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R Lemke

Showing results (201-210 of 342) with videos related to

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European Psychiatry : the Journal of the Association of European Psychiatrists|June 30, 2009
Early improvement as a predictor of remission and response in schizophrenia: Results from a naturalistic studyM Jäger, M Schmauss, G Laux, et al.
International Journal of Obesity (2005)|June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individualsRobert Künzel, Helene Faust, Linnaeus Bundalian, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Distances from ligands as main predictive features for pathogenicity and functional effect of variants in NMDA receptorsLudovica Montanucci, Tobias Brünger, Nisha Bhattarai, et al.
Human Molecular Genetics|November 13, 2024
Ligand distances as key predictors of pathogenicity and function in NMDA receptorsLudovica Montanucci, Tobias Brünger, Nisha Bhattarai, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities?Karl Hackmann, Andreas Rump, Stefan A Haas, et al.
Bioinformatics (Oxford, England)|April 27, 2023
CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants onlineMarie Macnee, Eduardo Pérez-Palma, Tobias Brünger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Clinical Genetics|October 3, 2022
The constitutional gain-of-function variant p.Glu1099Lys in NSD2 is associated with a novel syndromeBernt Popp, Melanie Brugger, Sibylle Poschmann, et al.
Pharmacopsychiatry|September 3, 2008
Standardized remission criteria in schizophrenia: descriptive validity and comparability with previously used outcome measuresM Jäger, T Messer, G Laux, et al.
European Journal of Human Genetics : EJHG|December 23, 2022
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsyJohannes Luppe, Heinrich Sticht, François Lecoquierre, et al.
Pageof 35

Showing results (201-210 of 342) with videos related to

Sort By:
Pageof 35
European Psychiatry : the Journal of the Association of European Psychiatrists|June 30, 2009
Early improvement as a predictor of remission and response in schizophrenia: Results from a naturalistic studyM Jäger, M Schmauss, G Laux, et al.
International Journal of Obesity (2005)|June 16, 2025
Detecting monogenic obesity: a systematic exome-wide workup of over 500 individualsRobert Künzel, Helene Faust, Linnaeus Bundalian, et al.
Medrxiv : the Preprint Server for Health Sciences|May 20, 2024
Distances from ligands as main predictive features for pathogenicity and functional effect of variants in NMDA receptorsLudovica Montanucci, Tobias Brünger, Nisha Bhattarai, et al.
Human Molecular Genetics|November 13, 2024
Ligand distances as key predictors of pathogenicity and function in NMDA receptorsLudovica Montanucci, Tobias Brünger, Nisha Bhattarai, et al.
American Journal of Medical Genetics. Part A|September 12, 2015
Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities?Karl Hackmann, Andreas Rump, Stefan A Haas, et al.
Bioinformatics (Oxford, England)|April 27, 2023
CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants onlineMarie Macnee, Eduardo Pérez-Palma, Tobias Brünger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsyHenrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Clinical Genetics|October 3, 2022
The constitutional gain-of-function variant p.Glu1099Lys in NSD2 is associated with a novel syndromeBernt Popp, Melanie Brugger, Sibylle Poschmann, et al.
Pharmacopsychiatry|September 3, 2008
Standardized remission criteria in schizophrenia: descriptive validity and comparability with previously used outcome measuresM Jäger, T Messer, G Laux, et al.
European Journal of Human Genetics : EJHG|December 23, 2022
Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsyJohannes Luppe, Heinrich Sticht, François Lecoquierre, et al.
Pageof 35