Associated Papers
The role of gene polymorphisms in the occurrence of gastroesophageal reflux disease: A systematic review and meta-analysis of genetic association studies.
Argyrou A et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2026
Current Perspectives in Peripartum Cardiomyopathy.
Goldsmith JG et al.
Reproduction (cambridge, England), 2026
A Narrative Review of the Genetic Architecture of Systemic Hypertension: From Candidate Genes to Biobank-Scale Genome-Wide Association Studies and Sequencing, With Translational Pathways to Precision Care.
Aldhufairi A et al.
Cureus, 2025
Pharmacogenomics in Diabetes: Population-Specific Insights from Colombia.
Hernandez-Paez DA et al.
Journal of Personalized Medicine, 2025
Pharmacogenetics and the Response to Antidepressants in Major Depressive Disorder.
Bertollo AG et al.
Pharmaceuticals (basel, Switzerland), 2025
Alternative Splicing Regulation in Metabolic Disorders.
Kaminska D
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity, 2025
Candidate gene polymorphisms and power athlete status: a meta-analytical approach.
İpekoğlu G et al.
Journal of Physiology and Biochemistry, 2025
Genetic variants of accessory proteins and G proteins in human genetic disease.
Thompson MD et al.
Critical Reviews in Clinical Laboratory Sciences, 2025
Interleukin-1β rs16944 and rs1143627 polymorphisms and risk of developing major depressive disorder: A case-control study among Bangladeshi population.
Toma FM et al.
Plos One, 2025
Influence of genetic polymorphism on sports talent performance versus non-athletes: a systematic review and meta-analysis.
Ferreira CP et al.
Bmc Sports Science, Medicine & Rehabilitation, 2024
Association of the Single Nucleotide Polymorphisms in the Renin-Angiotensin-Aldosterone System with Hypertension in the Uzbek Population.
Zakirova D et al.
Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir, 2024
Genetic Factors Contributing to the Pathogenesis of Essential Hypertension in Two African Populations.
Kalideen K et al.
Journal of Personalized Medicine, 2024
The prevalence and linkage disequilibrium of 21 genetic variations related to thrombophilia, folate cycle, and hypertension in reproductive age women of Rostov region (Russia).
Bordaeva OY et al.
Annals of Human Genetics, 2024
Association of GNB3, ACE polymorphisms with POAG and NTG.
Samoylov AN et al.
Ophthalmic Genetics, 2024
In the context of the triple burden of malnutrition: A systematic review of gene-diet interactions and nutritional status.
Tan PY et al.
Critical Reviews in Food Science and Nutrition, 2024
The single nucleotide polymorphism rs4986790 (c.896A>G) in the gene TLR4 as a protective factor in corona virus disease 2019 (COVID-19).
Zacher C et al.
Frontiers in Immunology, 2024
G Protein Subunit Beta 3 (GNB3) Variant Is Associated with Biochemical Changes in Brazilian Patients with Hypertension.
Agostini LDC et al.
Arquivos Brasileiros De Cardiologia, 2023
Single-Nucleotide Polymorphism in Genes Encoding G Protein Subunits GNB3 and GNAQ Increase the Risk of Cardiovascular Morbidity among Patients Undergoing Renal Replacement Therapy.
Birkner S et al.
International Journal of Molecular Sciences, 2023
Severe systemic adverse reactions to ophthalmic timolol in a CYP2D6 homozygous *4 allele carrier: a case report.
Bollinger A et al.
Pharmacogenomics, 2023
The Progress and Pitfalls of Pharmacogenetics-Based Precision Medicine in Schizophrenia Spectrum Disorders: A Systematic Review and Meta-Analysis.
Teng Y et al.
Journal of Personalized Medicine, 2023
Genetics of migraine: where are we now?
Grangeon L et al.
The Journal of Headache and Pain, 2023
Impact of pharmacogenetics on aspirin resistance: a systematic review.
Silva GFD et al.
Arquivos De Neuro-psiquiatria, 2023
Association polymorphism of guanine nucleotide-binding protein β3 subunit (GNB3) C825T and insertion/deletion of the angiotensin-converting enzyme (ACE) gene with peripartum cardiomyopathy.
Dewi IP et al.
Frontiers in Cardiovascular Medicine, 2023
Precision Medicine in Antidepressants Treatment.
Tsermpini EE et al.
Handbook of Experimental Pharmacology, 2023
The effect of angiotensin converting enzyme gene insertion/deletion polymorphism on anthropometric and biochemical parameters among hypertension patients: A case-control study from Northwest Ethiopia.
Birhan TA et al.
Plos One, 2023
Summary of Known Genetic and Epigenetic Modification Contributed to Hypertension.
Pratamawati TM et al.
International Journal of Hypertension, 2023
The Role of Single-Nucleotide Polymorphisms in Cholangiocarcinoma: A Systematic Review.
Wang G et al.
Cancers, 2022
Association between MTHFR C677T polymorphism and risk of coronary artery disease in the Chinese population: meta-analysis.
Li L et al.
Herz, 2022
CC Genotype of GNAS c.393C>T (rs7121) Polymorphism Has a Protective Effect against Development of BK Viremia and BKV-Associated Nephropathy after Renal Transplant
Peitz T et al.
Pathogens (basel, Switzerland), 2022
Genetics of long-distance runners and road cyclists-A systematic review with meta-analysis.
Konopka MJ et al.
Scandinavian Journal of Medicine & Science in Sports, 2022
GNB3 c.825C>T (rs5443) Polymorphism and Risk of Acute Cardiovascular Events after Renal Allograft Transplant
Peitz T et al.
International Journal of Molecular Sciences, 2022
Genetic polymorphisms in ADRB2 and ADRB1 are associated with differential survival in heart failure patients taking β-blockers.
Guerra LA et al.
The Pharmacogenomics Journal, 2022
Peripartum cardiomyopathy: a global effort to find the cause and cure for the rare and little understood disease.
Li A et al.
Biophysical Reviews, 2022
Sex and Gender Differences in Overlap Syndrome of Functional Gastrointestinal Disorder and Effect of Genetic Polymorphisms in South Korea: A Long-term Follow-up Study.
Lee JY et al.
Journal of Neurogastroenterology and Motility, 2022
Clinical Implication of Genetic Testing in Dilated Cardiomyopathy.
Lee JH et al.
International Journal of Heart Failure, 2022
Pathophysiological Role of Genetic Factors Associated With Gestational Diabetes Mellitus.
Ortega-Contreras B et al.
Frontiers in Physiology, 2022
The GNB3 c.825C>T (rs5443) polymorphism and protection against fatal outcome of corona virus disease 2019 (COVID-19).
Möhlendick B et al.
Frontiers in Genetics, 2022
Outcomes of Genetic Testing-Based Cardiac Rehabilitation Program in Patients with Acute Myocardial Infarction after Percutaneous Coronary Intervention.
Yu X et al.
Cardiology Research and Practice, 2022
GNB3 c.825c>T polymorphism influences T-cell but not antibody response following vaccination with the mRNA-1273 vaccine.
Čiučiulkaitė I et al.
Frontiers in Genetics, 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
Towards Understanding the Genetic Nature of Vasovagal Syncope.
Matveeva N et al.
International Journal of Molecular Sciences, 2021
Meta-analysis of the genetic association between maternal GNB3 C825T polymorphism and risk of pre-eclampsia.
Song J et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics, 2021
Genetic polymorphisms associated with obesity in the Arab world: a systematic review.
Younes S et al.
International Journal of Obesity (2005), 2021
The pharmacogenetics of treatment with olanzapine.
Zubiaur P et al.
Pharmacogenomics, 2021