Associated Papers
Sustained HIV-1 remission after heterozygous CCR5Δ32 stem cell transplantation.
Gaebler C et al.
Nature, 2026
Linking p53 rs1042522 Variant to Thyroid Cancer Risk: Insights from a Comprehensive Meta-Analysis of 2116 Cases.
Vakili-Ojarood M et al.
Cancer Investigation, 2026
Genetic analysis of two bladder exstrophy populations of South Asian and North American origin.
Weaver JK et al.
Journal of Pediatric Urology, 2025
Decoding the Impact of Genetic Polymorphisms in Xenobiotic Metabolizing Enzymes and Ovarian Cancer: A Comprehensive Review.
Sistla HC et al.
Environmental and Molecular Mutagenesis, 2025
Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS.
Abner E et al.
Nature Communications, 2025
Contrastive sequence signatures between the both sides of a recombination spot reveal an adaptation at PPARD locus from standing variation for pleiotropy since out-of-Africa dispersal.
Shou W et al.
Bmc Genomics, 2025
Pon1 and Sult1a1 Polymorphisms and Breast Cancer Among Young Women in Brazil.
da Costa RSS et al.
Journal of Adolescent and Young Adult Oncology, 2025
Impact of single nucleotide variants in estrogen genes on ovarian cancer risk: a systematic review and meta-analysis.
Aguiar MP et al.
Endocrine Oncology (bristol, England), 2025
Investigating the effects of cysteine-118 oxidation on G12D KRas structure and dynamics: insights from MD simulations.
Salamh S et al.
Journal of Biomolecular Structure & Dynamics, 2024
Genomic alterations in ovarian endometriosis and subsequently diagnosed ovarian carcinoma.
Linder A et al.
Human Reproduction (oxford, England), 2024
Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.
Zhang T et al.
Peerj, 2024
Meta-Analysis of 49 SNPs Covering 25,446 Cases and 41,106 Controls Identifies Polymorphisms in Hormone Regulation and DNA Repair Genes Associated with Increased Endometrial Cancer Risk.
Das AP et al.
Genes, 2023
Identifying polymorphic cis-regulatory variants as risk markers for lung carcinogenesis and chemotherapy responses in tobacco smokers from eastern India.
Sengupta D et al.
Scientific Reports, 2023
Probing the substrate binding modes and catalytic mechanisms of BLEG-1, a promiscuous B3 metallo-β-lactamase with glyoxalase II properties.
Au SX et al.
Plos One, 2023
Pharmacogenetics of human sulfotransferases and impact of amino acid exchange on Phase II drug metabolism.
Isvoran A et al.
Drug Discovery Today, 2022
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.
Hakkaart C et al.
Communications Biology, 2022
Predictive role of polymorphic variants of phase II drug metabolising enzyme in modulating toxicity in North Indian lung cancer patients undergoing chemotherapy.
Walia H et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems, 2022
SLC4A4, FRAS1, and SULT1A1 Genetic Variations Associated With Dabigatran Metabolism in a Healthy Chinese Population.
Xie Q et al.
Frontiers in Genetics, 2022
Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing.
Silgado-Guzmán DF et al.
Frontiers in Pharmacology, 2022
Pediatric Gliosarcoma With and Without Neurofibromatosis Type 1: A Whole-exome Comparison of 2 Patients.
Graham RT et al.
Journal of Pediatric Hematology/oncology, 2021
Genetic polymorphism of Arg213His variant in the SULT1A1 gene is associated with reduced susceptibility to lung cancer in North Indian population.
Walia HK et al.
Xenobiotica; the Fate of Foreign Compounds in Biological Systems, 2021
Peculiarities of Immune Regulation in Men of Perm Region with Atherosclerosis Related to Polymorphism of Candidate Genes.
Nikonoshina NA et al.
Bulletin of Experimental Biology and Medicine, 2021
Discovery of breast cancer risk genes and establishment of a prediction model based on estrogen metabolism regulation.
Zhao F et al.
Bmc Cancer, 2021
Pharmacogenetics of Direct Oral Anticoagulants: A Systematic Review.
Raymond J et al.
Journal of Personalized Medicine, 2021
Influence of SULT1A1*2 Polymorphism on Plasma Efavirenz Concentration in Thai HIV-1 Patients.
Chamnanphon M et al.
Pharmacogenomics and Personalized Medicine, 2021
Umbrella Review on Associations Between Single Nucleotide Polymorphisms and Lung Cancer Risk.
Li X et al.
Frontiers in Molecular Biosciences, 2021
Preliminary Pharmacogenomic-Based Predictive Models of Tamoxifen Response in Hormone-dependent Chilean Breast Cancer Patients.
Miranda C et al.
Frontiers in Pharmacology, 2021
Redundant meta-analyses are common in genetic epidemiology.
Sigurdson MK et al.
Journal of Clinical Epidemiology, 2020
Role of Genetic Variations in the Hepatic Handling of Drugs.
Marin JJG et al.
International Journal of Molecular Sciences, 2020
Cumulative Evidence for Associations between Genetic Variants and Risk of Esophageal Cancer.
Li G et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2020
Pharmacogene Variation in Thai Plasmodium vivax Relapse Patients Treated with a Combination of Primaquine and Chloroquine.
Chamnanphon M et al.
Pharmacogenomics and Personalized Medicine, 2020
Association of NAD (P) H Quinine Oxidoreductase 1 rs1800566 Polymorphism with Bladder and Prostate Cancers - a Systematic Review and Meta-Analysis.
Abedinzadeh M et al.
Klinicka Onkologie : Casopis Ceske a Slovenske Onkologicke Spolecnosti, 2020
Structural and Dynamic Characterizations Highlight the Deleterious Role of SULT1A1 R213H Polymorphism in Substrate Binding.
Dash R et al.
International Journal of Molecular Sciences, 2019
Steroid hormone-related polymorphisms associate with the development of bone erosions in rheumatoid arthritis and help to predict disease progression: Results from the REPAIR consortium.
Sánchez-Maldonado JM et al.
Scientific Reports, 2019
Adenomyosis: genetics of estrogen metabolism.
Artymuk N et al.
Hormone Molecular Biology and Clinical Investigation, 2019
Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients.
Canet LM et al.
The Pharmacogenomics Journal, 2019
Systematic Review of Genetic Factors in the Etiology of Esophageal Squamous Cell Carcinoma in African Populations.
Simba H et al.
Frontiers in Genetics, 2019
Population genetic difference of pharmacogenomic VIP gene variants in the Lisu population from Yunnan Province.
Zhang C et al.
Medicine, 2018
Association of Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism with Recurrent Pregnancy Loss: a Meta-Analysis of 26 Case-Control Studies.
Aslbahar F et al.
Revista Brasileira De Ginecologia E Obstetricia : Revista Da Federacao Brasileira Das Sociedades De Ginecologia E Obstetricia, 2018
Impact of Occupational Exposures and Genetic Polymorphisms on Recurrence and Progression of Non-Muscle-Invasive Bladder Cancer.
Carta A et al.
International Journal of Environmental Research and Public Health, 2018
Multi-ethnic SULT1A1 copy number profiling with multiplex ligation-dependent probe amplification.
Vijzelaar R et al.
Pharmacogenomics, 2018
The Interaction of Smoking with Gene Polymorphisms on Four Digestive Cancers: A Systematic Review and Meta-Analysis.
Du L et al.
Journal of Cancer, 2018
Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.
Zakerska-Banaszak O et al.
Scientific Reports, 2017
The significance of polymorphism and expression of oestrogen metabolism-related genes in Chinese women with premature ovarian insufficiency.
Qin C et al.
Reproductive Biomedicine Online, 2017
Association between SULT1A1 Arg213His (rs9282861) Polymorphism and Risk of Breast Cancer: A Systematic Review and Meta-Analysis.
Forat-Yazdi M et al.
Journal of Research in Health Sciences, 2017
Methyleugenol DNA adducts in human liver are associated with SULT1A1 copy number variations and expression levels.
Tremmel R et al.
Archives of Toxicology, 2017