Alia M. Albalawi

CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly

Sulman Basit, Khalid M. Al-Harbi, Sabri A. M. Alhijji et al. · Human Genetics · 2016 · 52 citations

Life Sciences, Genetics, Neuroscience +10

Exome sequencing identified rare variants in genes HSPG2 and ATP2B4 in a family segregating developmental dysplasia of the hip

Sulman Basit, Alia M. Albalawi, Essa Alharby et al. · BMC Medical Genetics · 2017 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole genome SNP genotyping in a family segregating developmental dysplasia of the hip detected runs of homozygosity on chromosomes 15q13.3 and 19p13.2

Sulman Basit, Essa Alharby, Alia M. Albalawi et al. · Congenital Anomalies · 2017 · 34 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel homozygous loss-of-function mutations in <i>RP1</i> and <i>RP1L1</i> genes in retinitis pigmentosa patients

Maan Abdullah Albarry, Jamil Amjad Hashmi, Ahdab Qasem Alreheli et al. · Ophthalmic Genetics · 2019 · 23 citations

Medicine, Genetics, Ophthalmology +17

A novel splice-site mutation in the <i>ASPM</i> gene underlies autosomal recessive primary microcephaly

Jamil Amjad Hashmi, Khalid M. Al-Harbi, Khushnooda Ramzan et al. · Annals of Saudi Medicine · 2016 · 22 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16