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Katarina Cisarova

Showing results (1-10 of 19) with videos related to

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Animal Biotechnology|August 17, 2013
A missense mutation in the rabbit melanocortin 4 receptor (MC4R) gene is associated with finishing weight in a meat rabbit lineLuca Fontanesi, Emilio Scotti, Katarina Cisarova, et al.
American Journal of Medical Genetics. Part A|October 30, 2024
Recurrent Increased Nuchal Translucency Led to the Identification of Novel NUP107 VariantsIsis Atallah, Katarina Cisarova, Cécile Guenot, et al.
American Journal of Human Genetics|October 7, 2017
DOMINO: Using Machine Learning to Predict Genes Associated with Dominant DisordersMathieu Quinodoz, Beryl Royer-Bertrand, Katarina Cisarova, et al.
Genes|September 28, 2021
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and LimitationsBeryl Royer-Bertrand, Katarina Cisarova, Florence Niel-Butschi, et al.
British Journal of Pharmacology|November 30, 2025
Targeting hexokinase 2 to induce breast cancer cell senescenceHelmut Bischof, Katarina Cisarova, Sandra Burgstaller, et al.
American Journal of Human Genetics|February 5, 2022
Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicityMathieu Quinodoz, Virginie G Peter, Katarina Cisarova, et al.
Cancers|March 25, 2022
Identification of New Vulnerabilities in Conjunctival Melanoma Using Image-Based High Content Drug ScreeningKatya Nardou, Michael Nicolas, Fabien Kuttler, et al.
American Journal of Medical Genetics. Part A|September 28, 2021
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasiaKatarina Cisarova, Livia Garavelli, Stefano Giuseppe Caraffi, et al.
PNAS Nexus|March 13, 2023
The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesisVirginie G Peter, Karolina Kaminska, Cristina Santos, et al.
Plos Genetics|December 31, 2020
Genomic and transcriptomic landscape of conjunctival melanomaKatarina Cisarova, Marc Folcher, Ikram El Zaoui, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Animal Biotechnology|August 17, 2013
A missense mutation in the rabbit melanocortin 4 receptor (MC4R) gene is associated with finishing weight in a meat rabbit lineLuca Fontanesi, Emilio Scotti, Katarina Cisarova, et al.
American Journal of Medical Genetics. Part A|October 30, 2024
Recurrent Increased Nuchal Translucency Led to the Identification of Novel NUP107 VariantsIsis Atallah, Katarina Cisarova, Cécile Guenot, et al.
American Journal of Human Genetics|October 7, 2017
DOMINO: Using Machine Learning to Predict Genes Associated with Dominant DisordersMathieu Quinodoz, Beryl Royer-Bertrand, Katarina Cisarova, et al.
Genes|September 28, 2021
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and LimitationsBeryl Royer-Bertrand, Katarina Cisarova, Florence Niel-Butschi, et al.
British Journal of Pharmacology|November 30, 2025
Targeting hexokinase 2 to induce breast cancer cell senescenceHelmut Bischof, Katarina Cisarova, Sandra Burgstaller, et al.
American Journal of Human Genetics|February 5, 2022
Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicityMathieu Quinodoz, Virginie G Peter, Katarina Cisarova, et al.
Cancers|March 25, 2022
Identification of New Vulnerabilities in Conjunctival Melanoma Using Image-Based High Content Drug ScreeningKatya Nardou, Michael Nicolas, Fabien Kuttler, et al.
American Journal of Medical Genetics. Part A|September 28, 2021
A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasiaKatarina Cisarova, Livia Garavelli, Stefano Giuseppe Caraffi, et al.
PNAS Nexus|March 13, 2023
The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesisVirginie G Peter, Karolina Kaminska, Cristina Santos, et al.
Plos Genetics|December 31, 2020
Genomic and transcriptomic landscape of conjunctival melanomaKatarina Cisarova, Marc Folcher, Ikram El Zaoui, et al.
Pageof 2