Alessia Fiorentino

6.7k total citations
15 papers, 335 citations indexed

About

Alessia Fiorentino is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Alessia Fiorentino has authored 15 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Alessia Fiorentino's work include Genetics and Neurodevelopmental Disorders (5 papers), Retinal Development and Disorders (4 papers) and Ion channel regulation and function (3 papers). Alessia Fiorentino is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Retinal Development and Disorders (4 papers) and Ion channel regulation and function (3 papers). Alessia Fiorentino collaborates with scholars based in United Kingdom, Japan and Italy. Alessia Fiorentino's co-authors include Andrew McQuillin, Sally I. Sharp, Antonio Pizzuti, Caterina Catalanotto, Lorenzo Sinibaldi, Viviana Caputo, Carlo Cogoni, Chiara Parisi, Augusto Pasini and David Curtis and has published in prestigious journals such as PLoS ONE, American Journal of Ophthalmology and Investigative Ophthalmology & Visual Science.

In The Last Decade

Alessia Fiorentino

14 papers receiving 331 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alessia Fiorentino United Kingdom 9 200 89 62 58 48 15 335
Lalit Kaurani Germany 10 207 1.0× 62 0.7× 68 1.1× 33 0.6× 36 0.8× 16 387
Shaomin Zhu China 12 212 1.1× 75 0.8× 26 0.4× 132 2.3× 10 0.2× 14 396
Daniëlle G.M. Bosch Netherlands 10 183 0.9× 133 1.5× 10 0.2× 47 0.8× 54 1.1× 12 374
Jue Ji China 12 177 0.9× 148 1.7× 19 0.3× 68 1.2× 11 0.2× 27 378
Andrea Christoforou United States 15 290 1.4× 157 1.8× 24 0.4× 38 0.7× 5 0.1× 23 559
Stephen I. Levin United States 8 238 1.2× 57 0.6× 9 0.1× 189 3.3× 12 0.3× 10 376
Tammi L. Reza United States 6 308 1.5× 18 0.2× 43 0.7× 118 2.0× 28 0.6× 6 494
Sahba Seddighi United States 7 108 0.5× 15 0.2× 15 0.2× 32 0.6× 15 0.3× 8 293
Debora Napoli Italy 9 184 0.9× 68 0.8× 18 0.3× 69 1.2× 29 0.6× 16 281
Jianmin Yuan China 12 207 1.0× 114 1.3× 68 1.1× 58 1.0× 2 0.0× 28 375

Countries citing papers authored by Alessia Fiorentino

Since Specialization
Citations

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

Fields of papers citing papers by Alessia Fiorentino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessia Fiorentino

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

All Works

15 of 15 papers shown
1.
Giannini, Giulia, Raffaella Minardi, Giorgio Barletta, et al.. (2024). The Degree of Cardiovascular Autonomic Dysfunction is not Different in GBA-Related and Idiopathic Parkinson’s Disease Patients: A Case-Control Instrumental Evaluation. Journal of Parkinson s Disease. 14(2). 335–346. 3 indexed citations
2.
Georgiou, Michalis, Sarah Hull, Anthony G. Robson, et al.. (2019). GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel Therapies. American Journal of Ophthalmology. 210. 59–70. 41 indexed citations
3.
Sharp, Sally I., Alessia Fiorentino, Niamh L. O’Brien, et al.. (2019). GENETIC ASSOCIATION AND FUNCTIONAL CHARACTERIZATION OF A VARIANT IN THE MCPH1 GENE IN BIPOLAR DISORDER AND SCHIZOPHRENIA. European Neuropsychopharmacology. 29. S966–S967.
4.
Sharp, Sally I., Niamh L. O’Brien, Alessia Fiorentino, et al.. (2019). Genetic association and functional characterization of MCPH1 gene variation in bipolar disorder and schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(4). 258–265. 2 indexed citations
5.
Fiorentino, Alessia, Jing Yu, Gavin Arno, et al.. (2018). Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa.. PubMed. 24. 603–612. 6 indexed citations
6.
O’Brien, Niamh L., Alessia Fiorentino, David Curtis, et al.. (2018). Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder. Schizophrenia Research. 199. 181–188. 7 indexed citations
7.
Fiorentino, Alessia, Sally I. Sharp, Niamh L. O’Brien, et al.. (2017). Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. Annals of Human Genetics. 82(2). 88–92. 16 indexed citations
8.
Fiorentino, Alessia, Gavin Arno, Nikolas Pontikos, et al.. (2017). Mutations in the X-linked gene PRPS1 cause retinal degeneration in females. Investigative Ophthalmology & Visual Science. 58(8). 1243–1243. 1 indexed citations
9.
Fiorentino, Alessia, Kaoru Fujinami, Gavin Arno, et al.. (2017). Missense variants in the X-linked genePRPS1cause retinal degeneration in females. Human Mutation. 39(1). 80–91. 23 indexed citations
10.
Arno, Gavin, Graham E. Holder, Christina Chakarova, et al.. (2016). Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3). JAMA Ophthalmology. 134(8). 924–924. 18 indexed citations
11.
Fiorentino, Alessia, Niamh L. O’Brien, Sally I. Sharp, et al.. (2016). Genetic variation in the miR‐708 gene and its binding targets in bipolar disorder. Bipolar Disorders. 18(8). 650–656. 10 indexed citations
12.
Fiorentino, Alessia, Niamh L. O’Brien, Devin P. Locke, et al.. (2014). Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data. Bipolar Disorders. 16(6). 583–591. 36 indexed citations
13.
Fiorentino, Alessia, Sally I. Sharp, & Andrew McQuillin. (2014). Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia. European Journal of Human Genetics. 23(9). 1200–1206. 45 indexed citations
14.
Kandaswamy, Radhika, Andrew McQuillin, Sally I. Sharp, et al.. (2013). Genetic Association, Mutation Screening, and Functional Analysis of a Kozak Sequence Variant in the Metabotropic Glutamate Receptor 3 Gene in Bipolar Disorder. JAMA Psychiatry. 70(6). 591–591. 24 indexed citations
15.
Caputo, Viviana, Lorenzo Sinibaldi, Alessia Fiorentino, et al.. (2011). Brain Derived Neurotrophic Factor (BDNF) Expression Is Regulated by MicroRNAs miR-26a and miR-26b Allele-Specific Binding. PLoS ONE. 6(12). e28656–e28656. 103 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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