Ivana Ricca

945 total citations
20 papers, 303 citations indexed

About

Ivana Ricca is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ivana Ricca has authored 20 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Ivana Ricca's work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ivana Ricca is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Ivana Ricca collaborates with scholars based in Italy, United States and France. Ivana Ricca's co-authors include Orsetta Zuffardi, Filippo M. Santorelli, Roberto Ciccone, Annalisa Vetro, Daniela Toniolo, Anna Verri, Federica Morani, Emma Burkitt‐Wright, Sahar Mansour and Sarah Walters and has published in prestigious journals such as Scientific Reports, Movement Disorders and Neurobiology of Disease.

In The Last Decade

Ivana Ricca

20 papers receiving 302 citations

Peers

Ivana Ricca

GENET

CMN

NEURO

Tyrone DeSpenza United States

Joseph Goodliffe United States

Niklas Schwarz Germany

Silvia Marenna Italy

Danielle S. Rudd United States

Ábel Vértesy Austria

Margaret Maronski United States

Maria Chiara Malaguti Italy

Kazue Kimura Japan

Anke Van Dijck Belgium

Tyrone DeSpenza United States

Ivana Ricca

156 ×1.0

79 ×0.6

GENET

77 ×1.0

CMN

49 ×0.9

10 ×0.4

NEURO

Citations per year, relative to Ivana Ricca Ivana Ricca (= 1×) peers Tyrone DeSpenza

Countries citing papers authored by Ivana Ricca

Since Specialization

Citations

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

Fields of papers citing papers by Ivana Ricca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivana Ricca

This figure shows the co-authorship network connecting the top 25 collaborators of Ivana Ricca. A scholar is included among the top collaborators of Ivana Ricca 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 Ivana Ricca. Ivana Ricca 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

Ugga, Lorenzo, Mirco Cosottini, Ivana Ricca, et al.. (2024). MRI‐ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study. Movement Disorders. 39(8). 1343–1351. 2 indexed citations

Branchu, Julien, Ivana Ricca, Karim Dorgham, et al.. (2024). Decreasing ganglioside synthesis delays motor and cognitive symptom onset in Spg11 knockout mice. Neurobiology of Disease. 199. 106564–106564. 1 indexed citations

Torella, Annalaura, Ivana Ricca, Giulio Piluso, et al.. (2023). A new genetic cause of spastic ataxia: the p.Glu415Lys variant in TUBA4A. Journal of Neurology. 270(10). 5057–5063. 4 indexed citations

Cosottini, Mirco, Graziella Donatelli, Ivana Ricca, et al.. (2022). Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases. European Radiology. 32(12). 8058–8064. 4 indexed citations

Todiere, Giancarlo, Maria Aurora Morales, Andrea Barison, et al.. (2022). Cardiac magnetic resonance findings in neuronal ceroid lipofuscinosis: A case report. Frontiers in Neurology. 13. 942667–942667. 1 indexed citations

Chilosi, Anna Maria, Ivana Ricca, A Comparini, et al.. (2022). Differences and Commonalities in Children with Childhood Apraxia of Speech and Comorbid Neurodevelopmental Disorders: A Multidimensional Perspective. Journal of Personalized Medicine. 12(2). 313–313. 11 indexed citations

Donato, Ilaria Di, Antonio Gallo, Ivana Ricca, et al.. (2021). POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients. Neurological Sciences. 43(2). 1071–1077. 9 indexed citations

Michele, Giovanna De, Daniele Galatolo, Serena Galosi, et al.. (2021). Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations. Journal of Neurology. 269(3). 1476–1484. 5 indexed citations

Riso, Vittorio, Daniele Galatolo, Melissa Barghigiani, et al.. (2021). A next generation sequencing‐based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21. European Journal of Neurology. 28(8). 2784–2788. 6 indexed citations

10.

Ricca, Ivana, et al.. (2021). Clinical Characterization of a 6-Year-Old Patient with Autism and Two Adjacent Duplications on 10q11.22q11.23. A Case Report. Children. 8(6). 518–518. 3 indexed citations

11.

Srivastava, Siddharth, Angelica D’Amore, Julie S. Cohen, et al.. (2020). Expansion of the genetic landscape of ERLIN2‐related disorders. Annals of Clinical and Translational Neurology. 7(4). 573–578. 13 indexed citations

12.

Ricca, Ivana, Alessandra Tessa, Rosanna Trovato, Giacomo Maria Bacci, & Filippo M. Santorelli. (2020). Docosahexaenoic acid in ARSACS: observations in two patients. BMC Neurology. 20(1). 215–215. 5 indexed citations

13.

Calderoni, Sara, Ivana Ricca, Giulia Balboni, et al.. (2020). Evaluation of Chromosome Microarray Analysis in a Large Cohort of Females with Autism Spectrum Disorders: A Single Center Italian Study. Journal of Personalized Medicine. 10(4). 160–160. 10 indexed citations

14.

Ricca, Ivana, Federica Morani, Giacomo Maria Bacci, et al.. (2019). Clinical and molecular studies in two new cases of ARSACS. Neurogenetics. 20(1). 45–49. 12 indexed citations

15.

Morani, Federica, Stefano Doccini, Francesco Pezzini, et al.. (2019). Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy. Scientific Reports. 9(1). 11878–11878. 27 indexed citations

16.

Grieco, Giulio, Stella Gagliardi, Ivana Ricca, et al.. (2018). New CACNA1A deletions are associated to migraine phenotypes. The Journal of Headache and Pain. 19(1). 75–75. 17 indexed citations

17.

Pichiecchio, Anna, Roberta La Piana, Daniel Doherty, et al.. (2012). COL4A1-Related Disease: Raised Creatine Kinase and Cerebral Calcification as Useful Pointers. Neuropediatrics. 43(5). 283–288. 16 indexed citations

18.

Rossi, Elena, Anna Verri, Maria Grazia Patricelli, et al.. (2008). A 12 Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea. European Journal of Medical Genetics. 51(6). 631–638. 59 indexed citations

19.

Clayton‐Smith, Jill, Sarah Walters, Emma Hobson, et al.. (2008). Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance. European Journal of Human Genetics. 17(4). 434–443. 64 indexed citations

20.

Torniero, Claudia, Bernardo Dalla Bernardina, Francesca Novara, et al.. (2006). Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams–Beuren locus. European Journal of Human Genetics. 15(1). 62–67. 34 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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