ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum by Philippe A. Salles, Philippe A. Salles, Ignacio F. Mata, Tobias Brünger, Dennis Lal, Hubert H. Fernandez

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals by Ludovica Montanucci, David Lewis-Smith, Ryan L. Collins, Lisa-Marie Niestroj, Shridhar Parthasarathy, Julie Xian, Shiva Ganesan, Marie Macnee, Tobias Brünger, Rhys H. Thomas, Michael Talkowski, Epi25 Collaborative, Ingo Helbig, Costin Leu, Dennis Lal

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P369: SATB2-associated syndrome severity score: Genotype/phenotype correlations and the SATB2 portal by Yuri Zarate, Katherine Bosanko, Amrit Kannan, Ashlen Thomason, Beth Nutt, Nihit Kumar, Kirk Simmons, Aaron Hiegert, Larry Hartzell, Adam Johnson, Tabitha Prater, Jillian Kimberlain, Aisling Caffrey, Arthur Stefanski, Tobias Brünger, Eduardo Pérez-Palma, Dennis Lal

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Scanning mutagenesis of the voltage-gated sodium channel NaV1.2 using base editing by Juan Lorenzo B. Pablo, Savannah L. Cornett, Lei A. Wang, Sooyeon Jo, Tobias Brünger, Nikita Budnik, Mudra Hegde, Jean-Marc DeKeyser, Christopher H. Thompson, John G. Doench, Dennis Lal, Alfred L. George, Jr., Jen Q. Pan

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Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFR by Christian M. Boßelmann, Costin Leu, Tobias Brünger, Lucas Hoffmann, Sara Baldassari, Mathilde Chipaux, Roland Coras, Katja Kobow, Hajo Hamer, Daniel Delev, Karl Rössler, Christian G. Bien, Thilo Kalbhenn, Tom Pieper, Till Hartlieb, Kerstin Becker, Lisa Ferguson, Robyn M. Busch, Stéphanie Baulac, Peter Nürnberg, Imad Najm, Ingmar Blümcke, Dennis Lal

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