citations
7.
Masnada, Silvia, Paola Anna Erba, Anna Camporesi, et al.. (2023). FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. Neurological Sciences. 44(9). 3037–3043. 4 indexed citations
8.
Tonduti, Davide, et al.. (2023). Establishing Patient-Centered Outcomes for MCT8 Deficiency: Stakeholder Engagement and Systematic Literature Review. Neuropsychiatric Disease and Treatment. Volume 19. 2195–2216. 5 indexed citations
9.
Iascone, Maria, Luigina Spaccini, Davide Tonduti, et al.. (2022). Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child. Genes. 13(3). 442–442. 14 indexed citations
10.
Viri, Maurizio, Leone Giordano, Roberta La Piana, et al.. (2022). The Epileptology of Aicardi–Goutières Syndrome: Electroclinical Phenotype and Clinical–Radiological Correlation. Neuropediatrics. 53(S 01). S1–S6.
11.
Gavazzi, Francesco, Holly Dubbs, Valentina De Giorgis, et al.. (2020). Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features. Pediatric Neurology. 115. 1–6. 17 indexed citations
12.
Giorgis, Valentina De, Costanza Varesio, Maurizio Viri, et al.. (2020). The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings. Seizure. 86. 197–209. 3 indexed citations
13.
Masnada, Silvia, Veronica Saletti, Luisa Chiapparini, et al.. (2019). Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency. Metabolic Brain Disease. 34(6). 1565–1575. 15 indexed citations
14.
Ardissone, Anna, Davide Tonduti, Andrea Legati, et al.. (2018). KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literature. Orphanet Journal of Rare Diseases. 13(1). 45–45. 28 indexed citations
15.
Ciaccio, Claudia, Veronica Saletti, Stefano D’Arrigo, et al.. (2018). Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience. European Journal of Medical Genetics. 62(12). 103596–103596. 43 indexed citations
16.
Invernizzi, Federica, Celeste Panteghini, Luisa Chiapparini, et al.. (2017). Thiamine-responsive disease due to mutation of tpk1 : Importance of avoiding misdiagnosis. Neurology. 89(8). 870–871. 13 indexed citations
17.
Tonduti, Davide, Simona Orcesi, Emma M. Jenkinson, et al.. (2016). Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome. European Journal of Paediatric Neurology. 20(4). 604–610. 24 indexed citations
18.
Piana, Roberta La, C. Uggetti, Ivana Olivieri, et al.. (2013). Bilateral striatal necrosis in two subjects with Aicardi–Goutières syndrome due to mutations in ADAR1 (AGS6). American Journal of Medical Genetics Part A. 164(3). 815–819. 27 indexed citations
19.
Vanderver, Adeline, Davide Tonduti, Sarah Auerbach, et al.. (2012). Neurotransmitter abnormalities and response to supplementation in SPG11. Molecular Genetics and Metabolism. 107(1-2). 229–233. 11 indexed citations
20.
Tétreault, Martine, Karine Choquet, Simona Orcesi, et al.. (2011). Recessive Mutations in POLR3B, Encoding the Second Largest Subunit of Pol III, Cause a Rare Hypomyelinating Leukodystrophy. The American Journal of Human Genetics. 89(5). 652–655. 110 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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