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Neuroscience

D-Index
55
Citations
14131
World Ranking
4652
National Ranking
2095

Overview

Giuseppe Capovilla is affiliated with Boston Children's Hospital in the United States and has a research focus primarily in the field of Medicine. Their work spans several subfields, including Surgery, Psychiatry and Mental Health, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology and Child Health, and Gastroenterology.

The scientist's research encompasses a range of topics, most notably in Epilepsy research and treatment, Esophageal and Gastrointestinal Pathology, Gastroesophageal reflux and treatments, Esophageal Cancer Research and Treatment, Pharmacological Effects and Toxicity Studies, Eosinophilic Esophagitis, and Neuroscience and Neuropharmacology Research.

The following recent papers illustrate the scope and diversity of their research contributions:

  • "Epilepsy Course and Developmental Trajectories in STXBP1 -DEE" (2022) published in Neurology Genetics
  • "Genotype-phenotype correlations in patients with de novo KCNQ2 pathogenic variants" (2020) published in Neurology Genetics
  • "Myoclonus: Differential diagnosis and current management" (2024) published in Epilepsia Open
  • "An Italian consensus on the management of Lennox-Gastaut syndrome" (2022) published in Seizure
  • "Appropriate use of generic and branded antiseizure medications in epilepsy: Updated recommendations from the Italian League Against Epilepsy (LICE)" (2021) published in Epilepsy & Behavior

Giuseppe Capovilla frequently collaborates with several co-authors, including Michele Valmasoni, Renato Salvador, Antonella Riva, Lucia Moletta, and Elisa Sefora Pierobon. These partnerships reflect ongoing research networks in their areas of study.

The scientist's work is also regularly published in several prominent venues, highlighting their research dissemination channels. Frequent publication venues include:

  • Diseases of the Esophagus
  • Epilepsy & Behavior
  • Epilepsia Open
  • Neurology Genetics
  • Seizure

Best Publications

  • ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.

    Ingrid E. Scheffer;Samuel Berkovic;Giuseppe Capovilla;Mary B. Connolly

  • STXBP1 encephalopathy A neurodevelopmental disorder including epilepsy

    Hannah Stamberger;Marina Nikanorova;Marjolein H. Willemsen;Patrizia Accorsi

  • Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy

    Rima Nabbout;E. Gennaro;B. Dalla Bernardina;O. Dulac

  • Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.

    Marcella Zollino;Rosetta Lecce;Rita Fischetto;Marina Murdolo

  • Recommendations for the management of “febrile seizures” Ad hoc Task Force of LICE Guidelines Commission

    Giuseppe Capovilla;Massimo Mastrangelo;Antonino Romeo;Federico Vigevano

  • AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

    Vincenzo Salpietro;Vincenzo Salpietro;Vincenzo Salpietro;Christine L Dixon;Hui Guo;Hui Guo;Oscar D Bello

  • Methodology of photic stimulation revisited: Updated European algorithm for visual stimulation in the EEG laboratory

    Dorothée Kasteleijn-Nolst Trenité;Guido Rubboli;Edouard Hirsch;Antonio Martins da Silva

  • Epilepsy, seizures, physical exercise, and sports: A report from the ILAE Task Force on Sports and Epilepsy

    Giuseppe Capovilla;Kenneth R. Kaufman;Emilio Perucca;Solomon L. Moshé

  • Experience with immunomodulatory treatments in Rasmussen’s encephalitis

    Tiziana Granata;L. Fusco;G. Gobbi;E. Freri

  • Diagnostic imaging in 13 cases of Rasmussen's encephalitis: can early MRI suggest the diagnosis?

    L. Chiapparini;T. Granata;L. Farina;E. Ciceri

  • The system epilepsies: A pathophysiological hypothesis

    Giuliano Avanzini;Paolo Manganotti;Stefano Meletti;Solomon L. Moshé

  • Eyelid myoclonia with absences (Jeavons syndrome): a well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?

    Salvatore Striano;Giuseppe Capovilla;Vito Sofia;Antonino Romeo

  • Rasmussen’s encephalitis Early characteristics allow diagnosis

    Tiziana Granata;G. Gobbi;R. Spreafico;F. Vigevano

  • Withdrawal of antiepileptic drugs: guidelines of the Italian League Against Epilepsy.

    Ettore Beghi;Giorgia Giussani;Salvatore Grosso;Alfonso Iudice

  • Topiramate as add-on drug in severe myoclonic epilepsy in infancy: An Italian multicenter open trial

    Giangennaro Coppola;Giuseppe Capovilla;Alessandra Montagnini;Antonino Romeo

  • Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

    Michael Steffens;Costin Leu

  • CHD2 variants are a risk factor for photosensitivity in epilepsy

    Elizabeth C. Galizia;Candace T. Myers;Costin Leu;Carolien G F de Kovel

  • Genetic testing in benign familial epilepsies of the first year of life : Clinical and diagnostic significance

    Federico Zara;Nicola Specchio;Pasquale Striano;Angela Robbiano

  • An open-label trial of levetiracetam in severe myoclonic epilepsy of infancy.

    P. Striano;A. Coppola;M. Pezzella;C. Ciampa

  • Continuous spike-and-wave activity during slow-wave sleep : syndrome or EEG pattern?

    Pierangelo Veggiotti;Francesca Beccaria;Renzo Guerrini;Giuseppe Capovilla

Frequent Co-Authors

Pasquale Striano
Pasquale Striano University of Genoa
Pierangelo Veggiotti
Pierangelo Veggiotti University of Milan
Federico Vigevano
Federico Vigevano Bambino Gesù Children's Hospital
Federico Zara
Federico Zara University of Genoa
Giangennaro Coppola
Giangennaro Coppola University of Salerno
Pasquale Parisi
Pasquale Parisi Sapienza University of Rome
Giuseppe Gobbi
Giuseppe Gobbi University of Bologna
Antonio Gambardella
Antonio Gambardella Magna Graecia University
Salvatore Striano
Salvatore Striano University of Naples Federico II
Renzo Guerrini
Renzo Guerrini University of Florence

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