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Volumn 14, Issue 1, 2013, Pages 75-

Mining electronic health records: An additional perspective

Author keywords

[No Author keywords available]

Indexed keywords

AUTOIMMUNE DISEASE; BREAST CANCER; CANCER REGISTRY; DATA BASE; ELECTRONIC MEDICAL RECORD; GASTROENTEROLOGY; GENE SEQUENCE; GERIATRIC NURSING; GYNECOLOGY; HUMAN; INCIDENCE; LETTER; ONCOGENE; OPHTHALMOLOGY; PRIORITY JOURNAL; STANDARD; TUMOR SUPPRESSOR GENE;

EID: 84871279032     PISSN: 14710056     EISSN: 14710064     Source Type: Journal    
DOI: 10.1038/nrg3208-c1     Document Type: Letter
Times cited : (7)

References (13)
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  • 2
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  • 3
    • 0027954465 scopus 로고
    • A large kindred with 17q linked breast and ovarian cancer: Genetic, phenotypic, and genealogical analysis
    • Goldgar, D. E. et al. A large kindred with 17q linked breast and ovarian cancer: Genetic, phenotypic, and genealogical analysis. J. Natl Cancer Institute 86, 200-209 (1994
    • (1994) J. Natl Cancer Institute , vol.86 , pp. 200-209
    • Goldgar, D.E.1
  • 4
    • 19144362921 scopus 로고    scopus 로고
    • Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study
    • Neuhausen, S. L. et al. Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study. Am. J. Hum. Genet. 58, 271 (1996
    • (1996) Am. J. Hum. Genet , vol.58 , pp. 271
    • Neuhausen, S.L.1
  • 5
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    • The complete BRCA2 gene and mutations in chromosome 13q linked kindreds
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    • (1996) Nature Genet , vol.12 , pp. 333-337
    • Tavtigian, S.1
  • 6
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    • Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis
    • Allen-Brady, K. et al. Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstetr. Gynecol. 118, 1345 (2011
    • (2011) Obstetr. Gynecol , vol.118 , pp. 1345
    • Allen-Brady, K.1
  • 7
    • 77954239390 scopus 로고    scopus 로고
    • Heritability of vasculopathy, autoimmune disease, and fibrosis in systemic sclerosis: A population-Based study
    • Frech, T. et al. Heritability of vasculopathy, autoimmune disease, and fibrosis in systemic sclerosis: A population-Based study. Arthritis Rheum. 62, 2109-2116 (2010
    • (2010) Arthritis Rheum , vol.62 , pp. 2109-2116
    • Frech, T.1
  • 8
    • 84655168099 scopus 로고    scopus 로고
    • Evidence of an inherited predisposition for cervical spondylotic myelopathy
    • Patel, A. A., Spiker, W. R., Daubs, M., Brodke, D. S. & Cannon-Albright, L. A. Evidence of an inherited predisposition for cervical spondylotic myelopathy. Spine 37, 26 (2012
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  • 9
    • 78149408871 scopus 로고    scopus 로고
    • Using the Utah Population Database to assess familial risk of primary open angle glaucoma
    • Wang, X. et al. Using the Utah Population Database to assess familial risk of primary open angle glaucoma. Vision Res. 50, 2391-2395 (2010
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    • Wang, X.1
  • 11
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    • Genome-wide study replicates linkage of 3p22 24 to extreme longevity in humans and identifies possible additional loci
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  • 13
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.