Heba Hassan

7PUBLICATIONS
35CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Medical biotechnology not elsewhere classifiedDevelopmental genetics (incl. sex determination)
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Publications (7)

|Jul 27, 2026
Further characterization of the BRSK2-associated neurodevelopmental disorder.

|Feb 27, 2026
Novel Homozygous DLX5 and WNT10B Variants Expand the Genetic and Phenotypic Spectrum of Autosomal Recessive Split-Hand/Foot Malformations (SHFM1D and SHFM6).

Heba A Hassan, Asmaa M Esmail, Mervat Elbelbesy

|Feb 16, 2026
Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.

Wessam E Sharaf-Eldin, Nirmeen A Kishk, Noura R Eissa

|Mar 25, 2024
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.

Heba Amin Hassan, Inas Mazen, Aya Elaidy

|Mar 20, 2021
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development.

Inas Mazen, Mona Mekkawy, Alaa Kamel

|Jul 16, 2020
Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I.

Heba Amin Hassan, M L Essawi, M K Mekkawy

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Frequent Collaborators

1 joint publications

Wessam E Sharaf-Eldin

1 joint publications

Nirmeen A Kishk

1 joint publications

Tzung-Chien Hsieh

1 joint publications

Marta Viggiano