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Hagit Baris

Showing results (71-80 of 96) with videos related to

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Breast Cancer Research and Treatment|August 2, 2019
The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patientsRinat Bernstein-Molho, Inbal Barnes-Kedar, Mark D Ludman, et al.
Annals of Internal Medicine|December 23, 2024
Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail SyndromeAlina Kurolap, Chofit Chai Gadot, Orly Eshach Adiv, et al.
Movement Disorders Clinical Practice|June 5, 2025
High Genetic Diagnostic Yield for Patients with Rare Movement Disorders at a Single-Center Neurogenetics ClinicDvir Penn, Yam Amir, Gil Ben David, et al.
Breast Cancer Research and Treatment|April 19, 2020
Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variantsRinat Bernstein-Molho, Eitan Friedman, Inbal Kedar, et al.
European Journal of Neurology|June 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From IsraelDror Shir, Noa Bregman, Aya Bar David, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2018
Two separate functions of NME3 critical for cell survival underlie a neurodegenerative disorderChih-Wei Chen, Hong-Ling Wang, Ching-Wen Huang, et al.
Human Genetics|March 25, 2024
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyCharlotte Herbst, Viktoria Bothe, Meret Wegler, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Human Mutation|February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytesRichard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Breast Cancer Research and Treatment|August 2, 2019
The yield of full BRCA1/2 genotyping in Israeli Arab high-risk breast/ovarian cancer patientsRinat Bernstein-Molho, Inbal Barnes-Kedar, Mark D Ludman, et al.
Annals of Internal Medicine|December 23, 2024
Impaired Wnt/Planar Cell Polarity Signaling in Yellow Nail SyndromeAlina Kurolap, Chofit Chai Gadot, Orly Eshach Adiv, et al.
Movement Disorders Clinical Practice|June 5, 2025
High Genetic Diagnostic Yield for Patients with Rare Movement Disorders at a Single-Center Neurogenetics ClinicDvir Penn, Yam Amir, Gil Ben David, et al.
Breast Cancer Research and Treatment|April 19, 2020
Diagnostic yield of multigene panel testing in an Israeli cohort: enrichment of low-penetrance variantsRinat Bernstein-Molho, Eitan Friedman, Inbal Kedar, et al.
European Journal of Neurology|June 23, 2026
A Practice Framework for Genetic Testing in Asymptomatic Relatives of Patients With Creutzfeldt-Jakob Disease: Experience and Insights From IsraelDror Shir, Noa Bregman, Aya Bar David, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2018
Two separate functions of NME3 critical for cell survival underlie a neurodegenerative disorderChih-Wei Chen, Hong-Ling Wang, Ching-Wen Huang, et al.
Human Genetics|March 25, 2024
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyCharlotte Herbst, Viktoria Bothe, Meret Wegler, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Human Mutation|February 12, 2019
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytesRichard Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
Pageof 10