|
| 34797200 | Potential added value of combined DPYD/DPD genotyping and phenotyping to prevent severe toxicity in patients with a variant and decreased dihydropyrimidine dehydrogenase enzyme activity. | Journal of Oncology Pharmacy Practice | 2023 |
| 37587271 | Genome-wide association study on pharmacological outcomes of musculoskeletal pain in UK Biobank. | | 2023 |
| 37988848 | A common germline variant in CYP11B1 is associated with adverse clinical outcome of treatment with abiraterone or enzalutamide. | | 2023 |
| 37551646 | Influence of genetic variants on the pharmacokinetics and pharmacodynamics of sirolimus: a systematic review. | | 2023 |
| 37551203 | Evaluating the Frequencies of , and Variant Alleles and Their Association with L-Asparaginase Hypersensitivity in Pediatric Acute Lymphoblastic Leukemia in Addis Ababa, Ethiopia. | | 2023 |
| 37768317 | Drug interaction potential of high-dose rifampicin in patients with pulmonary tuberculosis. | | 2023 |
| 37155164 | Effectiveness of Genotype-Specific Tricyclic Antidepressant Dosing in Patients With Major Depressive Disorder: A Randomized Clinical Trial. | | 2023 |
| 37144689 | A systematic review of genome-wide association studies for pain, nociception, neuropathy, and pain treatment responses. | | 2023 |
| 37267380 | Incidence and determinants of hematotoxicity in acute lymphoblastic leukemia children who received 6-mercaptopurine based maintenance therapy in Addis Ababa, Ethiopia. | | 2023 |
| 36699085 | Genome-wide analyses of platinum-induced ototoxicity in childhood cancer patients: Results of GO-CAT and United Kingdom MAGIC consortia. | Front Pharmacol | 2023 |
| 37251339 | Genetic variants of genes involved in thiopurine metabolism pathway are associated with 6-mercaptopurine toxicity in pediatric acute lymphoblastic leukemia patients from Ethiopia. | | 2023 |
| 35328824 | Molecular Processes in Stress Urinary Incontinence: A Systematic Review of Human and Animal Studies. | International Journal of Molecular Sciences | 2022 |
| 35396281 | From basic to advanced computerised intravenous to oral switch for paracetamol and antibiotics: an interrupted time series analysis. | BMJ Open | 2022 |
| 35743677 | Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in <i>RBMS3</i> and Acute Kidney Injury. | J Pers Med | 2022 |
| 36438828 | <i>SLC7A8</i> coding for LAT2 is associated with early disease progression in osteosarcoma and transports doxorubicin. | Front Pharmacol | 2022 |
| 36438788 | Editorial: Translation and implementation of pharmacogenomic testing in daily clinical practice: Considering current challenges and future needs. | Frontiers in Pharmacology | 2022 |
| 36446453 | Pain predict genetics: protocol for a prospective observational study of clinical and genetic factors to predict the development of postoperative pain. | BMJ Open | 2022 |
| 36536332 | Pharmacogenetics of chemotherapy treatment response and -toxicities in patients with osteosarcoma: a systematic review. | | 2022 |
| 35151671 | The Potential of Polygenic Risk Scores to Predict Antidepressant Treatment Response in Major Depression: A Systematic Review. | Journal of Affective Disorders | 2022 |
| 35150001 | Contribution of common and rare genetic variants in CEP72 on vincristine-induced peripheral neuropathy in brain tumour patients. | Br J Clin Pharmacol | 2022 |
| 35330732 | Editorial: Pharmacogenomics of Adverse Drug Reactions. | Front Genet | 2022 |
| 34423321 | Association of the neutrophil to lymphocyte ratio and white blood cell count with response to pharmacotherapy in unipolar psychotic depression: An exploratory analysis. | Brain, Behavior, and Immunity - Health | 2021 |
| 34267341 | Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis. | Eur J Hum Genet | 2021 |
| 33993873 | Methodology of the DCCSS later fatigue study: a model to investigate chronic fatigue in long-term survivors of childhood cancer. | BMC Medical Research Methodology | 2021 |
| 34024776 | Ancestral Origin of the First Indian Families with Myotonic Dystrophy Type 2. | Journal of Neuromuscular Diseases | 2021 |
| 33305616 | Pharmacogenetics of inflammatory bowel disease. | Pharmacogenomics | 2021 |
| 32717343 | Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK Consortium. | Ophthalmology | 2021 |
| 34777329 | Validation of GWAS-Identified Variants for Anti-TNF Drug Response in Rheumatoid Arthritis: A Meta-Analysis of Two Large Cohorts. | Frontiers in Immunology | 2021 |
| 32949220 | Genetic variants and expression changes in urgency urinary incontinence: A systematic review. | Neurourology and Urodynamics | 2020 |
| 31895215 | Dosage of 6-Mercaptopurine in Relation to Genetic TPMT and ITPA Variants: Toward Individualized Pediatric Acute Lymphoblastic Leukemia Maintenance Treatment. | Journal of Pediatric Hematology/Oncology | 2020 |
| 32231244 | The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. | Nat Commun | 2020 |
| 32152480 | NFKB2 polymorphisms associate with the risk of developing rheumatoid arthritis and response to TNF inhibitors: Results from the REPAIR consortium. | Scientific Reports | 2020 |
| 32903464 | Analysis of Drug Metabolizing Gene Panel in Osteosarcoma Patients Identifies Association Between Variants in and and Methotrexate Levels and Toxicities. | Frontiers in Pharmacology | 2020 |
| 30994858 | Association of HLA-C*06:02 Status With Differential Response to Ustekinumab in Patients With Psoriasis: A Systematic Review and Meta-analysis. | JAMA Dermatology | 2019 |
| 31616008 | 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. | Scientific Reports | 2019 |
| 32039286 | genotyping in Caucasian patients can help to optimise thiopurine treatment in patients with inflammatory bowel disease. | | 2019 |
| 30510603 | Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time. | Current Therapeutic Research | 2019 |
| 30287909 | Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients. | Pharmacogenomics Journal | 2019 |
| 30760878 | Correction: Polymorphisms at phase I-metabolizing enzyme and hormone receptor loci influence the response to anti-TNF therapy in rheumatoid arthritis patients. | Pharmacogenomics Journal | 2019 |
| 30698675 | Genotype-Guided Thiopurine Dosing Does not Lead to Additional Costs in Patients With Inflammatory Bowel Disease. | | 2019 |
| 30999660 | Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy (The PRONE Study). | Cancers (Basel) | 2019 |
| 28045129 | The glutathione transferase Mu null genotype leads to lower 6-MMPR levels in patients treated with azathioprine but not with mercaptopurine. | Pharmacogenomics Journal | 2018 |
| 28646581 | A systematic review of pharmacogenetic studies on the response to biologics in patients with psoriasis. | British Journal of Dermatology | 2018 |
| 30384381 | Cost-Effectiveness Analysis of Genotype-Guided Treatment Allocation in Patients with Alcohol Use Disorders Using Naltrexone or Acamprosate, Using a Modeling Approach. | European Addiction Research | 2018 |
| 30425331 | Unravelling the pharmacogenomics of TNF inhibition. | Nature reviews. Rheumatology | 2018 |
| 29120908 | Patients' beliefs about medicine are associated with early thiopurine discontinuation in patients with inflammatory bowel diseases. | European Journal of Gastroenterology and Hepatology | 2018 |
| 29844438 | Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus. | Scientific Reports | 2018 |
| 28134327 | IL-32 promoter SNP rs4786370 predisposes to modified lipoprotein profiles in patients with rheumatoid arthritis. | Scientific Reports | 2017 |
| 28692628 | Genetic determinants of impaired awareness of hypoglycemia in type 1 diabetes. | Pharmacogenet Genomics | 2017 |
| 28914446 | Risk factors for thiopurine-induced myelosuppression and infections in inflammatory bowel disease patients with a normal TPMT genotype. | Alimentary Pharmacology and Therapeutics | 2017 |