Hala Abalkhail - Concepedia

Author

Hala Abalkhail

King Faisal Specialist Hospital & Research Centre

Also Known As

H Abalkhail, H Abdullah Abalkhail, H. Abalkhail, Hala A. Abalkhail, Hala Abalkhail

Publications

243

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University Queen's University Umm al-Qura University University Health Network

About

Hala Abalkhail is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	169
2	Epidemiology	3	3	77
3	Public Health	2	2	55
4	Health Sciences	1	1	20
5	Cellular Therapies	1	1	20

Hala Abalkhail

Publications

236

Citations

H-Index

Page 1

	Year	Citations
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, Gene Genome-wide Association StudyEpidemiologyNext GenerationGenetic DeterminantCardiovascular Disease	2015	38
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency Muhammad Faiyaz‐Ul‐Haque, Mohammed Al‐Owain, Fouad Al‐Dayel, European Journal of Pediatrics Genetic DisorderGeneticsInherited Metabolic DiseaseBiochemical GeneticsPathology	2009	35
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, Clinical Genetics	2009	29
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, Human Genome Variation	2014	23
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, Genomics Familial HypercholesterolemiaGenetic DisorderGeneticsCardiovascular GeneticsMolecular Genetics	2015	22
Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria SHE Zaidi, Muhammad Faiyaz‐Ul‐Haque, Taghreed Shuaib, Clinical Genetics Molecular FindingsCbs Gene MutationsDisease MechanismGenetic DisorderSaudi Arabia	2011	21
Chimerism Analysis of Cell-Free DNA in Patients Treated with Hematopoietic Stem Cell Transplantation May Predict Early Relapse in Patients with Hematologic Malignancies Mahmoud Aljurf, Hala Abalkhail, Amal Al-Seraihy, Biotechnology Research International Cell TherapyPathologyDna ChimerismMyeloid NeoplasiaHematological Malignancy	2016	20
Compound heterozygous LDLR variant in severely affected familial hypercholesterolemia patient. Faisal A. Al-Allaf, Abdullah Al‐Ashwal, Zainularifeen Abduljaleel, Acta Biochimica Polonica Family MedicineGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1970	17
A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations Muhammad Faiyaz‐Ul‐Haque, Abdullah Al‐Jefri, Fouad Al‐Dayel, European Journal of Pediatrics Rare DiseasesMendelian DisorderGenetic DisorderGeneticsHematology	2010	16
Detection of mutations in <i><scp>JAK</scp>2</i> exons 12–15 by Sanger sequencing Nahlah AlGhasham, Yasmeen Alnouri, Hala Abalkhail, International Journal of Laboratory Hematology	2015	15

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