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Genomic analysis of breast cancer heralds a changing treatment paradigm.
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Int J Technol Assess Health Care. 2014 Apr;30(2):179-87. doi: 10.1017/S0266462314000142. Epub 2014 May 7.
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Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.
Clin Pharmacol Ther. 2014 Apr;95(4):394-402. doi: 10.1038/clpt.2013.226. Epub 2014 Feb 19.
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Translating genomics in cancer care.
J Natl Compr Canc Netw. 2013 Nov;11(11):1343-53. doi: 10.6004/jnccn.2013.0158.
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Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.
PLoS Biol. 2013 Nov;11(11):e1001699. doi: 10.1371/journal.pbio.1001699. Epub 2013 Nov 5.
9
The promise and challenges of next-generation genome sequencing for clinical care.
JAMA Intern Med. 2014 Feb 1;174(2):275-80. doi: 10.1001/jamainternmed.2013.12048.
10
Multigene assays in metastatic colorectal cancer.
J Natl Compr Canc Netw. 2013 Sep;11 Suppl 4:S9-17. doi: 10.6004/jnccn.2013.0221.

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