Co-Authors
                            
                            
                                This is a "connection" page, showing publications co-authored by   MICHAEL WANGLER   and   LINYAN MENG.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            0.381
         
        
        
     
 
    
        
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            MED27 Variants Cause Developmental Delay, Dystonia, and Cerebellar Hypoplasia. Ann Neurol. 2021 04; 89(4):828-833.
            
            
                Score: 0.180
             
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            Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management. JAMA Pediatr. 2017 12 04; 171(12):e173438.
            
            
                Score: 0.145
             
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            AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI. 2024 May; 1(5).
            
            
                Score: 0.056