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Journal of Genetic Counseling|June 25, 2020
The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle EastKhalsa Al-Kharusi, Zandre Bruwer, Tina-Marié WesselsOman Medical Journal|May 11, 2016
Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 DiseasePatrick Scott, Zandre Bruwer, Khalsa Al-Kharusi, et al.Genetics in Medicine Open|December 23, 2024
Genetic counseling development and milestone in OmanKhalsa Al-Kharusi, Chantel Van Wyk, Mariya Al Hinai, et al.European Journal of Medical Genetics|November 5, 2021
Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesisBushra Al-Shamsi, Ghalia Al-Kasbi, Adila Al-Kindi, et al.Neurosciences (Riyadh, Saudi Arabia)|April 5, 2012
Trinucleotide repeat analysis of spinocerebellar ataxia patients in OmanJacob P Chacko, Shanmugakonar Muralitharan, Alia Al-Ansari, et al.Clinical Genetics|November 16, 2020
Deficiency of acyl-CoA synthetase 5 is associated with a severe and treatable failure to thrive of neonatal onsetKhalid Al-Thihli, Cassian Afting, Nadia Al-Hashmi, et al.Journal of Perinatal Medicine|August 20, 2017
Inborn errors of metabolism in a cohort of pregnancies with non-immune hydrops fetalis: a single center experienceZandrè Bruwer, Nihal Al Riyami, Tamima Al Dughaishi, et al.Pediatric Hematology and Oncology|September 17, 2005
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemiaZakia Al-Lamki, Yasser A Wali, Shah M Wasifuddin, et al.Scientific Reports|November 7, 2022
The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern familiesGhalia Al-Kasbi, Fathiya Al-Murshedi, Adila Al-Kindi, et al.Journal of Community Genetics|February 18, 2022
Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year periodZandré Bruwer, Salwa Al Ubaidani, Khalsa Al Kharusi, et al.Pageof 1