Hala Abalkhail

Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease

Faisal A. Al-Allaf, Mohammad Athar, Zainularifeen Abduljaleel et al. · Gene · 2015 · 38 citations

Life Sciences, Genetics, Molecular Genetics +15

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

Muhammad Faiyaz‐Ul‐Haque, Mohammed Al‐Owain, Fouad Al‐Dayel et al. · European Journal of Pediatrics · 2009 · 35 citations

Life Sciences, Genetics, Molecular Genetics +16

Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients

Muhammad Faiyaz‐Ul‐Haque, Bassam Bin‐Abbas, A Al‐Abdullatif et al. · Clinical Genetics · 2009 · 29 citations

Life Sciences, Genetics, Molecular Genetics +15

Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia

Faisal A. Al-Allaf, Mohammad Athar, Zainularifeen Abduljaleel et al. · Human Genome Variation · 2014 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children

Faisal A. Al-Allaf, Abdullah Al‐Ashwal, Zainularifeen Abduljaleel et al. · Genomics · 2015 · 22 citations

Life Sciences, Genetics, Molecular Genetics +16