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 70 Citations 18,672 409 World Ranking 1446 National Ranking 11
Medicine D-index 76 Citations 21,715 458 World Ranking 13921 National Ranking 174

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Gene
  • Mutation

The scientist’s investigation covers issues in Epilepsy, Pregnancy, Pediatrics, Genetics and Anesthesia. His biological study spans a wide range of topics, including Cognition and Electroencephalography. His research in Pregnancy intersects with topics in Cancer, Psychiatry, Anxiety and Cohort study.

His studies deal with areas such as Neurocognitive, Ataxia and Genetic heterogeneity as well as Pediatrics. His Genetics research is multidisciplinary, incorporating elements of Molecular biology and Immunology. His biological study spans a wide range of topics, including Clinical trial, Adverse effect, Lennox–Gastaut syndrome, Neurological disorder and Symptomatic generalised epilepsy.

His most cited work include:

  • Operational classification of seizure types by the International League Against Epilepsy: position paper of the ILAE Commission for Classification and Terminology (975 citations)
  • De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. (924 citations)
  • Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response. (502 citations)

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

Lieven Lagae spends much of his time researching Epilepsy, Pediatrics, Anesthesia, Electroencephalography and Neuroscience. His Epilepsy study contributes to a more complete understanding of Psychiatry. His Pediatrics study which covers Pregnancy that intersects with Cancer.

The Anesthesia study combines topics in areas such as Adverse effect and Fenfluramine. His research in Electroencephalography intersects with topics in Audiology, Artificial intelligence and Pattern recognition. He specializes in Neuroscience, namely Visual cortex.

He most often published in these fields:

  • Epilepsy (31.13%)
  • Pediatrics (19.18%)
  • Anesthesia (11.96%)

What were the highlights of his more recent work (between 2016-2021)?

  • Epilepsy (31.13%)
  • Pediatrics (19.18%)
  • Dravet syndrome (8.87%)

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

His primary areas of investigation include Epilepsy, Pediatrics, Dravet syndrome, Fenfluramine and Tuberous sclerosis. The various areas that Lieven Lagae examines in his Epilepsy study include Adverse effect, Pharmacology, Intensive care medicine and Electroencephalography. His Electroencephalography study integrates concerns from other disciplines, such as Audiology, Artificial intelligence and Pattern recognition.

Lieven Lagae has researched Pediatrics in several fields, including Pregnancy, Cancer, Disease and Intellectual disability. Lieven Lagae interconnects Epilepsy syndromes, Clinical trial, Serotonergic and Cohort in the investigation of issues within Dravet syndrome. His Fenfluramine study combines topics in areas such as Anesthesia and Open label, Extension study.

Between 2016 and 2021, his most popular works were:

  • Operational classification of seizure types by the International League Against Epilepsy: position paper of the ILAE Commission for Classification and Terminology (975 citations)
  • Instruction manual for the ILAE 2017 operational classification of seizure types (292 citations)
  • Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. (219 citations)

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

  • Internal medicine
  • Gene
  • Mutation

His primary areas of investigation include Epilepsy, Dravet syndrome, Fenfluramine, Pediatrics and Anesthesia. His research integrates issues of Position paper, Pharmacology and Electroencephalography in his study of Epilepsy. His studies in Dravet syndrome integrate themes in fields like Cannabidiol, Alternative splicing, Exon, Intensive care medicine and Cohort.

Lieven Lagae has included themes like Retrospective cohort study, Quality of life, Tuberous sclerosis and Intellectual disability in his Pediatrics study. His Anesthesia research is multidisciplinary, incorporating perspectives in Randomized controlled trial, Adverse effect, Pulmonary hypertension, Effective dose and Epilepsy syndromes. His Eyelid myoclonia research integrates issues from Epileptic spasms, Cognition and Audiology.

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

Operational classification of seizure types by the International League Against Epilepsy: position paper of the ILAE Commission for Classification and Terminology

Robert S. Fisher;J. Helen Cross;Jacqueline A. French;Norimichi Higurashi.
Epilepsia (2017)

2142 Citations

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.

Lieve Claes;Jurgen Del-Favero;Berten Ceulemans;Lieven Lagae.
American Journal of Human Genetics (2001)

1368 Citations

Instruction manual for the ILAE 2017 operational classification of seizure types

Robert S. Fisher;J. Helen Cross;Carol D'Souza;Jacqueline A. French.
Epilepsia (2017)

764 Citations

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.

Gillian I Rice;Jacquelyn Bond;Aruna Asipu;Rebecca L Brunette.
Nature Genetics (2009)

699 Citations

Antenatal Maternal Anxiety is Related to HPA-Axis Dysregulation and Self-Reported Depressive Symptoms in Adolescence: A Prospective Study on the Fetal Origins of Depressed Mood

Bea R H Van den Bergh;Ben Van Calster;Tim Smits;Sabine Van Huffel.
Neuropsychopharmacology (2008)

548 Citations

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

Gillian I Rice;Yoandris del Toro Duany;Yoandris del Toro Duany;Emma M Jenkinson;Gabriella M A Forte.
Nature Genetics (2014)

482 Citations

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Sarah Weckhuysen;Simone Mandelstam;Arvid Suls;Dominique Audenaert;Dominique Audenaert.
Annals of Neurology (2012)

468 Citations

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Yanick J. Crow;Diana S. Chase;Johanna Lowenstein Schmidt;Marcin Szynkiewicz.
(2015)

428 Citations

Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

Gillian Rice;Teresa Patrick;Rekha Parmar;Claire F Taylor.
(2007)

392 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)

357 Citations

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