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5. Juli 2024 (Treat-ION)
Persistent sodium currents in neurons: potential mechanisms and pharmacological blockers
Pflugers Arch. 2024 Jul 5. >>Pubmed-Link<<
Peter Müller, Andreas Draguhn, Alexei V Egorov
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1. Juli 2024 (Treat-ION)
Cenobamate: real-world data from a retrospective multicenter study
J Neurol. 2024 Jul 1. >>Pubmed-Link<<
Stephan Lauxmann, David Heuer, Jan Heckelmann, Florian P Fischer, Melanie Schreiber, Elisabeth Schriewer, Guido Widman, Yvonne Weber, Holger Lerche, Michael Alber, Sigrid Schuh-Hofer, Stefan Wolking
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1. Juni 2024 (Treat-ION)
Retigabine and gabapentin restore channel function and neuronal firing in a cellular model of an epilepsy-associated dominant-negative KCNQ5 variant
Neuropharmacology. 2024 Jun 1. >>Pubmed-Link<<
Johanna Krüger, Holger Lerche
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20. März 2024 (Treat-ION)
Complex biophysical changes and reduced neuronal firing in an SCN8A variant associated with developmental delay and epilepsy
Biochim Biophys Acta Mol Basis Dis. 2024 Mar 20. >>PubMed-Link<<
Shir Quinn, Nan Zhang, Timothy A Fenton, Marina Brusel, Preethi Muruganandam, Yoav Peleg, Moshe Giladi, Yoni Haitin, Holger Lerche, Haim Bassan, Yuanyuan Liu, Roy Ben-Shalom, Moran Rubinstein
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1. Dezember 2023 (Treat-ION)
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis
Brain. 2023 Dec 1. >>PubMed-Link<<
Arthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner, Katrine M Johannesen, Kimberly Goodspeed, Marie Macnee, Alexander T Deng, Ángel Aledo-Serrano, Artem Borovikov, Maina Kava, Arjan M Bouman, M J Hajianpour, Deb K Pal, Marc Engelen, Eveline E O Hagebeuk, Marwan Shinawi, Alexis R Heidlebaugh, Kathryn Oetjens, Trevor L Hoffman, Pasquale Striano, Amanda S Freed, Line Futtrup, Thomas Balslev, Anna Abulí, Leslie Danvoye, Damien Lederer, Tugce Balci, Maryam Nabavi Nouri, Elizabeth Butler, Sarah Drewes, Kalene van Engelen, Katherine B Howell, Jean Khoury, Patrick May, Marena Trinidad, Steven Froelich, Johannes R Lemke 5, Jacob Tiller, Amber N Freed, Jing-Qiong Kang, Arthur Wuster, Rikke S Møller, Dennis Lal
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1. Dezember 2023 (Treat-ION)
Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia
eBioMedicine 2023;98:104855. >>Journal-Link<<
Hang Lyu, Christian M. Boßelmann, Katrine M. Johannesen, Mahmoud Koko, Juan Dario Ortigoza-Escobar, Sergio Aguilera-Albesa, Deyanira Garcia-Navas Núñez, Tarja Linnankivi, Eija Gaily, Henriette J. A. van Ruiten, Ruth Richardson, Cornelia Betzler, Gabriella Horvath, Eva Brilstra,m Niels Geerdink, Daniele Orsucci, Alessandra Tessa, Elena Gardella, Zofia Fleszar, Ludger Schöls, Holger Lerche, Rikke S. Møller, Yuanyuan Liu
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11. Oktober 2023 (Treat-ION)
Voltage-gated calcium channels in genetic epilepsies
J Neurochem. 2023 Oct 11. >>PubMed-Link<<
Robert J Lauerer, Holger Lerche
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19. Juli 2023 (Treat-ION)
Apo state pore opening as functional basis of increased EAAT anion channel activity in episodic ataxia 6
Front Physiol. 2023 Jul 19. >>PubMed-Link<<
Mariia Suslova, Daniel Kortzak, Jan-Philipp Machtens, Peter Kovermann, Christoph Fahlke
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9. Juni 2023 (Treat-ION)
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
Front Neurol. 2023 Jun 9. >>PubMed-Link<<
Simone Seiffert, Manuela Pendziwiat, Ulrike B S Hedrich, Ingo Helbig, Yvonne Weber, Niklas Schwarz
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24. Mai 2023 (Treat-ION)
Loss or gain of function? Effects of ion channel mutations on neuronal firing depend on the neuron type
Front Neurol. 2023 May 24. >>PubMed-Link<<
Nils A Koch, Lukas Sonnenberg, Ulrike B S Hedrich, Stephan Lauxmann, Jan Benda
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4. Mai 2023 (Treat-ION)
CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online
Bioinformatics. 2023 May 4 >>PubMed-Link<<
Marie Macnee, Eduardo Pérez-Palma, Tobias Brünger, Chiara Klöckner, Konrad Platzer, Arthur Stefanski, Ludovica Montanucci, Allan Bayat, Maximilian Radtke, Ryan L Collins, Michael Talkowski, Daniel Blankenberg, Rikke S Møller, Johannes R Lemke, Michael Nothnagel, Patrick May, Dennis Lal
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10. April 2023 (Treat-ION)
Expansion-enhanced super-resolution radial fluctuations enable nanoscale molecular profiling of pathology specimens
Nat Nanotechnol. 2023 Apr >>PubMed-Link<<
Dominik Kylies, Marina Zimmermann, Fabian Haas, Maria Schwerk, Malte Kuehl, Michael Brehler, Jan Czogalla, Lola C Hernandez, Leonie Konczalla, Yusuke Okabayashi, Julia Menzel, Ilka Edenhofer, Sam Mezher, Hande Aypek, Bernhard Dumoulin, Hui Wu, Smilla Hofmann, Oliver Kretz, Nicola Wanner, Nicola M Tomas, Susanne Krasemann, Markus Glatzel, Christoph Kuppe, Rafael Kramann, Bella Banjanin, Rebekka K Schneider, Christopher Urbschat, Petra Arck, Nicola Gagliani, Marc van Zandvoort, Thorsten Wiech, Florian Grahammer, Pablo J Sáez, Milagros N Wong, Stefan Bonn, Tobias B Huber, Victor G Puelles
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6. März 2023 (Treat-ION)
Predicting functional effects of ion channel variants using new phenotypic machine learning methods
PLoS Comput Biol. 2023 Mar 6. >>PubMed-Link<<
Christian Malte Boßelmann, Ulrike B S Hedrich, Holger Lerche, Nico Pfeifer
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1. März 2023 (Treat-ION)
Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutation
Stem Cell Res. 2023 Mar. >>PubMed-Link<<
Carolin Haag, Betül Uysal, Justus Marquetand, Heidi Löffler, Ulrike A Mau-Holzmann, Holger Lerche, Niklas Schwarz
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15. Februar 2023 (Treat-ION)
KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine
Ann Clin Transl Neurol. 2023 Feb 15. >>PubMed-Link<<
Peter Müller, Danielle S Takacs, Ulrike B S Hedrich, Rohini Coorg, Laura Masters, Kevin E Glinton, Hongzheng Dai, Jon A Cokley, James J Riviello, Holger Lerche, Edward C Cooper
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13. Februar 2023 (Treat-ION)
Delineation of functionally essential protein regions for 242 neurodevelopmental genes
Brain. 2023 Feb 13. >>PubMed-Link<<
Sumaiya Iqbal, Tobias Brünger, Eduardo Pérez-Palma, Marie Macnee, Andreas Brunklaus, Mark J Daly, Arthur J Campbell, David Hoksza, Patrick May, Dennis Lal
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30. Januar 2023 (Treat-ION)
Gentherapien für Epilepsie: Klinische Studien sind auf dem Weg [Gene Therapy for Epilepsy: Clinical Studies are on the Road]
Fortschr Neurol Psychiatr. 2023 Jan 30. >>PubMed-Link<<
Peter Müller, Holger Lerche
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1. Januar 2023 (Treat-ION)
Data-driven historical characterization of epilepsy-associated genes
Eur J Paediatr Neurol. 2023 Jan. >>PubMed-Link<<
Marie Macnee, Eduardo Pérez-Palma, Javier A López-Rivera, Alina Ivaniuk, Patrick May, Rikke S Møller, Dennis Lal
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2. November 2022 (Treat-ION)
In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders
Br J Pharmacol. 2022 Nov 2. >>PubMed-Link<<
Erva Bayraktar, Yuanyuan Liu, Lukas Sonnenberg, Ulrike B S Hedrich, Yildirim Sara, Ahmed Eltokhi, Hang Lyu, Holger Lerche, Thomas V Wuttke, Stephan Lauxmann
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1. Oktober 2022 (Treat-ION)
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies
EBioMedicine. 2022 Oct. >>PubMed-Link<<
Artikel in der Rubrik „Gesichter der Gesundheitsforschung“ des BMBF
Johanna Krüger, Julian Schubert, Josua Kegele, Audrey Labalme, Miaomiao Mao, Jacqueline Heighway, Guiscard Seebohm, Pu Yan, Mahmoud Koko, Kezban Aslan-Kara, Hande Caglayan, Bernhard J Steinhoff, Yvonne G Weber, Pascale Keo-Kosal, Samuel F Berkovic, Michael S Hildebrand, Steven Petrou, Roland Krause, Patrick May, Gaetan Lesca, Snezana Maljevic, Holger Lerche
Details
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1. September 2022 (Treat-ION)
Modulating effects of FGF12 variants on NaV1.2 and NaV1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case series
EBioMedicine. 2022 Sep. >>PubMed-Link<<
Simone Seiffert, Manuela Pendziwiat, Tatjana Bierhals, Himanshu Goel, Niklas Schwarz, Amelie van der Ven, Christian Malte Boßelmann, Johannes Lemke, Steffen Syrbe, Marjolein Hanna Willemsen, Ulrike Barbara Stefanie Hedrich, Ingo Helbig, Yvonne Weber
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29. August 2022 (Treat-ION)
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes
Brain. 2022 Aug 29. >>PubMed-Link<<
Tobias Brünger, Eduardo Pérez-Palma, Ludovica Montanucci, Michael Nothnagel, Rikke S Møller, Stephanie Schorge, Sameer Zuberi, Joseph Symonds, Johannes R Lemke, Andreas Brunklaus, Stephen F Traynelis, Patrick May, Dennis Lal
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26. August 2022 (Treat-ION)
Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype
Front Pediatr. 2022 Aug 26. >>PubMed-Link<<
Veronika M Berghold, Mahmoud Koko, Riccardo Berutti, Barbara Plecko
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19. Juli 2022 (Treat-ION)
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood
Neurology. 2022 Jul 19. >>PubMed-Link<<
Hannah Stamberger, David Crosiers, Ganna Balagura, Claudia M Bonardi, Anna Basu, Gaetano Cantalupo, Valentina Chiesa, Jakob Christensen, Bernardo Dalla Bernardina, Colin A Ellis, Francesca Furia, Fiona Gardiner, Camille Giron, Renzo Guerrini, Karl Martin Klein, Christian Korff, Hana Krijtova, Melanie Leffner, Holger Lerche, Gaetan Lesca, David Lewis-Smith, Carla Marini, Dragan Marjanovic, Laure Mazzola, Sarah McKeown Ruggiero, Fanny Mochel, Francis Ramond, Philipp S Reif, Aurélie Richard-Mornas, Felix Rosenow, Christian Schropp, Rhys H Thomas, Aglaia Vignoli, Yvonne Weber, Elizabeth Palmer, Ingo Helbig, Ingrid E Scheffer, Pasquale Striano, Rikke S Møller, Elena Gardella, Sarah Weckhuysen
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1. Juli 2022 (Treat-ION)
Predicting the functional effects of voltage-gated potassium channel missense variants with multi-task learning
EBioMedicine. 2022 Jul. >>PubMed-Link<<
Christian Malte Boßelmann, Ulrike B S Hedrich, Peter Müller, Lukas Sonnenberg, Shridhar Parthasarathy, Ingo Helbig, Holger Lerche, Nico Pfeifer
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18. Juni 2022 (Treat-ION)
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progress
Epilepsia. 2022 Jun 18. >>PubMed-Link<<
Juliet K Knowles, Ingo Helbig, Cameron S Metcalf, Laura S Lubbers, Lori L Isom, Scott Demarest, Ethan M Goldberg, Alfred L George Jr, Holger Lerche, Sarah Weckhuysen, Vicky Whittemore, Samuel F Berkovic, Daniel H Lowenstein
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26. Mai 2022 (Treat-ION)
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
Clin Genet. 2022 May 26. >>PubMed-Link<<
Christensen, M. B., Levy, A. M., Mohammadi, N. A., Niceta, M., Kaiyrzhanov, R., Dentici, M. L., Al Alam, C., Alesi, V., Benoit, V., Bhatia, K. P., Bierhals, T., Boßelmann, C. M., Buratti, J., Callewaert, B., Ceulemans, B., Charles, P., De Wachter, M., Dehghani, M., D’Haenens, E., Doco-Fenzy, M., Geßner, M., Gobert, C., Guliyeva, U., Haack, T. B., Hammer, T. B., Heinrich, T., Hempel, M., Herget, T., Hoffmann, U., Horvath, J., Houlden, H., Keren, B., Kresge, C., Kumps, C., Lederer, D., Lermine, A., Magrinelli, F., Maroofian, R., Vahidi Mehrjardi, M. Y., Moudi, M., Müller, A. J., Oostra, A. J., Pletcher, B. A., Ros-Pardo, D., Samarasekera, S., Tartaglia, M., Van Schil, K., Vogt, J., Wassmer, E., Winkelmann, J., Zaki, M. S., Zech, M., Lerche, H., Radio F. C., Gomez-Puertas, P., Møller, R. S., Tümer, Z.
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17. Mai 2022 (Treat-ION)
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants
Neurology. 2022 May 17. >>PubMed-Link<<
Niklas Schwarz, Simone Seiffert, Manuela Pendziwiat, Annika Verena Rademacher, Tobias Brünger, Ulrike B S Hedrich, Paul B Augustijn, Hartmut Baier, Allan Bayat, Francesca Bisulli, Russell J Buono, Ben Zeev Bruria, Michael G Doyle, Renzo Guerrini, Gali Heimer, Michele Iacomino, Hugh Kearney, Karl Martin Klein, Ioanna Kousiappa, Wolfram S Kunz, Holger Lerche, Laura Licchetta, Ebba Lohmann, Raffaella Minardi, Marie McDonald, Sarah Montgomery, Lejla Mulahasanovic, Renske Oegema, Barel Ortal, Savvas S Papacostas, Francesca Ragona, Tiziana Granata, Phillip S Reif, Felix Rosenow, Annick Rothschild, Paolo Scudieri, Pasquale Striano, Paolo Tinuper, George A Tanteles, Annalisa Vetro, Felix Zahnert, Ethan M Goldberg, Federico Zara, Dennis Lal, Patrick May, Hiltrud Muhle, Ingo Helbig, Yvonne Weber
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15. März 2022 (Treat-ION)
Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related Epilepsies
Neurology. 2022 Mar 15. Epub 2022 Jan 24. >>PubMed-Link<<
Andreas Brunklaus, Eduardo Pérez-Palma, Ismael Ghanty, Ji Xinge, Eva Brilstra, Berten Ceulemans, Nicole Chemaly, Iris de Lange, Christel Depienne, Renzo Guerrini, Davide Mei, Rikke S Møller, Rima Nabbout, Brigid M Regan, Amy L Schneider, Ingrid E Scheffer, An-Sofie Schoonjans, Joseph D Symonds, Sarah Weckhuysen, Michael W Kattan, Sameer M Zuberi, Dennis Lal
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1. März 2022 (Treat-ION)
Reply to: Genotype-phenotype correlations in SCN8A-related epilepsy: a cohort study of Chinese children in southern China
Bain. 2022 Mar 1. >>PubMed-Link<<
Katrine M Johannesen, Yuanyuan Liu, Elena Gardella, Holger Lerch, Rikke S Møller
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1. Februar 2022 (Treat-ION)
Genetic testing before epilepsy surgery-An exploratory survey and case collection from German epilepsy centers
Seizure-European Journal of Epilepsy. 2022 Feb. Epub 2021 Dec 17. >>PubMed-Link<<
Christian Malte Boßelmann, Victoria San Antonio-Arce, Andreas Schulze-Bonhage, Susanne Fauser, Pia Zacher, Thomas Mayer, Javier Aparicio, Kristina Albers, Thomas Cloppenborg, Wolfram Kunz, Rainer Surges, Steffen Syrbe, Yvonne Weber, Stefan Wolking
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26. Januar 2022 (Treat-ION)
Pyridoxine or pyridoxal-5-phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort study
Dev Med Child Neurol. 2022 Jan 26. >>PubMed-Link<<
Allan Bayat, Angel Aledo-Serrano, Antonio Gil-Nagel, Christian M Korff, Ashley Thomas, Christian Boßelmann, Yvonne Weber, Elena Gardella, Allan M Lund, Monique G M de Sain-van der Velden, Rikke S Møller
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6. Januar 2022 (Treat-ION)
Cellular Physiology and Pathophysiology of EAAT Anion Channels
Front Cell Nerurosci. 2022 Jan 6. >>PubMed-Link<<
Peter Kovermann, Miriam Engels, Frank Müller, Christoph Fahlke
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28. Dezember 2021 (Treat-ION)
Mutations associated with epileptic encephalopathy modify EAAT2 anion channel function
Epilepsia. 2021 Dec 28. >>PubMed-Link<<
Peter Kovermann, Yulia Kolobkova, Arne Franzen, Christoph Fahlke
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2. Dezember 2021 (Treat-ION)
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia
Am J Hum Genet. 2021 Dec 2. >>PubMed-Link<<
Zheng Yie Yap, Stephanie Efthymiou, Simone Seiffert, Karen Vargas Parra, Sukyeong Lee, Alessia Nasca, Reza Maroofian, Isabelle Schrauwen, Manuela Pendziwiat, Sunhee Jung, Elizabeth Bhoj, Pasquale Striano, Kshitij Mankad, Barbara Vona, Sanmati Cuddapah, Anja Wagner, Javeria Raza Alvi, Elham Davoudi-Dehaghani, Mohammad-Sadegh Fallah, Srinitya Gannavarapu, Costanza Lamperti, Andrea Legati, Bibi Nazia Murtaza, Muhammad Shahid Nadeem, Mujaddad Ur Rehman, Kolsoum Saeidi, Vincenzo Salpietro, Sarah von Spiczak, Abigail Sandoval, Sirous Zeinali, Massimo Zeviani, Adi Reich, SYNaPS Study Group; University of Washington Center for Mendelian Genomics; Cholsoon Jang, Ingo Helbig, Tahsin Stefan Barakat, Daniele Ghezzi, Suzanne M Leal, Yvonne Weber, Henry Houlden, Wan Hee Yoon
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26. November 2021 (Treat-ION)
Genetic generalized epilepsies in adults – challenging assumptions and dogmas
Nat Rev Neurol. 2021 Nov 26. >>PubMed-Link<<
Bernd J Vorderwülbecke , Britta Wandschneider, Yvonne Weber, Martin Holtkamp
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1. November 2021 (Treat-ION)
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
J Clin Invest. 2021 Nov 1. >>PubMed-Link<<
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, Daniela Miely, Bernhard Groschup, Thomas V Wuttke, Niklas Vogel, Philipp Lührs, Ilaria Zanardi, Sara Bertelli, Nadine Spielmann, Valerie Gailus-Durner, Helmut Fuchs, Martin Hrabě de Angelis, Michael Pusch, Martin Dichgans, Holger Lerche, Paola Gavazzo, Nikolaus Plesnila, Tobias Freilinger
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9. September 2021 (Treat-ION)
Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature
Front Neurol. 2021 Sep 9. >>PubMed-Link<<
Stephan Lauxmann, Lukas Sonnenberg, Nils A Koch, Christian Bosselmann, Natalie Winter, Niklas Schwarz, Thomas V Wuttke, Ulrike B S Hedrich, Yuanyuan Liu, Holger Lerche, Jan Benda, Josua Kegele
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1. September 2021 (Treat-ION)
4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy
Science Translational Medicine. 2021 Sep. >>PubMed-Link<<
U. B. S. Hedrich, S. Lauxmann, M. Wolff, M. Synofzik, T. Bast, A. Binelli, J. M. Serratosa, P. Martínez-Ulloa, N. M. Allen, M. D. King, K. M. Gorman, B. B. Zeev, M. Tzadok, L. Wong-Kisiel, D. Marjanovic, G. Rubboli, S. M. Sisodiya, F. Lutz, H. P. Ashraf, K. Torge, P. Yan, C. Bosselmann, N. Schwarz, M. Fudali, H. Lerche
Details
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25. August 2021 (Treat-ION)
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Brain. 2021 Aug 25. >>PubMed-Link<<
Katrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, Cathrine E Gjerulfsen, Lukas Sonnenberg, Julian Schubert, Christina D Fenger, Ahmed Eltokhi, Maert Rannap, Nils A Koch, Stephan Lauxmann, Johanna Krüger, Josua Kegele, Laura Canafoglia, Silvana Franceschetti, Thomas Mayer, Johannes Rebstock, Pia Zacher, Susanne Ruf, Michael Alber, Katalin Sterbova, Petra Lassuthová, Marketa Vlckova, Johannes R Lemke, Konrad Platzer, Ilona Krey, Constanze Heine, Dagmar Wieczorek, Judith Kroell-Seger, Caroline Lund, Karl Martin Klein, P Y Billie Au, Jong M Rho, Alice W Ho, Silvia Masnada, Pierangelo Veggiotti, Lucio Giordano, Patrizia Accorsi, Christina E Hoei-Hansen, Pasquale Striano, Federico Zara, Helene Verhelst, Judith S Verhoeven, Bert van der Zwaag, Aster V E Harder, Eva Brilstra, Manuela Pendziwiat, Sebastian Lebon, Maria Vaccarezza, Ngoc Minh Le, Jakob Christensen, Sabine Grønborg, Stephen W Scherer, Jennifer Howe, Walid Fazeli, Katherine B Howell, Richard Leventer, Chloe Stutterd, Sonja Walsh, Marion Gerard, Bénédicte Gerard, Sara Matricardi, Claudia M Bonardi, Stefano Sartori, Andrea Berger, Dorota Hoffman-Zacharska, Massimo Mastrangelo, Francesca Darra, Arve Vøllo, M Mahdi Motazacker, Phillis Lakeman, Mathilde Nizon, Cornelia Betzler, Cecilia Altuzarra, Roseline Caume, Agathe Roubertie, Philippe Gélisse, Carla Marini, Renzo Guerrini, Frederic Bilan, Daniel Tibussek, Margarete Koch-Hogrebe, M Scott Perry, Shoji Ichikawa, Elena Dadali, Artem Sharkov, Irina Mishina, Mikhail Abramov, Ilya Kanivets, Sergey Korostelev, Sergey Kutsev, Karen E Wain, Nancy Eisenhauer, Monisa Wagner, Juliann M Savatt, Karen Müller-Schlüter, Haim Bassan, Artem Borovikov, Marie-Cecile Nassogne, Anne Destrée, An-Sofie Schoonjans, Marije Meuwissen, Marga Buzatu, Anna Jansen, Emmanuel Scalais, Siddharth Srivastava, Wen-Hann Tan, Heather E Olson, Tobias Loddenkemper, Annapurna Poduri, Katherine L Helbig, Ingo Helbig, Mark P Fitzgerald, Ethan M Goldberg, Timo Roser, Ingo Borggraefe, Tobias Brünger, Patrick May, Dennis Lal, Damien Lederer, Guido Rubboli, Henrike O Heyne, Gaetan Lesca, Ulrike B S Hedrich, Jan Benda, Elena Gardella, Holger Lerche, Rikke S Møller
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8. August 2021 (Treat-ION)
Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations
Mol Genet Metab. Sep-Oct 2021. >>PubMed-Link<<
Alexander Tobias Kaczmarek, Nike Bahlmann, Besarta Thaqi, Patrick May, Guenter Schwarz
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8. Juli 2021 (Treat-ION)
Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related Disorders
Front Neurol. 2021 Jul 8. >>PubMed-Link<<
Josua Kegele, Johanna Krüger, Mahmoud Koko, Lara Lange, Ana Victoria Marco Hernandez, Francisco Martinez, Alexander Münchau, Holger Lerche, Stephan Lauxmann
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23. April 2021 (Treat-ION)
Präzisionsmedizin in der Epileptologie – wie weit sind wir wirklich?
Zeitschrift für Epileptologie. 2021 Apr 23.
Holger Lerche
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1. April 2021 (Treat-ION)
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study
EBioMedicine. 2021 Apr. >>PubMed-Link<<
Sana Amanat, Alvaro Gallego-Martinez, Joseph Sollini, Patricia Perez-Carpena, Juan M Espinosa-Sanchez, Ismael Aran, Andres Soto-Varela, Angel Batuecas-Caletrio, Barbara Canlon, Patrick May, Christopher R Cederroth, Jose A Lopez-Escamez
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1. November 2020 (Treat-ION)
Drug-resistant epilepsy – time to target mechanisms
Nat Rev Neurol. 2020 Nov. >>PubMed-Link<<
Holger Lerche
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12. Oktober 2020 (Treat-ION)
CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons
Dis Model Mech. 2020 Oct 12. >>PubMed-Link<<
S Schuster, E Heuten, A Velic, J Admard, M Synofzik, S Ossowski, B Macek, S Hauser, L Schöls
joint publication Treat-ION/TreatHSP.net
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12. August 2020 (Treat-ION)
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
Sci Transl Med. 2020 Aug 12. [Epub ahead of print] >>PubMed-Link<<
Henrike O Heyne, David Baez-Nieto, Sumaiya Iqbal, Duncan S Palmer, Andreas Brunklaus, Patrick May, Epi25 Collaborative; Katrine M Johannesen, Stephan Lauxmann, Johannes R Lemke, Rikke S Møller, Eduardo Pérez-Palma, Ute I Scholl, Steffen Syrbe, Holger Lerche, Dennis Lal, Arthur J Campbell, Hao-Ran Wang, Jen Pan, Mark J Daly
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2. August 2020 (Treat-ION)
Functional consequences of SLC1A3 mutations associated with episodic ataxia 6
Hum Mutat. 2020 Aug 2. [Epub ahead of print] >>PubMed-Link<<
Aparna Sharma Chivukula, Mariia Suslova, Daniel Kortzak, Peter Kovermann, Christoph Fahlke
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9. Juni 2020 (Treat-ION)
In Vitro Differentiated Human Stem Cell-Derived Neurons Reproduce Synaptic Synchronicity Arising During Neurodevelopment
Stem Cell Reports, 2020 Jun 9. [Epub ahead of print]>>PubMed-Link<<
Filip Rosa, Ashutosh Dhingra, Betül Uysal, G Dulini C Mendis, Heidi Loeffler, Gina Elsen, Stephan Mueller, Niklas Schwarz, Melissa Castillo-Lizardo, Claire Cuddy, Felicitas Becker, Peter Heutink, Christopher A Reid, Steven Petrou, Holger Lerche, Snezana Maljevic
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13. Mai 2020 (Treat-ION)
MISCAST: MIssense variant to protein StruCture Analysis web SuiTe
Nucleic Acids Res. 2020 May 13 [Epub ahead of print] >>PubMed-Link<<
Iqbal S, Hoksza D, Pérez-Palma E, May P, Jespersen JB, Ahmed SS, Rifat ZT, Heyne HO, Rahman MS, Cottrell JR, Wagner FF, Daly MJ, Campbell AJ, Lal D.
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17. März 2020 (Treat-ION)
Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders
Genome Med. 2020 Mar 17. >>PubMed-Link<<
Dennis Lal, Patrick May, Eduardo Perez-Palma, Kaitlin E. Samocha, Jack A. Kosmicki, Elise B. Robinson, Rikke S. Møller, Roland Krause, Peter Nürnberg, Sarah Weckhuysen, Peter De Jonghe, Renzo Guerrini, Lisa M. Niestroj, Juliana Du, Carla Marini, EuroEPINOMICS-RES Consortium, James S. Ware, Mitja Kurki, Padhraig Gormley, Sha Tang, Sitao Wu, Saskia Biskup, Annapurna Poduri, Bernd A. Neubauer, Bobby P. C. Koeleman, Katherine L. Helbig, Yvonne G. Weber, Ingo Helbig, Amit R. Majithia, Aarno Palotie, and Mark J. Daly
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4. März 2020 (Treat-ION)
Increased glutamate transporter-associated anion currents cause glial apoptosis in episodic ataxia 6
Brain Communications Vol 2(1) 2020 >>PubMed-Link<<
Kovermann P, Untiet V, Kolobkova Y, Engels M, Baader S, Schilling K, and Fahlke C.
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1. Januar 2020 (Treat-ION)
Genetic Potassium Channel-Associated Epilepsies: Clinical Review of the Kv Family
Eur J Paediatr Neurol. 2020 Jan [Epub ahead of print] >>PubMed-Link<<
Nicholas M Allen, Sarah Weckhuysen, Kathleen Gorman, Mary D King, Holger Lerche
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1. Dezember 2019 (Treat-ION)
SCN2A channelopathies: Mechanisms and models
Epilepsia. 2019 Dec. >>PubMed-Link<<
Hedrich UBS, Lauxmann S, Lerche H.
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8. November 2019 (Treat-ION)
Novel treatment approaches and pediatric research networks in status epilepticus
Epilepsy Behav. 2019 Dec. [Epub ahead of print] >>PubMed-Link<<
Bialer M, Cross H, Hedrich UBS, Lagae L, Lerche H, Loddenkemper T.
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1. Oktober 2019 (Treat-ION)
Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutation
Stem Cell Res. 2019 Oct. [Epub ahead of print] >>PubMed-Link<<
Uysal B, Löffler H, Rosa F, Lerche H, Schwarz N
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1. Juli 2019 (Treat-ION)
KCNC1-related disorders: new de novo variants expand the phenotypic spectrum
Ann Clin Transl Neurol. 2019 Jul. [Epub ahead of print] >>PubMed-Link<<
Joohyun Park, Mahmoud Koko, Ulrike B S Hedrich, Andreas Hermann, Kirsten Cremer, Edda Haberlandt, Mona Grimmel, Bader Alhaddad, Stefanie Beck-Woedl, Merle Harrer, Daniela Karall, Lisa Kingelhoefer, Andreas Tzschach, Lars C Matthies, Tim M Strom, Erich Bernd Ringelstein, Marc Sturm, Hartmut Engel, Markus Wolff, Holger Lerche, Tobias B Haack
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1. Mai 2019 (Treat-ION)
Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutation
Stem Cell Res. 2019 May. [Epub ahead of print] >>PubMed-Link<<
Schwarz N, Uysal B, Rosa F, Löffler H, Mau-Holzmann UA, Liebau S, Lerche H.