D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Neuroscience D-index 41 Citations 6,535 166 World Ranking 4584 National Ranking 8

Overview

What is he best known for?

The fields of study he is best known for:

  • Epilepsy
  • Internal medicine
  • Disease

Roberto Caraballo mainly focuses on Epilepsy, Pediatrics, Ketogenic diet, Status epilepticus and Anesthesia. His work on Landau–Kleffner syndrome as part of general Epilepsy research is frequently linked to GRIN2A, bridging the gap between disciplines. His Pediatrics research includes themes of Central nervous system disease, Surgery, West Syndrome and Age of onset.

His work deals with themes such as Discontinuation, Dravet syndrome, Tolerability, Adverse effect and Family medicine, which intersect with Ketogenic diet. He interconnects Internal medicine and Rolandic epilepsy, Electroencephalography in the investigation of issues within Status epilepticus. His work is dedicated to discovering how Anesthesia, Prospective cohort study are connected with Vomiting and other disciplines.

His most cited work include:

  • Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group (398 citations)
  • Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes (269 citations)
  • Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions (192 citations)

What are the main themes of his work throughout his whole career to date?

His primary scientific interests are in Epilepsy, Pediatrics, Electroencephalography, Anesthesia and Ketogenic diet. His Epilepsy research is multidisciplinary, incorporating perspectives in Tolerability, Encephalopathy and Surgery. His Pediatrics study which covers Epileptic spasms that intersects with Cortical dysplasia.

While the research belongs to areas of Electroencephalography, he spends his time largely on the problem of Psychomotor learning, intersecting his research to questions surrounding Neurological examination. In his research, Epileptic encephalopathy is intimately related to Refractory, which falls under the overarching field of Anesthesia. His research in Ketogenic diet intersects with topics in Dravet syndrome, Drug Resistant Epilepsy, Refractory epilepsy, Intensive care medicine and Prospective cohort study.

He most often published in these fields:

  • Epilepsy (61.90%)
  • Pediatrics (54.17%)
  • Electroencephalography (27.38%)

What were the highlights of his more recent work (between 2017-2021)?

  • Epilepsy (61.90%)
  • Pediatrics (54.17%)
  • Ketogenic diet (16.67%)

In recent papers he was focusing on the following fields of study:

His primary areas of investigation include Epilepsy, Pediatrics, Ketogenic diet, Electroencephalography and Intensive care medicine. His Epilepsy research integrates issues from Tolerability, Discontinuation and Etiology. His work carried out in the field of Pediatrics brings together such families of science as Epileptic spasms, Adverse effect, Lennox–Gastaut syndrome, Valproic Acid and Prospective cohort study.

His Ketogenic diet study also includes fields such as

  • Refractory epilepsy which is related to area like Neurological disorder,
  • Drug Resistant Epilepsy which connect with Osteoporosis, Malnutrition and Acute illness. The study incorporates disciplines such as Neurocognitive, Cognition and Neurological examination in addition to Electroencephalography. His studies in Intensive care medicine integrate themes in fields like Clinical trial and Encephalopathy.

Between 2017 and 2021, his most popular works were:

  • Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group (152 citations)
  • Dravet syndrome: Treatment options and management of prolonged seizures. (17 citations)
  • Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses. (12 citations)

In his most recent research, the most cited papers focused on:

  • Epilepsy
  • Internal medicine
  • Disease

His primary areas of study are Epilepsy, Ketogenic diet, Pediatrics, Intensive care medicine and Discontinuation. Roberto Caraballo studies Refractory epilepsy which is a part of Epilepsy. His Ketogenic diet research includes elements of Drug Resistant Epilepsy, Intractable epilepsy and Neurological disorder.

Roberto Caraballo has included themes like Tolerability, Gastrointestinal tract, Paediatric patients, Parenteral nutrition and Epilepsy syndromes in his Pediatrics study. His Intensive care medicine research is multidisciplinary, relying on both Clinical trial, Status epilepticus and Landau–Kleffner syndrome. His Discontinuation research is multidisciplinary, incorporating elements of Guideline, Adverse effect, Childhood epilepsy and Protocol.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group

Eric H. Kossoff;Beth A. Zupec-Kania;Per E. Amark;Karen R. Ballaban-Gil.
Epilepsia (2009)

650 Citations

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

Johannes R Lemke;Dennis Lal;Eva M Reinthaler;Isabelle Steiner.
Nature Genetics (2013)

423 Citations

Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group

Eric H. Kossoff;Beth A. Zupec‐Kania;Stéphane Auvin;Karen R. Ballaban‐Gil.
Epilepsia Open , 3 (2) pp. 175-192. (2018) (2018)

343 Citations

Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

Hsien Yang Lee;Yong Huang;Yong Huang;Nadine Bruneau;Patrice Roll.
Cell Reports (2012)

275 Citations

Atypical evolutions of benign localization-related epilepsies in children: are they predictable?

Natalio Fejerman;Roberto Caraballo;Silvia N. Tenembaum.
Epilepsia (2000)

207 Citations

GRIN2B mutations in West syndrome and intellectual disability with focal epilepsy.

Johannes R Lemke;Rik Hendrickx;Kirsten Geider;Bodo Laube.
Annals of Neurology (2014)

205 Citations

Panayiotopoulos syndrome: a consensus view

Colin Ferrie;Roberto Caraballo;Athanasios Covanis;Veysi Demirbilek.
Developmental Medicine & Child Neurology (2006)

196 Citations

Ketogenic Diet in Patients with Dravet Syndrome

Roberto Horacio Caraballo;Ricardo Oscar Cersósimo;Diego Sakr;Araceli Cresta.
Epilepsia (2005)

185 Citations

Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome

Roberto Caraballo;Sylvana Pavek;Arnaud Lemainque;Marguerite Gastaldi.
American Journal of Human Genetics (2001)

174 Citations

Autonomic status epilepticus in panayiotopoulos syndrome and other childhood and adult epilepsies: A consensus view

Colin D. Ferrie;Roberto Caraballo;Athanasios Covanis;Veysi Demirbilek.
Epilepsia (2007)

136 Citations

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