Lieven Lagae

Active 1989–2025

166
Papers
23,258
Citations
80
h-index
145
i10-index

Citations

Citations per year for Lieven Lagae1980: 1 citations1990: 1 citations1991: 1 citations1992: 2 citations1993: 5 citations1994: 10 citations1995: 22 citations1996: 25 citations1997: 30 citations1998: 38 citations1999: 37 citations2000: 19 citations2001: 37 citations2002: 33 citations2003: 40 citations2004: 39 citations2005: 50 citations2006: 60 citations2007: 70 citations2008: 87 citations2009: 101 citations2010: 85 citations2011: 124 citations2012: 159 citations2013: 175 citations2014: 182 citations2015: 230 citations2016: 213 citations2017: 212 citations2018: 222 citations2019: 836 citations2020: 915 citations2021: 969 citations2022: 814 citations2023: 562 citations2024: 954 citations2025: 433 citations2026: 21 citations1981–1989: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,417 citing papers, 21.5% of this breakdownUnited Kingdom: 976 citing papers, 8.7% of this breakdownItaly: 753 citing papers, 6.7% of this breakdownGermany: 709 citing papers, 6.3% of this breakdownChina: 582 citing papers, 5.2% of this breakdownFrance: 577 citing papers, 5.1% of this breakdownBelgium: 519 citing papers, 4.6% of this breakdownAustralia: 494 citing papers, 4.4% of this breakdownNetherlands: 453 citing papers, 4% of this breakdownCanada: 450 citing papers, 4% of this breakdownSpain: 258 citing papers, 2.3% of this breakdownJapan: 241 citing papers, 2.1% of this breakdown
0%21.5%Other 25.1%

Fields

  • Medicine46.9%
  • Neuroscience24.1%
  • Biochemistry, Genetics and Molecular Biology17.2%
  • Immunology and Microbiology6.7%
  • Computer Science1.8%
  • Psychology1%
  • Other2.3%

Topics

  • Epilepsy research and treatment12.5%
  • Neuroscience and Neuropharmacology Research4.9%
  • EEG and Brain-Computer Interfaces4.2%
  • Pharmacological Effects and Toxicity Studies3.4%
  • Genetics and Neurodevelopmental Disorders2.5%
  • interferon and immune responses2.5%
  • Other70%

Coauthors

All papers

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  1. Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

    Authors: , , , , , , , , , , , - Epilepsia 2017 cited by 3,392

  2. Instruction manual for the ILAE 2017 operational classification of seizure types

    Authors: , , , , , , , , , , , , , , , , , - Epilepsia 2017 cited by 980

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez and 36 more - American Journal of Medical Genetics Part A 2015 cited by 613

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Miriam Döcker, Thomas Bast, Tobias Loddenkemper, Lily C. Wong‐Kisiel, Friedrich Baumeister, Walid Fazeli, Pasquale Striano, Robertino Dilena, Elena Fontana, Federico Zara, Gerhard Kurlemann, Joerg Klepper, Jess G. Thoene, Daniel H. Arndt, Nicolas Deconinck, Thomas Schmitt‐Mechelke, Oliver Maier, Hiltrud Muhle, Beverly Wical, C. Finetti, Reinhard Brückner, Joachim Pietz, G. Golla, Dinesh Jillella, Karen Markussen Linnet, Perrine Charles, Ute Moog, Eve Õiglane‐Shlik, John F. Mantovani, Kristen Park, Marie Deprez, Damien Lederer, Sandrine Mary, Emmanuel Scalais, Laila Selim, Rudy Van Coster, Lieven Lagae, Marina Nikanorova, Helle Hjalgrim, Georg-Christoph Korenke, Marina Trivisano, Nicola Specchio, Berten Ceulemans, Thomas Dorn, Katherine L. Helbig, Katia Hardies, Hannah Stamberger, Peter De Jonghe, Sarah Weckhuysen, Johannes R. Lemke, Ingeborg Krägeloh‐Mann, Ingo Helbig, Gerhard Kluger, Holger Lerche, Rikke S. Møller - Brain 2017 cited by 575

  5. Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial

    Authors: , , , , , , , , , , , , , , , , , , , - The Lancet 2019 cited by 366

  6. Proposed consensus definitions for new‐onset refractory status epilepticus (NORSE), febrile infection‐related epilepsy syndrome (FIRES), and related conditions

    Authors: , , , , , , , , , , , , , , , , , - Epilepsia 2018 cited by 518

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Iain B. McInnes, Manoj P. Menezes, Cyril Mignot, James O’Sullivan, Simona Orcesi, Paolo Picco, Enrica Riva, Robert A. Robinson, Diana Rodriguez, E. Salvatici, Christiaan Scott, Marta Szybowska, John Tolmie, Adeline Vanderver, Catherine Vanhulle, José Pedro Vieira, Kate Webb, Robyn Whitney, Simon G. Williams, Lynne A. Wolfe, Sameer M. Zuberi, Sun Hur, Yanick J. Crow - Nature Genetics 2014 cited by 591

  8. De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

    Authors: , , , , , - The American Journal of Human Genetics 2001 cited by 1,275

  9. Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome

    Authors: , , , , , , , , , , , , , , , , , - JAMA Neurology 2022 cited by 124

  10. Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP Trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Annals of Neurology 2020 cited by 258

  11. Impact of fenfluramine on the expected SUDEP mortality rates in patients with Dravet syndrome

    Authors: , , , , , , , , , , , , - Seizure 2021 cited by 80

  12. Pediatric Outcome after Maternal Cancer Diagnosed during Pregnancy

    Authors: , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2015 cited by 367

  13. Automated detection of absence seizures using a wearable electroencephalographic device: a phase 3 validation study and feasibility of automated behavioral testing

    Authors: , , , , , , , , , , , - Epilepsia 2022 cited by 70

  14. Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hiltrud Muhle, Hande Çağlayan, Katalin Štěrbová, Dana Craiu, Dorota Hoffman, Anna‐Elina Lehesjoki, Kaja Kristine Selmer, Christel Depienne, Johannes R. Lemke, Carla Marini, Renzo Guerrini, Bernd A. Neubauer, Tiina Talvik, Eric Leguern, Peter De Jonghe, Sarah Weckhuysen - The American Journal of Human Genetics 2018 cited by 122

  15. Serotonin receptors in epilepsy: Novel treatment targets?

    Authors: , - Epilepsia Open 2022 cited by 72

  16. Accurate detection of typical absence seizures in adults and children using a two‐channel electroencephalographic wearable behind the ears

    Authors: , , , , , , , , , , , , - Epilepsia 2021 cited by 73

  17. Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo‐controlled clinical trial

    Authors: , , , , , , , , , , , , , , , , , , - Epilepsia 2023 cited by 47

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , P. Landrieu, Charles Marques Lourenço, Daphna Marom, Michael McDermott, William van der Merwe, Simona Orcesi, Julie Prendiville, Magnhild Rasmussen, Stavit A. Shalev, Doriette Soler, Marwan Shinawi, Ronen Spiegel, Tiong Yang Tan, Adeline Vanderver, Emma Wakeling, Evangeline Wassmer, Elizabeth Whittaker, Pierre Lebon, Daniel B. Stetson, David T. Bonthron, Yanick J. Crow - Nature Genetics 2009 cited by 684

  19. Vagus nerve stimulation for drug‐resistant epilepsy: A European long‐term study up to 24 months in 347 children

    Authors: , , , , , , , , , , , , , - Epilepsia 2014 cited by 267

  20. Dravet syndrome: A systematic literature review of the illness burden

    Authors: , , , , , , - Epilepsia Open 2023 cited by 62

  21. Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , John Dean, Corinne De Laet, Claudine De Praeter, Catherine Déry, Colin D. Ferrie, Kim Flintoff, Suzanna G.M. Frints, Àngels García‐Cazorla, Blanca Gener, Cyril Goizet, Françoise Goutières, Andrew Green, Agnès Guët, Ben C.J. Hamel, Bruce E. Hayward, Arvid Heiberg, Raoul C. M. Hennekam, Marie Husson, Andrew P. Jackson, Rasieka Jayatunga, Yong‐hui Jiang, Sarina G. Kant, Amy Kao, Mary D. King, Helen Kingston, Joerg Klepper, Marjo S. van der Knaap, Andrew J. Kornberg, Dieter Kotzot, W Kratzer, Didier Lacombe, Lieven Lagae, P. Landrieu, Giovanni Lanzi, Andrea Leitch, Ming Lim, John H. Livingston, Charles Marques Lourenço, E G Hermione Lyall, Sally Ann Lynch, Michael J. Lyons, Daphna Marom, John P. McClure, Robert McWilliam, Serge B. Melançon, Leena Mewasingh, Marie‐Laure Moutard, Ken K. Nischal, John R. Østergaard, Julie Prendiville, Magnhild Rasmussen, R. Curtis Rogers, Dominique Roland, Elisabeth Rosser, Kevin Rostásy, Agathe Roubertie, Amparo Sanchís, Raphael Schiffmann, Sabine Scholl‐Bürgi, Sunita Seal, Stavit A. Shalev, Concepción Sierra Córcoles, Gyan P. Sinha, Doriette Soler, Ronen Spiegel, John B.P. Stephenson, Uta Tacke, Tiong Yang Tan, Marianne Till, John Tolmie and 18 more - The American Journal of Human Genetics 2007 cited by 450

  22. Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey

    Authors: , , , , - Developmental Medicine & Child Neurology 2017 cited by 188

  23. Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox–Gastaut syndrome: Interim analysis of an open‐label extension study

    Authors: , , , , , , , , , , , , , , , , , , - Epilepsia 2022 cited by 49

  24. Updated classification of epileptic seizures: Position paper of the International League Against Epilepsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Angélica Lizcano, Aileen McGonigal, Katerina Tanya Perez‐Gosiengfiao, Philippe Ryvlin, Nicola Specchio, Michael R. Sperling, H. Stefan, William O. Tatum, Manjari Tripathi, Elza Márcia Targas Yacubian, Samuel Wiebe, Jo M. Wilmshurst, Dong Zhou, J. Helen Cross - Epilepsia 2025 cited by 305