Nehal Hassib

6PUBLICATIONS
14CO-AUTHORS
Cellular nervous systemMajor global burdens of diseaseGene mappingMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Sep 26, 2023
A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management.

Rasha M Elhossini, Inas M Sayed, Usama Saad Hellal

|Jun 24, 2022
Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.

Eman A Rabie, Inas S M Sayed, Khalda Amr

|Mar 12, 2022
Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum.

Ghada A Otaify, Mohamed S Abdel-Hamid, Nehal F Hassib

|Dec 13, 2021
Oro-dental features in Egyptian patients with familial mediterranean fever.

Maha Abouzaid, Nehal Hassib, Khaled Hamed

|Sep 28, 2021
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.

Hoda A Ahmed, Ghada Y El-Kamah, Eman Rabie

|Oct 27, 2019
Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.

Asia Parveen, Sher Alam Khan, Muhammad Usman Mirza

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Frequent Collaborators

2 joint publications

Eman Rabie

2 joint publications

Rasha M Elhossini

2 joint publications

Mohamed S Abdel-Hamid

1 joint publications

Asia Parveen