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Volumn 371, Issue 7, 2014, Pages 593-596

Genotype-phenotype correlation - Promiscuity in the era of next-generation sequencing

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; CORRELATIONAL STUDY; EXOME; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENETICS; GENOTYPE; HUMAN; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SHORT SURVEY; ARTICLE; ECONOMICS; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC SCREENING; GENOTYPING TECHNIQUE; HIGH THROUGHPUT SEQUENCING; METHODOLOGY; MUTATION;

EID: 84906079809     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMp1400788     Document Type: Article
Times cited : (73)

References (5)
  • 1
    • 79959829340 scopus 로고    scopus 로고
    • Exome sequencing identifies ZNF644 mutations in high myopia
    • Shi Y, Li Y, Zhang D, et al. Exome sequencing identifies ZNF644 mutations in high myopia. PLoS Genet 2011;7(6):e1002084 (http://dx.plos.org/10.1371/ journal.pgen.1002084).
    • (2011) PLoS Genet , vol.7 , Issue.6
    • Shi, Y.1    Li, Y.2    Zhang, D.3
  • 2
    • 80053549439 scopus 로고    scopus 로고
    • Clan genomics and the complex architecture of human disease
    • Lupski JR, Belmont JW, Boerwinkle E, Gibbs RA. Clan genomics and the complex architecture of human disease. Cell 2011; 147(1):32-43 (http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3656718&tool= pmcentrez&rendertype=abstract).
    • (2011) Cell , vol.147 , Issue.1 , pp. 32-43
    • Lupski, J.R.1    Belmont, J.W.2    Boerwinkle, E.3    Gibbs, R.A.4
  • 3
    • 84862507047 scopus 로고    scopus 로고
    • The ciliopathies: A transitional model into systems biology of human genetic disease
    • Davis EE, Katsanis N. The ciliopathies: a transitional model into systems biology of human genetic disease. Curr Opin Genet Dev 2012;22(3):290-303 (http://www.pubmedcentral.nih.gov/articlerender.fcgi? artid=3509787&tool= pmcentrez&rendertype=abstract).
    • (2012) Curr Opin Genet Dev , vol.22 , Issue.3 , pp. 290-303
    • Davis, E.E.1    Katsanis, N.2
  • 4
    • 84885785987 scopus 로고    scopus 로고
    • Clinical whole-exome sequencing for the diagnosis of mendelian disorders
    • Yang Y, Muzny DM, Reid JG, et al. Clinical whole-exome sequencing for the diagnosis of mendelian disorders. N Engl J Med 2013;369:1502-11.
    • (2013) N Engl J Med , vol.369 , pp. 1502-1511
    • Yang, Y.1    Muzny, D.M.2    Reid, J.G.3
  • 5
    • 84893378179 scopus 로고    scopus 로고
    • Searching for missing heritability: Designing rare variant association studies
    • Zuk O, Schaffner SF, Samocha K, et al. Searching for missing heritability: designing rare variant association studies. Proc Natl Acad Sci U S A 2014;111(4):E455E464 (http://www.pubmedcentral.nih.gov/articlerender.fcgi? artid=3910587&tool=pmcentrez&rendertype=abstract).
    • (2014) Proc Natl Acad Sci U S A , vol.111 , Issue.4
    • Zuk, O.1    Schaffner, S.F.2    Samocha, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.