# Hagar Mor‐Shaked
**Type:** Researchers
**Canonical URL:** https://scholariq.org/researchers/hagar-mor-shaked/
## Facts
| Field | Value |
| --- | --- |
| Citations | 692 |
| Field | Genomics and Rare Diseases |
| h-index | 15 |
| i10-index | 26 |
| Last Known Institution | Hebrew University of Jerusalem |
| OpenAlex ID | https://openalex.org/A5086624955 |
| ORCID iD | 0000-0001-6631-0376 |
| Works | 57 |
## Researcher papers
- [FMR1 Epigenetic Silencing Commonly Occurs in Undifferentiated Fragile X-Affected Embryonic Stem Cells](https://scholariq.org/papers/fmr1-epigenetic-silencing-commonly-occurs-in-undifferentiated-fragile-x-affected/)
- [Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy](https://scholariq.org/papers/loss-of-function-mutations-in-udp-glucose-6-dehydrogenase-cause-recessive/)
- [Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction](https://scholariq.org/papers/mutation-specific-pathophysiological-mechanisms-define-different/)
- [Whole-exome sequencing accuracy in the diagnosis of primary ciliary dyskinesia](https://scholariq.org/papers/whole-exome-sequencing-accuracy-in-the-diagnosis-of-primary-ciliary-dyskinesia/)
- [Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis](https://scholariq.org/papers/mutations-in-mylpf-cause-a-novel-segmental-amyoplasia-that-manifests-as-distal/)
- [The G-rich Repeats in FMR1 and C9orf72 Loci Are Hotspots for Local Unpairing of DNA](https://scholariq.org/papers/the-g-rich-repeats-in-i-fmr1-i-and-i-c9orf72-i-loci-are-hotspots-for-local/)
- [Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome](https://scholariq.org/papers/reevaluation-of-fmr1-hypermethylation-timing-in-fragile-x-syndrome/)
- [Exome sequencing for structurally normal fetuses—yields and ethical issues](https://scholariq.org/papers/exome-sequencing-for-structurally-normal-fetuses-yields-and-ethical-issues/)
- [Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder](https://scholariq.org/papers/rare-germline-heterozygous-missense-variants-in-brca1-associated-protein-1-bap1/)
- [Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells](https://scholariq.org/papers/modeling-fragile-x-syndrome-using-human-pluripotent-stem-cells/)
- [Clinical presentation and analysis of genotype-phenotype correlations in patients with malignant infantile osteopetrosis](https://scholariq.org/papers/clinical-presentation-and-analysis-of-genotype-phenotype-correlations-in/)
## Researcher topics
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
## Researcher university
- [Hebrew University of Jerusalem](https://scholariq.org/institutions/hebrew-university-of-jerusalem/)
---
Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.