Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Rotem Greenberg

3PUBLICATIONS
15CO-AUTHORS
Counselling psychologyNeurology and neuromuscular diseasesCardiology (incl. cardiovascular diseases)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (3)

Sort by Publication Date:
|Apr 01, 2026
Psychologically informed reminder messages for promoting BRCA1/2 carrier screening: evidence from a large-scale population-based study.

Tom Mushkat, Rotem Greenberg, Ofer Isakov

|Sep 30, 2025
N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder.

Asier Iturrate, Nurit Assia Batzir, Ranit Jaron

|Jan 27, 2025
Mono and Biallelic Variants in <i>TRIM63</i> Are Frequently Associated With a Unique Form of Hypertrophic Cardiomyopathy.

Noa Ruhrman Shahar, Dina Marek-Yagel, Rotem Greenberg

Pageof 1

Frequent Collaborators

2 joint publications

Ofer Isakov

2 joint publications

Lina Basel-Salmon

2 joint publications

Shay Ben-Shachar

1 joint publications

Noa Ruhrman Shahar

1 joint publications

Lily Bazak

1 joint publications

Daniel Monakier

1 joint publications

Amitai Segev

1 joint publications

Lilach Benyamini

1 joint publications

Adel Shalata

1 joint publications

Asier Iturrate

Frequent Collaborators

2 joint publications

Ofer Isakov

2 joint publications

Lina Basel-Salmon

2 joint publications

Shay Ben-Shachar

1 joint publications

Noa Ruhrman Shahar

Top Related Videos

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of <em>BRCA1</em>, <em>BRCA2</em>, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of <em>BRCA1</em>, <em>BRCA2</em>, and 9 Genes Involved in DNA Damage Repair

Published on : Oct 06, 2014

12.8K
In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>

Published on : Aug 20, 2019

14.2K
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on : Aug 08, 2022

3.0K
See more related videos

Top Related Videos

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of <em>BRCA1</em>, <em>BRCA2</em>, and 9 Genes Involved in DNA Damage Repair
08:15

gDNA Enrichment by a Transposase-based Technology for NGS Analysis of the Whole Sequence of <em>BRCA1</em>, <em>BRCA2</em>, and 9 Genes Involved in DNA Damage Repair

Published on : Oct 06, 2014

12.8K
In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using <em>Drosophila</em>

Published on : Aug 20, 2019

14.2K
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on : Aug 08, 2022

3.0K
See more related videos