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Juliane Winkelmann

Showing results (81-90 of 290) with videos related to

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Neurogenetics|March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variantIvana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
Journal of Neurology|May 12, 2011
Parkinson's disease risk score: moving to a premotor diagnosisJürgen Winkler, Reinhard Ehret, Thomas Büttner, et al.
Human Molecular Genetics|December 10, 2021
Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulationDaniel D Lam, Ana Antic Nikolic, Chen Zhao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2005
Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndromeJuliane Winkelmann, Peter Lichtner, Benno Pütz, et al.
Science Advances|June 13, 2025
Beyond volume: Unraveling the genetics of human brain geometrySabrina A Primus, Felix Hoffstaedter, Federico Raimondo, et al.
Scientific Reports|November 23, 2024
RLS-associated MEIS transcription factors control distinct processes in human neural stem cellsVolker Kittke, Chen Zhao, Daniel D Lam, et al.
Gene|November 1, 2024
Variants that get straight to your heart - Cardiogenetic secondary findings in exome sequencingKirsten Wenderholm, Theresa Brunet, Elisabeth Graf, et al.
Case Reports in Genetics|December 8, 2017
<i>SOX5</i>-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral AbnormalitiesMichael Zech, Katharina Poustka, Sylvia Boesch, et al.
Frontiers in Public Health|January 23, 2023
Perspective: Lessons from COVID-19 of countries in the European region in light of findings from the health system response monitorFlorian Tille, Ewout Van Ginneken, Juliane Winkelmann, et al.
Parkinsonism & Related Disorders|July 13, 2020
Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrierJán Necpál, Michael Zech, Alica Valachová, et al.
Pageof 29

Showing results (81-90 of 290) with videos related to

Sort By:
Pageof 29
Neurogenetics|March 7, 2021
Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variantIvana Dzinovic, Tereza Serranová, Clement Prouteau, et al.
Journal of Neurology|May 12, 2011
Parkinson's disease risk score: moving to a premotor diagnosisJürgen Winkler, Reinhard Ehret, Thomas Büttner, et al.
Human Molecular Genetics|December 10, 2021
Intronic elements associated with insomnia and restless legs syndrome exhibit cell-type-specific epigenetic features contributing to MEIS1 regulationDaniel D Lam, Ana Antic Nikolic, Chen Zhao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2005
Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndromeJuliane Winkelmann, Peter Lichtner, Benno Pütz, et al.
Science Advances|June 13, 2025
Beyond volume: Unraveling the genetics of human brain geometrySabrina A Primus, Felix Hoffstaedter, Federico Raimondo, et al.
Scientific Reports|November 23, 2024
RLS-associated MEIS transcription factors control distinct processes in human neural stem cellsVolker Kittke, Chen Zhao, Daniel D Lam, et al.
Gene|November 1, 2024
Variants that get straight to your heart - Cardiogenetic secondary findings in exome sequencingKirsten Wenderholm, Theresa Brunet, Elisabeth Graf, et al.
Case Reports in Genetics|December 8, 2017
<i>SOX5</i>-Null Heterozygous Mutation in a Family with Adult-Onset Hyperkinesia and Behavioral AbnormalitiesMichael Zech, Katharina Poustka, Sylvia Boesch, et al.
Frontiers in Public Health|January 23, 2023
Perspective: Lessons from COVID-19 of countries in the European region in light of findings from the health system response monitorFlorian Tille, Ewout Van Ginneken, Juliane Winkelmann, et al.
Parkinsonism & Related Disorders|July 13, 2020
Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrierJán Necpál, Michael Zech, Alica Valachová, et al.
Pageof 29