Lieven Lagae
Active 1989–2025
- 166
- Papers
- 23,258
- Citations
- 80
- h-index
- 145
- i10-index
Citations
Citation sources
Countries
Institutions
- Inserm1.1%
- KU Leuven0.9%
- University College London0.9%
- Harvard University0.8%
- Université Paris Cité0.7%
- The University of Melbourne0.7%
- Other94.9%
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
- Berten Ceulemans41
- Sabine Van Huffel30
- Bart Vanrumste21
- Rima Nabbout21
- Floor E. Jansen18
- Anna Jansen17
- Anouk Van de Vel16
- J. Helen Cross16
- Kate Riney14
- Martha Feucht14
- Ingrid E. Scheffer13
- Katrien Jansen13
- Paolo Curatolo13
- Katarzyna Kotulska12
- Kris Cuppens12
- Sergiusz Jóźwiak12
- David J. Kwiatkowski11
- Eleonora Aronica11
- Jo Sourbron11
- Pavel Kršek11
- Stéphane Auvin11
- Bernhard Weschke10
- Christoph Hertzberg10
- Frédéric Amant10
All papers
- Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology
Authors: Robert S. Fisher, J. Helen Cross, Jacqueline A. French, Norimichi Higurashi, Édouard Hirsch, Floor E. Jansen, Lieven Lagae, Solomon L. Moshé, Jukka Peltola, Eliane Roulet Perez, Ingrid E. Scheffer, Sameer M. Zuberi - Epilepsia 2017 cited by 3,392
- Instruction manual for the ILAE 2017 operational classification of seizure types
Authors: Robert S. Fisher, J. Helen Cross, Carol D’Souza, Jacqueline A. French, Sheryl R. Haut, Norimichi Higurashi, Édouard Hirsch, Floor E. Jansen, Lieven Lagae, Solomon L. Moshé, Jukka Peltola, Eliane Roulet Perez, Ingrid E. Scheffer, Andreas Schulze‐Bonhage, Ernest Somerville, Michael R. Sperling, Elza Márcia Targas Yacubian, Sameer M. Zuberi - Epilepsia 2017 cited by 980
- Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Authors: Yanick J. Crow, Diana Chase, Johanna L. Schmidt, Marcin Szynkiewicz, Gabriella Forte, Hannah Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine S. W. Albin, Stavit A. Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul‐Hirji, Eileen Baildam, Nadia Bahi‐Buisson, Kathryn Bailey, Christine Barnérias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, 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
- Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Authors: Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaëtan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard, Alexandra Afenjar, Sandra Chantot‐Bastaraud, Cyril Mignot, Caroline Lardennois, Caroline Nava, Niklas Schwarz, Marion Gérard, Laurence Perrin, Diane Doummar, Stéphane Auvin, María J. Miranda, Maja Hempel, Eva H. Brilstra, Nine Knoers, Nienke E. Verbeek, Marjan van Kempen, Kees P. J. Braun, Grazia M.S. Mancini, Saskia Biskup, Konstanze Hörtnagel, 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
- Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial
Authors: Lieven Lagae, Joseph Sullivan, Kelly G. Knupp, Linda Laux, Tilman Polster, Marina Nikanorova, Orrin Devinsky, J. Helen Cross, Renzo Guerrini, Dinesh Talwar, Ian Miller, Gail Farfel, Bradley S. Galer, Arnold R. Gammaitoni, Arun Mistry, Glenn Morrison, Michael Lock, Anupam Agarwal, Wyman W. Lai, Berten Ceulemans - The Lancet 2019 cited by 366
- Proposed consensus definitions for new‐onset refractory status epilepticus (NORSE), febrile infection‐related epilepsy syndrome (FIRES), and related conditions
Authors: Lawrence J. Hirsch, Nicolas Gaspard, Andreas van Baalen, Rima Nabbout, Sophie Demeret, Tobias Loddenkemper, Vincent Navarro, Nicola Specchio, Lieven Lagae, Andrea O. Rossetti, Sara E. Hocker, Teneille Gofton, Nicholas S. Abend, Emily J. Gilmore, Cecil D. Hahn, Houman Khosravani, Felix Rosenow, Eugen Trinka - Epilepsia 2018 cited by 518
- Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling
Authors: Gillian Rice, Yoandris del Toro Duany, Emma M. Jenkinson, Gabriella Forte, Beverley Anderson, Giada Ariaudo, Brigitte Bader‐Meunier, Eileen Baildam, Roberta Battini, Michael W. Beresford, Manuela Casarano, Mondher Chouchane, Rolando Cimaz, Abigail E. Collins, Nuno Cordeiro, Russell C. Dale, Joyce Davidson, Liesbeth De Waele, Isabelle Desguerre, Laurence Faivre, Elisa Fazzi, Bertrand Isidor, Lieven Lagae, Andrew Latchman, Pierre Lebon, Chumei Li, John H. Livingston, Charles Marques Lourenço, Maria Margherita Mancardi, Alice Masurel‐Paulet, 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
- De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
Authors: Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans, Lieven Lagae, Christine Van Broeckhoven, Peter De Jonghe - The American Journal of Human Genetics 2001 cited by 1,275
- Efficacy and Safety of Fenfluramine for the Treatment of Seizures Associated With Lennox-Gastaut Syndrome
Authors: Kelly G. Knupp, Ingrid E. Scheffer, Berten Ceulemans, Joseph Sullivan, Katherine Nickels, Lieven Lagae, Renzo Guerrini, Sameer M. Zuberi, Rima Nabbout, Kate Riney, Svetlana Shore, Anupam Agarwal, Michael Lock, Gail Farfel, Bradley S. Galer, Arnold R. Gammaitoni, Ronald L. Davis, António Gil‐Nagel - JAMA Neurology 2022 cited by 124
- Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP Trial
Authors: Katarzyna Kotulska, David J. Kwiatkowski, Paolo Curatolo, Bernhard Weschke, Kate Riney, Floor E. Jansen, Martha Feucht, Pavel Kršek, Rima Nabbout, Anna Jansen, Konrad Wojdan, Kamil Sijko, Jagoda Głowacka‐Walas, Julita Borkowska, Krzysztof Sadowski, Dorota Domańska‐Pakieła, Romina Moavero, Christoph Hertzberg, Hanna M. Hulshof, Theresa O. Scholl, Barbora Beňová, Eleonora Aronica, Jessie De Ridder, Lieven Lagae, Sergiusz Jóźwiak, the EPISTOP Investigators - Annals of Neurology 2020 cited by 258
- Impact of fenfluramine on the expected SUDEP mortality rates in patients with Dravet syndrome
Authors: J. Helen Cross, Bradley S. Galer, António Gil‐Nagel, Orrin Devinsky, Berten Ceulemans, Lieven Lagae, An‐Sofie Schoonjans, Elizabeth Donner, Elaine Wirrell, Sanjeev V. Kothare, Anupam Agarwal, Michael Lock, Arnold R. Gammaitoni - Seizure 2021 cited by 80
- Pediatric Outcome after Maternal Cancer Diagnosed during Pregnancy
Authors: Frédéric Amant, Tineke Vandenbroucke, Magali Verheecke, Monica Fumagalli, M Halaška, Ingrid Boere, Sileny Han, Mina Mhallem Gzirí, Fedro A. Peccatori, Lukáš Rob, Christianne Lok, Petronella O. Witteveen, Jens‐Uwe Voigt, Gunnar Naulaers, Lore Vallaeys, Frank Van den Heuvel, Lieven Lagae, Luc Mertens, Laurence Claes, Kristel Van Calsteren - New England Journal of Medicine 2015 cited by 367
- Automated detection of absence seizures using a wearable electroencephalographic device: a phase 3 validation study and feasibility of automated behavioral testing
Authors: Giorgi Japaridze, Dirk Loeckx, Tim Buckinx, Sidsel Armand Larsen, Renée Proost, Katrien Jansen, Paul MacMullin, Natália Gimenez Paiva, Sofia Kasradze, Alexander Rotenberg, Lieven Lagae, Sándor Beniczky - Epilepsia 2022 cited by 70
- Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies
Authors: Gemma L. Carvill, Krysta L. Engel, Aishwarya Ramamurthy, J. Nicholas Cochran, Jolien Roovers, Hannah Stamberger, Nicholas Lim, Amy Schneider, Georgie Hollingsworth, Dylan H. Holder, Brigid M. Regan, James M.J. Lawlor, Lieven Lagae, Berten Ceulemans, E. Martina Bebin, John Nguyen, Gregory S. Barsh, Sarah Weckhuysen, Miriam H. Meisler, Samuel F. Berkovic, Peter De Jonghe, Ingrid E. Scheffer, R Myers, Gregory M. Cooper, Heather C. Mefford, Pasquale Striano, Federico Zara, Ingo Helbig, Rikke S. Møller, Sarah von Spiczak, 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
- Serotonin receptors in epilepsy: Novel treatment targets?
Authors: Jo Sourbron, Lieven Lagae - Epilepsia Open 2022 cited by 72
- Accurate detection of typical absence seizures in adults and children using a two‐channel electroencephalographic wearable behind the ears
Authors: Lauren Swinnen, Christos Chatzichristos, Katrien Jansen, Lieven Lagae, Chantal Depondt, Laura Seynaeve, Evelien Vancaester, Annelies Van Dycke, Jaiver Macea, Kaat Vandecasteele, Victoria Broux, Maarten De Vos, Wim Van Paesschen - Epilepsia 2021 cited by 73
- Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo‐controlled clinical trial
Authors: Joseph Sullivan, Lieven Lagae, J. Helen Cross, Orrin Devinsky, Renzo Guerrini, Kelly G. Knupp, Linda Laux, Marina Nikanorova, Tilman Polster, Dinesh Talwar, Berten Ceulemans, Rima Nabbout, Gail Farfel, Bradley S. Galer, Arnold R. Gammaitoni, Michael Lock, Anupam Agarwal, Ingrid E. Scheffer, the FAiRE DS Study Group - Epilepsia 2023 cited by 47
- Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response
Authors: Gillian Rice, Jacquelyn Bond, Aruna Asipu, Rebecca Brunette, Iain W. Manfield, Ian Carr, Jonathan C. Fuller, Richard M. Jackson, Teresa M. Lamb, Tracy A. Briggs, Manir Ali, Hannah Gornall, Lydia R Couthard, Alec Aeby, Simon Attard-Montalto, Enrico Bertini, Christine Bodemer, Knut Brockmann, Louise Brueton, Peter Corry, Isabelle Desguerre, Elisa Fazzi, Àngels García Cazorla, Blanca Gener, Ben C.J. Hamel, Arvid Heiberg, Matthew F. Hunter, Marjo S. van der Knaap, Ram Kumar, Lieven Lagae, 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
- Vagus nerve stimulation for drug‐resistant epilepsy: A European long‐term study up to 24 months in 347 children
Authors: Iren Orosz, David McCormick, Nelia Zamponi, Sophia Varadkar, Martha Feucht, D. Parain, Roger Griens, Louis Vallée, Paul Boon, Christopher Rittey, Amara K. Jayewardene, Mark Bunker, Alexis Arzimanoglou, Lieven Lagae - Epilepsia 2014 cited by 267
- Dravet syndrome: A systematic literature review of the illness burden
Authors: Adam Strzelczyk, Lieven Lagae, Jo M. Wilmshurst, Andreas Brunklaus, Pasquale Striano, Felix Rosenow, Susanne Schubert‐Bast - Epilepsia Open 2023 cited by 62
- Clinical and Molecular Phenotype of Aicardi-Goutières Syndrome
Authors: Gillian Rice, Teresa Patrick, Rekha Parmar, Claire Taylor, Alec Aeby, Jean Aicardi, Rafael Artuch, Simon Attard Montalto, Carlos A. Bacino, Bruno Barroso, Peter Baxter, Willam S. Benko, Carsten Bergmann, Enrico Bertini, Roberta Biancheri, Edward Blair, Nenad Blau, David T. Bonthron, Tracy A. Briggs, Louise Brueton, Han G. Brunner, Christopher J. Burke, Ian Carr, Daniel R. Carvalho, Kate Chandler, H.‐J. Christen, Peter Corry, Frances M. Cowan, Helen Cox, Stefano D’Arrigo, 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
- Quality of life and comorbidities associated with Dravet syndrome severity: a multinational cohort survey
Authors: Lieven Lagae, Isabella Brambilla, Ana Mingorance, Eddie Gibson, Alysia Battersby - Developmental Medicine & Child Neurology 2017 cited by 188
- 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: Kelly G. Knupp, Ingrid E. Scheffer, Berten Ceulemans, Joseph Sullivan, Katherine Nickels, Lieven Lagae, Renzo Guerrini, Sameer M. Zuberi, Rima Nabbout, Kate Riney, Anupam Agarwal, Michael Lock, David Dai, Gail Farfel, Bradley S. Galer, Arnold R. Gammaitoni, Shikha Polega, Ronald L. Davis, António Gil‐Nagel - Epilepsia 2022 cited by 49
- Updated classification of epileptic seizures: Position paper of the International League Against Epilepsy
Authors: Sándor Beniczky, Eugen Trinka, Elaine Wirrell, Fatema Abdulla, Raidah Albaradie, Mario Alonso‐Vanegas, Stéphane Auvin, Mamta Bhushan Singh, Hal Blumenfeld, Alicia Bogacz Fressola, Roberto Caraballo, Mar Carreño, Fernando Cendes, Augustina Charway‐Felli, Mark Cook, Dana Craiu, Birinus Ezeala‐Adikaibe, Birgit Frauscher, Jacqueline A. French, M. V. Gule, Norimichi Higurashi, Akio Ikeda, Floor E. Jansen, Barbara C. Jobst, Philippe Kahane, Nirmeen A. Kishk, Ching Soong Khoo, Kollencheri Puthenveettil Vinayan, Lieven Lagae, Kheng Seang Lim, 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
