Sulman Basit
44PUBLICATIONS
52CO-AUTHORS
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Publications (44)
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|Jan 06, 2025
Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi families.Abdulfatah M Alayoubi, Ambreen Ijaz, Abdul Wali
|Jan 02, 2025
Biallelic Variant in the AGXT Gene in a Family Segregating Primary Hyperoxaluria; Accurate Genetic Diagnosis and Carrier Detection.Jamil A Hashmi, Sibtan Afzal, Reham M Balahmar
|Jul 27, 2024
Exome Sequence Analysis to Characterize Undiagnosed Family Segregating Motor Impairment and Dystonia.Ahmad M Almatrafi, Abdulfatah M Alayoubi, Majed Alluqmani
|Apr 27, 2024
Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women.Ahmed M Almatrafi, Ali M Hibshi, Sulman Basit
|Apr 09, 2024
Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia.Muhammad Latif, Jamil Amjad Hashmi, Abdulfatah M Alayoubi
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Frequent Collaborators
7 joint publications
Wasim Ahmad
5 joint publications
Ahmed M Almatrafi
3 joint publications
Asmat Ullah
2 joint publications
Muhammad Latif
2 joint publications
Abdulfatah M Alayoubi
2 joint publications
Naveed Wasif
2 joint publications
Shaheen Shahzad
2 joint publications
Majed M Alluqmani
2 joint publications
Abdul Nasir
2 joint publications
Jamil A Hashmi
