H-Index & Metrics Top Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Neuroscience H-index 144 Citations 69,289 547 World Ranking 49 National Ranking 2
Medicine H-index 148 Citations 74,814 632 World Ranking 454 National Ranking 17

Research.com Recognitions

Awards & Achievements

2017 - Member of the National Academy of Medicine (NAM)

2007 - Fellow of the Royal Society, United Kingdom

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Gene
  • Epilepsy

His primary scientific interests are in Epilepsy, Genetics, Pediatrics, Generalized epilepsy with febrile seizures plus and Generalized epilepsy. His Epilepsy research is multidisciplinary, incorporating elements of Internal medicine, Central nervous system disease and Electroencephalography. His study in Childhood absence epilepsy extends to Genetics with its themes.

His Pediatrics research integrates issues from Seizure types, Psychiatry, Myoclonus, Age of onset and Neurological disorder. His biological study spans a wide range of topics, including Exon, GABRG2, SCN1B and Myoclonic epilepsy. His studies deal with areas such as Idiopathic generalized epilepsy, Gene mutation, Genetic architecture and Dravet syndrome as well as Generalized epilepsy.

His most cited work include:

  • Revised Terminology and Concepts for Organization of Seizures and Epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009 (3024 citations)
  • ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology (1414 citations)
  • De novo mutations in epileptic encephalopathies (1040 citations)

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

Samuel F. Berkovic mainly investigates Epilepsy, Genetics, Pediatrics, Neuroscience and Internal medicine. His Epilepsy research includes themes of Central nervous system disease and Electroencephalography. His Pediatrics study integrates concerns from other disciplines, such as Surgery, Seizure types, Dravet syndrome, Psychiatry and Age of onset.

Specifically, his work in Neuroscience is concerned with the study of Idiopathic generalized epilepsy. In his study, Autosomal dominant nocturnal frontal lobe epilepsy is strongly linked to Endocrinology, which falls under the umbrella field of Internal medicine. His research in Temporal lobe intersects with topics in Ictal, Magnetic resonance imaging, Hippocampal formation and Pathology.

He most often published in these fields:

  • Epilepsy (67.32%)
  • Genetics (25.55%)
  • Pediatrics (21.40%)

What were the highlights of his more recent work (between 2015-2021)?

  • Epilepsy (67.32%)
  • Genetics (25.55%)
  • Gene (8.86%)

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

Epilepsy, Genetics, Gene, Pediatrics and Exome sequencing are his primary areas of study. Samuel F. Berkovic combines subjects such as Mutation, Missense mutation and Bioinformatics with his study of Epilepsy. Samuel F. Berkovic has researched Mutation in several fields, including Cortical dysplasia and Germline.

The concepts of his Germline study are interwoven with issues in Germline mutation and Neuroscience. His Juvenile myoclonic epilepsy research extends to the thematically linked field of Genetics. In his work, Incidence is strongly intertwined with Etiology, which is a subfield of Pediatrics.

Between 2015 and 2021, his most popular works were:

  • ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology (1414 citations)
  • Analysis of shared heritability in common disorders of the brain (726 citations)
  • High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies (175 citations)

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

  • Gene
  • Internal medicine
  • Mutation

His primary areas of investigation include Epilepsy, Genetics, Bioinformatics, Gene and Exome sequencing. His work carried out in the field of Epilepsy brings together such families of science as Exome and Electroencephalography. The study incorporates disciplines such as Batten disease, Disease, Mutation, Proband and Mutation in addition to Bioinformatics.

Samuel F. Berkovic has included themes like Computational biology and Neurotransmission in his Gene study. The various areas that Samuel F. Berkovic examines in his Exome sequencing study include Alternative splicing, Exon, DNA sequencing and Genomics. The Generalized epilepsy study combines topics in areas such as Genetic data, Generalized epilepsy with febrile seizures plus, Immunology, Focal Epilepsies and Genetic testing.

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.

Top Publications

Revised Terminology and Concepts for Organization of Seizures and Epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009

Anne T. Berg;Anne T. Berg;Samuel F. Berkovic;Martin J. Brodie;Jeffrey Buchhalter.
Epilepsia (2010)

4738 Citations

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.
Epilepsia (2017)

2120 Citations

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Robyn H. Wallace;Dao W. Wang;Rita Singh;Rita Singh;Ingrid E. Scheffer;Ingrid E. Scheffer;Ingrid E. Scheffer.
Nature Genetics (1998)

1282 Citations

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Ortrud K. Steinlein;John C. Mulley;Peter Propping;Robyn H. Wallace;Robyn H. Wallace.
Nature Genetics (1995)

1244 Citations

A potassium channel mutation in neonatal human epilepsy.

Christian Biervert;Björn C. Schroeder;Christian Kubisch;Samuel F. Berkovic.
Science (1998)

1239 Citations

doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

Joseph G Gleeson;Joseph G Gleeson;Kristina M Allen;Jeremy W Fox;Edward D Lamperti.
Cell (1998)

1076 Citations

De novo mutations in epileptic encephalopathies

Andrew S. Allen;Samuel F. Berkovic;Patrick Cossette;Norman Delanty.
Nature (2013)

1040 Citations

Generalized epilepsy with febrile seizures plus: A genetic disorder with heterogeneous clinical phenotypes

I E Scheffer;S F Berkovic.
Brain (1997)

957 Citations

Mutant GABA A receptor γ2-subunit in childhood absence epilepsy and febrile seizures

Robyn H. Wallace;Carla Marini;Steven Petrou;Louise A. Harkin;Louise A. Harkin.
Nature Genetics (2001)

922 Citations

Mutations in filamin 1 Prevent Migration of Cerebral Cortical Neurons in Human Periventricular Heterotopia

Jeremy W Fox;Jeremy W Fox;Edward D Lamperti;Yaman Z Ekşioğlu;Susan E Hong.
Neuron (1998)

878 Citations

Profile was last updated on December 6th, 2021.
Research.com Ranking is based on data retrieved from the Microsoft Academic Graph (MAG).
The ranking h-index is inferred from publications deemed to belong to the considered discipline.

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