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UnknownExamining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.
Not available
S-EPMC4334677 | biostudies-literature
UnknownA genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record.
Not available
S-EPMC4433536 | biostudies-literature
UnknownA juxtamembrane mutation in the N terminus of the dopamine transporter induces preference for an inward-facing conformation.
Not available
S-EPMC2684905 | biostudies-literature
UnknownA prognostic model based on readily available clinical data enriched a pre-emptive pharmacogenetic testing program.
Not available
S-EPMC4779720 | biostudies-literature
UnknownDeciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action.
Not available
S-EPMC4470683 | biostudies-literature
UnknownPredicting clopidogrel response using DNA samples linked to an electronic health record.
Not available
S-EPMC3621954 | biostudies-literature
UnknownAssessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical records.
Not available
S-EPMC3725600 | biostudies-literature
UnknownSLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.
Not available
S-EPMC4350523 | biostudies-literature
UnknownOptimizing drug outcomes through pharmacogenetics: a case for preemptive genotyping.
Not available
S-EPMC3785311 | biostudies-literature
UnknownGenotype and risk of major bleeding during warfarin treatment.
Not available
S-EPMC4304738 | biostudies-literature
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