Pharmacogenetics and Genomics

Papers
(The median citation count of Pharmacogenetics and Genomics is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Impact of UGT1A4 and UGT2B7 polymorphisms on lamotrigine plasma concentration in patients with bipolar disorder85
Body weight changes and bipolar disorder: a molecular pathway analysis11
Clozapine metabolism may be affected by Gilbert’s syndrome: case report and discussion11
Association of ATP8B3 gene polymorphisms with aspirin-exacerbated respiratory disease in asthmatics10
Psychotropic prescribing rates and pharmacogenomic testing implications for autism in the Canadian primary care sentinel surveillance network9
Genome-wide DNA methylation profile of peripheral blood lymphocytes from subjects with nonsteroidal anti-inflammatory drug-induced respiratory diseases7
Attitudes on pharmacogenomic results as secondary findings among medical geneticists7
Effect of CYP3A4*22, CYP3A5*3 and POR*28 genetic polymorphisms on calcineurin inhibitors dose requirements in early phase renal transplant patients6
Attempted replication of pharmacogenetic association of variants in PPP1R14C and CCDC148 with aromatase inhibitor-induced musculoskeletal symptoms6
Contribution of APOA5, APOC3, CETP, ABCA1 and SIK3 genetic variants to hypertriglyceridemia development in Mexican HIV-patients receiving antiretroviral therapy6
MEG3 in hematologic malignancies: from the role of disease biomarker to therapeutic target6
Pharmacogenetic study in gastric cancer patients treated with adjuvant fluorouracil/leucovorin or epirubicin/cisplatin/fluorouracil before and after chemoradiation on CALGB 80101 (Alliance)6
PharmGKB summary: heparin-induced thrombocytopenia pathway, adverse drug reaction6
Real-world pharmacogenetics of statin intolerance: effects of SLCO1B1, ABCG2, and CYP2C9 variants5
Association between opioid and dopamine receptor gene polymorphisms OPRM1rs1799971, DAT VNTR9-10 repeat allele, DRD1 rs4532 and DRD2 rs1799732 and alcohol dependence: an ethnicity oriented meta-analys5
Evaluation of ADRB2 and OATP2A1 genetic polymorphisms in Indian patients with primary open-angle glaucoma5
Development of an ARMS multiplex real-time PCR assay for the detection of HLA-B*13:01 genotype by detecting highly specific SNPs4
Pharmacogenetic study of methadone treatment for heroin addiction: associations between drug-metabolizing gene polymorphisms and treatment efficacy4
Effect of CYP2C19 genetic variants on bleeding and major adverse cardiovascular events in a cohort of Arab patients undergoing percutaneous coronary intervention and stent implantation4
Cytochrome P4503A4 gene polymorphisms guide safe sufentanil analgesic doses in pregnant Chinese mothers: a multicenter, randomized, prospective study4
Healthcare provider and patient perspectives on the implementation of pharmacogenetic-guided treatment in routine clinical practice4
Establishing national reference materials for genetic testing of cytochrome P4504
Effects of CYP2C19, CYP2C9 and CYP3A4 gene polymorphisms on plasma voriconazole levels in Chinese pediatric patients4
Differential distribution of NAT2 polymorphisms and NAT2 acetylator phenotypes among indigenous populations of the Brazilian Amazon4
Pregnane X receptor gene variant rs7643645 and total mortality in subjects with nonalcoholic fatty liver disease4
N-acetyltransferase 2 haplotype modifies risks for both dyslipidemia and urinary bladder cancer4
Novel variant in Nudix hydrolase 15 gene influences 6-mercaptopurine toxicity in childhood acute lymphoblastic leukemia patients3
Pan-cancer single-cell landscape of drug-metabolizing enzyme genes3
Pharmacogenomic allele coverage of genome-wide genotyping arrays: a comparative analysis2
The reduced function allele SLCO1B1 c.521T>C is of no practical relevance for the renal graft function over the first post-transplant year in patients treated with mycophenolic acid2
Genetic polymorphisms effect on cyclophosphamide’s tolerability and clinical efficacy in Egyptian patients with lupus nephritis2
PharmGKB summary: acyclovir/ganciclovir pathway2
Investigation of pharmacologic interactions between omeprazole and tacrolimus in a membranous nephropathy patient with CYP3A5 nonexpresser: a case report2
Proposals for a standardized procedure of validation of DNA extraction and allelic discrimination assays in pharmacogenomics according to ISO15189 requirements2
Pharmacogenomics and major depressive disorder: time to take a stance?2
Diversity of oncopharmacogenetic profile within Spanish population2
Comparative performance of pharmacogenetics-based warfarin dosing algorithms in Chinese population: use of a pharmacokinetic/pharmacodynamic model to explore dosing regimen through clinical trial simu2
Philadelphia chromosome-positive or Philadelphia chromosome-like B-cell precursor acute lymphoblastic leukemia with multilineage involvement in pediatric patients: a report of two cases and literature2
Histone acetylation at the sulfotransferase 1a1 gene is associated with its hepatic expression in normal aging2
Influence of CYP2B6 and CYP3A4 polymorphisms on the virologic and immunologic responses of patients treated with efavirenz-containing regimen2
Pharmacogenetic interactions of efavirenz or rifampin and isoniazid with levonorgestrel emergency contraception during treatment of HIV or tuberculosis2
Prevalence of CYP2D6 structural variation in large retrospective study2
Proximal tubular dysfunction related to tenofovir in people living with HIV/AIDS: a pharmacogenetic study2
Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stabi2
Association of ADH1B and ALDH2 genotypes with the risk of lung adenocarcinoma2
Sulfamethoxazole-trimethoprim-induced liver injury and genetic polymorphisms of NAT2 and CYP2C9 in Taiwan2
The Pharmacogenomics Global Research Network Implementation Working Group: global collaboration to advance pharmacogenetic implementation2
Pharmacogenetics to prevent hypersensitivity reactions to antiepileptic drugs: is testing performed when indicated?1
The c.415C>T polymorphism in NUDT15 is more frequent than the polymorphisms in TPMT in Chilean patients who use thiopurine drugs1
Unraveling the genetic link: an umbrella review on HLA-B*15:02 and antiepileptic drug-induced Stevens–Johnson syndrome/toxic epidermal necrolysis1
Background sensitivity to chemotherapy-induced nausea and vomiting and response to antiemetics in paediatric patients: a genetic association study1
Composite CYP3A phenotypes influence tacrolimus dose-adjusted concentration in lung transplant recipients1
HDL-C and creatinine levels at 1 month are associated with patient 12-month survival rate after kidney transplantation1
Implementation of upfront DPYD genotyping with a low-cost and high-throughput assay to guide fluoropyrimidine treatment in cancer patients1
Single Nucleotide Polymorphisms (SNPs) in PRKG1 & SPATA13-AS1 are associated with bronchodilator response: a pilot study during acute asthma exacerbations in African American children1
Prenatal efavirenz exposure is independently associated with maternal, but not fetal CYP2B6 genotype1
Differential expression of NAT1 pharmacogene in hormone receptor positive vs. negative female breast tumors may affect drug treatment1
Genome-wide association study of letrozole plasma concentrations identifies non-exonic variants that may affect CYP2A6 metabolic activity1
Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans1
Luteal phase stimulation in double ovarian stimulation cycles is not affected by the follicle-stimulating hormone (FSH) receptor genotype: double ovarian stimulation is beneficial independently of the1
The functional role of inherited CDKN2A variants in childhood acute lymphoblastic leukemia1
Exploring CYP2D6 polymorphisms and angiotensin receptor blocker response in the Bai hypertensive population1
Impact of cytochrome P450 2C19 polymorphisms on the clinical efficacy and safety of voriconazole: an update systematic review and meta-analysis1
Metabolic effects of heterocyclic amines on insulin‑induced AKT phosphorylation and gluconeogenic gene expression are modified by N-acetyltransferase 2 genetic polymorphism1
Common dihydropyrimidinase (DPYS) genetic variations do not predict fluoropyrimidine-related chemotherapy toxicity in a Canadian cohort1
Comparison of clinical pharmacogenetic recommendations across therapeutic areas1
Updated analysis of the pharmacogenomics of pediatric bronchodilator response1
Incorporating G6PD genotyping to identify patients with G6PD deficiency1
Mouse nerve growth factor suppresses neuronal apoptosis in valproic acid-induced autism spectrum disorder rats by regulating the phosphoinositide-3-kinase/serine/threonine kinase signaling pathway1
Cisplatin-induced ototoxicity: a novel approach to an ancient problem1
Impact of CYP3A5 genotype on de-novo LCP tacrolimus dosing and monitoring in kidney transplantation1
Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease1
The c.415C>T polymorphism in NUDT15 is more frequent than the polymorphisms in TPMT in Chilean patients who use thiopurine drugs1
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