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Clinical, Cosmetic and Investigational Dermatology|June 26, 2024
First Cousin Marriages and the Risk of Childhood-Onset Vitiligo: Exploring the Genetic Background: A Cross-Sectional StudyAmr Molla, Abdulfatah M Alayoubi, Raed Jannadi
Frontiers in Genetics|November 21, 2024
De novo SCN1A missense variant in a patient with Parkinson's diseaseMajed Alluqmani, Abdulfatah M Alayoubi, Jamil A Hashmi, et al.
Journal of Clinical Medicine|April 9, 2024
Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi ArabiaMuhammad Latif, Jamil Amjad Hashmi, Abdulfatah M Alayoubi, et al.
Annals of Hematology|September 22, 2023
CRISPR-Cas9 system: a novel and promising era of genotherapy for beta-hemoglobinopathies, hematological malignancy, and hemophiliaAbdulfatah M Alayoubi, Zakaria Y Khawaji, Mohammed A Mohammed, et al.
Journal of Clinical Medicine|July 27, 2024
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and DystoniaAhmad M Almatrafi, Abdulfatah M Alayoubi, Majed Alluqmani, et al.
Annals of Medicine|January 6, 2025
Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi familiesAbdulfatah M Alayoubi, Ambreen Ijaz, Abdul Wali, et al.
Scientific Reports|October 25, 2024
A homozygous variant in ARHGAP39 is associated with lethal cerebellar vermis hypoplasia in a consanguineous Saudi familyAbdulfatah M Alayoubi, Fatima Alfadhli, Mehnaz, et al.
International Journal of Biological Macromolecules|April 29, 2023
Controlled drug release contenders comprising starch/poly(allylamine hydrochloride) biodegradable composite filmsMuhammad Sohail Sarwar, Abdul Ghaffar, Qingrong Huang, et al.
JIMD Reports|June 27, 2019
Hematopoietic stem cell transplant does not prevent neurological deterioration in infants with Farber disease: Case report and literature reviewCatherine Goudie, Abdulfatah M Alayoubi, Pauline Tibout, et al.
Scientific Reports|March 8, 2024
Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorderAbdulfatah M Alayoubi, Muhammad Iqbal, Hassan Aman, et al.
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