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Sandra Jansen

Showing results (31-40 of 62) with videos related to

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The Journal of Clinical Investigation|February 6, 2002
Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoformsIngeborg Stalmans, Yin-Shan Ng, Richard Rohan, et al.
Human Mutation|January 12, 2017
Quantification of Phenotype Information Aids the Identification of Novel Disease GenesAnneke T Vulto-van Silfhout, Christian Gilissen, Jelle J Goeman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disordersAlexander J M Dingemans, Max Hinne, Sandra Jansen, et al.
American Journal of Medical Genetics. Part A|January 13, 2021
Human disease genes website series: An international, open and dynamic library for up-to-date clinical informationAlexander J M Dingemans, Diante E Stremmelaar, Lisenka E L M Vissers, et al.
HGG Advances|July 21, 2022
Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.
HGG Advances|January 20, 2022
Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2013
Thick-shelled, grazer-protected diatoms decouple ocean carbon and silicon cycles in the iron-limited Antarctic Circumpolar CurrentPhilipp Assmy, Victor Smetacek, Marina Montresor, et al.
American Journal of Human Genetics|November 7, 2017
Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain PhenotypeIdeke J C Lamers, Margot R F Reijnders, Hanka Venselaar, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
<i>SOD1</i> is a synthetic lethal target in <i>PPM1D</i>-mutant leukemia cellsLinda Zhang, Joanne I Hsu, Etienne D Braekeleer, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|February 6, 2002
Arteriolar and venular patterning in retinas of mice selectively expressing VEGF isoformsIngeborg Stalmans, Yin-Shan Ng, Richard Rohan, et al.
Human Mutation|January 12, 2017
Quantification of Phenotype Information Aids the Identification of Novel Disease GenesAnneke T Vulto-van Silfhout, Christian Gilissen, Jelle J Goeman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disordersRoos van der Donk, Sandra Jansen, Janneke H M Schuurs-Hoeijmakers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Phenotype based prediction of exome sequencing outcome using machine learning for neurodevelopmental disordersAlexander J M Dingemans, Max Hinne, Sandra Jansen, et al.
American Journal of Medical Genetics. Part A|January 13, 2021
Human disease genes website series: An international, open and dynamic library for up-to-date clinical informationAlexander J M Dingemans, Diante E Stremmelaar, Lisenka E L M Vissers, et al.
HGG Advances|July 21, 2022
Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.
HGG Advances|January 20, 2022
Discovery of a neuromuscular syndrome caused by biallelic variants in <i>ASCC3</i>Divya Nair, Dong Li, Hannah Erdogan, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 20, 2013
Thick-shelled, grazer-protected diatoms decouple ocean carbon and silicon cycles in the iron-limited Antarctic Circumpolar CurrentPhilipp Assmy, Victor Smetacek, Marina Montresor, et al.
American Journal of Human Genetics|November 7, 2017
Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain PhenotypeIdeke J C Lamers, Margot R F Reijnders, Hanka Venselaar, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
<i>SOD1</i> is a synthetic lethal target in <i>PPM1D</i>-mutant leukemia cellsLinda Zhang, Joanne I Hsu, Etienne D Braekeleer, et al.
Pageof 7