Salanti, G.* ; Southam, L.* ; Altshuler, D.* ; Ardlie, K.* ; Barroso, I.* ; Boehnke, M.* ; Cornelis, M.C.* ; Frayling, T.M.* ; Grallert, H. ; Grarup, N.* ; Groop, L.* ; Hansen, T.* ; Hattersley, A.T.* ; Hu, F.B.* ; Hveem, K.* ; Illig, T. ; Kuusisto, J.* ; Laakso, M.* ; Langenberg, C.* ; Lyssenko, V.* ; McCarthy, M.I.* ; Morris, A.* ; Morris, A.D.* ; Palmer, C.N.A.* ; Payne, F.* ; Platou, C.G.P.* ; Scott, L.J.* ; Voight, B.F.* ; Wareham, N.J.* ; Zeggini, E.* ; Ioannidis, J.P.A.*
     
 
    
        
Underlying genetic models of inheritance in established type 2 diabetes associations.
    
    
        
    
    
        
        Am. J. Epidemiol. 170, 537-545 (2009)
    
    
		
		
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			Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
		
     
    
		
		
			
				For most associations of common single nucleotide polymorphisms (SNPs) with common diseases, the genetic model of inheritance is unknown. The authors extended and applied a Bayesian meta-analysis approach to data from 19 studies on 17 replicated associations with type 2 diabetes. For 13 SNPs, the data fitted very well to an additive model of inheritance for the diabetes risk allele; for 4 SNPs, the data were consistent with either an additive model or a dominant model; and for 2 SNPs, the data were consistent with an additive or recessive model. Results were robust to the use of different priors and after exclusion of data for which index SNPs had been examined indirectly through proxy markers. The Bayesian meta-analysis model yielded point estimates for the genetic effects that were very similar to those previously reported based on fixed- or random-effects models, but uncertainty about several of the effects was substantially larger. The authors also examined the extent of between-study heterogeneity in the genetic model and found generally small between-study deviation values for the genetic model parameter. Heterosis could not be excluded for 4 SNPs. Information on the genetic model of robustly replicated association signals derived from genome-wide association studies may be useful for predictive modeling and for designing biologic and functional experiments.
			
			
				
			
		 
		
			
				
					
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        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
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        Schlagwörter
        Bayes theorem; diabetes mellitus; type 2; meta-analysis; models; genetic; polymorphism; genetic; population characteristics; genome-wide association; molecular association; metaanalysis; replication; loci; polymorphisms; epidemiology; challenges; variants; disease
    
 
    
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        Veröffentlichungsjahr
        2009
    
 
    
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        2009
    
 
    
    
        ISSN (print) / ISBN
        0002-9262
    
 
    
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        1476-6256
    
 
    
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	    Band: 170,  
	    Heft: 5,  
	    Seiten: 537-545 
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	    Supplement: ,  
	
    
 
  
        
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            Verlag
            Oxford University Press
        
 
        
            Verlagsort
            Oxford
        
 
	
        
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        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Epidemiology (EPI)
    
 
    
        POF Topic(s)
        30503 - Chronic Diseases of the Lung and Allergies
    
 
    
        Forschungsfeld(er)
        Genetics and Epidemiology
    
 
    
        PSP-Element(e)
        G-503900-003
    
 
    
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        Erfassungsdatum
        2009-11-26