| Title | Author(s) | Year | View Count |
 | Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease | 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 | 48 |
| Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liability | 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 | 594 |
| Long-range regulation at the SOX9 locus in development and disease | Gordon, CT; Tan, TY; Benko, S; Fitzpatrick, D; Lyonnet, S; Farlie, PG | 2009 | 51 |
 | Hirschsprung disease, associated syndromes and genetics: A review | 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 | 345 |
 | The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease | 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 | 122 |
| Higher prevalence of Hirschsprung disease in China explained by a common RET mutation | Garcia-Barcelo, MM; Amiel, J; Antinolo, G; Borrego, S; Burzynski, G; Ceccherini, I; Emison, E; Eng, C; Fernandez, R; Griseri, P; Hofstra, R; Kashuk, C; Lantien, F; Lyonnet, S; Miao, X; Tam, PKH; Tullio-Pelet, A; West, K; Chakravarti, A | 2006 | 121 |
| Differential liabilities of coding and non-coding mutations in complex disease | 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 | 90 |
| Differential liabilities of rare coding and common non-coding RET mutations explain the multifactorial genetics of Hirschsprung disease. | 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 | 90 |
| Heterozygous endothelin receptor B mutation in isolated Hirschsprung's disease | Amiel, J; Attie, T; Burge, D; Griffiths, M; Lyonnet, S; Tam, PKH | 1996 | 73 |
| Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung's disease | Amiel, J; Attie, T; Jan, D; Pelet, A; Edery, P; Bidaud, C; Lacombe, D; Tam, PKH; Simeoni, J; Flori, E; Nihoul-Fekete, C; Munnich, A; Lyonnet, S | 1996 | 103 |
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