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Tobias Brünger

Showing results (1-10 of 26) with videos related to

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Frontiers in Neurology|April 19, 2021
ATP1A3-Related Disorders: An Ever-Expanding Clinical SpectrumPhilippe A Salles, Ignacio F Mata, Tobias Brünger, et al.
Epilepsia|October 23, 2024
Evaluating novel in silico tools for accurate pathogenicity classification in epilepsy-associated genetic missense variantsLudovica Montanucci, Tobias Brünger, Christian M Boßelmann, et al.
Brain : a Journal of Neurology|October 18, 2022
Delineation of functionally essential protein regions for 242 neurodevelopmental genesSumaiya Iqbal, Tobias Brünger, Eduardo Pérez-Palma, et al.
Genome Biology|July 7, 2025
Conserved missense variant pathogenicity and correlated phenotypes across paralogous genesTobias Brünger, Alina Ivaniuk, Eduardo Pérez-Palma, et al.
Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Genotype-specific communication profiles in 79,518 individuals with neurodevelopmental disordersCristiane Hsu, Alina Ivaniuk, Andres Jimenez-Gomez, et al.
Epilepsia|May 7, 2026
The International Classification of Cognitive Disorders in Epilepsy (IC-CoDE) Portal: An open source resource for neuropsychological research in epilepsyRobyn M Busch, Tobias Brünger, Kayela Arrotta, et al.
Brain : a Journal of Neurology|August 29, 2022
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypesTobias Brünger, Eduardo Pérez-Palma, Ludovica Montanucci, et al.
Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.
Human Mutation|April 14, 2025
Quantitative Phenotype Morbidity Description of <i>SATB2</i>-Associated SyndromeYuri A Zarate, Katherine Bosanko, Amrit Kannan, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Frontiers in Neurology|April 19, 2021
ATP1A3-Related Disorders: An Ever-Expanding Clinical SpectrumPhilippe A Salles, Ignacio F Mata, Tobias Brünger, et al.
Epilepsia|October 23, 2024
Evaluating novel in silico tools for accurate pathogenicity classification in epilepsy-associated genetic missense variantsLudovica Montanucci, Tobias Brünger, Christian M Boßelmann, et al.
Brain : a Journal of Neurology|October 18, 2022
Delineation of functionally essential protein regions for 242 neurodevelopmental genesSumaiya Iqbal, Tobias Brünger, Eduardo Pérez-Palma, et al.
Genome Biology|July 7, 2025
Conserved missense variant pathogenicity and correlated phenotypes across paralogous genesTobias Brünger, Alina Ivaniuk, Eduardo Pérez-Palma, et al.
Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Medrxiv : the Preprint Server for Health Sciences|February 12, 2026
Genotype-specific communication profiles in 79,518 individuals with neurodevelopmental disordersCristiane Hsu, Alina Ivaniuk, Andres Jimenez-Gomez, et al.
Epilepsia|May 7, 2026
The International Classification of Cognitive Disorders in Epilepsy (IC-CoDE) Portal: An open source resource for neuropsychological research in epilepsyRobyn M Busch, Tobias Brünger, Kayela Arrotta, et al.
Brain : a Journal of Neurology|August 29, 2022
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypesTobias Brünger, Eduardo Pérez-Palma, Ludovica Montanucci, et al.
Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.
Human Mutation|April 14, 2025
Quantitative Phenotype Morbidity Description of <i>SATB2</i>-Associated SyndromeYuri A Zarate, Katherine Bosanko, Amrit Kannan, et al.
Pageof 3