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Showing results 1 to 8 of 8

	Title	Author(s)	Issue Date
	Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liability Journal:American Journal of Human Genetics	Emison, ES GarciaBarcelo, M Grice, EA Lantieri, F Amiel, J Burzynski, G Fernandez, RM Hao, L Kashuk, C West, K Miao, X Tam, PKH Griseri, P Ceccherini, I Pelet, A Jannot, AS De Pontual, L HenrionCaude, A Lyonnet, S Verheij, JBGM Hofstra, RMW Antiñolo, G Borrego, S McCallion, AS Chakravarti, A	2010
	Differential liabilities of coding and non-coding mutations in complex disease Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2005	Burzynski, G Amiel, J Antinolo, G Borrego,, S Ceccherini, I Emison, E Eng, C Fernandez, R Garcia-Barcelo, MM Griseri, P Hofstra, R Kashuk, C Lantieri, F Lyonnet, S Tam, PKH Tullio-Pelet, A West, K Chakravarti, A	2005
	Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung diseases Proceeding/Conference:GRC on Human Genetics & Genomics	Emison, E Burzynski, G Amiel, J Borrego, S Ceccherini,, I Fernandez, R Garcia-Barcelo, MM Griseri, P Hofstra, R Kashuk, CS Lantieri, F Lyonnet, S Tam, PKH Pecina, A Tullio-Pelet,, A West, K Chakravarti, A	2005
	Hirschsprung disease, associated syndromes and genetics: A review Journal:Journal of Medical Genetics	Amiel, J SproatEmison, E GarciaBarcelo, M Lantieri, F Burzynski, G Borrego, S Pelet, A Arnold, S Miao, X Griseri, P Brooks, AS Antinolo, G De Pontual, L ClementZiza, M Munnich, A Kashuk, C West, K Wong, KKY Lyonnet, S Chakravarti, A Tam, PKH Ceccherini, I Hofstra, RMW Fernandez, R	2008
	The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease Proceeding/Conference:Annual International Congress of the British Association of Paediatric Suregons, BAPS 2006	Tam, PKH Garcia-Barcelo, MM Tullio-Pelet, A Lyonnet, S Lantieri, F Kashuk, C Hofstra, R Griseri, P Fernandez, R Eng, C Emison, E Burzynski, G Ceccherini, I Borrego, S Antinolo, G Amiel, J West, K Chakravarti, A	2006
	Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease Journal:European Journal of Human Genetics	Jannot, AS Amiel, J Pelet, A Lantieri, F Fernandez, RM Verheij, JBGM GarciaBarcelo, M Arnold, S Ceccherini, I Borrego, S Hofstra, RMW Tam, PKH Munnich, A Chakravarti, A ClergetDarpoux, F Lyonnet, S	2012
	Systems biology approaches to the search for disease genes in Hirschsprung‘s disease Proceeding/Conference:European Journal of Human Genetics	Luzon-Toro, B Bleda, M Fernandez, RM Garcia-Alonso, L Arnold, S Sribudiani, Y Besmond, C Lantieri, F Torroglosa, A Enguix-Riego, M Garcia-Barcelo, MM Tam, PKH Ceccherini, I Lyonnet, S Hofstra, RM Chakravarti, A Antinolo, G Dopazo, J Borrego, S	2014
	Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease Journal:Human Molecular Genetics	Tang, SM Gui, H Kapoor, A Kim, JH Luzon-Toro, B Pelet, A Burzynski, G Lantieri, F So, MT Berrios, C Shin, HD Fernandez, RM Le, TL Verheij, JBGM Matera, I Cherny, SS Nandakumar, P Cheong, HS Antinolo, G Amiel, J Seo, JM Kim, DY Oh, JT Lyonnet, S Borrego, S Ceccherini, I Hofstra, RMW Chakravarti, A Kim, HY Sham, PC Tam, PKH Garcia-Barcelo, MM	2016

Showing results 1 to 8 of 8