195 results on '"Al-Ali, Amein K."'
Search Results
2. Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts
3. Oral microbiota analyses of paediatric Saudi population reveals signatures of dental caries
4. Gut microbiota analyses of inflammatory bowel diseases from a representative Saudi population
5. Whole‐exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk
6. Elevated plasma level of the glycolysis byproduct methylglyoxal on admission is an independent biomarker of mortality in ICU COVID-19 patients
7. Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci
8. Gut microbiota analyses of Saudi populations for type 2 diabetes-related phenotypes reveals significant association
9. Evaluating the molecular diagnostic yield of joint genotyping–based approach for detecting rare germline pathogenic and putative loss-of-function variants
10. The role of MicroRNA as a potential diagnostic and prognostic biomarker for cerebral aneurysms
11. Family-base rare variant association analysis in Saudi Arabian hydrocephalus subjects using whole exome sequencing
12. Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls
13. Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients
14. A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population
15. Comparative and molecular analysis of MRSA isolates from infection sites and carrier colonization sites
16. Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype
17. Reply to the Letter to the Editor: “It is urgent to evaluate the efficacy and safety of genotype guided antiplatelet therapy in patients after percutaneous coronary intervention in East Asian”
18. Elevated Plasma Level of the Glycolysis Byproduct Methylglyoxal on Admission Is an Independent Biomarker of Mortality in ICU COVID-19 Patients
19. Bedside testing of CYP2C19 vs. conventional clopidogrel treatment to guide antiplatelet therapy in ST-segment elevation myocardial infarction patients
20. Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia
21. Prevalence of CYP2C19*2 carriers in Saudi ischemic stroke patients and the suitability of using genotyping to guide antiplatelet therapy in a university hospital setup
22. Exome sequencing in high and low fetal haemoglobin Arab–Indian haplotype sickle cell disease
23. Early detection of SARS‐CoV‐2 and other infections in solid organ transplant recipients and household members using wearable devices
24. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign
25. Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features
26. Molecular bases of β-thalassemia in the Eastern Province of Saudi Arabia
27. Detection of Pathogenic Variants With Germline Genetic Testing Using Deep Learning vs Standard Methods in Patients With Prostate Cancer and Melanoma
28. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0 thalassemia
29. Prevalence of CYP2C19*2 carriers in Saudi ischemic stroke patients and the suitability of using genotyping to guide antiplatelet therapy in a university hospital setup.
30. Adeno-Associated Viral Transfer of Glyoxalase-1 Blunts Carbonyl and Oxidative Stresses in Hearts of Type 1 Diabetic Rats
31. Bedside testing of CYP2C19 gene for treatment of patients with PCI with antiplatelet therapy
32. Prevalence and Diversity of Haplotypes of Sickle Cell Disease in the Eastern Province of Saudi Arabia
33. Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA2 in β-thalassaemia carriers.
34. Design and Implementation of the International Genetics and Translational Research in Transplantation Network
35. Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients
36. Exome sequencing of Saudi Arabian patients with ADPKD
37. Prevalence of CYP2C19*2carriers in Saudi ischemic stroke patients and the suitability of using genotyping to guide antiplatelet therapy in a university hospital setup
38. Assessment of low vitamin D among Saudi Arabians
39. Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia
40. Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT)
41. KLF1 gene and borderline hemoglobin A2 in Saudi population
42. Variants of ZBTB7A (LRF) and its β-Globin Gene Cluster Binding Motifs in Sickle Cell Anemia: —ZBTB7A and Sickle Cell Anemia
43. A phased SNP-based classification of sickle cell anemia HBB haplotypes
44. Association of MBL2 Gene Polymorphism with Dental Caries in Saudi Children
45. A candidate transacting modulator of fetal hemoglobin gene expression in the Arab-Indian haplotype of sickle cell anemia
46. Homozygosity for a haplotype in theHBG2-OR51B4region is exclusive to Arab-Indian haplotype sickle cell anemia
47. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies
48. Hemoglobin A2 (HbA2) has a measure of unreliability in diagnosing β-thalassemia trait (β-TT).
49. The -α3.7 deletion in α-globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population.
50. gene and borderline hemoglobin A2 in Saudi population.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.