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期刊名:Pharmacogenomics journal

缩写:PHARMACOGENOMICS J

ISSN:1470-269X

e-ISSN:1473-1150

IF/分区:2.9/Q2

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共收录本刊相关文章索引1106
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Emma F Magavern,Faiza Durrani,Mehru Raza et al. Emma F Magavern et al.
Background: South Asian ancestry populations are underrepresented in genomic studies and therapeutics trials. British South Asians suffer from multi-morbidity leading to polypharmacy. Our objective was to elucidate Britis...
George P Patrinos,Negar Sarhangi,Behnaz Sarrami et al. George P Patrinos et al.
Personalized medicine is a novel frontier in health care that is based on each person's unique genetic makeup. It represents an exciting opportunity to improve the future of individualized health care for all individuals. Pharmacogenomics, ...
Michael T Eadon,Marc B Rosenman,Pengyue Zhang et al. Michael T Eadon et al.
Adverse drug events (ADEs) account for a significant mortality, morbidity, and cost burden. Pharmacogenetic testing has the potential to reduce ADEs and inefficacy. The objective of this INGENIOUS trial (NCT02297126) analysis was to determi...
Debleena Guin,Yasha Hasija,Ritushree Kukreti Debleena Guin
Epilepsy treatment is challenging due to heterogeneous syndromes, different seizure types and higher inter-individual variability. Identification of genetic variants predicting drug efficacy, tolerability and risk of adverse-effects for ant...
Song Li,Geert Poelmans,Regina L M van Boekel et al. Song Li et al.
The pharmacological management of musculoskeletal pain starts with NSAIDs, followed by weak or strong opioids until the pain is under control. However, the treatment outcome is usually unsatisfying due to inter-individual differences. To in...
Fumiko Shimoda,Takeo Naito,Yoichi Kakuta et al. Fumiko Shimoda et al.
Recently, the HLA-DQA1*05 (rs2097432) genetic variation has been reported to be linked to early infliximab (IFX) treatment failure in the Caucasian Crohn's disease (CD) population, but that evidence is scarce in the Asian population. This s...
Emma F Magavern,David A van Heel;Genes & Health Research Team;Damian Smedley,Mark J Caulfield Emma F Magavern
Background: Reported association between statin use and cataract risk is controversial. The SLCO1B1 gene encodes a transport protein responsible for statin clearance. The aim of this study was to investigate a possible as...
Young Ho Lee,Gwan Gyu Song Young Ho Lee
Objectives: To investigate the association between the functional Fc gamma receptor 3 A (FCGR3A) V158F and FCGR2A R131H polymorphisms and rituximab therapy in patients with autoimmune diseases. ...
Chen Li,Xiaona Su,Qidi Sun et al. Chen Li et al.
Pharmacogenomics (PGx) is rapidly growing branch of molecular genetics with high potentials to influence therapeutics. This review evaluates knowledge and attitudes of medical and pharmacy students about PGx. A literature search was conduct...