Alessandro Iodice

586 total citations
24 papers, 212 citations indexed

About

Alessandro Iodice is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Alessandro Iodice has authored 24 papers receiving a total of 212 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Rheumatology. Recurrent topics in Alessandro Iodice's work include Epilepsy research and treatment (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Pregnancy and preeclampsia studies (3 papers). Alessandro Iodice is often cited by papers focused on Epilepsy research and treatment (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Pregnancy and preeclampsia studies (3 papers). Alessandro Iodice collaborates with scholars based in Italy, United States and Canada. Alessandro Iodice's co-authors include Carlo Fusco, Carlotta Spagnoli, Francesco Pisani, Daniele Frattini, Grazia Salerno, Laura Andréoli, Mario Motta, Cecilia Nalli, Elisa Fazzi and Andrea Lojacono and has published in prestigious journals such as European Journal of Pharmaceutics and Biopharmaceutics, Parkinsonism & Related Disorders and Lupus.

In The Last Decade

Alessandro Iodice

21 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessandro Iodice Italy 8 61 61 54 52 44 24 212
Ichraf Kraoua Tunisia 9 112 1.8× 111 1.8× 54 1.0× 28 0.5× 50 1.1× 64 270
Shakti Agrawal United Kingdom 11 73 1.2× 143 2.3× 67 1.2× 47 0.9× 23 0.5× 16 305
Esther Ganelin‐Cohen Israel 10 106 1.7× 71 1.2× 49 0.9× 40 0.8× 38 0.9× 26 274
Anaita Hegde India 10 58 1.0× 84 1.4× 24 0.4× 11 0.2× 31 0.7× 32 240
Kurt Schlachter Austria 8 77 1.3× 59 1.0× 31 0.6× 73 1.4× 79 1.8× 12 346
Qi‐Lun Lai China 11 62 1.0× 162 2.7× 41 0.8× 15 0.3× 21 0.5× 37 295
Amina Gargouri Tunisia 10 36 0.6× 138 2.3× 32 0.6× 29 0.6× 29 0.7× 70 284
Andrea Guerin Canada 8 99 1.6× 17 0.3× 103 1.9× 24 0.5× 33 0.8× 30 336
Mara Lúcia Schmitz Ferreira Santos Brazil 8 101 1.7× 70 1.1× 23 0.4× 28 0.5× 31 0.7× 37 276
Tjalf Ziemssen Germany 9 66 1.1× 53 0.9× 11 0.2× 27 0.5× 22 0.5× 26 237

Countries citing papers authored by Alessandro Iodice

Since Specialization
Citations

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

Fields of papers citing papers by Alessandro Iodice

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandro Iodice

This figure shows the co-authorship network connecting the top 25 collaborators of Alessandro Iodice. A scholar is included among the top collaborators of Alessandro Iodice 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 Alessandro Iodice. Alessandro Iodice 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.
Maines, Evelina, Annalisa Campomori, Alessandro Iodice, et al.. (2024). Formulation and clinical evaluation of carbidopa/levodopa oral solution for the treatment of sepiapterin reductase deficiency. European Journal of Pharmaceutics and Biopharmaceutics. 203. 114429–114429. 1 indexed citations
2.
Iodice, Alessandro, Margherita Nosadini, Irene Toldo, et al.. (2024). PPP3CA gene-related developmental and epileptic encephalopathy: Expanding the electro-clinical phenotype. Seizure. 121. 253–261. 1 indexed citations
3.
4.
Frattini, Daniele, et al.. (2023). Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 157–157. 1 indexed citations
5.
Iodice, Alessandro, Sara Signa, Mariasavina Severino, et al.. (2021). Combined medical therapy and neurosurgical revascularization preventing stroke in post-varicella angiopathy: Case report and review of literature. Brain and Development. 43(10). 1051–1056.
6.
Iodice, Alessandro, et al.. (2021). Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization.. Seizure. 94. 161–164. 3 indexed citations
7.
Iodice, Alessandro, Carlotta Spagnoli, Grazia Salerno, et al.. (2020). Long-term follow-up in infantile-onset SCAR18: A case report. Journal of Clinical Neuroscience. 77. 232–234. 3 indexed citations
8.
Iodice, Alessandro & Francesco Pisani. (2019). Status dystonicus: management and prevention in children at high risk.. PubMed. 90(3). 207–212. 7 indexed citations
9.
Iodice, Alessandro, Miryam Carecchio, Giovanna Zorzi, et al.. (2018). Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum. Brain and Development. 41(3). 250–256. 6 indexed citations
10.
Farnetti, Enrico, Davide Nicoli, Elena Pavlidis, et al.. (2018). Co-occurrence of an HSPG2 Missense Variant and Functional Polymorphisms in Atypical Schwartz–Jampel Syndrome Type 1 with Obesity: A Case Report. Journal of Pediatric Neurology. 17(4). 149–152. 1 indexed citations
11.
Carecchio, Miryam, Niccolò E. Mencacci, Alessandro Iodice, et al.. (2017). ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients. Parkinsonism & Related Disorders. 41. 37–43. 56 indexed citations
12.
Spagnoli, Carlotta, Grazia Salerno, Alessandro Iodice, et al.. (2017). KCNQ2 encephalopathy: A case due to a de novo deletion. Brain and Development. 40(1). 65–68. 17 indexed citations
13.
Nalli, Cecilia, Alessandro Iodice, Laura Andréoli, et al.. (2017). Long-term neurodevelopmental outcome of children born to prospectively followed pregnancies of women with systemic lupus erythematosus and/or antiphospholipid syndrome. Lupus. 26(5). 552–558. 19 indexed citations
14.
Giustina, Elvio Della, Alessandro Iodice, Carlotta Spagnoli, et al.. (2017). “Minimal” holoprosencephaly in a 14q deletion syndrome patient. American Journal of Medical Genetics Part A. 173(12). 3216–3220. 1 indexed citations
15.
Iodice, Alessandro, et al.. (2016). Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy. European Journal of Paediatric Neurology. 20(3). 454–456. 15 indexed citations
16.
Iodice, Alessandro, Carlotta Spagnoli, Grazia Salerno, et al.. (2016). Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis. Brain and Development. 39(2). 93–100. 25 indexed citations
17.
Ivanovski, Ivan, Alessandro Iodice, Simonetta Rosato, et al.. (2016). Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review. Molecular Syndromology. 7(6). 337–343. 3 indexed citations
18.
Spagnoli, Carlotta, Alessandro Iodice, Grazia Salerno, et al.. (2015). CMV-associated axonal sensory-motor Guillain–Barré syndrome in a child: Case report and review of the literature. European Journal of Paediatric Neurology. 20(1). 168–175. 13 indexed citations
19.
Nalli, Cecilia, Alessandro Iodice, Laura Andréoli, et al.. (2014). Children born to SLE and APS mothers. Lupus. 23(12). 1246–1248. 3 indexed citations
20.
Giordano, Lucio, Anna Molinaro, Alessandro Iodice, et al.. (2013). 17p13.1 microdeletion: Genetic and clinical findings in a new patient with epilepsy and comparison with literature. American Journal of Medical Genetics Part A. 164(1). 225–230. 6 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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