Watfa Al‐Mamari

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits

Maryam Al‐Nabhani, Samiya Al‐Rashdi, Fathiya Al Murshedi et al. · Clinical Genetics · 2018 · 72 citations

Genome-wide Association Study, Intellectual Impairment, Sequencing +15

Revisiting the Prevalence of Autism Spectrum Disorder among Omani Children: A multicentre study

Watfa Al‐Mamari, Ahmed B. Idris, Samar Dakak et al. · Sultan Qaboos University medical journal · 2019 · 66 citations · Full text

THUMPD1 bi-allelic variants cause loss of tRNA acetylation and a syndromic neurodevelopmental disorder

Martin Broly, Bogdan Polevoda, Kamel Awayda et al. · The American Journal of Human Genetics · 2022 · 43 citations · Full text

Trna Acetylation, Developmental Biology, Syndromic Neurodevelopmental Disorder +9

Consanguinity, Endogamy and Inborn Errors of Metabolism in Oman: A Cross-Sectional Study

Khalid Al‐Thihli, Fathiya Al-Murshedi, Nadia Alhashmi et al. · Human Heredity · 2014 · 35 citations

Nutrition, Family Medicine, Metabolic Disorder +22

The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families

Ghalia Al‐Kasbi, Fathiya Al-Murshedi, Adila Al‐Kindi et al. · Scientific Reports · 2022 · 29 citations · Full text