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Unsettling the treatment imperative? Chemotherapy decision-making in the wake of genomic techniques.
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Kernel Fusion Method for Detecting Cancer Subtypes via Selecting Relevant Expression Data.
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The nuanced negative: Meanings of a negative diagnostic result in clinical exome sequencing.
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Trust in standards: transitioning clinical exome sequencing from bench to bedside.
Soc Stud Sci. 2015 Feb;45(1):77-99. doi: 10.1177/0306312714559323.
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Return of results: ethical and legal distinctions between research and clinical care.
Am J Med Genet C Semin Med Genet. 2014 Mar;166C(1):105-11. doi: 10.1002/ajmg.c.31393. Epub 2014 Mar 10.
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Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
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Implementing genomic medicine in the clinic: the future is here.
Genet Med. 2013 Apr;15(4):258-67. doi: 10.1038/gim.2012.157. Epub 2013 Jan 10.
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Customers or research participants? Guidance for research practices in commercialization of personal genomics.
Genet Med. 2012 Oct;14(10):833-5. doi: 10.1038/gim.2012.64. Epub 2012 Jun 14.
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"If I could in a small way help": motivations for and beliefs about sample donation for genetic research.
J Empir Res Hum Res Ethics. 2011 Jun;6(2):57-70. doi: 10.1525/jer.2011.6.2.57.
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Genomics. Deflating the genomic bubble.
Science. 2011 Feb 18;331(6019):861-2. doi: 10.1126/science.1198039.

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