Chiara Pantaleoni

4.7k total citations
84 papers, 1.5k citations indexed

About

Chiara Pantaleoni is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Chiara Pantaleoni has authored 84 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 28 papers in Genetics and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Chiara Pantaleoni's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and Mitochondrial Function and Pathology (10 papers). Chiara Pantaleoni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (13 papers) and Mitochondrial Function and Pathology (10 papers). Chiara Pantaleoni collaborates with scholars based in Italy, United Kingdom and United States. Chiara Pantaleoni's co-authors include Daria Riva, Stefano D’Arrigo, Sara Bulgheroni, Chiara Vago, Silvana Franceschetti, Veronica Saletti, N. Milani, Francesca Nichelli, Enrico Alfei and Monica Devoti and has published in prestigious journals such as Neurology, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Chiara Pantaleoni

81 papers receiving 1.4k citations

Peers

Countries citing papers authored by Chiara Pantaleoni

Since Specialization

Citations

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

Fields of papers citing papers by Chiara Pantaleoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Pantaleoni

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Developmental profiles of young children with autism spectrum disorder and global developmental delay: A study with the GriffithsIIIscales 2023 ·Autism Research ·(unknown), Sara Bulgheroni, Enrico Toffalini, Chiara Pantaleoni, Silvia Lanfranchi	8
2	Periventricular heterotopia in a male child with USP9X missense variant 2023 ·American Journal of Medical Genetics Part A ·(unknown), Claudia Ciaccio, Alessandra Erbetta, Michele Pinelli, Vincenzo Nigro, Chiara Pantaleoni, Stefano D’Arrigo	1
3	Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center Experience 2023 ·Diagnostics ·(unknown), Silvia Esposito, Gianluca Marucci, Alessandra Erbetta, Paolo Ferroli, Laura Grazia Valentini, Chiara Pantaleoni, Stefano D’Arrigo, Veronica Saletti, Bianca Pollo, Rosina Paterra, Daria Riva, Sara Bulgheroni	1
4	Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3 -Related Syndrome 2023 ·Neurology Genetics ·Claudia Ciaccio, Chiara Pantaleoni, Marco Moscatelli, Luisa Chiapparini, Vincenzo Nigro, Enza Maria Valente, Francesca L. Sciacca, Laura Canafoglia, Sara Bulgheroni, Stefano D’Arrigo	1
5	Clinical features and magnesium levels: Novel insights in 15q11.2 BP1–BP2 copy number variants 2023 ·Journal of Intellectual Disability Research ·(unknown), (unknown), Claudia Ciaccio, Margherita Estienne, Rosamaria Silipigni, Francesca L. Sciacca, Chiara Pantaleoni, Stefano D’Arrigo, Donatella Milani	1
6	Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmus 2023 ·Frontiers in Neurology ·(unknown), Claudia Ciaccio, Barbara Castellotti, Francesca L. Sciacca, Chiara Pantaleoni, Stefano D’Arrigo	2
7	Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients 2021 ·Molecular Genetics and Metabolism ·(unknown), Francesco Nicita, Silvia Masnada, Roberta Battini, (unknown), Martino Montomoli, Angela Berardinelli, Chiara Pantaleoni, Anna Ardissone, Thomas Foiadelli, (unknown), Ettore Salsano, Pierangelo Veggiotti, Isabella Ceccherini, Isabella Moroni, Enrico Bertini, Davide Tonduti	6
8	Teaching NeuroImages: Symmetrical abnormalities of the globi pallidi in succinic semialdehyde dehydrogenase deficiency 2020 ·Neurology ·Silvia Esposito, Marco Moscatelli, Claudio Caccia, (unknown), Chiara Pantaleoni, Anna Ardissone, Cinzia Gellera, Laura Farina	2
9	Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients 2020 ·Biomedicines ·Silvia Bonanno, Stefania Marcuzzo, (unknown), (unknown), Riccardo Masson, Riccardo Zanin, Maria Teresa Arnoldi, Francesca Andreetta, Ornella Simoncini, Anna Venerando, Cinzia Gellera, Chiara Pantaleoni, Renato Mantegazza, Pia Bernasconi, Giovanni Baranello, Lorenzo Maggi	38
10	Chromosomal Microarray Analysis Has a Poor Diagnostic Yield in Children with Developmental Delay/Intellectual Disability When Concurrent Cerebellar Anomalies Are Present 2020 ·The Cerebellum ·Claudia Ciaccio, Chiara Pantaleoni, Sara Bulgheroni, Francesca L. Sciacca, Stefano D’Arrigo	2
11	Chiari I malformation in defined genetic syndromes in children: are there common pathways? 2019 ·Child s Nervous System ·Veronica Saletti, Ilaria Viganò, Giulia Melloni, Chiara Pantaleoni, Ignazio G. Vetrano, Laura Grazia Valentini	12
12	Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome 2018 ·International Journal of Molecular Sciences ·Francesca L. Sciacca, (unknown), Gloria Bedini, Fioravante Capone, Vincenzo Di Lazzaro, Sara Nava, Francesco Acerbi, Davide Rossi Sebastiano, S. Binelli, Giuseppe Faragò, (unknown), Marina Grisoli, Maria Grazia Bruzzone, Paolo Ferroli, Chiara Pantaleoni, (unknown), (unknown), Eugenio Parati, Anna Bersano	6
13	Outcome measures for children with movement disorders 2018 ·European Journal of Paediatric Neurology ·Emanuela Pagliano, Giovanni Baranello, Riccardo Masson, Maria Foscan, Maria Teresa Arnoldi, (unknown), (unknown), Chiara Pantaleoni	2
14	Vasculogenic and Angiogenic Pathways in Moyamoya Disease 2016 ·Current Medicinal Chemistry ·Gloria Bedini, Kinga Blecharz, Sara Nava, Peter Vajkoczy, Giulio Alessandri, Michela Ranieri, Francesco Acerbi, Paolo Ferroli, Daria Riva, Silvia Esposito, Chiara Pantaleoni, Nardo Nardocci, Federica Zibordi, Elisa Ciceri, Eugenio Parati, Anna Bersano	42
15	Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum 2015 ·European Journal of Paediatric Neurology ·Federica Natacci, Enrico Alfei, (unknown), Stefano D’Arrigo, Orsetta Zuffardi, Barbara Gentilin, Chiara Pantaleoni	19
16	POMK mutations disrupt muscle development leading to a spectrum of neuromuscular presentations 2014 ·Human Molecular Genetics ·Stefania Di Costanzo, Anuradha Balasubramanian, (unknown), Anete Rozkalne, Chiara Pantaleoni, S. Saredi, Vandana Gupta, (unknown), Timothy W. Yu, Peter B. Kang, Mustafa A. Salih, Marina Mora, Emanuela Gussoni, Christopher A. Walsh, M. Chiara Manzini	58
17	5p13 microduplication syndrome: A new case and better clinical definition of the syndrome 2012 ·European Journal of Medical Genetics ·Francesca Novara, Enrico Alfei, Stefano D’Arrigo, Chiara Pantaleoni, Silvana Beri, (unknown), Francesca L. Sciacca, Roberto Giorda, Orsetta Zuffardi, Roberto Ciccone	24
18	Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease 2012 ·Journal of the Neurological Sciences ·S. Saredi, Anna Ardissone, Alessandra Ruggieri, (unknown), Laura Farina, Rita Rinaldi, Evelina Silvestri, (unknown), Stefano D’Arrigo, Franco Salerno, Lucía Morandi, Paola Grammatico, Chiara Pantaleoni, Isabella Moroni, Marina Mora	20
19	Oligoyric microcephaly in a child with Williams syndrome 2002 ·American Journal of Medical Genetics Part A ·Francesca Faravelli, Stefano D’Arrigo, Irene Bagnasco, Angelo Selicorni, Ludovico D’Incerti, Daria Riva, Chiara Pantaleoni	3
20	Late neuropsychological and behavioural outcome of children surgically treated for craniopharyngioma 1998 ·Child s Nervous System ·Daria Riva, Chiara Pantaleoni, Monica Devoti, Veronica Saletti, Francesca Nichelli, Cesare Giorgi	66

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.

Explore authors with similar magnitude of impact