Yusra Alyafee

Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay

Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet et al. · The American Journal of Human Genetics · 2013 · 120 citations

Life Sciences, Genetics, Molecular Genetics +14

Non-invasive prenatal testing for autosomal recessive disorders: A new promising approach

Yusra Alyafee, Abeer Al Tuwaijri, Muhammad Umair et al. · Frontiers in Genetics · 2022 · 47 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Next Generation Sequencing Based Non-invasive Prenatal Testing (NIPT): First Report From Saudi Arabia

Yusra Alyafee, Abeer Al Tuwaijri, Qamre Alam et al. · Frontiers in Genetics · 2021 · 46 citations · Full text

Medicine, Genetics, Obstetrics +17

<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 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia

Yusra Alyafee, Qamre Alam, Abeer Al Tuwaijri et al. · Genes · 2021 · 39 citations · Full text

Veterinary Medicine, Genetics, Molecular Genetics +15