Mohammed Bellaoui - Publications

JAK2 mutational status and the contribution of TERT and JAK2 polymorphisms to the occurrence of myeloproliferative neoplasms in Eastern Morocco.

Journal: African health sciences

Published: August 08, 2025

Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan Patients.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation

Published: June 17, 2025

Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic Diagnosis.

Journal: Molecular syndromology

Published: April 08, 2025

Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic Review.

Journal: Biochemical genetics

Published: September 14, 2024

Prevalence of anaemia among blood donors in eastern Morocco: The need for pre-donation haemoglobin assessment.

Journal: Transfusion medicine (Oxford, England)

Published: September 02, 2024

Carrier frequency and molecular basis of hemoglobinopathies among blood donors in eastern Morocco: Implications for blood donation and genetic diagnosis.

Journal: Clinical biochemistry

Published: August 12, 2024

Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis.

Journal: Molecular syndromology

Published: June 19, 2023

A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias.

Journal: Bone

Published: June 05, 2023

First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: April 06, 2023

Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: February 17, 2023

New N-Alkylated Heterocyclic Compounds as Prospective NDM1 Inhibitors: Investigation of In Vitro and In Silico Properties.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: February 18, 2022

Molecular heterogeneity of β-thalassemia variants in the Eastern region of Morocco.

Journal: Molecular genetics & genomic medicine

Published: November 29, 2021