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    Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.
        
        Mol. Psychiatry 23, 1169-1180 (2018)
    
    
				Anorexia nervosa (AN) is a complex neuropsychiatric disorder presenting with dangerously low body weight, and a deep and persistent fear of gaining weight. To date, only one genome-wide significant locus associated with AN has been identified. We performed an exome-chip based genome-wide association studies (GWAS) in 2158 cases from nine populations of European origin and 15 485 ancestrally matched controls. Unlike previous studies, this GWAS also probed association in low-frequency and rare variants. Sixteen independent variants were taken forward for in silico and de novo replication (11 common and 5 rare). No findings reached genome-wide significance. Two notable common variants were identified: rs10791286, an intronic variant in OPCML (P=9.89 × 10(-6)), and rs7700147, an intergenic variant (P=2.93 × 10(-5)). No low-frequency variant associations were identified at genome-wide significance, although the study was well-powered to detect low-frequency variants with large effect sizes, suggesting that there may be no AN loci in this genomic search space with large effect sizes.
			
			
		Impact Factor
					Scopus SNIP
					Web of Science
Times Cited
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					Cited By
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					2.395
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
     
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2018
    
 
    
        Prepublished im Jahr 
        2017
    
 
    
        HGF-Berichtsjahr
        2017
    
 
    
    
        ISSN (print) / ISBN
        1359-4184
    
 
    
        e-ISSN
        1476-5578
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Molecular Psychiatry
    
 
		
    
        Quellenangaben
        
	    Band: 23,  
	    Heft: 5,  
	    Seiten: 1169-1180 
	    
	    
	
    
 
  
         
        
            Verlag
            Nature Publishing Group
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)
 
    Institute of Epidemiology (EPI)
        POF Topic(s)
        30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
30202 - Environmental Health
 
    30202 - Environmental Health
        Forschungsfeld(er)
        Genetics and Epidemiology
    
 
    
        PSP-Element(e)
        G-504100-001
G-504000-007
 
     
     	
    
    G-504000-007
        WOS ID
        WOS:000431614600009
    
    
        PubMed ID
        29155802
    
    
        Erfassungsdatum
        2017-11-27