Taghrid Aloraini

Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing

Ahmed Alfares, Taghrid Aloraini, Lamia Al subaie et al. · Genetics in Medicine · 2018 · 167 citations · Full text

Long-read Sequencing, Sequencing, Whole-exome Sequencing +9

<scp><i>EMC10</i></scp> homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay

Muhammad Umair, Mariam Ballow, Abdulaziz Asiri et al. · Clinical Genetics · 2020 · 39 citations · Full text

Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

William L. Macken, Annie Godwin, Gabrielle Wheway et al. · Genome Medicine · 2021 · 37 citations · Full text

Common disease-associated gene variants in a Saudi Arabian population

Mariam M. AlEissa, Taghrid Aloraini, Lamia Alsubaie et al. · Annals of Saudi Medicine · 2022 · 28 citations · Full text

What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations

Ahmed Alfares, Lamia Alsubaie, Taghrid Aloraini et al. · BMC Medical Genomics · 2020 · 17 citations · Full text