Hala Abalkhail

King Faisal Specialist Hospital & Research Centre — Saudi Arabia

Medicine · Health Sciences

10h-index243citations18works0.02yr avg
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Research Topics

Acute Myeloid Leukemia Research(5), Lipoproteins and Cardiovascular Health(4), Chronic Myeloid Leukemia Treatments(3), Cancer Genomics and Diagnostics(3), Hematopoietic Stem Cell Transplantation(2)

Publications18 total

Chimerism Analysis of Cell-Free DNA in Patients Treated with Hematopoietic Stem Cell Transplantation May Predict Early Relapse in Patients with Hematologic Malignancies
Biotechnology Research International·2016· 20 citedOpen Access
Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs*33)) causing familial hypercholesterolemia in Saudi Arab homozygous children
Genomics·2015· 22 cited
Detection of mutations in <i><scp>JAK</scp>2</i> exons 12–15 by Sanger sequencing
International Journal of Laboratory Hematology·2015· 15 citedOpen Access
Next generation sequencing to identify novel genetic variants causative of autosomal dominant familial hypercholesterolemia associated with increased risk of coronary heart disease
Gene·2015· 38 cited
Identification of a novel nonsense variant c.1332dup, p.(D445*) in the LDLR gene that causes familial hypercholesterolemia
Human Genome Variation·2014· 23 citedOpen Access
Donor-derived extramedullary acute promyelocytic leukemia post kidney transplant
Annals of Hematology·2014· 5 cited
Noval Mutation in Four Saudi Families with Glanzmann Thrombasthenia
Blood·2011· 1 cited
Clinical Relevance of IDH1 and IDH2 Mutations and Single Nucleotide Polymorphism (SNP) rs11554137 in Patients with Acute Myeloid Leukemia Treated with Stem Cell Transplant in First Complete Remission
Blood·2011
The AG Genotype of the Wilms Tumor-1 rs16754 SNP Is Associated with Poor Outcome in Pediatric AML Patients Treated with Stem Cell Transplantation but Not in Adults
Blood·2011· 1 cited
Chimerism Analysis of Free Circulating DNA in the Prediction of Relapse in Patients with Acute Leukemia Treated with Stem Cell Transplantation,
Blood·2011
FLT3 Internal Tandem Duplication and Kinase Domain Mutations Remain Poor Prognostic Markers in Intermediate Cytogenetic AML After Treatment with Transplant in First Remission
Blood·2011
Most Risk-Stratification Molecular Markers in Acute Myeloid Leukemia (AML) Are Rarely Found in Early Childhood AML in the Middle Eastern Population
Blood·2011
CEBPA Single Nucleotide Polymorphism (SNP) rs34529039 As An Independent Adverse Prognostic Factor in Acute Myeloid Leukemia Treated with Allogeneic Hematopoietic Stem Cell Transplantation
Blood·2011
Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria
Clinical Genetics·2011· 21 cited
A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations
European Journal of Pediatrics·2010· 16 cited
Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
Clinical Genetics·2009· 29 cited
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency
European Journal of Pediatrics·2009· 35 cited
Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient.
Acta Biochimica Polonica·1970· 17 citedOpen Access

Frequent Co-authors

Mahmoud Aljurf(7), Claudia Walter(7), Naeem Chaudhri(7), Fahed Almhareb(6), Maher Albitar(6), Abdullah Al‐Jefri(5), Faisal A. Al-Allaf(4), Mohammad Athar(4), Zainularifeen Abduljaleel(4), Mohiuddin M. Taher(4), Abdullah Al‐Ashwal(4), Muhammad Faiyaz‐Ul‐Haque(4), Iskra Peltekova(4), Amal Al-Seraihy(4), Said Mohamed(4), Mouhab Ayas(4), Fahad Alsharif(4), Ali Alahmari(4), Asim Belgaumi(4), Hassan El‐Solh(4)