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Isabell Schumann

Showing results (11-20 of 20) with videos related to

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Human Mutation|July 18, 2025
Incorporating Nanopore Sequencing Into a Diverse Diagnostic Toolkit for Incontinentia PigmentiSimone Ahting, Denny Popp, Henry Oppermann, et al.
Journal of Neurogenetics|January 25, 2020
Food restriction reconfigures naïve and learned choice behavior in <i>Drosophila</i> larvaeBenita Brünner, Juliane Saumweber, Merve Samur, et al.
Human Genetics|July 16, 2024
Automatized detection of uniparental disomies in a large cohortJohanna Moch, Maximilian Radtke, Thomas Liehr, et al.
Proceedings. Biological Sciences|July 11, 2019
Origin of ecdysis: fossil evidence from 535-million-year-old scalidophoran wormsDeng Wang, Jean Vannier, Isabell Schumann, et al.
European Journal of Medical Genetics|August 24, 2025
Overview and expansion of CEP85L-associated lissencephalyIsabell Schumann, Rami Abou Jamra, Robin-Tobias Jauss, et al.
Frontiers in Genetics|January 8, 2024
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in <i>PARD6G-AS1</i> promotor in a case with arthrogryposisJohanna Moch, Maximilian Radtke, Janina Gburek-Augustat, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Tagungsbericht GfH-Juniorakademie 2025: Junge Humangenetik auf Schloss Buchenau: Austausch, Vernetzung und neue PerspektivenIsabell Schumann, Hanna Salchow, Simone Ahting, et al.
Journal of Neurogenetics|February 25, 2025
<i>Drosophila WDFY3</i>/<i>Bchs</i> overexpression impairs neural functionMarek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Human Mutation|July 18, 2025
Incorporating Nanopore Sequencing Into a Diverse Diagnostic Toolkit for Incontinentia PigmentiSimone Ahting, Denny Popp, Henry Oppermann, et al.
Journal of Neurogenetics|January 25, 2020
Food restriction reconfigures naïve and learned choice behavior in <i>Drosophila</i> larvaeBenita Brünner, Juliane Saumweber, Merve Samur, et al.
Human Genetics|July 16, 2024
Automatized detection of uniparental disomies in a large cohortJohanna Moch, Maximilian Radtke, Thomas Liehr, et al.
Proceedings. Biological Sciences|July 11, 2019
Origin of ecdysis: fossil evidence from 535-million-year-old scalidophoran wormsDeng Wang, Jean Vannier, Isabell Schumann, et al.
European Journal of Medical Genetics|August 24, 2025
Overview and expansion of CEP85L-associated lissencephalyIsabell Schumann, Rami Abou Jamra, Robin-Tobias Jauss, et al.
Frontiers in Genetics|January 8, 2024
Case report: Complete paternal isodisomy on chromosome 18 induces methylation changes in <i>PARD6G-AS1</i> promotor in a case with arthrogryposisJohanna Moch, Maximilian Radtke, Janina Gburek-Augustat, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
Tagungsbericht GfH-Juniorakademie 2025: Junge Humangenetik auf Schloss Buchenau: Austausch, Vernetzung und neue PerspektivenIsabell Schumann, Hanna Salchow, Simone Ahting, et al.
Journal of Neurogenetics|February 25, 2025
<i>Drosophila WDFY3</i>/<i>Bchs</i> overexpression impairs neural functionMarek B Körner, Akhil Velluva, Linnaeus Bundalian, et al.
Medrxiv : the Preprint Server for Health Sciences|September 15, 2025
Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Nature Genetics|March 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathiesElsa Leitão, Amandine Santini, Benjamin Cogne, et al.
Pageof 2