Paolo Alfieri

1.9k total citations
69 papers, 1.1k citations indexed

About

Paolo Alfieri is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Paolo Alfieri has authored 69 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 31 papers in Genetics and 17 papers in Cognitive Neuroscience. Recurrent topics in Paolo Alfieri's work include Genetics and Neurodevelopmental Disorders (27 papers), Protein Tyrosine Phosphatases (16 papers) and Autism Spectrum Disorder Research (15 papers). Paolo Alfieri is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Protein Tyrosine Phosphatases (16 papers) and Autism Spectrum Disorder Research (15 papers). Paolo Alfieri collaborates with scholars based in Italy, United States and United Kingdom. Paolo Alfieri's co-authors include Stefano Vicari, Giorgia Piccini, Eugenio Mercuri, Marco Tartaglia, M. Cristina Digilio, Enrico Bertini, Giuseppe Zampino, Deny Menghini, Chiara Leoni and Marika Pane and has published in prestigious journals such as PLoS ONE, The Journal of Physiology and International Journal of Molecular Sciences.

In The Last Decade

Paolo Alfieri

62 papers receiving 1.0k citations

Peers

Paolo Alfieri

GENET

CMN

PMH

Simon Girard Canada

Fabien Fauchereau France

Zoran Brkanac United States

Maria T. Acosta United States

Erwin Petek Austria

Lorenzo Sinibaldi Italy

Željka Krsnik Croatia

María Dolores Rubio Spain

Jennifer Brown United States

Simon Girard Canada

Paolo Alfieri

537 ×0.8

238 ×0.7

GENET

415 ×2.2

127 ×0.9

CMN

100 ×0.9

PMH

Citations per year, relative to Paolo Alfieri Paolo Alfieri (= 1×) peers Simon Girard

Countries citing papers authored by Paolo Alfieri

Since Specialization

Citations

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

Fields of papers citing papers by Paolo Alfieri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paolo Alfieri

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

Rose, Paola De, et al.. (2024). Differences and similarities between children and adolescent exposed to interpersonal traumas with and without Intellectual Disability: An explorative study. Research in Developmental Disabilities. 154. 104860–104860.

Alesi, Viola, Charles E. Schwartz, Cindy Skinner, et al.. (2024). PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports. Frontiers in Psychiatry. 14. 1327802–1327802. 1 indexed citations

Catteruccia, Michela, Daria Diodato, Francesco Nicita, et al.. (2024). Evolution of neuropsychological and behavioral profile in a cohort of pediatric patients with Becker muscular dystrophy in a longitudinal study. Neuromuscular Disorders. 36. 33–37.

Alfieri, Paolo, Marina Macchiaiolo, Marcella Zollino, et al.. (2023). Behavioral profiling in children and adolescents with Malan syndrome. PubMed. 2. 1106228–1106228. 2 indexed citations

Fucà, Elisa, et al.. (2023). Assessment of oppositional defiant disorder and oppositional behavior in children and adolescents with Down syndrome. Frontiers in Psychiatry. 13. 1062201–1062201. 1 indexed citations

Alfieri, Paolo, et al.. (2023). “Corp-Osa-Mente”, a Combined Psychosocial–Neuropsychological Intervention for Adolescents and Young Adults with Fragile X Syndrome: An Explorative Study. Brain Sciences. 13(2). 277–277. 3 indexed citations

Alfieri, Paolo, Maria Lisa Dentici, M. Cristina Digilio, et al.. (2021). Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study. Journal of Clinical Medicine. 10(7). 1523–1523. 2 indexed citations

Alfieri, Paolo, Lorenzo Sinibaldi, Giovanni Valeri, et al.. (2020). Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases. Genes Brain & Behavior. 19(7). e12687–e12687. 5 indexed citations

Sferra, Antonella, Stefania Petrini, Emanuele Bellacchio, et al.. (2020). TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. International Journal of Molecular Sciences. 21(4). 1385–1385. 26 indexed citations

10.

Dentici, Maria Lisa, Paola De Rose, Viola Alesi, et al.. (2020). 7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling. Brain Sciences. 10(11). 839–839. 5 indexed citations

11.

Nicita, Francesco, Emanuele Bellacchio, Paolo Alfieri, et al.. (2019). Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia. Clinical Genetics. 96(2). 169–175. 20 indexed citations

12.

Stregapede, Fabrizia, Lorena Travaglini, Adriana Rebelo, et al.. (2019). Hereditary spastic paraplegia is a novel phenotype for germline de novo ATP1A1 mutation. Clinical Genetics. 97(3). 521–526. 11 indexed citations

13.

Lepri, Francesca Romana, Dario Cocciadiferro, Bartolomeo Augello, et al.. (2017). Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature. International Journal of Molecular Sciences. 19(1). 82–82. 17 indexed citations

14.

Compagnucci, Claudia, Sabina Barresi, Stefania Petrini, et al.. (2016). Rho Kinase Inhibition Is Essential During In Vitro Neurogenesis and Promotes Phenotypic Rescue of Human Induced Pluripotent Stem Cell-Derived Neurons With Oligophrenin-1 Loss of Function. Stem Cells Translational Medicine. 5(7). 860–869. 18 indexed citations

15.

Alfieri, Paolo, Giorgia Piccini, Maria Luigia Gambardella, et al.. (2014). Behavioral Profile in RASopathies. American Journal of Medical Genetics Part A. 164(4). 934–942. 64 indexed citations

16.

Fusco, Carmela, Lucia Micale, Bartolomeo Augello, et al.. (2013). Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits. European Journal of Human Genetics. 22(1). 64–70. 47 indexed citations

17.

Marca, Giacomo Della, Chiara Leoni, Serena Dittoni, et al.. (2011). Increased Sleep Spindle Activity in Patients With Costello Syndrome (HRAS Gene Mutation). Journal of Clinical Neurophysiology. 28(3). 314–318. 9 indexed citations

18.

Alfieri, Paolo, Laura Cesarini, Paola De Rose, et al.. (2011). Visual processing in Noonan syndrome: Dorsal and ventral stream sensitivity. American Journal of Medical Genetics Part A. 155(10). 2459–2464. 13 indexed citations

19.

Rose, Paola De, Donatella Lettori, Paolo Alfieri, et al.. (2010). Visual and visuoperceptual function in children with Panayiotopoulos syndrome. Epilepsia. 51(7). 1205–1211. 9 indexed citations

20.

Alfieri, Paolo. (2008). La formazione morale e patriottica della gioventù cattolica nella rivista degli oratori milanesi (1907-1917). 1000–1029.

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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