Spectrum of genetic variants in bilateral sensorineural hearing lossAmanat Ali, Hiba Alblooshi, Mohammed Tabouni et al.|Frontiers in Genetics|2024Cited by 8
Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrumPraseetha Kizhakkedath, Hiba Alblooshi, Watfa AlDhaheri et al.|Frontiers in Genetics|2023Cited by 5
Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational analysisFeda E. Mohamed, Fatma Al‐Jasmi, Mohammad A. Ghattas et al.|Frontiers in Pediatrics|2023Cited by 4
A novel LACC1 variant c.658G>A (p. Asp220Asn) in familial juvenile arthritis: identification and functional analysisHiba Alblooshi, Najla Aljaberi|Human Genomics|2025Cited by 4
Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health recordsNadia Akawi, Fatma Al Jasmi, Ghadeera Al Mansoori et al.|Frontiers in Molecular Biosciences|2024Cited by 3