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Author

Saida Lhousni

Observed name: S., Lhousni
Observed institution: Mohamed I University
ORCID: 0000-0002-4479-3853
Observed ORCID: 0000-0002-4479-3853
OpenAlex ID: A5062191252
Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco
2020 · Saida Lhousni, Fatiha Daoudi, et al. · Biopreservation and Biobanking · 21
Morocco’s First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges
2020 · Saida Lhousni, Karam Yahya Belmokhtar, et al. · BioMed Research International · 18
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Assessment of Knowledge, Attitudes and Support of Health Professionals towards Biobanks in Eastern Morocco
2019 · Saida Lhousni, Redouane Boulouiz, et al. · Open Journal of Epidemiology · 13
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Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis
2023 · Karam Yahya Belmokhtar, Imane Cherkaoui, et al. · Molecular Syndromology · 9
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Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco
2022 · Ihab Belmokhtar, Saida Lhousni, et al. · Molecular Genetics & Genomic Medicine · 8
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
2024 · Manal Elidrissi Errahhali, Mounia Elidrissi Errahhali, et al. · Archives de Pédiatrie · 4
A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias
2023 · Saida Lhousni, Majida Charif, et al. · Bone · 4
Utility of liquid biopsy for EGFR mutation testing in lung adenocarcinoma in a resource-limited setting
2025 · Mounia Elidrissi Errahhali, Karam Yahya Belmokhtar, et al. · LabMed discovery. · 2
Environmental and genetic interactions underlying the morphological and genetic variability of the red juniper (Juniperus turbinata Guss.) in northeastern Morocco: implications for conservation
2025 · Mehdi Boumediene, Chaymae Benkirane, et al. · Scientific African · 2
Clinical and Molecular Spectrum of Wilson Disease in the Arab World: A Systematic Review
2025 · Halima Benzine, Saida Lhousni, et al. · Biochemical Genetics · 2
JAK2 mutational status and the contribution of TERT and JAK2 polymorphisms to the occurrence of myeloproliferative neoplasms in Eastern Morocco
2024 · Karam Yahya Belmokhtar, Mounia Elidrissi Errahhali, et al. · African Health Sciences · 2
Identification of Novel and Known Variants in Epigenetic Genes Associated with Syndromic 46,XY Differences of Sex Development among Moroccan Patients
2026 · Imane Cherkaoui, Saida Lhousni, et al. · Sexual Development · 1
Prevalence of anaemia among blood donors in eastern Morocco: The need for pre‐donation haemoglobin assessment
2025 · Ihab Belmokhtar, Karam Yahya Belmokhtar, et al. · Transfusion Medicine · 1
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Carrier frequency and molecular basis of hemoglobinopathies among blood donors in eastern Morocco: Implications for blood donation and genetic diagnosis
2024 · Ihab Belmokhtar, Karam Yahya Belmokhtar, et al. · Clinical Biochemistry · 1
Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
2026 · Imane Cherkaoui, Saida Lhousni, et al. · Journal of Rare Diseases
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Additional file 1 of Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
2026 · Imane Cherkaoui, Saida Lhousni, et al. · Figshare
Identification of a novel homozygous RAB3GAP1 variant associated with Warburg micro syndrome type 1 in a Moroccan patient and a literature review
2026 · Imane Cherkaoui, Saida Lhousni, et al. · Figshare
Identification of the Genetic Causes of Inherited Diseases in a North African Biobank: Implications for Genetic Diagnosis
2025 · Majida Charif, Saida Lhousni, et al. · Molecular Syndromology
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Supplementary Material for: Triple-A syndrome in Morocco: founder effect, age estimation of the AAAS c.1331+1G>A variant and implications for genetic diagnosis
2023 · K.Y., Belmokhtar, I., Cherkaoui, et al. · Figshare
Works count: 20
Citation count: 88
H-index: 5
I10-index: 3
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