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Volumn 171, Issue 10, 2010, Pages 1155-1156

Three authors reply

Author keywords

[No Author keywords available]

Indexed keywords

CROHN DISEASE; GENE FREQUENCY; GENE IDENTIFICATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC VARIABILITY; GENOTYPE; HERITABILITY; INHERITANCE; LETTER; NON INSULIN DEPENDENT DIABETES MELLITUS; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77952379127     PISSN: 00029262     EISSN: 14766256     Source Type: Journal    
DOI: 10.1093/aje/kwq059     Document Type: Letter
Times cited : (1)

References (7)
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    • Re: "Underlying genetic models of inheritance in established type 2 diabetes associations" [letter]
    • Hemminki K, Försti A, Bermejo JL. Re: "Underlying genetic models of inheritance in established type 2 diabetes associations" [letter]. Am J Epidemiol. 2010;171(0):000-000
    • (2010) Am J Epidemiol. , pp. 171
    • Hemminki, K.1    Försti, A.2    Bermejo, J.L.3
  • 2
    • 70249146533 scopus 로고    scopus 로고
    • Underlying genetic models of inheritance in established type 2 diabetes associations
    • Salanti G, Southam L, Altshuler D, et al. Underlying genetic models of inheritance in established type 2 diabetes associations. Am J Epidemiol. 2009;170(5):537-545.
    • (2009) Am J Epidemiol , vol.170 , Issue.5 , pp. 537-545
    • Salanti, G.1    Southam, L.2    Altshuler, D.3
  • 3
    • 65249164859 scopus 로고    scopus 로고
    • Validating, augmenting and refining genome-wide association signals
    • Ioannidis JP, Thomas G, Daly MJ. Validating, augmenting and refining genome-wide association signals. Nat Rev Genet. 2009;10(5):318-329.
    • (2009) Nat Rev Genet , vol.10 , Issue.5 , pp. 318-329
    • Ioannidis, J.P.1    Thomas, G.2    Daly, M.J.3
  • 4
    • 0035978651 scopus 로고    scopus 로고
    • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
    • Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature. 2001;411(6837):599-603.
    • (2001) Nature , vol.411 , Issue.6837 , pp. 599-603
    • Hugot, J.P.1    Chamaillard, M.2    Zouali, H.3
  • 5
    • 0035978533 scopus 로고    scopus 로고
    • A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
    • Ogura Y, Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001;411(6837):603- 606.
    • (2001) Nature , vol.411 , Issue.6837 , pp. 603-606
    • Ogura, Y.1    Bonen, D.K.2    Inohara, N.3
  • 6
    • 67249117049 scopus 로고    scopus 로고
    • Potential etio-logic and functional implications of genome-wide association loci for human diseases and traits
    • Hindorff LA, Sethupathy P, Junkins HA, et al. Potential etio-logic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA. 2009;106(23):9362-9367.
    • (2009) Proc Natl Acad Sci USA , vol.106 , Issue.23 , pp. 9362-9367
    • Hindorff, L.A.1    Sethupathy, P.2    Junkins, H.A.3
  • 7
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    • Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes
    • Nejentsev S, Walker N, Riches D, et al. Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes. Science. 2009;324(5925):387-389.
    • (2009) Science , vol.324 , Issue.5925 , pp. 387-389
    • Nejentsev, S.1    Walker, N.2    Riches, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.