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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
A J Risselada,J Vehof,R Bruggeman et al. A J Risselada et al.
In two previous studies we found an association between HTR2C polymorphisms and the prevalence of the metabolic syndrome in patients using antipsychotics. In this study, we set out to replicate our findings in a third separate sample of pat...
M Chierici,K Miclaus,S Vega et al. M Chierici et al.
The discordance in results between independent genome-wide association studies (GWAS) indicates the potential for Type I and Type II errors. To identify the causes of variability underlying lack of reproducibility, here we present the resul...
L Zhang,S Yin,K Miclaus et al. L Zhang et al.
The robustness of genome-wide association study (GWAS) results depends on the genotyping algorithms used to establish the association. This paper initiated the assessment of the impact of the Corrected Robust Linear Model with Maximum Likel...
K Miclaus,R Wolfinger,S Vega et al. K Miclaus et al.
The Affymetrix GeneChip Human Mapping 500K array is common for genome-wide association studies (GWASs). Recent findings highlight the importance of accurate genotype calling algorithms to reduce the inflation in Type I and Type II error rat...
K Miclaus,M Chierici,C Lambert et al. K Miclaus et al.
The Genome-Wide Association Working Group (GWAWG) is part of a large-scale effort by the MicroArray Quality Consortium (MAQC) to assess the quality of genomic experiments, technologies and analyses for genome-wide association studies (GWASs...
W Shi,M Bessarabova,D Dosymbekov et al. W Shi et al.
Gene expression signatures of toxicity and clinical response benefit both safety assessment and clinical practice; however, difficulties in connecting signature genes with the predicted end points have limited their application. The Microar...
R M Parry,W Jones,T H Stokes et al. R M Parry et al.
In the clinical application of genomic data analysis and modeling, a number of factors contribute to the performance of disease classification and clinical outcome prediction. This study focuses on the k-nearest neighbor (KNN) modeling stra...
J Luo,M Schumacher,A Scherer et al. J Luo et al.
Batch effects are the systematic non-biological differences between batches (groups) of samples in microarray experiments due to various causes such as differences in sample preparation and hybridization protocols. Previous work focused mai...
J Huang,W Shi,J Zhang et al. J Huang et al.
Genomic biomarkers for the detection of drug-induced liver injury (DILI) from blood are urgently needed for monitoring drug safety. We used a unique data set as part of the Food and Drug Administration led MicroArray Quality Control Phase-I...
A Oberthuer,D Juraeva,L Li et al. A Oberthuer et al.
Microarray-based prediction of clinical endpoints may be performed using either a one-color approach reflecting mRNA abundance in absolute intensity values or a two-color approach yielding ratios of fluorescent intensities. In this study, a...