Hicham Mansour

Benha University — Egypt

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index1.3kcitations73works0.42yr avg
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Research Topics

Metabolism and Genetic Disorders(7), Regulation of Appetite and Obesity(6), Genomics and Rare Diseases(6), Genetics and Neurodevelopmental Disorders(6), Mitochondrial Function and Pathology(5)

Publications73 total

Compound Heterozygous SLC22A5 Pathogenic Variants Presenting with ADHD and Silent Hyperammonemia in a Lebanese Child
SVOA Paediatrics·2025Open Access
Medication Expiration and Stockout Reduction in Moroccan Healthcare: A DMAIC-Driven Optimization of Pharmaceutical Supply Chain at CHU Oujda
2025
Mutational profiling using liquid biopsy to guide targeted therapy in patients with metastatic cancer
Scientific Reports·2025· 1 citedOpen Access
Identification of two previously unreported Duchenne muscular dystrophy gene variants in a patient diagnosed with a dystrophinopathy: a case report
Journal of Medical Case Reports·2025· 1 citedOpen Access
Effect of Instructional Guidelines on Prevention of Dengue Fever among Rural Women
Assiut Scientific Nursing Journal·2025Open Access
Is the development of liquid biopsy for the early detection and the monitoring of breast cancers on its way of overtaking mammography?
Frontiers in Medicine·2024· 1 citedOpen Access
The significance of using liquid biopsy to improve treatment outcomes for metastatic patients
2024Open Access
AARS Novel Homozygous Variant in Two Lebanese Siblings with Isolated Transient Neonatal Axial Hypotonia
SVOA Paediatrics·2024Open Access
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SVOA Paediatrics·2023Open Access
Cox10 Novel Variant in a Lebanese Female Patient with Congenital Cataracts
SVOA Paediatrics·2023Open Access
A Novel Variant of ASL Gene Mutation in a Lebanese Neonate with Severe Argininosuccinic Aciduria Phenotype
SVOA Paediatrics·2023Open Access
A Case of Cardiac Regression in a Lebanese Patient with Duchenne Muscular Dystrophy Following the Discontinuation of Ataluren
SVOA Paediatrics·2023Open Access
Adenovirus-induced Acute Necrotizing Encephalopathy in a Previously Healthy Infant- A case report
International Journal of Integrative Pediatrics and Environmental Medicine·2023Open Access
Novel USP9X Mutation in A Lebanese Patient with Delay and Microcephaly: Case Report and Review of Literature
SVOA Paediatrics·2023Open Access
A Novel PSAP Gene Mutation in A Lebanese Patient with A Limited Phenotypic Expression
SVOA Paediatrics·2023Open Access
First Reported Lebanese Patient with Dihydrolipoamide Dehydrogenase Deficiency
Journal of Rare Diseases and Orphan Drugs·2023Open Access
Supplementary Figure 2 from Leptin Receptor–Related Immune Response in Colorectal Tumors: The Role of Colonocytes and Interleukin-8
2023Open Access
Data from Leptin Receptor–Related Immune Response in Colorectal Tumors: The Role of Colonocytes and Interleukin-8
2023Open Access
Supplementary Figure 1 from Leptin Receptor–Related Immune Response in Colorectal Tumors: The Role of Colonocytes and Interleukin-8
2023Open Access
Data from Leptin Receptor–Related Immune Response in Colorectal Tumors: The Role of Colonocytes and Interleukin-8
2023Open Access
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Frequent Co-authors

Roberto Incitti(8), André Mégarbané(6), Dominique Desvaux(5), Vincent Audard(5), Philippe Lang(5), Philippe Grimbert(5), Michael L. Berumen(5), Iradj Sobhani(4), Valérie Delague(4), Abdelhak Ouhajjou(4), Sandra Sabbagh(4), Stephany El‐Hayek(4), Hugo B. Harrison(4), Geoffrey P. Jones(4), Sabine Le Gouvello(3), Nabiha Salem(3), Sébastien Homs(3), Karine Dahan(3), Nijez Aloulou(3), Marie Thérèse Chaumette(3)