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1
Research ethics and the challenge of whole-genome sequencing.
Nat Rev Genet. 2008 Feb;9(2):152-6. doi: 10.1038/nrg2302.
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3
Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Am J Med Genet A. 2011 Dec;155A(12):2916-24. doi: 10.1002/ajmg.a.34357. Epub 2011 Oct 28.
4
Clinical research in Chile: do not block the way of inquiry.
Lancet. 2020 Sep 5;396(10252):668. doi: 10.1016/S0140-6736(20)31829-8.
5
Potāto, potăto, proxy consent, permission -- just don't call the a whole thing off.
Crit Care. 2005 Apr;9(2):123-4. doi: 10.1186/cc3037. Epub 2005 Jan 7.
8
Ethical issues raised by whole genome sequencing.
Best Pract Res Clin Gastroenterol. 2014 Apr;28(2):269-79. doi: 10.1016/j.bpg.2014.02.004. Epub 2014 Mar 12.
10
Considering the Benefits and Risks of Research Participants' Access to Sequence Data.
Genet Test Mol Biomarkers. 2017 Dec;21(12):717-721. doi: 10.1089/gtmb.2017.0143. Epub 2017 Oct 18.

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Genomics in Pancreas-Kidney Transplantation: From Risk Stratification to Personalized Medicine.
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Circulating tumor DNA in cholangiocarcinoma: current clinical applications and future perspectives.
Front Cell Dev Biol. 2025 Jul 2;13:1616064. doi: 10.3389/fcell.2025.1616064. eCollection 2025.
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Circulating tumor DNA in lymphoma: technologies and applications.
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From code to care: Clinician and researcher perspectives on an optimal therapeutic web portal for acute myeloid leukemia.
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Liquid biopsy in T-cell lymphoma: biomarker detection techniques and clinical application.
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Research progress of CTC, ctDNA, and EVs in cancer liquid biopsy.
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Liquid-based biomarkers in breast cancer: looking beyond the blood.
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Minimal residual disease in solid tumors: an overview.
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Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies.
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When Not to Ask: A Defense of Choice-Masking Nudges in Medical Research.
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本文引用的文献

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Personalized medicine in the era of genomics.
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Medicine. The future of personal genomics.
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The diploid genome sequence of an individual human.
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Celebrity genomes alarm researchers.
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Prohibiting genetic discrimination.
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Medicine. Reestablishing the researcher-patient compact.
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Educating health-care professionals about genetics and genomics.
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Meeting the growing demands of genetic research.
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Disclosing individual genetic results to research participants.
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