Salomon R - Search Results

1

Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease.

Pelet A, de Pontual L, Clément-Ziza M, Salomon R, Mugnier C, Matsuda F, Lathrop M, Munnich A, Feingold J, Lyonnet S, Abel L, Amiel J. Pelet A, et al. Among authors: salomon r. J Med Genet. 2005 Mar;42(3):e18. doi: 10.1136/jmg.2004.028746. J Med Genet. 2005. PMID: 15744028 Free PMC article. No abstract available.

2

Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.

Salomon R, Attié T, Pelet A, Bidaud C, Eng C, Amiel J, Sarnacki S, Goulet O, Ricour C, Nihoul-Fékété C, Munnich A, Lyonnet S. Salomon R, et al. Nat Genet. 1996 Nov;14(3):345-7. doi: 10.1038/ng1196-345. Nat Genet. 1996. PMID: 8896569

3

Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease.

Doray B, Salomon R, Amiel J, Pelet A, Touraine R, Billaud M, Attié T, Bachy B, Munnich A, Lyonnet S. Doray B, et al. Among authors: salomon r. Hum Mol Genet. 1998 Sep;7(9):1449-52. doi: 10.1093/hmg/7.9.1449. Hum Mol Genet. 1998. PMID: 9700200

4

Investigation of germline GFR alpha-1 mutations in Hirschsprung disease.

Myers SM, Salomon R, Goessling A, Pelet A, Eng C, von Deimling A, Lyonnet S, Mulligan LM. Myers SM, et al. Among authors: salomon r. J Med Genet. 1999 Mar;36(3):217-20. J Med Genet. 1999. PMID: 10204848 Free PMC article.

5

Segregation at three loci explains familial and population risk in Hirschsprung disease.

Gabriel SB, Salomon R, Pelet A, Angrist M, Amiel J, Fornage M, Attié-Bitach T, Olson JM, Hofstra R, Buys C, Steffann J, Munnich A, Lyonnet S, Chakravarti A. Gabriel SB, et al. Among authors: salomon r. Nat Genet. 2002 May;31(1):89-93. doi: 10.1038/ng868. Epub 2002 Apr 15. Nat Genet. 2002. PMID: 11953745

6

[Genetics of Hirschsprung disease].

Attié T, Amiel J, Jan D, Edery P, Pelet A, Salomon R, Munnich A, Lyonnet S, Nihoul-Fékété C. Attié T, et al. Among authors: salomon r. Ann Chir. 1996;50(7):538-41. Ann Chir. 1996. PMID: 9035423 French.

7

[Genetics of Hirschsprung disease].

Attié T, Salomon R, Amiel J, Edery P, Pelet A, Nihoul-Fékété C, Munnich A, Lyonnet S. Attié T, et al. Among authors: salomon r. C R Seances Soc Biol Fil. 1996;190(5-6):549-56. C R Seances Soc Biol Fil. 1996. PMID: 9074720 Review. French.

8

[From monogenic to polygenic: model of Hirschsprung disease].

Salomon R, Amiel J, Attié T, Pelet A, Munnich A, Lyonnet S. Salomon R, et al. Pathol Biol (Paris). 1998 Nov;46(9):705-7. Pathol Biol (Paris). 1998. PMID: 9885824 Review. French.

9

A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.

Bolk S, Pelet A, Hofstra RM, Angrist M, Salomon R, Croaker D, Buys CH, Lyonnet S, Chakravarti A. Bolk S, et al. Among authors: salomon r. Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):268-73. doi: 10.1073/pnas.97.1.268. Proc Natl Acad Sci U S A. 2000. PMID: 10618407 Free PMC article.

10

Mutations of the RET-GDNF signaling pathway in Ondine's curse.

Amiel J, Salomon R, Attié T, Pelet A, Trang H, Mokhtari M, Gaultier C, Munnich A, Lyonnet S. Amiel J, et al. Among authors: salomon r. Am J Hum Genet. 1998 Mar;62(3):715-7. doi: 10.1086/301759. Am J Hum Genet. 1998. PMID: 9497256 Free PMC article. No abstract available.

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