Connection
 
																	
																		  Pei-San  Tsai  to  Humans 
																	
																		
																	 
																	
																		 This is a "connection" page, showing publications  Pei-San  Tsai  has written about  Humans.   
																	
																		
																	 
																	
																			
																					
	
						
				
		
			
			
			| 
				
				
			 | 
			
				
				
					|   | 
					Connection Strength  | 
					  | 
				 
				
					  | 
					   | 
					  | 
				 
				
					|   | 
					0.030  | 
					  | 
				 
				 
			 | 
			
				
				
			 | 
			 
			 
		 
	 	
	
	
		
		
			- 
				Tsai PS, Brooks LR, Rochester JR, Kavanaugh SI, Chung WC. Fibroblast growth factor signaling in the developing neuroendocrine hypothalamus. Front Neuroendocrinol. 2011 Jan; 32(1):95-107.	
				
				
					Score: 0.009
				 
			 
		
			- 
				Chung WC, Matthews TA, Tata BK, Tsai PS. Compound deficiencies in multiple fibroblast growth factor signalling components differentially impact the murine gonadotrophin-releasing hormone system. J Neuroendocrinol. 2010 Aug; 22(8):944-50.	
				
				
					Score: 0.008
				 
			 
		
			- 
				Tsai PS, Gill JC. Mechanisms of disease: Insights into X-linked and autosomal-dominant Kallmann syndrome. Nat Clin Pract Endocrinol Metab. 2006 Mar; 2(3):160-71.	
				
				
					Score: 0.006
				 
			 
		
			- 
				Miraoui H, Dwyer AA, Sykiotis GP, Plummer L, Chung W, Feng B, Beenken A, Clarke J, Pers TH, Dworzynski P, Keefe K, Niedziela M, Raivio T, Crowley WF, Seminara SB, Quinton R, Hughes VA, Kumanov P, Young J, Yialamas MA, Hall JE, Van Vliet G, Chanoine JP, Rubenstein J, Mohammadi M, Tsai PS, Sidis Y, Lage K, Pitteloud N. Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism. Am J Hum Genet. 2013 May 02; 92(5):725-43.	
				
				
					Score: 0.003
				 
			 
		
			- 
				McCabe MJ, Gaston-Massuet C, Tziaferi V, Gregory LC, Alatzoglou KS, Signore M, Puelles E, Gerrelli D, Farooqi IS, Raza J, Walker J, Kavanaugh SI, Tsai PS, Pitteloud N, Martinez-Barbera JP, Dattani MT. Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction. J Clin Endocrinol Metab. 2011 Oct; 96(10):E1709-18.	
				
				
					Score: 0.002
				 
			 
		
			- 
				Falardeau J, Chung WC, Beenken A, Raivio T, Plummer L, Sidis Y, Jacobson-Dickman EE, Eliseenkova AV, Ma J, Dwyer A, Quinton R, Na S, Hall JE, Huot C, Alois N, Pearce SH, Cole LW, Hughes V, Mohammadi M, Tsai P, Pitteloud N. Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice. J Clin Invest. 2008 Aug; 118(8):2822-31.	
				
				
					Score: 0.002
				 
			 
		
		 
	 
																				
                                                                            
																		
																	 
																 
															 | 
		
																
																	
																		
																			
																					    Connection Strength   
  The connection strength for concepts is the sum of the scores for each matching publication.  
     Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.   
																				
																		
																	 
																 
															 |