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Volumn 107, Issue 17, 2010, Pages 7898-7903

Anonymization of electronic medical records for validating genome-wide association studies

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BIOMEDICINE; CLINICAL FEATURE; DATA ANALYSIS; ELECTRONIC MEDICAL RECORD; GENE SEQUENCE; HUMAN; INFORMATION PROCESSING; PRIORITY JOURNAL; RISK ASSESSMENT;

EID: 77952390550     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0911686107     Document Type: Article
Times cited : (103)

References (17)
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  • 3
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    • Mailman MD, et al. (2007) The NCBI dbGaP database of genotypes and phenotypes. Nat Genet 39:1181-1186.
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    • Mailman, M.D.1
  • 5
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    • Standards for privacy of individually identifiable health information; final rule
    • US Department of Health and Human Services (2002), parts 160 and 164
    • US Department of Health and Human Services (2002) Standards for privacy of individually identifiable health information; final rule. Federal Register 45 (2002), parts 160 and 164.
    • (2002) Federal Register , vol.45
  • 6
    • 84888124568 scopus 로고    scopus 로고
    • Department of Biomedical Informatics, Vanderbilt University School of Medicine. Available at Accessed February 16, 2010
    • Department of Biomedical Informatics, Vanderbilt University School of Medicine. Electronic Medical Records and Genomics (eMERGE) Network Available at. http:// www.gwas.net. Accessed February 16, 2010.
    • Electronic Medical Records and Genomics (EMERGE) Network
  • 7
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    • The disclosure of diagnosis codes can breach research participants' privacy
    • in press
    • Loukides G, Denny JC, Malin B (2009) The disclosure of diagnosis codes can breach research participants' privacy. J Am Med Inform Assoc, in press.
    • (2009) J Am Med Inform Assoc
    • Loukides, G.1    Denny, J.C.2    Malin, B.3
  • 11
    • 33745534521 scopus 로고    scopus 로고
    • Quality assurance of medical ontologies
    • Rogers JE (2006) Quality assurance of medical ontologies. Methods Inf Med 45: 267-274.
    • (2006) Methods Inf Med , vol.45 , pp. 267-274
    • Rogers, J.E.1
  • 12
    • 34249885875 scopus 로고    scopus 로고
    • A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
    • Scott LJ, et al. (2007) A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316:1341-1345.
    • (2007) Science , vol.316 , pp. 1341-1345
    • Scott, L.J.1
  • 13
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    • Development of a large-scale de-identified DNA biobank to enable personalized medicine
    • Roden DM, et al. (2008) Development of a large-scale de-identified DNA biobank to enable personalized medicine. Clin Pharmacol Ther 84:362-369.
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  • 14
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    • A HapMap harvest of insights into the genetics of common disease
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    • Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.