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Overview

Stéphane Auvin is affiliated with Université Paris Cité in France and has a focused body of research within medicine, particularly relating to epilepsy and associated neurological disorders. Their work spans multiple subfields including psychiatry and mental health, pediatrics, perinatology and child health, genetics, molecular biology, and cellular and molecular neuroscience.

The scientist's publication record includes numerous contributions to epilepsy research and treatment, pharmacological effects and toxicity studies, neuroscience and neuropharmacology research, neonatal and fetal brain pathology, metabolism and genetic disorders, genetics and neurodevelopmental disorders, and diet and metabolism studies.

Major recent papers authored or co-authored by Stéphane Auvin include:

  • International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions (2022, Epilepsia)
  • ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions (2022, Epilepsia)
  • ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions (2022, Epilepsia)
  • Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group (2020, Epilepsia Open)
  • International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions (2022, Epilepsia)

Frequent co-authors in their research include:

  • Nicola Specchio
  • Blandine Dozières-Puyravel
  • Rima Nabbout
  • J. Helen Cross
  • Lieven Lagae

The main publication venues where Stéphane Auvin's work appears are:

  • Epilepsia
  • Epilepsy & Behavior
  • European Journal of Paediatric Neurology
  • Epilepsia Open
  • Neurology

The scientist's fields of study demonstrate a significant interdisciplinary approach, integrating medicine with biochemistry, genetics, and molecular biology. Their work covers a broad spectrum of neurological and genetic disorders, with a particular emphasis on conditions related to epilepsy syndromes across different age groups, including neonates, infants, and children.

Stéphane Auvin's contributions have helped define classification systems and position statements for epilepsy syndromes under the International League Against Epilepsy, indicating a role in shaping clinical frameworks and guidelines in this domain. Their research also addresses genetic metabolic conditions such as Glut1 Deficiency Syndrome, further illustrating the intersection of metabolic and neurological research in their profile.

Best Publications

  • International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions

    Unknown

  • ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions

    Unknown

  • 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

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

    Markus Wolff;Katrine M Johannesen;Ulrike B S Hedrich;Silvia Masnada

  • ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions

    Unknown

  • High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies

    Fadi F. Hamdan;Candace T. Myers;Patrick Cossette;Philippe Lemay

  • International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions

    Unknown

  • MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

    Nathalie Le Meur;Muriel Holder-Espinasse;Sylvie Jaillard;Alice Goldenberg

  • Incidence, clinical presentation and location at diagnosis of pediatric inflammatory bowel disease: a prospective population-based study in northern France (1988-1999).

    Stéphane Auvin;Florence Molinié;Corinne Gower-Rousseau;Franck Brazier

  • Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group.

    Joerg Klepper;Cigdem Akman;Marisa Armeno;Stéphane Auvin

  • Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial.

    Rima Nabbout;Arun Mistry;Sameer Zuberi;Nathalie Villeneuve

  • Ketogenic diet exhibits anti-inflammatory properties.

    Nina Dupuis;Nina Dupuis;Niccolo Curatolo;Jean-François Benoist;Stéphane Auvin;Stéphane Auvin

  • Ketogenic diet guidelines for infants with refractory epilepsy

    Elles van der Louw;Dorine van den Hurk;Elizabeth Neal;Bärbel Leiendecker

  • Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study.

    Rima Nabbout;Elena Belousova;Mirjana P. Benedik;Tom Carter

  • Functional ultrasound imaging of brain activity in human newborns.

    Charlie Demene;Jérome Baranger;Miguel Bernal;Catherine Delanoe

  • Expert Opinion on the Management of Lennox–Gastaut Syndrome: Treatment Algorithms and Practical Considerations

    J Helen Cross;Stéphane Auvin;Mercè Falip;Pasquale Striano

  • TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

    Petrus J de Vries;Elena Belousova;Mirjana P Benedik;Tom Carter

  • International consensus recommendations for management of new onset refractory status epilepticus (NORSE) including febrile infection‐related epilepsy syndrome (FIRES): Summary and clinical tools

    Unknown

  • International consensus recommendations for management of new onset refractory status epilepticus including febrile infection‐related epilepsy syndrome: Statements and supporting evidence

    Unknown

  • Inflammation induced by LPS enhances epileptogenesis in immature rat and may be partially reversed by IL1RA

    Stéphane Auvin;Don Shin;Andrey Mazarati;Raman Sankar

  • Polyunsaturated fatty acids and epilepsy.

    Ameer Y. Taha;W. McIntyre Burnham;Stéphane Auvin

  • Ketogenic diet and Neuroinflammation

    Sookyong Koh;Nina Dupuis;Stéphane Auvin

  • Finding a better drug for epilepsy: Antiepileptogenesis targets

    Katja Kobow;Stéphane Auvin;Frances Jensen;Wolfgang Löscher

  • Novel KCNQ2 and KCNQ3 Mutations in a Large Cohort of Families with Benign Neonatal Epilepsy: First Evidence for an Altered Channel Regulation by Syntaxin‐1A

    Maria Virginia Soldovieri;Nadia Boutry-Kryza;Mathieu Milh;Diane Doummar

  • Comparison of seizure reduction and serum fatty acid levels after receiving the ketogenic and modified Atkins diet

    Natacha Porta;Louis Vallée;Elisabeth Boutry;Monique Fontaine

  • Kindling epileptogenesis in immature rats leads to persistent depressive behavior.

    Andréy Mazarati;Don Shin;Stéphane Auvin;Rochelle Caplan

Frequent Co-Authors

Andrey Mazarati
Andrey Mazarati University of California, Los Angeles
Mathieu Milh
Mathieu Milh Aix-Marseille University
Don Shin
Don Shin University of California, Los Angeles
Rima Nabbout
Rima Nabbout Université Paris Cité
Raman Sankar
Raman Sankar University of California, Los Angeles
Catherine Chiron
Catherine Chiron Assistance Publique – Hôpitaux de Paris
Nathalie Villeneuve
Nathalie Villeneuve Hôpital Européen
J. Helen Cross
J. Helen Cross Great Ormond Street Hospital
Ingrid E. Scheffer
Ingrid E. Scheffer University of Melbourne
Gaetan Lesca
Gaetan Lesca Claude Bernard University Lyon 1

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