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本文引用的文献

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The mathematical limits of genetic prediction for complex chronic disease.复杂慢性疾病遗传预测的数学极限
J Epidemiol Community Health. 2015 Jun;69(6):574-9. doi: 10.1136/jech-2014-204983. Epub 2015 Feb 3.
2
A new initiative on precision medicine.一项关于精准医学的新倡议。
N Engl J Med. 2015 Feb 26;372(9):793-5. doi: 10.1056/NEJMp1500523. Epub 2015 Jan 30.
3
Non-invasive blood glucose monitor based on spectroscopy using a smartphone.基于光谱技术并使用智能手机的无创血糖监测仪。
Annu Int Conf IEEE Eng Med Biol Soc. 2014;2014:3695-8. doi: 10.1109/EMBC.2014.6944425.
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Epigenetics: modifying the genetic blueprint.表观遗传学:修改基因蓝图。
Mo Med. 2014 Sep-Oct;111(5):428-33.
5
Blue Button use by patients to access and share health record information using the Department of Veterans Affairs' online patient portal.患者使用“蓝按钮”通过退伍军人事务部的在线患者门户访问和共享健康记录信息。
J Am Med Inform Assoc. 2014 Jul-Aug;21(4):657-63. doi: 10.1136/amiajnl-2014-002723. Epub 2014 Apr 16.
6
Ivacaftor for the treatment of patients with cystic fibrosis and the G551D mutation: a systematic review and cost-effectiveness analysis.依伐卡托特治疗囊性纤维化和 G551D 突变患者:系统评价和成本效益分析。
Health Technol Assess. 2014 Mar;18(18):1-106. doi: 10.3310/hta18180.
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Gene-environment interaction in autoimmune disease.自身免疫性疾病中的基因-环境相互作用。
Expert Rev Mol Med. 2014 Mar 7;16:e4. doi: 10.1017/erm.2014.5.
8
Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies.验证 PhenX 措施在个性化医学研究项目中的有效性,以用于基因/环境研究。
BMC Med Genomics. 2014 Jan 14;7:3. doi: 10.1186/1755-8794-7-3.
9
A pharmacogenetic versus a clinical algorithm for warfarin dosing.基于药理学的华法林剂量调整算法与临床算法的比较。
N Engl J Med. 2013 Dec 12;369(24):2283-93. doi: 10.1056/NEJMoa1310669. Epub 2013 Nov 19.
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A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.非简并性的孟德尔遗传位点有害变异编码有助于复杂疾病风险。
Cell. 2013 Sep 26;155(1):70-80. doi: 10.1016/j.cell.2013.08.030.

News from the NIH: potential contributions of the behavioral and social sciences to the precision medicine initiative.

作者信息

Riley William T, Nilsen Wendy J, Manolio Teri A, Masys Daniel R, Lauer Michael

机构信息

Office of Behavioral and Social Sciences Research, National Institutes of Health, 30 Center Dr., Bethesda, MD USA.

Division of Genomic Medicine, National Human Genome Research Institute, 5635 Fishers Lane MSC 9305, Bethesda, MD 20892-9305 USA.

出版信息

Transl Behav Med. 2015 Sep;5(3):243-6. doi: 10.1007/s13142-015-0320-5.

DOI:10.1007/s13142-015-0320-5
PMID:26327928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4537462/
Abstract
摘要