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World Journal of Stem Cells
|
July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells
Shira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
HGG Advances
|
February 24, 2022
CRISPR/Cas9-induced gene conversion between <i>ATAD3</i> paralogs
Shira 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 impairments
Liya 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 features
Jonathan 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 patients
Shira 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 delay
Hagar 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 Disorder
Shira 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 syndrome
Avivit 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 zebrafish
Shlomit 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 delay
Alisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
World Journal of Stem Cells
|
July 2, 2015
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells
Shira Yanovsky-Dagan, Hagar Mor-Shaked, Rachel Eiges
HGG Advances
|
February 24, 2022
CRISPR/Cas9-induced gene conversion between <i>ATAD3</i> paralogs
Shira 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 impairments
Liya 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 features
Jonathan 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 patients
Shira 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 delay
Hagar 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 Disorder
Shira 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 syndrome
Avivit 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 zebrafish
Shlomit 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 delay
Alisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.
Page
of 3