Nofar Mor

Sheba Medical Center — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

13h-index3.1kcitations33works5.62yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Pluripotent Stem Cells Research(12), CRISPR and Genetic Engineering(9), RNA Research and Splicing(7), Renal and related cancers(6), RNA modifications and cancer(5)

Publications33 total

Knock-in Mouse Model of Hereditary Myopathy with Early Respiratory Failure Carrying the Titin Variant Corresponding to Human p.N31786K
2026Open Access
Design and Preliminary Screen of Antisense Oligonucleotides
Methods in molecular biology·2025
Personalized allele-specific antisense oligonucleotides for GNAO1-neurodevelopmental disorder
Molecular Therapy — Nucleic Acids·2024· 7 citedOpen Access
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
Human Genetics and Genomics Advances·2024· 5 citedOpen Access
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
The American Journal of Human Genetics·2024· 16 citedOpen Access
Intellectual disability syndrome associated with a homozygous founder variant in <i>SGSM3</i> in Ashkenazi Jews
Journal of Medical Genetics·2023· 1 cited
Adult-onset Alexander disease among patients of Jewish Syrian descent
Neurogenetics·2023· 5 cited
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure
Kidney International Reports·2023· 11 citedOpen Access
GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis
Frontiers in Immunology·2022· 7 citedOpen Access
FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases
Nephrology Dialysis Transplantation·2022
A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights
Pediatric Nephrology·2022· 21 cited
SUMOylation of linker histone H1 drives chromatin condensation and restriction of embryonic cell fate identity
Molecular Cell·2021· 33 citedOpen Access
A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies
Scientific Reports·2021· 26 citedOpen Access
Principles of signaling pathway modulation for enhancing human naive pluripotency induction
Cell stem cell·2021· 151 citedOpen Access
Context-dependent functional compensation between Ythdf m<sup>6</sup>A reader proteins
Genes & Development·2020· 245 citedOpen Access
Context-dependent functional compensation between Ythdf m6A readers
2020· 10 citedOpen Access
Tripartite Inhibition of SRC-WNT-PKC Signalling Consolidates Human Naïve Pluripotency
2020· 5 citedOpen Access
Supplementary materials for Perl et al 2019
Zenodo (CERN European Organization for Nuclear Research)·2019Open Access
Human non-olfactory cognition phase-locked with inhalation
Nature Human Behaviour·2019· 219 cited
Supplementary materials for Perl et al 2019
2019Open Access
page 1 of 2Next →

Frequent Co-authors

Jacob H. Hanna(16), Vladislav Krupalnik(15), Noa Novershtern(15), Sergey Viukov(14), Mirie Zerbib(14), Yoach Rais(12), Alejandro Aguilera-Castrejon(11), Shay Geula(10), Jonathan Bayerl(10), Elad Chomsky(9), Asaf Zviran(9), Ohad Gafni(9), Daoud Sheban(9), Rada Massarwa(8), Shani Peles(8), Dan Dominissini(7), Leehee Weinberger(7), Lior Lasman(7), Tom Shani(7), Suhair Hanna(7)