Pasquale Striano

Active 1999–2025

334
Papers
24,672
Citations
89
h-index
298
i10-index

Citations

Citations per year for Pasquale Striano1991: 1 citations1996: 2 citations1999: 3 citations2000: 2 citations2001: 3 citations2002: 1 citations2003: 3 citations2004: 1 citations2005: 3 citations2006: 8 citations2007: 24 citations2008: 36 citations2009: 87 citations2010: 93 citations2011: 68 citations2012: 51 citations2013: 67 citations2014: 79 citations2015: 138 citations2016: 141 citations2017: 153 citations2018: 138 citations2019: 691 citations2020: 884 citations2021: 1,052 citations2022: 1,077 citations2023: 882 citations2024: 1,478 citations2025: 608 citations2026: 21 citations1992–1995: no citations, so these years are not shown1997–1998: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,223 citing papers, 18.9% of this breakdownUnited Kingdom: 982 citing papers, 8.3% of this breakdownItaly: 942 citing papers, 8% of this breakdownGermany: 749 citing papers, 6.4% of this breakdownChina: 702 citing papers, 6% of this breakdownAustralia: 518 citing papers, 4.4% of this breakdownCanada: 517 citing papers, 4.4% of this breakdownFrance: 499 citing papers, 4.2% of this breakdownNetherlands: 404 citing papers, 3.4% of this breakdownSpain: 288 citing papers, 2.4% of this breakdownSwitzerland: 258 citing papers, 2.2% of this breakdownBelgium: 236 citing papers, 2% of this breakdown
0%18.9%Other 29.4%

Fields

  • Medicine46.5%
  • Biochemistry, Genetics and Molecular Biology35.2%
  • Neuroscience13.4%
  • Immunology and Microbiology1.2%
  • Psychology0.6%
  • Agricultural and Biological Sciences0.6%
  • Other2.5%

Topics

  • Epilepsy research and treatment10.9%
  • Neuroscience and Neuropharmacology Research5.5%
  • Genetics and Neurodevelopmental Disorders5.5%
  • Genomics and Rare Diseases5.1%
  • Pharmacological Effects and Toxicity Studies3%
  • Genomic variations and chromosomal abnormalities2.5%
  • Other67.5%

Coauthors

All papers

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  1. Mapping the human genetic architecture of COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Younghun Han, Mohammed Jashim Uddin, George Davey Smith, Cristen J. Willer, Joseph D. Buxbaum, Analysis group, Manuscript analyses team leader, Manuscript analyses team member: meta-analysis, Juha Mehtonen, Manuscript analyses team member: heritability, methods and supplements, Manuscript analyses team member: PHEWAS, Manuscript analyses team member: Mendelian randomization, Manuscript analyses team member: PC projection and gene prioritization, Manuscript analyses team member: gene prioritization, Hilary K. Finucane, Manuscript analyses team member: sensitivity analysis, Mattia Cordioli, Manuscript analyses team members: PC projection, Alicia R. Martin, Wei Zhou, In silico analysis team members, Bogdan Paşaniuc, Hanna Julienne, Hugues Aschard, Huwenbo Shi, Loïc Yengo, Renato Polimanti, Maya Ghoussaini, Jeremy Schwartzentruber, Ian Dunham, Project management group, Project management leader, Project management support, Karolina Chwiałkowska, Margherita Francescatto, Amy Trankiem, Mary K. Balaconis, Phenotype steering group, Lea K. Davis, Sulggi A. Lee, James R. Priest, Alessandra Renieri, Vijay G. Sankaran, David A. van Heel, Patrick Deelen, J. Brent Richards, Tomoko Nakanishi, Les Biesecker, V. Eric Kerchberger, J. Kenneth Baillie, Data dictionary, Francesca Mari, Anna Bernasconi, J. Kenneth Baillie, Arif Canakoglu, Scientific communication group, Scientific communication leaders, Brooke Wolford, Scientific communication members, Annika Faucon, Atanu Kumar Dutta, Claudia Schurmann, Emi N. Harry, Ewan Birney, Huy Nguyen, Jamal Nasir, Mari Kaunisto, Matthew Solomonson, Nicole Dueker, Nirmal Vadgama and 3,796 more - Nature 2021 cited by 1,127

  2. 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

  3. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sönke Langner, Matteo Lenge, Kelly M. Leyden, Min Liu, Richard Q. Loi, Pascal Martin, Mario Mascalchi, Márcia Elisabete Morita, José C. Pariente, Raúl Rodríguez‐Cruces, Christian Rummel, Taavi Saavalainen, Mira Semmelroch, Mariasavina Severino, Rhys H. Thomas, Manuela Tondelli, Domenico Tortora, Anna Elisabetta Vaudano, Lucy Vivash, Felix von Podewils, Jan Wagner, Bernd Weber, Yi Yao, Clarissa Lin Yasuda, Guohao Zhang, Núria Bargalló, Benjamin Bender, Neda Bernasconi, Andrea Bernasconi, Boris C. Bernhardt, Ingmar Blümcke, Chad Carlson, Gianpiero L. Cavalleri, Fernando Cendes, Luis Concha, Norman Delanty, Chantal Depondt, Orrin Devinsky, Colin P. Doherty, Niels K. Focke, Antonio Gambardella, Renzo Guerrini, Khalid Hamandi, Graeme D. Jackson, Reetta Kälviäinen, Peter Kochunov, Patrick Kwan, Angelo Labate, Carrie R. McDonald, Stefano Meletti, Terence J. O’Brien, Sébastien Ourselin, Mark P. Richardson, Pasquale Striano, Thomas Thesen, Roland Wiest, Junsong Zhang, Annamaria Vezzani, Mina Ryten, Paul M. Thompson, Sanjay M. Sisodiya - Brain 2017 cited by 531

  4. Interpretable surface-based detection of focal cortical dysplasias: a Multi-centre Epilepsy Lesion Detection study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eugenio Abela, Nandini Mullatti, Jonathan O’Muircheartaigh, Katy Vecchiato, Yawu Liu, Maria Eugenia Caligiuri, Ben Sinclair, Lucy Vivash, Anna Willard, Jothy Kandasamy, Ailsa McLellan, Drahoslav Sokol, Mira Semmelroch, Ane Kloster, Giske Opheim, Letícia Ribeiro, Clarissa Lin Yasuda, Maria Camilla Rossi‐Espagnet, Khalid Hamandi, Anna Tietze, Carmen Barba, Renzo Guerrini, William D. Gaillard, Xiaozhen You, Irène Wang, Sofía González‐Ortiz, Mariasavina Severino, Pasquale Striano, Domenico Tortora, Reetta Kälviäinen, Antonio Gambardella, Angelo Labate, Patricia Desmond, Elaine Lui, Terence J. O’Brien, Jay Shetty, Graeme D. Jackson, John S. Duncan, Gavin P. Winston, Lars H. Pinborg, Fernando Cendes, Fabian J. Theis, Russell T. Shinohara, J. Helen Cross, Torsten Baldeweg, Sophie Adler, Konrad Wagstyl - Brain 2022 cited by 132

  5. White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Renzo Guerrini, Khalid Hamandi, Akari Ishikawa, Simon S. Keller, Peter Kochunov, Raviteja Kotikalapudi, Barbara A. K. Kreilkamp, Patrick Kwan, Angelo Labate, Sönke Langner, Matteo Lenge, Min Liu, Elaine Lui, Pascal Martin, Mario Mascalchi, José C.V. Moreira, Marcia Morita‐Sherman, Terence J. O’Brien, Heath Pardoe, José C. Pariente, Letícia Ribeiro, Mark P. Richardson, Cristiane S. Rocha, Raúl Rodríguez‐Cruces, Felix Rosenow, Mariasavina Severino, Benjamin Sinclair, Hamid Soltanian‐Zadeh, Pasquale Striano, Peter N. Taylor, Rhys H. Thomas, Domenico Tortora, Dennis Velakoulis, Annamaria Vezzani, Lucy Vivash, Felix von Podewils, Sjoerd B. Vos, Bernd Weber, Gavin P. Winston, Clarissa Lin Yasuda, Alyssa H. Zhu, Paul M. Thompson, Christopher D. Whelan, Neda Jahanshad, Sanjay M. Sisodiya, Carrie R. McDonald - Brain 2020 cited by 233

  6. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michal Tzadok, Kristin G. Monaghan, Teresa Santiago‐Sim, Richard Person, Megan T. Cho, Rebecca Willaert, Yongjin Yoo, Jong‐Hee Chae, Yingting Quan, Huidan Wu, Tianyun Wang, Raphael Bernier, Kun Xia, Alyssa Blesson, Mahim Jain, Mohammad Mahdi Motazacker, Bregje Jaeger, Amy Schneider, Katja Boysen, Alison M. Muir, Candace T. Myers, Ralitza H. Gavrilova, Lauren Gunderson, Laura Schultz‐Rogers, Eric W. Klee, David A. Dyment, Matthew Osmond, Mara Parellada, Cloe Llorente, Javier González‐Peñas, Ángel Carracedo, Arie van Haeringen, Claudia Ruivenkamp, Caroline Nava, Delphine Héron, Rosaria Nardello, Michele Iacomino, Carlo Minetti, Aldo Skabar, Antonella Fabretto, SYNAPS Study Group, Michael G. Hanna, Enrico Bugiardini, Isabel C. Hostettler, Benjamin O’Callaghan, Alaa Khan, Andrea Cortese, Emer O’Connor, Wai Y. Yau, Thomas Bourinaris, Rauan Kaiyrzhanov, Viorica Chelban, M Madej, Maria C. Diana, Maria S. Vari, Marina Pedemonte, Claudio Bruno, Ganna Balagura, Marcello Scala, Chiara Fiorillo, Lino Nobili, Nancy T. Malintan, M. Natalia Zanetti, Shyam S. Krishnakumar, Gabriele Lignani, James E.C. Jepson, Paolo Broda, Sımona Baldassari, Pia Rossi, Floriana Fruscione and 139 more - Nature Communications 2019 cited by 249

  7. The Pharmacoresistant Epilepsy: An Overview on Existent and New Emerging Therapies

    Authors: , , , , , , - Frontiers in Neurology 2021 cited by 262

  8. Microbiota-gut brain axis involvement in neuropsychiatric disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emilio Russo, Pasquale Striano - Expert Review of Neurotherapeutics 2019 cited by 177

  9. Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Olivier Vanakker, Marja W. Wessels, Suppachok Wetchaphanphesat, Michele Yang, François Boller, Dominique Campion, Didier Hannequin, Marc Sitbon, Daniel H. Geschwind, Jean‐Luc Battini, Giovanni Coppola - Nature Genetics 2015 cited by 316

  10. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anthony G Marson, Randy Stewart, Chantal Depondt, Dennis Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Kevin E. McKenna, Brigid M. Regan, Susannah T. Bellows, Costin Leu, Caitlin A. Bennett, Esther M.C. Johns, Alexandra MacDonald, Hannah Shilling, Rosemary Burgess, Dorien Weckhuysen, Melanie Bahlo, Terence J. O’Brien, Marian Todaro, Hannah Stamberger, Danielle M. Andrade, Tara Sadoway, Kelly Mo, Heinz Krestel, Sabina Gallati, Savvas Papacostas, Ioanna Kousiappa, George A. Tanteles, Katalin Štěrbová, Markéta Vlčková, Lucie Sedláčková, Petra Laššuthová, Karl Martin Klein, Felix Rosenow, Philipp S. Reif, Susanne Knake, Wolfram S. Kunz, Gábor Zsurka, Christian E. Elger, Jürgen Bauer, Michael Rademacher, Manuela Pendziwiat, Hiltrud Muhle, Annika Rademacher, Andreas van Baalen, Sarah von Spiczak, Ulrich Stephani, Zaid Afawi, Amos D. Korczyn, Moien Kanaan, Christina Canavati, Gerhard Kurlemann, Karen Müller‐Schlüter, Gerhard Kluger, Martin Häusler, Ilan Blatt, Johannes R. Lemke, Ilona Krey, Yvonne Weber, Stefan Wolking, Felicitas Becker, Christian Hengsbach, Sarah Rau, Ana F. Maisch, Bernhard J. Steinhoff, Andreas Schulze‐Bonhage, Susanne Schubert‐Bast, Herbert Schreiber, Ingo Borggräfe and 141 more - The American Journal of Human Genetics 2019 cited by 303

  11. Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mario Mascalchi, Mira Semmelroch, Rhys H. Thomas, Hamid Soltanian‐Zadeh, Esmaeil Davoodi‐Bojd, Junsong Zhang, Matteo Lenge, Renzo Guerrini, Emanuele Bartolini, Khalid Hamandi, Sonya Foley, Bernd Weber, Chantal Depondt, Julie Absil, Sarah J. A. Carr, Eugenio Abela, Mark P. Richardson, Orrin Devinsky, Mariasavina Severino, Pasquale Striano, Domenico Tortora, Sean N. Hatton, Sjoerd B. Vos, John S. Duncan, Christopher D. Whelan, Paul M. Thompson, Sanjay M. Sisodiya, Andrea Bernasconi, Angelo Labate, Carrie R. McDonald, Neda Bernasconi, Boris C. Bernhardt - Science Advances 2020 cited by 198

  12. Assessing the landscape of STXBP1-related disorders in 534 individuals

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Heather E. Olson, Emma Sexton, Beth Rosen Sheidley, Lacey Smith, Luiza Sotero, Hannah Stamberger, Steffen Syrbe, Kim Marie Thalwitzer, Annemiek A. van Berkel, Mieke M. van Haelst, Christopher J. Yuskaitis, Sarah Weckhuysen, Benjamin L. Prosser, Charlene Son Rigby, Scott Demarest, Samuel R. Pierce, Yuehua Zhang, Rikke S. Møller, Hilgo Bruining, Annapurna Poduri, Federico Zara, Matthijs Verhage, Pasquale Striano, Ingo Helbig - Brain 2021 cited by 122

  13. Genotype-phenotype correlations in SCN8A -related disorders reveal prognostic and therapeutic implications

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Karl Martin Klein, P Y Billie Au, Jong M. Rho, Alice Ho, Silvia Masnada, Pierangelo Veggiotti, Lucio Giordano, Patrizia Accorsi, Christina Engel Hoei‐Hansen, Pasquale Striano, Federico Zara, Hélène Verhelst, J. Verhoeven, Hilde M. H. Braakman, Bert van der Zwaag, Aster V. E. Harder, Eva H. Brilstra, Manuela Pendziwiat, Sebastian Lebon, María Vaccarezza, Ngọc Minh Lê, Jakob Christensen, Sabine Grønborg, Stephen W. Scherer, Jennifer Howe, Walid Fazeli, Katherine B. Howell, Richard J. Leventer, Chloe Stutterd, Sonja Walsh, Marion Gérard, Bénédicte Gérard, Sara Matricardi, Claudia Bonardi, Stefano Sartori, Andrea Berger, Dorota Hoffman‐Zacharska, Massimo Mastrangelo, Francesca Darra, Arve Vøllo, M. Mahdi Motazacker, Phillis Lakeman, Mathilde Nizon, Cornelia Betzler, Cécilia Altuzarra, Roseline Caume, Agathe Roubertie, Philippe Gélisse, Carla Marini, Renzo Guerrini, Frédéric Bilan, Daniel Tibussek, Margarete Koch‐Hogrebe, Μ. Scott Perry, Shoji Ichikawa, Е. Л. Дадали, Artem Sharkov, Irina Mishina, M. O. Abramov, Ilya Kanivets, С. А. Коростелев, Sergey I. Kutsev, Karen E. Wain, Nancy Eisenhauer, Monisa Wagner, Juliann M. Savatt, Karen Müller‐Schlüter, Haim Bassan, Artem Borovikov, Marie‐Cécile Nassogne and 29 more - Brain 2021 cited by 146

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

    Authors: , , , , - Frontiers in Neurology 2017 cited by 198

  15. A second update on mapping the human genetic architecture of COVID-19

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kumar Veerapen, Brooke N. Wolford, Scientific communication member, Hajar Fauzan Ahmad, Shea J. Andrews, Kathrin Aprile von Hohenstaufen Puoti, Cindy G. Boer, Palwendé Romuald Boua, Guillaume Butler‐Laporte, Carmen L. Cadilla, Karolina Chwiałkowska, Francesca Colombo, Venceslas Douillard, Nicole Dueker, Atanu Kumar Dutta, Yasser M. El‐Sherbiny, Madonna M. Eltoukhy, Sahar Esmaeeli, Annika Faucon, Marie-Julie Favé, Israel Fernández Cadenas, Margherita Francescatto, Laurent C. Francioli, Lude Franke, Macarena Fuentes, Rocío Gallego Durán, David Gómez-Cabrero, Emi N. Harry, Philip R. Jansen, József Szentpéteri, Elżbieta Kaja, Masahiro Kanai, Chloe Kirk, Athanasios Kousathanas, José Eduardo Krieger, Sanjay Patel, Audrey Lemaçon, Sophie Limou, Píetro Lió, Eirini Marouli, M. Marttila, Carolina Medina‐Gómez, Yael Michaeli, Isabelle Migeotte, Soumyajit Mondal, Andrés Moreno‐Estrada, Leire Moya, Tomoko Nakanishi, Jamal Nasir, Dorote Pasko, Nathaniel M. Pearson, Alexandre C. Pereira, James R. Priest, Vid Prijatelj, Ivana Nedeljković, Alexander Teumer, Réka Várnai, Manuel Romero-Gómez, Christina Roos, Jeffrey Rosenfeld, Ruolin Li, Eva C. Schulte, Claudia Schurmann, Bahareh Sedaghati-khayat, Doaa Shaheen, Ilangumaran Shivanathan, Csilla Sipeky, Zhou Sirui, Pasquale Striano, Yosuke Tanigawa and 3,785 more - Nature 2023 cited by 116

  16. Temporal Lobe Epilepsy and Psychiatric Comorbidity

    Authors: , , , , , , - Frontiers in Neurology 2021 cited by 127

  17. The landscape of epilepsy-related GATOR1 variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , E. Niks, Floor E. Jansen, Kees P. J. Braun, Daniëlle de Jong, Guido Rubboli, Inga Talvik, Valentin Sander, Peter Uldall, M. Jacquemont, Caroline Nava, Éric Leguern, Sophie Julia, Antonio Gambardella, G. D’Orsi, Giovanni Crichiutti, Laurence Faivre, Véronique Darmency, Barbora Beňová, Pavel Kršek, Arnaud Biraben, Anne-Sophie Lèbre, Mélanie Jennesson, Shifteh Sattar, Cécile Marchal, Douglas R. Nordli, Kristin Lindstrom, Pasquale Striano, Lysa Boissé Lomax, Courtney Kiss, Fabrice Bartoloméi, Anne Lépine, An‐Sofie Schoonjans, Katrien Stouffs, Anna Jansen, Eleni Panagiotakaki, Brigitte Ricard‐Mousnier, Julien Thévenon, Julitta de Bellescize, Hélène Catenoix, Thomas Dorn, Martin Zenker, Karen Müller‐Schlüter, Christian Brandt, Ilona Krey, Tilman Polster, Markus Wolff, Meral Balci, Kevin Rostásy, Guillaume Achaz, Pia Zacher, Thomas Becher, Thomas Cloppenborg, Christopher J. Yuskaitis, Sarah Weckhuysen, Annapurna Poduri, Johannes R. Lemke, Rikke S. Møller, Stéphanie Baulac - Genetics in Medicine 2018 cited by 239

  18. Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gianpiero L. Cavalleri, Norman Delanty, Reetta Kälviäinen, Graeme D. Jackson, Magdalena Kowalczyk, Mario Mascalchi, Mira Semmelroch, Rhys H. Thomas, Hamid Soltanian‐Zadeh, Esmaeil Davoodi‐Bojd, Junsong Zhang, Gavin P. Winston, Aoife Griffin, Aditi Singh, Vijay Tiwari, Barbara A. K. Kreilkamp, Matteo Lenge, Renzo Guerrini, Khalid Hamandi, Sonya Foley, Theodor Rüber, Bernd Weber, Chantal Depondt, Julie Absil, Sarah J. A. Carr, Eugenio Abela, Mark P. Richardson, Orrin Devinsky, Mariasavina Severino, Pasquale Striano, Domenico Tortora, Erik Kaestner, Sean N. Hatton, Sjoerd B. Vos, Lorenzo Caciagli, John S. Duncan, Christopher D. Whelan, Paul M. Thompson, Sanjay M. Sisodiya, Andrea Bernasconi, Angelo Labate, Carrie R. McDonald, Neda Bernasconi, Boris C. Bernhardt - Nature Communications 2022 cited by 105

  19. The burden of illness in Lennox–Gastaut syndrome: a systematic literature review

    Authors: , , , , - Orphanet Journal of Rare Diseases 2023 cited by 62

  20. STXBP1 encephalopathy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carlo Minetti, Hiltrud Muhle, Judith Phalin, Keri Ramsey, Antonino Romeo, Jens Schallner, Ina Schanze, Marwan Shinawi, Kristel Sleegers, Katalin Štěrbová, Steffen Syrbe, Monica Traverso, Andreas Tzschach, Peter Uldall, Rudy Van Coster, Hélène Verhelst, Maurizio Viri, Susan Winter, Markus Wolff, Martin Zenker, Leonardo Zoccante, Peter De Jonghe, Ingo Helbig, Pasquale Striano, Johannes R. Lemke, Rikke S. Møller, Sarah Weckhuysen - Neurology 2016 cited by 323

  21. Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications

    Authors: , , , , , , , , , , , - Frontiers in Neurology 2022 cited by 55

  22. 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

  23. Third-Generation Antiseizure Medications for Adjunctive Treatment of Focal-Onset Seizures in Adults: A Systematic Review and Network Meta-analysis

    Authors: , , , , , , , - Drugs 2022 cited by 115

  24. Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Maria Eugenia Caligiuri, Ben Sinclair, Lucy Vivash, Anna Willard, Jothy Kandasamy, Ailsa McLellan, Drahoslav Sokol, Mira Semmelroch, Ane Kloster, Giske Opheim, Clarissa Lin Yasuda, Kai Zhang, Khalid Hamandi, Carmen Barba, Renzo Guerrini, William D. Gaillard, Xiaozhen You, Irène Wang, Sofía González‐Ortiz, Mariasavina Severino, Pasquale Striano, Domenico Tortora, Reetta Kälviäinen, Antonio Gambardella, Angelo Labate, Patricia Desmond, Elaine Lui, Terry O'Brien, Jay Shetty, Graeme D. Jackson, John S. Duncan, Gavin P. Winston, Lars H. Pinborg, Fernando Cendes, J. Helen Cross, Torsten Baldeweg, Sophie Adler - Epilepsia 2021 cited by 107