Holger Lerche
Active 1989–2025
- 159
- Papers
- 21,370
- Citations
- 89
- h-index
- 154
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Medicine41.7%
- Biochemistry, Genetics and Molecular Biology35.9%
- Neuroscience19.6%
- Engineering0.7%
- Psychology0.4%
- Computer Science0.3%
- Other1.4%
Topics
- Epilepsy research and treatment12.4%
- Neuroscience and Neuropharmacology Research8.3%
- Ion channel regulation and function6.1%
- Genomics and Rare Diseases5.3%
- Genetics and Neurodevelopmental Disorders5.2%
- Pharmacological Effects and Toxicity Studies2.9%
- Other59.8%
Coauthors
- Yvonne Weber35
- Rikke S. Møller28
- Snezana Maljevic23
- Ulrike B. S. Hedrich17
- Felicitas Becker16
- Ingo Helbig16
- Samuel F. Berkovic16
- Bobby P.C. Koeleman15
- Dennis Lal15
- Sarah Weckhuysen15
- Federico Zara14
- Gianpiero L. Cavalleri14
- Pasquale Striano14
- Roland Krause14
- Sanjay M. Sisodiya14
- Thomas V. Wuttke14
- Hiltrud Muhle13
- Johannes R. Lemke13
- Patrick May13
- Stefan Wolking13
- Julian Schubert12
- Peter De Jonghe11
- Carolien G. F. de Kovel10
- Norman Delanty10
All papers
- Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
Authors: Ingmar Blümcke, Roberto Spreafico, Gerrit Haaker, Roland Coras, Katja Kobow, Christian G. Bien, Margarete Pfäfflin, Christian E. Elger, Guido Widman, Johannes Schramm, Albert J. Becker, Kees P. J. Braun, Frans S. S. Leijten, Johannes C. Baayen, Eleonora Aronica, Francine Chassoux, Hajo M. Hamer, Hermann Stefan, Karl Rössler, Maria Thom, Matthew C. Walker, Sanjay M. Sisodiya, John S. Duncan, Andrew W. McEvoy, Tom Pieper, Hans Holthausen, Manfred Kudernatsch, H. J. Meencke, Philippe Kahane, Andreas Schulze‐Bonhage, 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
- Incidence and mechanisms of cardiorespiratory arrests in epilepsy monitoring units (MORTEMUS): a retrospective study
Authors: Philippe Ryvlin, Lina Nashef, Samden D. Lhatoo, Lisa M. Bateman, Jonathan M. Bird, Andrew Bleasel, Paul Boon, Arielle Crespel, Barbara A. Dworetzky, Hans Høgenhaven, Holger Lerche, Louis Maillard, Michael P. Malter, Cécile Marchal, J. M. K. Murthy, Michael A. Nitsche, Ekaterina Pataraia, Terje Rabben, Sylvain Rheims, Bernard Sadzot, Andreas Schulze‐Bonhage, Masud Seyal, Elson L. So, Mark C. Spitz, Anna Szűcs, Meng H. Tan, James X. Tao, Torbjörn Tomson - The Lancet Neurology 2013 cited by 1,121
- 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
- Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Authors: Bassel Abou‐Khalil, Pauls Auce, Andreja Avberšek, Melanie Bahlo, David J. Balding, Thomas Bast, Larry Baum, Albert J. Becker, Felicitas Becker, Bianca Berghuis, Samuel F. Berkovic, Katja Boysen, Jonathan P. Bradfield, Lawrence C. Brody, Russell J. Buono, Ellen Campbell, Gregory D. Cascino, Claudia B. Catarino, Gianpiero L. Cavalleri, Stacey S. Cherny, Krishna Chinthapalli, Alison J. Coffey, Alastair Compston, Antonietta Coppola, Patrick Cossette, John Craig, Gerrit‐Jan de Haan, Peter De Jonghe, Carolien G. F. de Kovel, Norman Delanty, Chantal Depondt, Orrin Devinsky, Dennis Dlugos, Colin P. Doherty, Christian E. Elger, Johan G. Eriksson, Thomas N. Ferraro, Martha Feucht, Ben Francis, André Franke, Jacqueline A. French, Saskia Freytag, Verena Gaus, Eric B. Geller, Christian Gieger, Tracy A. Glauser, Simon Glynn, David B. Goldstein, Hongsheng Gui, Youling Guo, Kevin F. Haas, Håkon Håkonarson, Kerstin Hallmann, Sheryl R. Haut, Erin L. Heinzen, Ingo Helbig, Christian Hengsbach, Helle Hjalgrim, Michele Iacomino, Andrés Ingason, Jennifer Jamnadas-Khoda, Michael R. Johnson, Reetta Kälviäinen, Anne-Mari Kantanen, Dalia Kasperavičiūtė, Dorothée Kasteleijn‐Nolst Trenité, Heidi E. Kirsch, Robert C. Knowlton, Bobby P.C. Koeleman, Roland Krause, Martin Krenn, Wolfram S. Kunz, Ruben Kuzniecky, Patrick Kwan, Dennis Lal, YL Lau, Anna‐Elina Lehesjoki, Holger Lerche, Costin Leu, Wolfgang Lieb, Dick Lindhout, Warren Lo, Íscia Lopes‐Cendes, Daniel H. Lowenstein, Alberto Malovini, Anthony G Marson, Thomas Mayer, Mark McCormack, James L. Mills, Nasir Mirza, Martina Moerzinger, Rikke S. Møller, Anne M. Molloy, Hiltrud Muhle, Mark R. Newton, Ping-Wing Ng, Markus M. Nöthen, Peter Nürnberg, Terence J. O’Brien, Karen Oliver and 58 more - Nature Communications 2018 cited by 513
- GAA-FGF14 ataxia (SCA27B): phenotypic profile, natural history progression and 4-aminopyridine treatment response
Authors: Carlo Wilke, David Pellerin, David Mengel, Andreas Traschütz, Matt C. Danzi, Marie‐Josée Dicaire, Manuela Neumann, Holger Lerche, Benjamin Bender, Henry Houlden, RFC1 study group, Jennifer Faber, Richard Roxburgh, José Luiz Pedroso, Paula Camila Alvez, Orlando Graziani Póvoas Barsottini, Chiara Pane, Francesco Saccà, Alessandro Filla, Filippo M. Santorelli, Ivana Ricca, Stephan Züchner, Lüdger Schöls, Bernard Brais, Matthis Synofzik - Brain 2023 cited by 114
- Transcutaneous Vagus Nerve Stimulation (tVNS) for Treatment of Drug-Resistant Epilepsy: A Randomized, Double-Blind Clinical Trial (cMPsE02)
Authors: Sebastian Bauer, Hartmut Baier, Christian Baumgärtner, K. Bohlmann, Susanne Fauser, W. Graf, Barbara Hillenbrand, Martin Hirsch, Cynthia G. Last, Holger Lerche, T. Mayer, Andreas Schulze‐Bonhage, Bernhard J. Steinhoff, Yvonne Weber, Andreas Hartlep, Felix Rosenow, Hajo M. Hamer - Brain stimulation 2016 cited by 272
- Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress
Authors: Juliet K. Knowles, Ingo Helbig, Cameron S. Metcalf, Laura S. Lubbers, Lori L. Isom, Scott Demarest, Ethan M. Goldberg, Alfred L. George, Holger Lerche, Sarah Weckhuysen, Vicky Whittemore, Samuel F. Berkovic, Daniel H. Lowenstein - Epilepsia 2022 cited by 140
- Risk of Major Congenital Malformations and Exposure to Antiseizure Medication Monotherapy
Authors: Dina Battino, Torbjörn Tomson, Erminio Bonizzoni, John Craig, Emilio Perucca, Anne Sabers, Sanjeev V. Thomas, Silje Alvestad, Piero Perucca, Frank Vajda, EURAP Collaborators, Chiara Pantaleoni, Claudia Ciaccio, Silvia Kochen, Frank Vajda, Gerhard Luef, Alejandro de Marinis, Jana Zárubová, Anne Sabers, Reetta Kälviäinen, Sofia Kasradze, Bettina Schmitz, Sanjeev V. Thomas, Nasim Tabrizi, Lilach Goldstein, Barbara Mostacci, Hideyuki Ohtani, Gordana Kiteva‐Trenchevska, Eugène van Puijenbroek, Silje Alvestad, Maja Milovanović, Vladimír Šafčák, Meritxell Martínez Ferri, Torbjörn Tomson, Elisabeth Sellitto, Hsiang‐Yu Yu, Stephanie Hödl, Petr Marusič, Renata Listonova, Hana Krijtová, David Franc, Petr Bušek, Michaela Kajšová, Noémi Becser Andersen, Birthe Pedersen, Katarzyna Maria Mieszczanek, Katarzyna Cebula, Stefan Juhl, Birgitte Forsom Sondal, Karen Nielsen, Tatiana V. Danielsen, Elsebeth Bruun Christiansen, Jakob Christensen, Ovidio Solano Cabrera, Aleksei Rakitin, Anne Kirss, Anna Maija Saukkonen, Nino Gogatishvili, Dieter Dennig, Kerstin Erdmann, Christian M. Dippon, Bernhard J. Steinhoff, Lisa Langenbruch, Holger Lerche, Anja Herzer, Jan S. Gerdes, Elisa K. El-Allawy-Zielke, Hajo M. Hamer, Malgorzata Kalita, Martin Hirsch, Stephan Arnold, Hans‐Beatus Straub, Rebekka Lehmann, Christiane Asenbauer, Florian Losch, Wenke Grönheit, Matthias Lindenau, Ramshekhar N. Menon, Jafar Mehvari Habibabadi, Maria Paola Canevini, Elena Zambrelli, Katherine Turner, Michela Cecconi, A Paggi, Nicoletta Foschi, Antonio Gambardella, Simone Beretta, Angela Giglio, Gaia Fanella, Lorenzo Ferri, Francesca Bisulli, Alessandra Pistelli, Pietro Pignatta, Marta Maschio, Francesca Muzzi, Maria Sofia Cotelli, Etsuko Yamazaki, Kiyohito Terada, Yushi Inoue, Masahiro Mizobuchi and 56 more - JAMA Neurology 2024 cited by 113
- De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
Authors: Silke Appenzeller, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Petia Dimova, Tania Djémié, Padhraig Gormley, Renzo Guerrini, Ingo Helbig, Helle Hjalgrim, Dorota Hoffman-Zacharska, Johanna Jähn, Karl Martin Klein, Bobby Koeleman, Vladimir Komarek, Roland Krause, Gregor Kuhlenbäumer, Eric Leguern, Anna-Elina Lehesjoki, Johannes R. Lemke, Holger Lerche, Tarja Linnankivi, Carla Marini, Patrick May, Rikke S. Møller, Hiltrud Muhle, Deb Pal, Aarno Palotie, Manuela Pendziwiat, Angela Robbiano, Filip Roelens, Felix Rosenow, Kaja Selmer, Jose M. Serratosa, Sanjay Sisodiya, Ulrich Stephani, Katalin Sterbova, Pasquale Striano, Arvid Suls, Tiina Talvik, Sarah von Spiczak, Yvonne Weber, Sarah Weckhuysen, Federico Zara, Bassel Abou-Khalil, Brian K. Alldredge, Eva Andermann, Frederick Andermann, Dina Amron, Jocelyn F. Bautista, Samuel F. Berkovic, Judith Bluvstein, Alex Boro, Gregory Cascino, Damian Consalvo, Patricia Crumrine, Orrin Devinsky, Dennis Dlugos, Michael P. Epstein, Miguel Fiol, Nathan B. Fountain, Jacqueline French, Daniel Friedman, Eric B. Geller, Tracy Glauser, Simon Glynn, Kevin Haas, Sheryl R. Haut, Jean Hayward, Sandra L. Helmers, Sucheta Joshi, Andres Kanner, Heidi E. Kirsch, Robert C. Knowlton, Eric H. Kossoff, Rachel Kuperman, Ruben Kuzniecky, Daniel H. Lowenstein, Shannon M. McGuire, Paul V. Motika, Edward J. Novotny, Ruth Ottman, Juliann M. Paolicchi, Jack Parent, Kristen Park, Annapurna Poduri, Lynette Sadleir, Ingrid E. Scheffer, Renée A. Shellhaas, Elliott Sherr, Jerry J. Shih, Rani Singh, Joseph Sirven, Michael C. Smith, Joe Sullivan, Liu Lin Thio and 31 more - The American Journal of Human Genetics 2014 cited by 454
- Current practice in diagnostic genetic testing of the epilepsies
Authors: Ilona Krey, Konrad Platzer, Alina Esterhuizen, Samuel F. Berkovic, Ingo Helbig, Michael S. Hildebrand, Holger Lerche, Daniel H. Lowenstein, Rikke S. Møller, Annapurna Poduri, Lynette G. Sadleir, Sanjay M. Sisodiya, Sarah Weckhuysen, Jo M. Wilmshurst, Yvonne Weber, Johannes R. Lemke - Epileptic Disorders 2022 cited by 102
- Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies
Authors: Silvia Masnada, Ulrike B. S. Hedrich, Elena Gardella, Julian Schubert, Charu Kaiwar, Eric W. Klee, Brendan C. Lanpher, Ralitza H. Gavrilova, Matthis Synofzik, Thomas Bast, Kathleen M. Gorman, Mary D. King, Nicholas M. Allen, Judith Conroy, Bruria Ben Zeev, Michal Tzadok, Christian Korff, Fanny Dubois, Keri Ramsey, Vinodh Narayanan, José M. Serratosa, Beatriz G. Giráldez, Ingo Helbig, Eric D. Marsh, Margaret O’Brien, Christina A Bergqvist, Adrian Binelli, Brenda E. Porter, Eduardo José Bernardo Zaeyen, Dafne Dain Gandelman Horovitz, Markus Wolff, Dragan Marjanović, Hande Çağlayan, Mutluay Arslan, Sérgio D.J. Pena, Sanjay M. Sisodiya, Simona Balestrini, Steffen Syrbe, Pierangelo Veggiotti, Johannes R. Lemke, Rikke S. Møller, Holger Lerche, Guido Rubboli - Brain 2017 cited by 164
- A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Authors: Mikko Muona, Samuel F. Berkovic, Leanne M. Dibbens, Karen Oliver, Snezana Maljevic, Marta A. Bayly, Tarja Joensuu, Laura Canafoglia, Silvana Franceschetti, Roberto Michelucci, Salla Markkinen, Sarah E. Heron, Michael S. Hildebrand, Eva Andermann, Frédérick Andermann, Antonio Gambardella, Paolo Tinuper, Laura Licchetta, Ingrid E. Scheffer, Chiara Criscuolo, Alessandro Filla, Edoardo Ferlazzo, Jamil Ahmad, Adeel Ahmad, Betül Baykan, Edith Said, Meral Topçu, P. Riguzzi, Mary D. King, Çiğdem Özkara, Danielle M. Andrade, Bernt A. Engelsen, Arielle Crespel, Matthias Lindenau, Ebba Lohmann, Veronica Saletti, João Massano, Michael Privitera, Alberto J. Espay, Birgit Kauffmann, Michael Duchowny, Rikke S. Møller, Rachel Straussberg, Zaid Afawi, Bruria Ben‐Zeev, Kaitlin E. Samocha, Mark J. Daly, Steven Petrou, Holger Lerche, Aarno Palotie, Anna-Elina Lehesjoki - Nature Genetics 2014 cited by 315
- Phenotypic spectrum of GABRA1
Authors: Katrine M. Johannesen, Carla Marini, Siona Pfeffer, Rikke S. Møller, Thomas Dorn, Cristina Elena Niturad, Elena Gardella, Yvonne Weber, Marianne Søndergård, Helle Hjalgrim, Mariana Nikanorova, Felicitas Becker, Line H.G. Larsen, Hans A. Dahl, Oliver Maier, Davide Mei, Saskia Biskup, Karl Martin Klein, Philipp S. Reif, Felix Rosenow, Abdallah F. Elias, Cindy Hudson, Katherine L. Helbig, Susanne Schubert‐Bast, Maria Rosaria Scordo, Dana Craiu, Tania Djémié, Dorota Hoffman‐Zacharska, Hande Çağlayan, Ingo Helbig, José M. Serratosa, Pasquale Striano, Peter De Jonghe, Sarah Weckhuysen, Arvid Suls, Kai Muru, Inga Talvik, Tiina Talvik, Hiltrud Muhle, Ingo Borggraefe, Imma Rost, Renzo Guerrini, Holger Lerche, Johannes R. Lemke, Guido Rubboli, Snezana Maljevic - Neurology 2016 cited by 141
- Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
Authors: Yuanyuan Liu, Julian Schubert, Lukas Sonnenberg, Katherine L. Helbig, Christina Engel Hoei‐Hansen, Mahmoud Koko, Maert Rannap, Stephan Lauxmann, Mahbubul Huq, Michael C. Schneider, Katrine M. Johannesen, Gerhard Kurlemann, Elena Gardella, Felicitas Becker, Yvonne Weber, Jan Benda, Rikke S. Møller, Holger Lerche - Brain 2018 cited by 132
- Spectrum of GABAA receptor variants in epilepsy
Authors: Snezana Maljevic, Rikke S. Møller, Christopher A. Reid, Eduardo Pérez‐Palma, Dennis Lal, Patrick May, Holger Lerche - Current Opinion in Neurology 2019 cited by 87
- 4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2 -encephalopathy
Authors: Ulrike B. S. Hedrich, Stephan Lauxmann, Markus Wolff, Matthis Synofzik, Thomas Bast, Adrian Binelli, José M. Serratosa, Pedro Martínez-Ulloa, Nicholas M. Allen, Mary D. King, Kathleen M. Gorman, Bruria Ben Zeev, Michal Tzadok, Lily C. Wong‐Kisiel, Dragan Marjanović, Guido Rubboli, Sanjay M. Sisodiya, Florian Lutz, Harshad Pannikkaveettil Ashraf, Kirsten Torge, Pu Yan, Christian M. Boßelmann, Niklas Schwarz, Monika Fudali, Holger Lerche - Science Translational Medicine 2021 cited by 83
- Randomized phase III study 306
Authors: Gregory L. Krauss, José M. Serratosa, Vicente Villanueva, Milda Endzinienė, Zhen Hong, Jacqueline A. French, Haitao Yang, David Squillacote, Hannah B Edwards, Jin Zhu, Antonio Laurenza, Samuel F. Berkovic, Wendyl D’Souza, Terence J. O’Brien, Udaya Seneviratne, Martin Robinson, Plamen Bozinov, Ivan Milanov, Еkaterina Titianova, Zahari Zahariev, Liwen Wu, Xuefeng Wang, Dong Zhou, Jindriska Buresova, Jan Hadač, Petr Marusič, Hana Ošlejšková, Sulev Haldre, Ain Pajos, Valentin Sander, Inga Talvik, Stephan Arnold, A. Hufnagel, Frank Kerling, Holger Lerche, Soheyl Noachtar, Felix Rosenow, Joachim Springub, Bernhard J. Steinhoff, Konrad J. Werhahn, Raymond Tak Fai Cheung, Patrick Kwan, Ping Wing Ng, John S.D. Chan, Attila Balogh, István Kondákor, Magdolna Neuwirth, Péter Rajna, György Rásonyi, Joy Desai, Sudhir Kothari, Sita Sattaluri, Bhawna Sharma, Nandan Yardi, J. M. K. Murthy, Manmohan Mehndiratta, Kolichana Venkateshwaralu, Silvana Franceschetti, Guntis Karelis, Guntis Rozentals, Baiba Uskane, Rūta Mameniškienė, Irena Virketiene, Zariah Abdul Aziz, Kheng Seang Lim, Mei‐Ling Sharon Tai, Maria Epifania Collantes, Katerina Tanya P. Gosiengfiao, Anna Członkowska, Wiesław Drozdowski, Waldemar Fryze, Jacek Gawłowicz, Maria Mazurkiewicz‐Bełdzińska, E Motta, Carla Bentes, Luı́s Cunha, Georgine de Sousa, Jose Manuel Lopes Lima, Ioana Mı̂ndruță, Dezso Nagy, Sanda Maria Nica, E. D. Belousova, Kalinin Vv, Е. В. Левитина, Perunova Nb, Н. В. Пизова, И. Е. Повереннова, П. Н. Власов, Dragoslav Sokić, Ksenija Božić, N. Jović, Žarko Martinović, Mirjana Spasić, Seung Bong Hong, Joong Koo Kang, Sang Ho Kim, Sung Eun Kim, Byung-In Lee, Sang Kun Lee, Yong Won Cho and 25 more - Neurology 2012 cited by 429
- The phenotypic spectrum of SCN8A encephalopathy
Authors: Jan Larsen, Gemma L. Carvill, Elena Gardella, Gerhard Kluger, G. Schmiedel, Nina Barišić, Christel Depienne, Eva H. Brilstra, Yuan Mang, Jens Erik Nielsen, Martin Kirkpatrick, David Goudie, Rebecca Goldman, Johanna Jähn, Birgit Jepsen, Deepak Gill, Miriam Döcker, Saskia Biskup, Jacinta M. McMahon, Bobby P.C. Koeleman, M.L. Harris, Kees P. J. Braun, Carolien G. F. de Kovel, Carla Marini, Nicola Specchio, Tania Djémié, Sarah Weckhuysen, Niels Tommerup, M. Troncoso, L. Troncoso, Andrea Bevot, Markus Wolff, Helle Hjalgrim, Renzo Guerrini, Ingrid E. Scheffer, Heather C. Mefford, Rikke S. Møller, Aarno Palotie, Anna-Elina Lehesjoki, Arvid Suls, Bobby P.C. Koeleman, Carla Marini, Christel Depienne, Dana Craiu, Deb K. Pal, Dorota Hoffman‐Zacharska, Eric Leguern, Federico Zara, Felix Rosenow, Hande Çağlayan, Helle Hjalgrim, Hiltrud Muhle, Holger Lerche, Ingo Helbig, Johanna Jähn, Johannes R. Lemke, José M. Serratosa, Kaja Kristine Selmer, Karl Martin Klein, Katalin Štěrbová, Nina Barišić, Padhraig Gormley, Pasquale Striano, Patrick May, Peter De Jonghe, Renzo Guerrini, Rikke S. Møller, Roland Krause, Rudi Balling, Sanjay M. Sisodiya, Sarah von Spiczak, Sarah Weckhuysen, Stéphanie Baulac, Tiina Talvik, Ulrich Stephani, Vladimı́r Komárek, Yvonne Weber - Neurology 2015 cited by 285
- Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy
Authors: Philip K. Ahring, Vivian W. Y. Liao, Elena Gardella, Katrine M. Johannesen, Ilona Krey, Kaja Kristine Selmer, Barbro Stadheim, H. W. C. DAVIS, Charlotte Peinhardt, Mahmoud Koko, Rohini Coorg, Steffen Syrbe, Astrid Bertsche, Teresa Santiago‐Sim, Tue Diemer, Christina Fenger, Konrad Platzer, Evan E. Eichler, Holger Lerche, Johannes R. Lemke, Mary Chebib, Rikke S. Møller - Brain 2021 cited by 74
- Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Authors: Johannes R. Lemke, Dennis Lal, Eva M. Reinthaler, Isabelle Steiner, Michael Nothnagel, Michael Alber, Kirsten Geider, Bodo Laube, Michael Schwake, Katrin Finsterwalder, André Franke, Markus B. Schilhabel, Johanna Jähn, Hiltrud Muhle, Rainer Boor, Wim Van Paesschen, Roberto Caraballo, Natalio Fejerman, Sarah Weckhuysen, Peter De Jonghe, Jan Larsen, Rikke S. Møller, Helle Hjalgrim, Laura Addis, Shan Tang, Elaine Hughes, Deb K. Pal, Kadi Veri, Ulvi Vaher, Tiina Talvik, Petia Dimova, Rosa Guerrero, José M. Serratosa, Tarja Linnankivi, Anna‐Elina Lehesjoki, Susanne Ruf, Markus Wolff, Sarah E. Buerki, Gabriele Wohlrab, Judith Kroell, Alexandre Datta, Barbara Fiedler, Gerhard Kurlemann, Gerhard Kluger, Andreas Hahn, D Edda Haberlandt, Christina Kutzer, Jürgen Sperner, Felicitas Becker, Yvonne Weber, Martha Feucht, Hannelore Steinböck, Birgit Neophythou, Gabriel M. Ronen, U Gruber‐Sedlmayr, Julia Geldner, Robert J Harvey, Per Hoffmann, Stefan Herms, Janine Altmüller, Mohammad R. Toliat, Hölger Thiele, Peter Nürnberg, Christian Wilhelm, Ulrich Stephani, Ingo Helbig, Holger Lerche, Fritz Zimprich, Bernd A. Neubauer, Saskia Biskup, Sarah von Spiczak - Nature Genetics 2013 cited by 440
- Polygenic burden in focal and generalized epilepsies
Authors: Costin Leu, Remi Stevelink, Alexander C.W. Smith, Slavina B. Goleva, Masahiro Kanai, Lisa Ferguson, Ciarán Campbell, Yoichiro Kamatani, Yukinori Okada, Sanjay M. Sisodiya, Gianpiero L. Cavalleri, Bobby P.C. Koeleman, Holger Lerche, Lara Jehi, Lea K. Davis, Imad Najm, Aarno Palotie, Mark J Daly, Robyn M. Busch, Dennis Lal - Brain 2019 cited by 151
- Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Authors: Eva Auffenberg, Ulrike B. S. Hedrich, Raffaella Barbieri, Daniela Miely, Bernhard Groschup, Thomas V. Wuttke, Niklas Vogel, Philipp Lührs, Ilaria Zanardi, Sara Bertelli, Nadine Spielmann, Valérie Gailus‐Durner, Helmut Fuchs, Martin Hrabě de Angelis, Michael Pusch, Martin Dichgans, Holger Lerche, Paola Gavazzo, Nikolaus Plesnila, Tobias Freilinger - Journal of Clinical Investigation 2021 cited by 64
- Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals
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