Lamia Alsubaie

Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency

Musa Alharbi, Nahla Ali Mobark, Latifa AlMubarak et al. · The Oncologist · 2018 · 69 citations · Full text

Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders

Elizabeth J. Leslie, James O’Sullivan, Michael L. Cunningham et al. · American Journal of Medical Genetics Part A · 2015 · 49 citations · Full text

<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