Stefano D’Arrigo

5.6k citations

79 papers · 1.9k indexed · 1 hit paper · h-index 21

Impact in

Neurology top 2%
- Vestibular and auditory disorders
Cognitive Neuroscience top 5%
- Functional Brain Connectivity Studies

Papers in

Neurology 10
Genetics 26
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 8

Co-authors: Daria Riva Sara Bulgheroni Chiara Pantaleoni Deborah Ely Budding Nancy C. Andreasen Tadashi Yamazaki Leonard F. Koziol Jeremy D. Schmahmann
Journals: Journal of Child Neurology (9 papers)Neuropediatrics (4 papers)The Cerebellum (4 papers)Cephalalgia (3 papers)Brain and Development (3 papers)
Partner nations: Italy United Kingdom United States

In The Last Decade

Stefano D’Arrigo

76 papers receiving 1.9k citations

Hit Papers

align trajectories log scale

Consensus Paper: The Cerebellum's Role in Movement and Cognition 2013 · 775 citations

Peers

Countries citing papers authored by Stefano D’Arrigo

Since Specialization

Citations

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

Fields of papers citing papers by Stefano D’Arrigo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefano D’Arrigo. 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 Stefano D’Arrigo. The network helps show where Stefano D’Arrigo may publish in the future.

Co-authors

The 25 scholars most cited alongside Stefano D’Arrigo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stefano D’Arrigo Line = papers co-authored together Stefano D’Arrigo links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Periventricular heterotopia in a male child with USP9X missense variant American Journal of Medical Genetics Part A ·松本宣郎, Claudia Ciaccio, Alessandra Erbetta, Michele Pinelli, Vincenzo Nigro, Chiara Pantaleoni, Stefano D’Arrigo	2023	1
2	Cognitive and Behavioral Outcome of Pediatric Low-Grade Central Nervous System Tumors Treated Only with Surgery: A Single Center Experience Diagnostics ·M. Santhiya, 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	2023	1
3	Neurologic, Neuropsychologic, and Neuroradiologic Features of EBF3 -Related Syndrome 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	2023	1
4	Clinical features and magnesium levels: Novel insights in 15q11.2 BP1–BP2 copy number variants Journal of Intellectual Disability Research ·Doralba Jaramillo U., RW O'Neill, Claudia Ciaccio, Margherita Estienne, Rosamaria Silipigni, Francesca L. Sciacca, Chiara Pantaleoni, Stefano D’Arrigo, Donatella Milani	2023	1
5	Pediatric Slow-Progressive, but Not Non-Progressive Cerebellar Ataxia Delays Intra-Limb Anticipatory Postural Adjustments in the Upper Arm Brain Sciences ·Antonio Gutiérrez-Márquez, Roberto Esposti, В В Новохатский, Claudia Ciaccio, 松本宣郎, Stefano D’Arrigo, Paolo Cavallari	2023	0
6	Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmus Frontiers in Neurology ·Baolong Jia, Claudia Ciaccio, Barbara Castellotti, Francesca L. Sciacca, Chiara Pantaleoni, Stefano D’Arrigo	2023	2
7	Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol Seizure ·Elena Freri, Barbara Castellotti, Laura Canafoglia, Francesca Ragona, Roberta Solazzi, Fernando Mera González, Stefania Magri, K. Kleve, Stefano D’Arrigo, Cinzia Gellera, Jacopo C. DiFrancesco, Tiziana Granata	2021	7
8	CGH Findings in Children with Complex and Essential Autistic Spectrum Disorder Journal of Autism and Developmental Disorders ·Cristian Pinats, Sara Bulgheroni, Stefano D’Arrigo, Silvia Esposito, M. Santhiya, Veronica Saletti, Enrico Alfei, Francesca L. Sciacca, Abdullahi Rabi'u, Chiara Pantaleoni, Daria Riva	2021	4
9	Chromosomal Microarray Analysis Has a Poor Diagnostic Yield in Children with Developmental Delay/Intellectual Disability When Concurrent Cerebellar Anomalies Are Present The Cerebellum ·Claudia Ciaccio, Chiara Pantaleoni, Sara Bulgheroni, Francesca L. Sciacca, Stefano D’Arrigo	2020	2
10	EED and EZH2 constitutive variants: A study to expand the Cohen‐Gibson syndrome phenotype and contrast it with Weaver syndrome American Journal of Medical Genetics Part A ·Rae Ferguson, Chey Loveday, Anna Zachariou, Lucy‐Ann Behan, Kate Chandler, Trevor Cole, Stefano D’Arrigo, Andrea Dieckmann, Alison Foster, James Gibney, Matthew F. Hunter, Donatella Milani, Chiara Pantaleoni, Edna Roche, Endah Puspitotanti, Amanda Springer, Susan M. White, Katrina Tatton‐Brown	2019	23
11	Comprehensive molecular screening strategy of OCLN in band‐like calcification with simplified gyration and polymicrogyria Clinical Genetics ·Emma M. Jenkinson, John H. Livingston, Mary O’Driscoll, Isabelle Desguerre, Rima Nabbout, Nathalie Boddaert, Gabriela Soares, Makiko Nishida, Stefano D’Arrigo, Gillian Rice, Yanick J. Crow	2017	8
12	Cognitive, adaptive, and behavioral features in Joubert syndrome American Journal of Medical Genetics Part A ·Sara Bulgheroni, Stefano D’Arrigo, Sabrina Signorini, Marilena Briguglio, Alex. Anning, Manuela Casarano, Francesca Mancini, Marta Romani, Paolo Alfieri, Roberta Battini, C. P. Adithyaraj, Gaetano Tortorella, Enrico Bertini, Vincenzo Leuzzi, Enza Maria Valente, Daria Riva	2016	21
13	Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum European Journal of Paediatric Neurology ·Federica Natacci, Enrico Alfei, Jia-Qian Xie, Stefano D’Arrigo, Orsetta Zuffardi, Barbara Gentilin, Chiara Pantaleoni	2015	19
14	Consensus Paper: The Cerebellum's Role in Movement and Cognition The Cerebellum ·Leonard F. Koziol, Deborah Ely Budding, Nancy C. Andreasen, Stefano D’Arrigo, Sara Bulgheroni, Hiroshi Imamizu, Masao Ito, Mario Manto, Cherie L. Marvel, K L Parker, Giovanni Pezzulo, Narender Ramnani, Daria Riva, Jeremy D. Schmahmann, Larry R. Vandervert, Tadashi Yamazaki Hit paper breakdown →	2013	775
15	5p13 microduplication syndrome: A new case and better clinical definition of the syndrome European Journal of Medical Genetics ·Francesca Novara, Enrico Alfei, Stefano D’Arrigo, Chiara Pantaleoni, Silvana Beri, 李少梅, Francesca L. Sciacca, Roberto Giorda, Orsetta Zuffardi, Roberto Ciccone	2012	24
16	Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease Journal of the Neurological Sciences ·S. Saredi, Anna Ardissone, Alessandra Ruggieri, 黄德揆, Laura Farina, Rita Rinaldi, Evelina Silvestri, Marthe‐Elisabeth Eladari, Stefano D’Arrigo, Franco Salerno, Lucía Morandi, Paola Grammatico, Chiara Pantaleoni, Isabella Moroni, Marina Mora	2012	20
17	Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria The American Journal of Human Genetics ·Mary O’Driscoll, Sarah B. Daly, Jill Urquhart, Graeme C. Black, Daniela T. Pilz, Knut Brockmann, Meriel McEntagart, Ghada M. H. Abdel‐Salam, Maha S. Zaki, Nicole I. Wolf, Roger L. Ladda, Susan L. Sell, Stefano D’Arrigo, Waney Squier, William B. Dobyns, John H. Livingston, Yanick J. Crow	2010	92
18	The Effectiveness of Hospitalization in the Treatment of Paediatric Idiopathic Headache Patients Psychopathology ·G. Lanzi, Stefano D’Arrigo, Cristiano Termine, Wenjing Mo, Santi Ahmad, Carmelo Parisi, Andrea Millul, Ettore Beghi	2006	12
19	Oligoyric microcephaly in a child with Williams syndrome American Journal of Medical Genetics Part A ·Francesca Faravelli, Stefano D’Arrigo, Irene Bagnasco, Angelo Selicorni, Ludovico D’Incerti, Daria Riva, Chiara Pantaleoni	2002	3
20	Papillitis as an onset sign of Leber's hereditary optic neuropathy: a case report Brain and Development ·Chiara Pantaleoni, Stefano D’Arrigo, J. H. Kahodariya, Elena Piozzi, Franco Carrara, V. Scaioli, Daria Riva	2001	0

About Stefano D’Arrigo

Stefano D’Arrigo is a scholar working on Neurology, Genetics, Pediatrics, Perinatology and Child Health, Psychiatry and Mental health and Clinical Biochemistry, having authored 79 papers that have together received 1.9k indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (14 papers), Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (8 papers), Congenital heart defects research (8 papers), Epilepsy research and treatment (8 papers), Mitochondrial Function and Pathology (7 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Neurology (432 citations), Cognitive Neuroscience (504 citations), Psychiatry and Mental health (384 citations), Cellular and Molecular Neuroscience (319 citations) and Pediatrics, Perinatology and Child Health (315 citations). Stefano D’Arrigo has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Daria Riva, Sara Bulgheroni, Chiara Pantaleoni, Deborah Ely Budding, Nancy C. Andreasen, Tadashi Yamazaki, Leonard F. Koziol, Jeremy D. Schmahmann, Masao Ito and K L Parker. Their work appears in journals such as Journal of Child Neurology, Neuropediatrics, The Cerebellum, Cephalalgia and Brain and Development.

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