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Richard D. Hockett

Researcher at Eli Lilly and Company

Publications -  13
Citations -  3520

Richard D. Hockett is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Prasugrel & Clopidogrel. The author has an hindex of 10, co-authored 13 publications receiving 3359 citations.

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Cytochrome P-450 Polymorphisms and Response to Clopidogrel

TL;DR: Carriers of a reduced-function CYP2C19 allele had significantly lower levels of the active metabolite of clopidogrel, diminished platelet inhibition, and a higher rate of major adverse cardiovascular events, including stent thrombosis, than did noncarriers.
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Cytochrome P450 genetic polymorphisms and the response to prasugrel: relationship to pharmacokinetic, pharmacodynamic, and clinical outcomes.

TL;DR: Common functional CYP genetic variants do not affect active drug metabolite levels, inhibition of platelet aggregation, or clinical cardiovascular event rates in persons treated with prasugrel, and these pharmacogenetic findings are in contrast to observations with clopidogrel.
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The External RNA Controls Consortium: a progress report.

TL;DR: The External RNA Controls Consortium (ERCC) is developing commonly agreed-upon and tested controls for use in expression assays, a true industry-wide standard control.
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Comprehensive assessment of metabolic enzyme and transporter genes using the Affymetrix Targeted Genotyping System.

TL;DR: The Targeted Genotyping System provides a solution to this challenge, by combining molecular inversion probe technology with universal microarrays to provide a method that is capable of analyzing thousands of variants in a single reaction, while remaining relatively insensitive to cross-reactivity between reaction components.
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A Phase II Trial of Pemetrexed in Advanced Breast Cancer: Clinical Response and Association with Molecular Target Expression

TL;DR: Future trials examining expression levels of other genes important to the folate pathway and/or breast cancer may identify a more robust multigene profile that can better predict response to this novel antifolate.