Sanjay M. Sisodiya

Active 1986–2025

Also published as
Sanjay M Sisodiya
200
Papers
27,447
Citations
94
h-index
188
i10-index

Citations

Citations per year for Sanjay M. Sisodiya1978: 2 citations1987: 5 citations1988: 9 citations1989: 5 citations1990: 7 citations1991: 6 citations1992: 4 citations1993: 3 citations1994: 2 citations1995: 6 citations1996: 10 citations1997: 18 citations1998: 15 citations1999: 17 citations2000: 19 citations2001: 25 citations2002: 50 citations2003: 95 citations2004: 121 citations2005: 202 citations2006: 155 citations2007: 120 citations2008: 150 citations2009: 136 citations2010: 98 citations2011: 146 citations2012: 144 citations2013: 131 citations2014: 223 citations2015: 240 citations2016: 262 citations2017: 257 citations2018: 224 citations2019: 839 citations2020: 928 citations2021: 1,062 citations2022: 822 citations2023: 644 citations2024: 1,024 citations2025: 436 citations2026: 18 citations1979–1986: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,644 citing papers, 19.6% of this breakdownUnited Kingdom: 1,369 citing papers, 10.2% of this breakdownGermany: 1,016 citing papers, 7.5% of this breakdownChina: 840 citing papers, 6.2% of this breakdownItaly: 772 citing papers, 5.7% of this breakdownCanada: 651 citing papers, 4.8% of this breakdownAustralia: 596 citing papers, 4.4% of this breakdownFrance: 554 citing papers, 4.1% of this breakdownNetherlands: 518 citing papers, 3.9% of this breakdownSpain: 300 citing papers, 2.2% of this breakdownSwitzerland: 271 citing papers, 2% of this breakdownJapan: 241 citing papers, 1.8% of this breakdown
0%19.6%Other 27.6%

Fields

  • Medicine47.1%
  • Biochemistry, Genetics and Molecular Biology29.5%
  • Neuroscience16.6%
  • Computer Science1.8%
  • Pharmacology, Toxicology and Pharmaceutics1.6%
  • Environmental Science0.7%
  • Other2.7%

Topics

  • Epilepsy research and treatment12.2%
  • Neuroscience and Neuropharmacology Research5.9%
  • Genomics and Rare Diseases4.1%
  • Pharmacological Effects and Toxicity Studies3.8%
  • Genetics and Neurodevelopmental Disorders3.4%
  • Functional Brain Connectivity Studies3.1%
  • Other67.5%

Coauthors

All papers

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  1. Drug Resistance in Epilepsy: Clinical Impact, Potential Mechanisms, and New Innovative Treatment Options

    Authors: , , , - Pharmacological Reviews 2020 cited by 860

  2. Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Josef Zentner, Dieter Henrik Heiland, Horst Urbach, Bernhard J. Steinhoff, Thomas Bast, Laura Tassi, Giorgio Lo Russo, Çiğdem Özkara, Büğe Öz, Pavel Kršek, Silke Vogelgesang, Uwe Runge, Holger Lerche, Yvonne Weber, Mrinalini Honavar, José Pimentel, Alexis Arzimanoglou, Adriana Ulate-Campos, Soheyl Noachtar, Elisabeth Härtl, Olaf Schijns, Renzo Guerrini, Carmen Barba, Thomas S. Jacques, J. Helen Cross, Martha Feucht, Angelika Mühlebner, Thomas Grünwald, Eugen Trinka, Peter Winkler, António Gil‐Nagel, Rafael Toledano, Thomas Mayer, Martin Lutz, Basilios Zountsas, Kyriakos Garganis, Felix Rosenow, Anke Hermsen, Tim J. von Oertzen, Thomas L. Diepgen, G. Avanzini - New England Journal of Medicine 2017 cited by 917

  3. Comorbidities of epilepsy: current concepts and future perspectives

    Authors: , , - The Lancet Neurology 2015 cited by 762

  4. The ENIGMA Toolbox: multiscale neural contextualization of multisite neuroimaging datasets

    Authors: , , , , , , , , , , , , , , , - Nature Methods 2021 cited by 260

  5. 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

  6. International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from theILAECommission on Diagnostic Methods

    Authors: , , , , , , , , , , , , , , , , , , , , , - Epilepsia 2013 cited by 997

  7. 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

  8. De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Petr Danecek, Emmanuèle C. Délot, Kerith‐Rae Dias, Ellen Roy Elias, Frances Elmslie, Care-Anne Evans, Lisa Ewans, Kimberly Ezell, Jamie L. Fraser, Lyndon Gallacher, Casie A. Genetti, Anne Goriely, Christina Grant, Tobias B. Haack, Jenny Higgs, Anjali Gupta Hinch, Matthew E. Hurles, Alma Kuechler, Katherine Lachlan, Seema R. Lalani, François Lecoquierre, Elsa Leitão, Anna Le Fevre, Richard J. Leventer, Jan Liebelt, Sarah Lindsay, Paul J. Lockhart, Alan Ma, Ellen F. Macnamara, Sahar Mansour, Taylor Maurer, Rodrigo Mendez, Kay Metcalfe, Stephen B. Montgomery, Mariya Moosajee, Marie‐Cécile Nassogne, Serena Neumann, Michael O’Donoghue, Melanie O’Leary, Elizabeth E. Palmer, Nikhil Pattani, John Phillips, Georgia Pitsava, Ryan Pysar, Heidi L. Rehm, Chloe M. Reuter, Nicole Revençu, Angelika Rieß, Rocío Rius, Lance H. Rodan, Tony Roscioli, Jill A. Rosenfeld, Rani Sachdev, Charles Shaw‐Smith, Cas Simons, Sanjay M. Sisodiya, Penny Snell, Laura St Clair, Zornitza Stark, Helen Stewart, Tiong Yang Tan, Natalie B. Tan, Suzanna E.L. Temple, David R. Thorburn, Cynthia J. Tifft, Eloise Uebergang, Grace E. VanNoy, Pradeep Vasudevan, Éric Vilain, David Viskochil and 19 more - Nature 2024 cited by 118

  9. Local molecular and global connectomic contributions to cross-disorder cortical abnormalities

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 128

  10. Microbiota-gut brain axis involvement in neuropsychiatric disorders

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

  11. 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

  12. 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

  13. Precision medicine and therapies of the future

    Authors: - Epilepsia 2020 cited by 144

  14. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura Hernández-Hernández, Bridget H. Maher, Sanjay M. Sisodiya, Marius Kuhn, Dieter Glaeser, Sarah Weckhuysen, Candace T. Myers, Heather C. Mefford, Konstanze Hörtnagel, Saskia Biskup, EuroEPINOMICS-RES MAE working group, Johannes R. Lemke, Delphine Héron, Gerhard Kluger, Christel Depienne - Journal of Medical Genetics 2016 cited by 200

  15. 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

  16. 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

  17. Advances in the development of biomarkers for epilepsy

    Authors: , , , , , , , , , , , , , , - The Lancet Neurology 2016 cited by 364

  18. Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sara Larivière, Matteo Lenge, Elaine Lui, Pascal Martin, Mario Mascalchi, Stefano Meletti, Terence J. O’Brien, Heath Pardoe, José C. Pariente, Jun Rao, Mark P. Richardson, Raúl Rodríguez‐Cruces, Theodor Rüber, Ben Sinclair, Hamid Soltanian‐Zadeh, Dan J. Stein, Pasquale Striano, Peter N. Taylor, Rhys H. Thomas, Anna Elisabetta Vaudano, Lucy Vivash, Felix von Podewills, Sjoerd B. Vos, Bernd Weber, Yi Yao, Clarissa Lin Yasuda, Junsong Zhang, Paul M. Thompson, Sanjay M. Sisodiya, Carrie R. McDonald, Leonardo Bonilha, André Altmann, Chantal Depondt, Marian Galovic, Sophia I. Thomopoulos, Roland Wiest - NeuroImage Clinical 2021 cited by 77

  19. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Steven Van Vooren, Ronald J. Wapner, Andrew O.M. Wilkie, Caroline F. Wright, Anneke T. Vulto‐van Silfhout, Nicole de Leeuw, Bert B.A. de Vries, Nicole L. Washingthon, Cynthia L. Smith, Monte Westerfield, Paul N. Schofield, Barbara J. Ruef, Georgios V. Gkoutos, Melissa Haendel, Damian Smedley, Suzanna Lewis, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2013 cited by 837

  20. Current practice in diagnostic genetic testing of the epilepsies

    Authors: , , , , , , , , , , , , , , , - Epileptic Disorders 2022 cited by 102

  21. Climate change and epilepsy: Insights from clinical and basic science studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Roland Krause, Daniel H. Lowenstein, Despoina Mandelenaki, Carla Marini, Terence J. O’Brien, Adrian Pace, Luca De Palma, Piero Perucca, Asla Pitkänen, Finola Quinn, Kaja Kristine Selmer, Charles A. Steward, Nicola Swanborough, Roland D. Thijs, Phil Tittensor, Marina Trivisano, Sarah Weckhuysen, Federico Zara, Sanjay M. Sisodiya - Epilepsy & Behavior 2021 cited by 85

  22. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nardo Nardocci, Elisa De Grandis, E. Veneselli, Michela Stagnaro, Fiorella Gurrieri, Giovanni Neri, Federico Vigevano, Eleni Panagiotakaki, Claudia Oechsler, Alexis Arzimanoglou, Sophie Nicole, Melania Giannotta, Giuseppe Gobbi, Miriam Ninan, Brian Neville, Friedrich Ebinger, Carmen Fons, Jaume Campistol, David Kemlink, Soňa Nevšímalová, Laura Laan, Cacha Peeters‐Scholte, Arn van den Maagdenberg, Paul Casaer, Giorgio Casari, Guenter Sange, Georg Spiel, Filippo Martinelli Boneschi, Claudio Zucca, Maria Teresa Bassi, Tsveta Schyns, Francis P. Crawley, Dominique Poncelin, Rosaria Vavassori, Stefania Fiori, Emanuela Abiusi, Lorena Di Pietro, Matthew Sweney, Tara Newcomb, Louis Viollet, Chad D. Huff, Lynn B. Jorde, Sandra P. Reyna, Kelley J. Murphy, Kevin V. Shianna, Curtis Gumbs, Latasha Little, Kenneth Silver, Louis J. Ptáček, Joost Haan, Michel D. Ferrari, Ann M Bye, Geoffrey Herkes, Charlotte M Whitelaw, David Webb, Bryan J. Lynch, Peter Uldall, Mary D. King, Ingrid E. Scheffer, Giovanni Neri, Alexis Arzimanoglou, Arn M. J. M. van den Maagdenberg, Sanjay M. Sisodiya, Mohamad A. Mikati, David B. Goldstein - Nature Genetics 2012 cited by 423

  23. De novo variants in neurodevelopmental disorders with epilepsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2018 cited by 318

  24. Mortality in Dravet syndrome: A review

    Authors: , , , , - Epilepsy & Behavior 2016 cited by 185