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

Filters

Shira Yanovsky-Dagan

Showing results (1-10 of 22) with videos related to

Pageof 3
Sort By:
World Journal of Stem Cells|July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cellsShira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
HGG Advances|February 24, 2022
CRISPR/Cas9-induced gene conversion between <i>ATAD3</i> paralogsShira Yanovsky-Dagan, Ayala Frumkin, James R Lupski, et al.
Journal of Molecular Endocrinology|October 3, 2025
Intronic IGF1R variant causing aberrant splicing, short stature, and neurological impairmentsLiya Kerem, Jonathan Rips, Adam Zaretsky, et al.
American Journal of Medical Genetics. Part A|October 7, 2020
De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic featuresJonathan Rips, Hagar Mor-Shaked, Serkan Erdin, et al.
European Journal of Human Genetics : EJHG|November 15, 2021
DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patientsShira Yanovsky-Dagan, Eliora Cohen, Pauline Megalli, et al.
Clinical Genetics|January 7, 2021
Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delayHagar Mor-Shaked, Somaya Salah, Shira Yanovsky-Dagan, et al.
Human Mutation|December 24, 2025
Homozygous Deletion of the Epigenetic Regulator <i>PHF20</i> in Individuals With Neurodevelopmental DisorderShira Yanovsky Dagan, Hongwen Xuan, Jonathan Rips, et al.
European Journal of Human Genetics : EJHG|December 12, 2023
Complex rearrangement in TBC1D4 in an individual with diabetes due to severe insulin resistance syndromeAvivit Cahn, Hagar Mor-Shaked, Hallel Rosenberg-Fogler, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Allele-specific antisense oligonucleotide treatment rescues <i>atad3-</i> associated phenotype in zebrafishShlomit Ezer, Shira Yanovsky-Dagan, Amit Granit, et al.
Clinical Genetics|April 2, 2023
A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delayAlisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
World Journal of Stem Cells|July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cellsShira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
HGG Advances|February 24, 2022
CRISPR/Cas9-induced gene conversion between <i>ATAD3</i> paralogsShira Yanovsky-Dagan, Ayala Frumkin, James R Lupski, et al.
Journal of Molecular Endocrinology|October 3, 2025
Intronic IGF1R variant causing aberrant splicing, short stature, and neurological impairmentsLiya Kerem, Jonathan Rips, Adam Zaretsky, et al.
American Journal of Medical Genetics. Part A|October 7, 2020
De novo variant in AMOTL1 in infant with cleft lip and palate, imperforate anus and dysmorphic featuresJonathan Rips, Hagar Mor-Shaked, Serkan Erdin, et al.
European Journal of Human Genetics : EJHG|November 15, 2021
DMPK hypermethylation in sperm cells of myotonic dystrophy type 1 patientsShira Yanovsky-Dagan, Eliora Cohen, Pauline Megalli, et al.
Clinical Genetics|January 7, 2021
Biallelic deletion in a minimal CAPN15 intron in siblings with a recognizable syndrome of congenital malformations and developmental delayHagar Mor-Shaked, Somaya Salah, Shira Yanovsky-Dagan, et al.
Human Mutation|December 24, 2025
Homozygous Deletion of the Epigenetic Regulator <i>PHF20</i> in Individuals With Neurodevelopmental DisorderShira Yanovsky Dagan, Hongwen Xuan, Jonathan Rips, et al.
European Journal of Human Genetics : EJHG|December 12, 2023
Complex rearrangement in TBC1D4 in an individual with diabetes due to severe insulin resistance syndromeAvivit Cahn, Hagar Mor-Shaked, Hallel Rosenberg-Fogler, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2026
Allele-specific antisense oligonucleotide treatment rescues <i>atad3-</i> associated phenotype in zebrafishShlomit Ezer, Shira Yanovsky-Dagan, Amit Granit, et al.
Clinical Genetics|April 2, 2023
A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delayAlisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.
Pageof 3