M. Di Capua

2.0k total citations
53 papers, 1.3k citations indexed

About

M. Di Capua is a scholar working on Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Psychiatry and Mental health. According to data from OpenAlex, M. Di Capua has authored 53 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pediatrics, Perinatology and Child Health, 14 papers in Cellular and Molecular Neuroscience and 13 papers in Psychiatry and Mental health. Recurrent topics in M. Di Capua's work include Neonatal and fetal brain pathology (12 papers), Epilepsy research and treatment (12 papers) and Hereditary Neurological Disorders (9 papers). M. Di Capua is often cited by papers focused on Neonatal and fetal brain pathology (12 papers), Epilepsy research and treatment (12 papers) and Hereditary Neurological Disorders (9 papers). M. Di Capua collaborates with scholars based in Italy, Germany and France. M. Di Capua's co-authors include Federico Vigevano, Enrico Bertini, Lucia Fusco, Stefano Ricci, Filippo M. Santorelli, Odile Boespflug‐Tanguy, Éléonore Eymard-Pierre, Gaëtan Lesca, R. Sebastianelli and Sandra Dollet and has published in prestigious journals such as Neurology, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

M. Di Capua

51 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Di Capua Italy 20 454 406 377 310 256 53 1.3k
G Kurlemann Germany 17 399 0.9× 626 1.5× 250 0.7× 306 1.0× 189 0.7× 40 1.4k
Byung Chan Lim South Korea 23 750 1.7× 481 1.2× 375 1.0× 244 0.8× 244 1.0× 165 1.8k
Yong Seung Hwang South Korea 22 553 1.2× 367 0.9× 284 0.8× 135 0.4× 177 0.7× 89 1.4k
Dilek Yalnızoğlu Türkiye 17 200 0.4× 350 0.9× 267 0.7× 192 0.6× 233 0.9× 72 1.0k
Francesco Nicita Italy 23 412 0.9× 288 0.7× 188 0.5× 244 0.8× 239 0.9× 94 1.3k
Michael A. Nigro United States 21 618 1.4× 180 0.4× 139 0.4× 214 0.7× 221 0.9× 36 1.4k
Kenji Yokochi Japan 20 587 1.3× 285 0.7× 460 1.2× 131 0.4× 145 0.6× 72 1.4k
S. Binelli Italy 20 209 0.5× 387 1.0× 260 0.7× 185 0.6× 188 0.7× 43 926
Hadassa Goldberg‐Stern Israel 23 378 0.8× 790 1.9× 388 1.0× 429 1.4× 215 0.8× 51 1.6k
Agathe Roubertie France 28 769 1.7× 424 1.0× 173 0.5× 618 2.0× 713 2.8× 114 2.1k

Countries citing papers authored by M. Di Capua

Since Specialization
Citations

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

Fields of papers citing papers by M. Di Capua

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Di Capua. 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 M. Di Capua. The network helps show where M. Di Capua may publish in the future.

Co-authorship network of co-authors of M. Di Capua

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

All Works

20 of 20 papers shown
1.
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Dilena, Robertino, Federico Raviglione, Gaetano Cantalupo, et al.. (2021). Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates. Clinical Neurophysiology. 132(4). 886–903. 29 indexed citations
3.
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Cesaroni, Elisabetta, Pasquale Striano, Dario Pruna, et al.. (2019). De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort. Seizure. 73. 79–82. 4 indexed citations
5.
Dilena, Robertino, Paola De Liso, M. Di Capua, et al.. (2019). Influence of etiology on treatment choices for neonatal seizures: A survey among pediatric neurologists. Brain and Development. 41(7). 595–599. 9 indexed citations
6.
Chiabrando, Deborah, Marco Castori, Maja Di Rocco, et al.. (2016). Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception. PLoS Genetics. 12(12). e1006461–e1006461. 41 indexed citations
7.
Specchio, Nicola, Antonio Carotenuto, Marina Trivisano, et al.. (2011). Ring 21 chromosome presenting with epilepsy and intellectual disability: Clinical report and review of the literature. American Journal of Medical Genetics Part A. 155(4). 911–914. 11 indexed citations
8.
Quattrocchi, Carlo Cosimo, Daniela Longo, Maria Roberta Cilio, et al.. (2010). Dorsal Brain Stem Syndrome: MR Imaging Location of Brain Stem Tegmental Lesions in Neonates with Oral Motor Dysfunction. American Journal of Neuroradiology. 31(8). 1438–1442. 20 indexed citations
9.
Cilio, Maria Roberta, Roberto Bianchi, Martina Balestri, et al.. (2009). Intravenous levetiracetam terminates refractory status epilepticus in two patients with migrating partial seizures in infancy. Epilepsy Research. 86(1). 66–71. 31 indexed citations
10.
Plecko, Barbara, Eduard Paschke, Sylvia Stoeckler-Ipsiroglu, et al.. (2006). Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene. Human Mutation. 28(1). 19–26. 117 indexed citations
11.
Eymard-Pierre, Éléonore, Gaëtan Lesca, Sandra Dollet, et al.. (2002). Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene. The American Journal of Human Genetics. 71(3). 518–527. 175 indexed citations
12.
Piemonte, Fiorella, Carlo Casali, Rosalba Carrozzo, et al.. (2001). Respiratory chain defects in hereditary spastic paraplegias. Neuromuscular Disorders. 11(6-7). 565–569. 15 indexed citations
13.
Fusco, Lucia, et al.. (2001). Video/EEG aspects of early-infantile epileptic encephalopathy with suppression-bursts (Ohtahara syndrome). Brain and Development. 23(7). 708–714. 33 indexed citations
14.
Capua, M. Di & Enrico Bertini. (1995). Remission in dihydroxyphenylalanine‐responsive dystonia. Movement Disorders. 10(2). 223–223. 5 indexed citations
15.
Vigevano, Federico, M. Di Capua, Francesco Iorio, et al.. (1995). Hemimegalencephaly, hemihypertrophy and vascular lesions. European Journal of Pediatrics. 154(2). 134–137. 27 indexed citations
16.
Capua, M. Di, Lucia Fusco, Stefano Ricci, & Federico Vigevano. (1993). Benign neonatal sleep myoclonus: Clinical features and video‐polygraphic recordings. Movement Disorders. 8(2). 191–194. 34 indexed citations
17.
Bertini, Enrico, Raffaella Cusmai, Geneviève de Saint Basile, et al.. (1992). Congenital X‐linked ataxia, progressive myoclonic encephalopathy, macular degeneration and recurrent infections. American Journal of Medical Genetics. 43(1-2). 443–451. 14 indexed citations
18.
Vigevano, Federico, Enrico Bertini, Dianela Claps, et al.. (1991). EMIMEGALENCEFALIA: CORRELAZIONE TRA NEUROIMAGING, DATI NEUROFISIOLOGICI ED EVOLUZIONE CLINICA. 157–159. 1 indexed citations
19.
Vigevano, Federico, Enrico Bertini, Renata Boldrini, et al.. (1989). Hemimegalencephaly and Intractable Epilepsy: Benefits of Hemispherectomy. Epilepsia. 30(6). 833–843. 112 indexed citations
20.
Bertini, Enrico, G. Palmieri, Enzo Ricci, et al.. (1989). Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: A variant of infantile spinal muscular atrophy. American Journal of Medical Genetics. 33(3). 328–335. 37 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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