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Andreas Laner

Showing results (1-10 of 48) with videos related to

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Human Mutation|July 15, 2022
Human Mutation special issue on "Variant Effect Prediction"Andreas Laner, Ales Maver, Johan T den Dunnen
International Journal of Molecular Sciences|October 29, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic StrategiesLukas Neuhann, Andreas Laner, Elke Holinski-Feder, et al.
Cardiovascular Diagnosis and Therapy|May 10, 2021
Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counselingAngela Abicht, Ulrike Schön, Andreas Laner, et al.
The Journal of Gene Medicine|August 3, 2007
Targeting of the glucocorticoid hormone receptor with plasmid DNA comprising glucocorticoid response elements improves nonviral gene transfer efficiency in the lungs of micePetra Dames, Andreas Laner, Christof Maucksch, et al.
European Journal of Gastroenterology & Hepatology|December 3, 2008
Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancerMonika Morak, Andreas Laner, Michael Scholz, et al.
European Journal of Human Genetics : EJHG|March 11, 2026
Validation structures for sequence variants of uncertain significance in hereditary cancerMorghan C Lucas, Thomas Keßler, Anna Benet-Pagès, et al.
European Journal of Human Genetics : EJHG|May 13, 2021
Stepwise ABC system for classification of any type of genetic variantGunnar Houge, Andreas Laner, Sebahattin Cirak, et al.
The Journal of Gene Medicine|October 10, 2006
Interaction of polyamine gene vectors with RNA leads to the dissociation of plasmid DNA-carrier complexesStephanie Huth, Florian Hoffmann, Katharina von Gersdorff, et al.
European Journal of Human Genetics : EJHG|December 12, 2019
Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndromeAnke Marie Arnold, Monika Morak, Anna Benet-Pagès, et al.
Clinical Case Reports|November 21, 2018
Extending the critical regions for mutations in the non-coding gene <i>RNU4ATAC</i> in another patient with Roifman SyndromeAriane Hallermayr, Janine Graf, Udo Koehler, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Human Mutation|July 15, 2022
Human Mutation special issue on "Variant Effect Prediction"Andreas Laner, Ales Maver, Johan T den Dunnen
International Journal of Molecular Sciences|October 29, 2025
Next-Generation Sequencing in Congenital Eye Malformations: Identification of Genetic Causes and Comparison of Different Panel-Based Diagnostic StrategiesLukas Neuhann, Andreas Laner, Elke Holinski-Feder, et al.
Cardiovascular Diagnosis and Therapy|May 10, 2021
Actionable secondary findings in arrhythmogenic right ventricle cardiomyopathy genes: impact and challenge of genetic counselingAngela Abicht, Ulrike Schön, Andreas Laner, et al.
The Journal of Gene Medicine|August 3, 2007
Targeting of the glucocorticoid hormone receptor with plasmid DNA comprising glucocorticoid response elements improves nonviral gene transfer efficiency in the lungs of micePetra Dames, Andreas Laner, Christof Maucksch, et al.
European Journal of Gastroenterology & Hepatology|December 3, 2008
Report on de-novo mutation in the MSH2 gene as a rare event in hereditary nonpolyposis colorectal cancerMonika Morak, Andreas Laner, Michael Scholz, et al.
European Journal of Human Genetics : EJHG|March 11, 2026
Validation structures for sequence variants of uncertain significance in hereditary cancerMorghan C Lucas, Thomas Keßler, Anna Benet-Pagès, et al.
European Journal of Human Genetics : EJHG|May 13, 2021
Stepwise ABC system for classification of any type of genetic variantGunnar Houge, Andreas Laner, Sebahattin Cirak, et al.
The Journal of Gene Medicine|October 10, 2006
Interaction of polyamine gene vectors with RNA leads to the dissociation of plasmid DNA-carrier complexesStephanie Huth, Florian Hoffmann, Katharina von Gersdorff, et al.
European Journal of Human Genetics : EJHG|December 12, 2019
Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndromeAnke Marie Arnold, Monika Morak, Anna Benet-Pagès, et al.
Clinical Case Reports|November 21, 2018
Extending the critical regions for mutations in the non-coding gene <i>RNU4ATAC</i> in another patient with Roifman SyndromeAriane Hallermayr, Janine Graf, Udo Koehler, et al.
Pageof 5