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Tania Attié

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H K Benailly; Jean-Michel Lapierre; Béatrice Laudier; Jeanne Amiel; Tania Attié; Marie-Christine De Blois; Michel Vekemans; Serge Romana
PMX2B, a new candidate gene for Hirschsprung's disease.
Pierre F Ray; Frydman Nelly; Tania Attié; Samir Hamamah; Violaine Kerbrat; Gérard Tachdjian; Serge Romana; Michel Vekemans; René Frydman; Arnold Munnich
Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination.
Séverine Roselli; Olivier Gribouval; Nicolas Boute; Mireille Sich; France Benessy; Tania Attié; Marie-Claire Gubler; Corinne Antignac
Podocin localizes in the kidney to the slit diaphragm area.

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All Publications

2003: H K Benailly; Jean-Michel Lapierre; Béatrice Laudier; Jeanne Amiel; Tania Attié; Marie-Christine De Blois; Michel Vekemans; Serge Romana
PMX2B, a new candidate gene for Hirschsprung's disease.
Clinical genetics 2003;64(3):204-9.
2002: Pierre F Ray; Frydman Nelly; Tania Attié; Samir Hamamah; Violaine Kerbrat; Gérard Tachdjian; Serge Romana; Michel Vekemans; René Frydman; Arnold Munnich
Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination.
Molecular human reproduction 2002;8(7):688-94.
2002: Séverine Roselli; Olivier Gribouval; Nicolas Boute; Mireille Sich; France Benessy; Tania Attié; Marie-Claire Gubler; Corinne Antignac
Podocin localizes in the kidney to the slit diaphragm area.
The American journal of pathology 2002;160(1):131-9.
2000: Pierre F Ray; Nadine Gigarel; Jean-Paul Bonnefont; Tania Attié; Samir Hamamah; Frydman Nelly; Michel Vekemans; René Frydman; Arnold Munnich
First specific preimplantation genetic diagnosis for ornithine transcarbamylase deficiency.
Prenatal diagnosis 2000;20(13):1048-54.
2000: Marie-France Gagnadoux; Tania Attié; Jeanne Amiel; Nadine Gigarel; Jean-Paul Bonnefont; Arnold Munnich; Marie-Claire Gubler; Corinne Antignac
[Prenatal diagnosis of autosomal recessive polycystic kidney disease].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2000;7(9):942-7.
1998: S Chappuis-Flament; A Pasini; Gabriella De Vita; C Ségouffin-Cariou; Alfredo Fusco; Tania Attié; Gilbert M Lenoir; Massimo Santoro; Marc Billaud
Dual effect on the RET receptor of MEN 2 mutations affecting specific extracytoplasmic cysteines.
Oncogene 1998;17(22):2851-61.
1998: Rémi Salomon; Jeanne Amiel; Tania Attié; Anna Pelet; Arnold Munnich; Stanislas LYONNET
[From monogenic to polygenic: model of Hirschsprung disease].
Pathologie-biologie 1998;46(9):705-7.
1998: B Doray; Rémi Salomon; Jeanne Amiel; Anna Pelet; Renaud Touraine; Marc Billaud; Tania Attié; B Bachy; Arnold Munnich; Stanislas LYONNET
Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease.
Human molecular genetics 1998;7(9):1449-52.
1998: Jeanne Amiel; Rémi Salomon; Tania Attié; Anna Pelet; Ha Trang; M Mokhtari; Claude Gaultier; Arnold Munnich; Stanislas LYONNET
Mutations of the RET-GDNF signaling pathway in Ondine's curse.
American journal of human genetics 1998;62(3):715-7.
1998: Jeanne Amiel; D Lacombe; Tania Attié; A Munnich; Stanislas LYONNET
[Congenital malformations in pediatric tumors].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1998;5 Suppl 2():88s-89s.
1997: C Bidaud; Rémi Salomon; G Van Camp; Anna Pelet; Tania Attié; C Eng; M Bonduelle; Jeanne Amiel; C Nihoul-Fékété; P J Willems; Arnold Munnich; Stanislas LYONNET
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
European journal of human genetics : EJHG 1997;5(4):247-51.
1996: Rémi Salomon; Tania Attié; Anna Pelet; C Bidaud; Charis Eng; Jeanne Amiel; Sabine Sarnacki; Olivier Goulet; Claude Ricour; C Nihoul-Fékété; Arnold Munnich; Stanislas LYONNET
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
Nature genetics 1996;14(3):345-7.
1996: Philippe Caron; Tania Attié; D David; Jeanne Amiel; F Brousset; P Roger; A Munnich; Stanislas LYONNET
C618R mutation in exon 10 of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease.
The Journal of clinical endocrinology and metabolism 1996;81(7):2731-3.
1996: P Edery; Tania Attié; Jeanne Amiel; Anna Pelet; Charis Eng; R M Hofstra; H Martelli; C Bidaud; Arnold Munnich; Stanislas LYONNET
Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome).
Nature genetics 1996;12(4):442-4.
1996: Jeanne Amiel; Tania Attié; Dominique M. Jan; Anna Pelet; P Edery; C Bidaud; D Lacombe; P Tam; J Simeoni; E Flori; C Nihoul-Fékété; Arnold Munnich; Stanislas LYONNET
Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.
Human molecular genetics 1996;5(3):355-7.
1996: Tania Attié; Rémi Salomon; Jeanne Amiel; P Edery; Anna Pelet; C Nihoul-Fékété; Arnold Munnich; Stanislas LYONNET
[Genetics of Hirschsprung disease].
Comptes rendus des séances de la Société de biologie et de ses filiales 1996;190(5-6):549-56.
1996: Tania Attié; Jeanne Amiel; Dominique M. Jan; P Edery; Anna Pelet; Rémi Salomon; Arnold Munnich; Stanislas LYONNET; C Nihoul-Fékété
[Genetics of Hirschsprung disease].
Annales de chirurgie 1996;50(7):538-41.
1995: Tania Attié; M Till; Anna Pelet; Jeanne Amiel; P Edery; L Boutrand; Arnold Munnich; Stanislas LYONNET
Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.
Human molecular genetics 1995;4(12):2407-9.
1995: Tania Attié; Anna Pelet; P Edery; Charis Eng; Lois M Mulligan; Jeanne Amiel; L Boutrand; C Beldjord; C Nihoul-Fékété; Arnold Munnich
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
Human molecular genetics 1995;4(8):1381-6.
1995: Tania Attié; M Till; Anna Pelet; P Edery; J P Bonnet; Arnold Munnich; Stanislas LYONNET
Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung disease.
Journal of medical genetics 1995;32(4):312-3.
1994: Lois M Mulligan; Charis Eng; Tania Attié; Stanislas LYONNET; Deborah J Marsh; V J Hyland; Bruce G Robinson; A Frilling; C Verellen-Dumoulin; A Safar
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.
Human molecular genetics 1994;3(12):2163-7.
1994: P Edery; Tania Attié; Lois M Mulligan; Anna Pelet; Charis Eng; B A Ponder; Arnold Munnich; Stanislas LYONNET
A novel polymorphism in the coding sequence of the human RET proto-oncogene.
Human genetics 1994;94(5):579-80.
1994: P Edery; Anna Pelet; Lois M Mulligan; L Abel; Tania Attié; E Dow; D Bonneau; A David; W Flintoff; Dominique M. Jan
Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
Journal of medical genetics 1994;31(8):602-6.
1994: Tania Attié; P Edery; Stanislas LYONNET; C Nihoul-Fékété; Arnold Munnich
[Identification of mutation of RET proto-oncogene in Hirschsprung disease].
Comptes rendus des séances de la Société de biologie et de ses filiales 1994;188(5-6):499-504.