Mennat I Mehrez

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 8

Top Venues

Genes

American journal of medical genetics. Part A

National Research Centre

Cairo University, faculty of oral and dental medicine (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Research Centre Nov 01 2015

Egypt

Researcher :: Oro-Dental Genetics

Education History

Cairo University, faculty of oral and dental medicine

Egypt

MSC :: Oral Radiology

Publications

Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Khalda Sayed Amr, Hala T El-Bassyouni, Sawsan Abdel Hady, Mostafa I Mostafa, Mennat I Mehrez, Domenico A Coviello, Ghada Y El-Kamah
Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease. Genes 12 (10) (2021)
Hoda Abdalla Ahmed, Ghada Y El-Kamah, Eman A Rabie, Mostafa I Mostafa, Maha R Abouzaid, Nehal F Hassib, Mennat I Mehrez, Mohamed A Abdel-Kader, Yasmine H Mohsen, Suher K Zada, Khalda S Amr, Inas S M Sayed
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. Genes 12 (9) (2021)
Hanan H Afifi, Mohamed S Abdel-Hamid, Mennat I Mehrez, Ghada El-Kamah, Ghada M H Abdel-Salam
Lenz-Majewski syndrome in a patient from Egypt. American journal of medical genetics. Part A 179 (10) (2019)

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Publication Activity (10 Years)

Top Topics

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Mennat I Mehrez