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A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

artículo científico publicado en 2013

Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records

artículo científico publicado en 2013

Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins

artículo científico publicado en 2014

Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.

artículo científico publicado en 2014

Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting

artículo científico publicado en 2014

Genome-wide association of lipid-lowering response to statins in combined study populations

artículo científico publicado en 2010

High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE

artículo científico publicado en 2012

Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks

artículo científico publicado en 2011

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

artículo científico publicado en 2016

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

artículo científico publicado en 2014

Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality

artículo científico publicado en 2011

Quality control procedures for genome-wide association studies

artículo científico publicado en 2011

Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients

artículo científico publicado en 2014

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

artículo científico publicado en 2011

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