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 31 Citations 4,635 83 World Ranking 5180 National Ranking 33

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Epilepsy
  • Disease

His primary areas of study are Epilepsy, Pediatrics, Genetics, Encephalopathy and Anesthesia. Epilepsy is a primary field of his research addressed under Psychiatry. The Pediatrics study combines topics in areas such as Central nervous system disease, Status epilepticus, Lennox–Gastaut syndrome, Rufinamide and Disease.

His Genetics research is multidisciplinary, relying on both Corpus Callosum Agenesis and Developmental disorder. His work deals with themes such as Hypotonia, Epileptic spasms and Movement disorders, which intersect with Encephalopathy. His studies in Anesthesia integrate themes in fields like Epilepsy syndromes and Febrile infection related epilepsy syndrome.

His most cited work include:

  • Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology (287 citations)
  • Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes (269 citations)
  • Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome (249 citations)

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

Gerhard Kluger focuses on Epilepsy, Pediatrics, Anesthesia, Rufinamide and Psychiatry. His research in Epilepsy intersects with topics in Encephalopathy and Electroencephalography. His studies deal with areas such as Tolerability, Adverse effect, Retrospective cohort study and Dravet syndrome as well as Pediatrics.

Many of his studies involve connections with topics such as Convulsion and Anesthesia. His Rufinamide course of study focuses on Lennox–Gastaut syndrome and Placebo. His research in Status epilepticus is mostly focused on Febrile infection related epilepsy syndrome.

He most often published in these fields:

  • Epilepsy (50.66%)
  • Pediatrics (48.03%)
  • Anesthesia (17.76%)

What were the highlights of his more recent work (between 2018-2021)?

  • Epilepsy (50.66%)
  • Pediatrics (48.03%)
  • Dravet syndrome (9.87%)

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

Epilepsy, Pediatrics, Dravet syndrome, Cohort study and SYNGAP1 are his primary areas of study. Gerhard Kluger merges many fields, such as Epilepsy and Outcome, in his writings. He interconnects Epilepsy surgery, Electroencephalography and Topiramate in the investigation of issues within Pediatrics.

His Dravet syndrome research focuses on Quality of life and how it connects with Wakefulness, Activities of daily living and Psychiatry. In his study, Early disease, Clinical research, Tuberous sclerosis and Vigabatrin is inextricably linked to Medical prescription, which falls within the broad field of Cohort study. His SYNGAP1 research includes elements of Young adult, Treatment outcome, Term effect, Reflex and Rosuvastatin.

Between 2018 and 2021, his most popular works were:

  • Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. (78 citations)
  • Clinical and genetic spectrum of SCN2A-associated episodic ataxia. (17 citations)
  • Burden-of-illness and cost-driving factors in Dravet syndrome patients and carers: A prospective, multicenter study from Germany (13 citations)

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

  • Internal medicine
  • Epilepsy
  • Disease

Gerhard Kluger mainly investigates Epilepsy, Pediatrics, Dravet syndrome, Depression and Indirect costs. The concepts of his Epilepsy study are interwoven with issues in Episodic ataxia, Internal medicine, Cohort study, Cohort and Autism spectrum disorder. In the field of Internal medicine, his study on Acetazolamide overlaps with subjects such as Sleep deprivation.

Many of his studies on Pediatrics involve topics that are commonly interrelated, such as Electroencephalography. Gerhard Kluger has included themes like Hippocampal sclerosis, Temporal lobe, Reflex and Gene mutation in his Electroencephalography study. Gerhard Kluger combines subjects such as Quality of life, Univariate analysis and Encephalopathy with his study of Depression.

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

Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology

Alexis Arzimanoglou;Jacqueline French;Warren T. Blume;J. Helen Cross.
Lancet Neurology (2009)

415 Citations

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

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

372 Citations

Rufinamide for generalized seizures associated with Lennox–Gastaut syndrome

T. Glauser;G. Kluger;R. Sachdeo;G. Krauss.
Neurology (2008)

368 Citations

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Markus Wolff;Katrine M Johannesen;Ulrike B S Hedrich;Silvia Masnada.
Brain (2017)

261 Citations

Febrile infection-related epilepsy syndrome (FIRES): pathogenesis, treatment, and outcome: a multicenter study on 77 children.

Uri Kramer;Ching Shiang Chi;Kuang Lin Lin;Nicola Specchio.
Epilepsia (2011)

245 Citations

Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood.

Andreas Van Baalen;Martin Häusler;Rainer Boor;Axel Rohr.
Epilepsia (2010)

223 Citations

The phenotypic spectrum of SCN8A encephalopathy

Jan Larsen;Gemma L Carvill;Elena Gardella;Gerhard Kluger.
Neurology (2015)

206 Citations

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Fanny Kortüm;Soma Das;Max Flindt;Deborah J Morris-Rosendahl.
Journal of Medical Genetics (2011)

196 Citations

Limbic encephalitis in children and adolescents

E Haberlandt;T Bast;A Ebner;H Holthausen.
Archives of Disease in Childhood (2011)

186 Citations

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Arvid Suls;Johanna A. Jaehn;Angela Kecskés;Yvonne Weber.
American Journal of Human Genetics (2013)

183 Citations

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