Associated Papers
Association of MMP9 and NOS3 Polymorphisms with Distinct Clinical Forms of Juvenile Scleroderma and Characteristics of Humoral Immunity.
Osminina M et al.
International Journal of Molecular Sciences, 2026
Exploring IL-10 and NOS3 Genetic Variants as a Risk Factor for Neonatal Respiratory Distress Syndrome and Its Outcome.
Anciuc-Crauciuc M et al.
Diagnostics (basel, Switzerland), 2025
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.
Guo R et al.
Scientific Reports, 2025
NOS3 Gene Polymorphisms (rs2070744 and rs1799983) and Differentiated Thyroid Cancer: Investigating Associations with Clinical Outcomes.
Tiucă RA et al.
International Journal of Molecular Sciences, 2025
Single nucleotide polymorphism-based biomarker in primary hypertension.
Laxmi et al.
European Journal of Pharmacology, 2024
Genetic Factors Contributing to the Pathogenesis of Essential Hypertension in Two African Populations.
Kalideen K et al.
Journal of Personalized Medicine, 2024
Polymorphisms in Innate and Adaptive Immune Genes in Subjects with Allergic Bronchopulmonary Aspergillosis Complicating Asthma.
Kanaujia R et al.
Mycopathologia, 2024
Single Nucleotide Polymorphisms in Coronary Microvascular Dysfunction.
Stein AP et al.
Journal of the American Heart Association, 2024
Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases.
Mhatre I et al.
Scientific Reports, 2023
Male-biased association of endothelial nitric oxide synthase Asp298Glu substitution (NOS3-c.894G/T) with asthma risk and severity.
Aftabi Y et al.
The Journal of Asthma : Official Journal of the Association for the Care of Asthma, 2023
Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families.
Fang Y et al.
Frontiers in Genetics, 2023
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.
Boukhalfa W et al.
Frontiers in Aging Neuroscience, 2023
Genetic Determinants of Cardiovascular Disease: The Endothelial Nitric Oxide Synthase 3 (eNOS3), Krüppel-Like Factor-14 (KLF-14), Methylenetetrahydrofolate Reductase (MTHFR), MiRNAs27a and Their Association with the Predisposition and Susceptibility to Coronary Artery Disease.
Mir R et al.
Life (basel, Switzerland), 2022
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022
Endothelial nitric oxide synthase Asp298Glu (894G/T) gene polymorphism as a possible risk factor for the coronary slow flow phenomenon among Iranians.
Karimi Y et al.
Bmc Cardiovascular Disorders, 2022
Role of Pharmacogenetics in the Treatment of Acute Myeloid Leukemia: Systematic Review and Future Perspectives.
Pinto-Merino Á et al.
Pharmaceutics, 2022
Impact of Variants in the ATIC and ARID5B Genes on Therapeutic Failure with Imatinib in Patients with Chronic Myeloid Leukemia.
Cereja Pantoja KBC et al.
Genes, 2022
Clinical Implication of Genetic Testing in Dilated Cardiomyopathy.
Lee JH et al.
International Journal of Heart Failure, 2022
SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.
Drouet C et al.
Frontiers in Allergy, 2022
Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.
Liu YX et al.
Frontiers in Cardiovascular Medicine, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Variability in oxidative stress-related genes (SOD2, CAT, GPX1, GSTP1, NOS3, NFE2L2, and UCP2) and susceptibility to migraine clinical phenotypes and features.
Papasavva M et al.
Frontiers in Neurology, 2022
Genetic analysis of suicide: a sample study in Tuscany (Central Italy).
Focardi M et al.
Forensic Sciences Research, 2022
Multidisciplinary In-Depth Investigation in a Young Athlete Suffering from Syncope Caused by Myocardial Bridge.
Brancaccio M et al.
Diagnostics (basel, Switzerland), 2021
Genetic variations as molecular diagnostic factors for idiopathic male infertility: current knowledge and future perspectives.
Karimian M et al.
Expert Review of Molecular Diagnostics, 2021
Influence of polymorphisms in anthracyclines metabolism genes in the standard induction chemotherapy of acute myeloid leukemia.
Megías-Vericat JE et al.
Pharmacogenetics and Genomics, 2021
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome.
Jiménez-Jiménez FJ et al.
Frontiers in Pharmacology, 2021
Association of Genes Related to Oxidative Stress with the Extent of Coronary Atherosclerosis.
Racis M et al.
Life (basel, Switzerland), 2020
Dissecting Mechanisms of Melanoma Resistance to BRAF and MEK Inhibitors Revealed Genetic and Non-Genetic Patient- and Drug-Specific Alterations and Remarkable Phenotypic Plasticity.
Hartman ML et al.
Cells, 2020
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
Pediatric Anthracycline-Induced Cardiotoxicity: Mechanisms, Pharmacogenomics, and Pluripotent Stem-Cell Modeling.
Tripaydonis A et al.
Clinical Pharmacology and Therapeutics, 2019
Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population.
Hong EP et al.
Journal of Clinical Medicine, 2019
Genetic Association Study in Multigenerational Kindreds With Vasovagal Syncope: Evidence for Involvement of Sex-Specific Serotonin Signaling.
Sheldon R et al.
Circulation. Arrhythmia and Electrophysiology, 2019
The Associations of PMF1, ICAM1, AGT, TRIM65, FBF1, and ACOX1 Variants With Leukoaraiosis in Chinese Population.
Huang WQ et al.
Frontiers in Genetics, 2019
Polygenic Study of Endurance-Associated Genetic Markers NOS3 (Glu298Asp), BDKRB2 (-9/+9), UCP2 (Ala55Val), AMPD1 (Gln45Ter) and ACE (I/D) in Polish Male Half Marathoners.
Gronek P et al.
Journal of Human Kinetics, 2018
Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians.
Tang D et al.
Scientific Reports, 2018
Challenges imposed by minor reference alleles on the identification and reporting of clinical variants from exome data.
Koko M et al.
Bmc Genomics, 2018
Genetic Risk Factors in Cerebrovascular Disorders and Cognitive Deterioration.
Carril JC et al.
Current Genomics, 2017
Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis.
Azani A et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology, 2017
Functional PTGS2 polymorphism-based models as novel predictive markers in metastatic renal cell carcinoma patients receiving first-line sunitinib.
Cebrián A et al.
Scientific Reports, 2017
Influence of Genetic Risk Factors on Coronary Heart Disease Occurrence in Afro-Caribbeans.
Larifla L et al.
The Canadian Journal of Cardiology, 2016
Identification of candidate genes for familial early-onset essential tremor.
Liu X et al.
European Journal of Human Genetics : Ejhg, 2016
Association of eNOS gene polymorphisms and systemic lupus erythematosus in southeast Iran.
Sandoughi M et al.
International Journal of Rheumatic Diseases, 2016