Assessing the clinical impact of CYP2C9 pharmacogenetic variation on phenytoin prescribing practice and patient response in an integrated health system.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000383
CYP2D6 haplotypes with enhancer single-nucleotide polymorphism rs5758550 and rs16947 (*2 allele): implications for CYP2D6 genotyping panels
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000363
Assessment of provider-perceived barriers to clinical use of pharmacogenomics during participation in an institutional implementation study
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000362
Utility of human leukocyte antigen-B*58: 01 genotyping and patient outcomes
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000359
Gene expression changes in lymphoblastoid cell lines and primary B cells by dexamethasone
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000365
DNA methylation is associated with improvement in lung function on inhaled corticosteroids in pediatric asthmatics
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000366
Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000361
The N680S variant in the follicle-stimulating hormone receptor gene identifies hyperresponders to controlled ovarian stimulation
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000374
Targeted ultra-deep sequencing of a South African Bantu-speaking cohort to comprehensively map and characterize common and novel variants in 65 pharmacologically-related genes
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000380
The effect of the CYP2D6 genotype on the maintenance dose of metoprolol in a chronic Dutch patient population.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000381
Pharmacogeomic implications of population diversity in Latin America: TPMT and NUDT15 polymorphisms and thiopurine dosing
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000388
Effect of tacrolimus dispositional genetics on acute rejection in the first 2 weeks and estimated glomerular filtration rate in the first 3 months following kidney transplantation
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000360
International survey of patients undergoing percutaneous coronary intervention and their attitudes toward pharmacogenetic testing
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000368
Impact of SULT1A3/SULT1A4 genetic polymorphisms on the sulfation of phenylephrine and salbutamol by human SULT1A3 allozymes
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000371
Pharmacogenetic analysis of belimumab fails to identify robust genetic predictors of efficacy in lupus
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000378
N-acetyltransferase 2 acetylator genotype-dependent N-acetylation of 4-aminobiphenyl in cryopreserved human hepatocytes
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000394
Analysis of comprehensive pharmacogenomic profiling to impact in-hospital prescribing
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000346
PharmGKB summary: sertraline pathway, pharmacokinetics
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000392
The role of phase I and II genetic polymorphisms, smoking, alcohol and cancer family history, in the risk of developing testicular cancer.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000379
The relevance of the individual screening for genetic variants in predicting ovarian response.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/fpc.0000000000000386
Association between HNF4A mutations and bleeding complications in patients with stable international normalized ratio.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000384
HLA-B*58:01 carrier status of Hmong in Minnesota: first in Hmong genotyping for prevalence of this biomarker of risk for severe cutaneous adverse reactions caused by allopurinol
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000391
Association of FAM65B, AGBL4, and CUX2 genetic polymorphisms with susceptibility to antituberculosis drug-induced hepatotoxicity: validation study in a Chinese Han population
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000370
PharmGKB summary: methylphenidate pathway, pharmacokinetics/pharmacodynamics
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000376
Associations between TMEM196 polymorphisms and NSAID-exacerbated respiratory disease in asthma
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000367
Individuals with CYP2C8 and CYP2C9 reduced metabolism haplotypes self-adjusted ibuprofen dose in the Coriell Personalized Medicine Collaborative
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000364
N-acetyltransferase 2 enzyme genotype–phenotype discordances in both HIV-negative and HIV-positive Nigerians
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000373
A multiplex pharmacogenetics assay using the MinION nanopore sequencing device.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/fpc.0000000000000385
PharmGKB summary: very important pharmacogene information for CACNA1S
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000393
Fentanyl overdoses and pharmacogenetics
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000389
PharmGKB summary: Ondansetron and tropisetron pathways, pharmacokinetics and pharmacodynamics
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000369
Deep sequencing across germline genome-wide association study signals relating to breast cancer events in women receiving aromatase inhibitors for adjuvant therapy of early breast cancer.
来源期刊:Pharmacogenetics and genomicsDOI:10.1097/FPC.0000000000000382
Enriched developmental biology molecular pathways impact on antipsychotics-induced weight gain
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000390
An initial genetic analysis of gemcitabine-induced high-grade neutropenia in pancreatic cancer patients in CALGB 80303 (Alliance)
来源期刊:Pharmacogenetics and GenomicsDOI:10.1097/FPC.0000000000000375