# Mennat Mehrez

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/mennat-mehrez/

## Facts

| Field | Value |
| --- | --- |
| Citations | 264 |
| Field | Bone and Dental Protein Studies |
| h-index | 9 |
| i10-index | 9 |
| Last Known Institution | National Human Genome Research Institute |
| OpenAlex ID | https://openalex.org/A5044649842 |
| ORCID iD | 0000-0003-4500-4024 |
| Works | 27 |

## Researcher papers

- [Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium](https://scholariq.org/papers/specific-variants-in-wdr35-cause-a-distinctive-form-of-ellis-van-creveld/)
- [Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome](https://scholariq.org/papers/germline-and-mosaic-variants-in-prkaca-and-prkacb-cause-a-multiple-congenital/)
- [Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations](https://scholariq.org/papers/gene-mutations-of-the-three-ectodysplasin-pathway-key-players-eda-edar-and/)
- [Expanding the mutation and clinical spectrum of Roberts syndrome](https://scholariq.org/papers/expanding-the-mutation-and-clinical-spectrum-of-roberts-syndrome/)
- [Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect](https://scholariq.org/papers/genetic-study-of-eight-egyptian-patients-with-pycnodysostosis-identification-of/)
- [Generalised versus Regional Odontodysplasia: Diagnosis, Transitional Management, and Long-Term Followup—A Report of 2 Cases](https://scholariq.org/papers/generalised-versus-regional-odontodysplasia-diagnosis-transitional-management/)
- [Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel <i>ROR2</i> gene mutations](https://scholariq.org/papers/clinical-and-molecular-characterization-of-seven-egyptian-families-with/)
- [Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation](https://scholariq.org/papers/further-delineation-of-the-oculoauricular-syndrome-phenotype-a-new-family-with-a/)
- [Lenz–Majewski syndrome in a patient from Egypt](https://scholariq.org/papers/lenz-majewski-syndrome-in-a-patient-from-egypt/)
- [Lipoid proteinosis: A clinical and molecular study in Egyptian patients](https://scholariq.org/papers/lipoid-proteinosis-a-clinical-and-molecular-study-in-egyptian-patients/)
- [Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families](https://scholariq.org/papers/outlining-the-clinical-profile-of-tcirg1-14-variants-including-5-novels-with/)

## Researcher topics

- [Bone and Dental Protein Studies](https://scholariq.org/topics/bone-and-dental-protein-studies/)
- [dental development and anomalies](https://scholariq.org/topics/dental-development-and-anomalies/)
- [Wnt/β-catenin signaling in development and cancer](https://scholariq.org/topics/wnt-catenin-signaling-in-development-and-cancer/)
- [Bone health and treatments](https://scholariq.org/topics/bone-health-and-treatments/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)

## Researcher university

- [National Human Genome Research Institute](https://scholariq.org/institutions/national-human-genome-research-institute/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.