1. BRCA mutation screening and patterns among high-risk Lebanese subjects
    Chantal Farra et al, 2019, Hered Cancer Clin Pract CrossRef
  2. Characterization of BRCA1 and BRCA2 genetic variants in a cohort of Bahraini breast cancer patients using next‐generation sequencing
    Fatima Al Hannan et al, 2019, Mol Genet Genomic Med CrossRef
  3. Genetics and genomic medicine in Morocco: the present hope can make the future bright
    Khadija Belhassan et al, 2016, Mol Genet Genomic Med CrossRef
  4. High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast–ovarian cancer prevention and control
    Fatima-Zahra Laarabi et al, 2017, BMC Res Notes CrossRef
  5. Applications of Next Generation Sequencing to the Analysis of Familial Breast/Ovarian Cancer
    Veronica Zelli et al, 2020, High-Throughput CrossRef
  6. Teaching Pedigree Analysis and Risk Calculation for Diagnosis Purposes of Genetic Disease
    Noureddine Kerzazi et al, 2020 CrossRef
  7. Screening of BRCA1 and BRCA2 germline mutations in unselected triple‐negative breast cancer patients: A series from north of Morocco
    Mohammed Mansouri et al, 2020, Precision Medical Sciences CrossRef
  8. Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC)
    Fatima Zahra El Ansari et al, 2020, BMC Cancer CrossRef
  9. Contribution of BRCA1 and BRCA2 germline mutations to early onset breast cancer: a series from north of Morocco
    Joaira Bakkach et al, 2020, BMC Cancer CrossRef
  10. Tracing Ovarian Cancer Research in Morocco: A Bibliometric Analysis
    Khalid El Bairi et al, 2021, Gynecologic Oncology Reports CrossRef
  11. Prevalence of specific and recurrent/founder pathogenic variants in BRCA genes in breast and ovarian cancer in North Africa
    Oubaida ElBiad et al, 2022, BMC Cancer CrossRef
  12. A BRCA1 Splice Site Variant Responsible for Familial Ovarian Cancer in a Han-Chinese Family
    Peng-zhi Hu et al, 2022, CURR MED SCI CrossRef
  13. Prevalence of Clinically Relevant Germline BRCA Variants in a Large Unselected South African Breast and Ovarian Cancer Cohort: A Public Sector Experience
    Nerina C. Van der Merwe et al, 2022, Front. Genet. CrossRef
  14. Mutational spectrum of BRCA1/2 genes in Moroccan patients with hereditary breast and/or ovarian cancer, and review of BRCA mutations in the MENA region
    Siham Chafai Elalaoui et al, 2022, Breast Cancer Res Treat CrossRef
  15. Targeted Sequencing of Germline Breast Cancer Susceptibility Genes for Discovering Pathogenic/Likely Pathogenic Variants in the Jakarta Population
    Sonar Soni Panigoro et al, 2022, Diagnostics CrossRef
  16. The impact of consanguinity on human health and disease with an emphasis on rare diseases
    G. Temaj et al, 2022, J Rare Dis CrossRef
  17. Increased prevalence of the founder BRCA1 c.5309G>T and recurrent BRCA2 c.1310_1313delAAGA mutations in breast cancer families from Northerstern region of Morocco: evidence of geographical specificity and high relevance for genetic counseling
    Rahma Melki et al, 2023, BMC Cancer CrossRef
  18. Genetics of Breast Cancer Among Moroccan Women: a Literature Review
    Chaimaa Mounjid et al, 2022, JMSR CrossRef