Béroud C - Search Results

1

Actionable Genes, Core Databases, and Locus-Specific Databases.

Pinard A, Miltgen M, Blanchard A, Mathieu H, Desvignes JP, Salgado D, Fabre A, Arnaud P, Barré L, Krahn M, Grandval P, Olschwang S, Zaffran S, Boileau C, Béroud C, Collod-Béroud G. Pinard A, et al. Among authors: beroud c. Hum Mutat. 2016 Dec;37(12):1299-1307. doi: 10.1002/humu.23112. Epub 2016 Sep 26. Hum Mutat. 2016. PMID: 27600092

2

Software and database for the analysis of mutations in the human FBN1 gene.

Collod G, Béroud C, Soussi T, Junien C, Boileau C. Collod G, et al. Among authors: beroud c. Nucleic Acids Res. 1996 Jan 1;24(1):137-40. doi: 10.1093/nar/24.1.137. Nucleic Acids Res. 1996. PMID: 8594563 Free PMC article.

3

p53 and APC gene mutations: software and databases.

Béroud C, Soussi T. Béroud C, et al. Nucleic Acids Res. 1997 Jan 1;25(1):138. doi: 10.1093/nar/25.1.138. Nucleic Acids Res. 1997. PMID: 9016523 Free PMC article.

4

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene.

Collod-Béroud G, Béroud C, Adès L, Black C, Boxer M, Brock DJ, Godfrey M, Hayward C, Karttunen L, Milewicz D, Peltonen L, Richards RI, Wang M, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: beroud c. Nucleic Acids Res. 1997 Jan 1;25(1):147-50. doi: 10.1093/nar/25.1.147. Nucleic Acids Res. 1997. PMID: 9016526 Free PMC article.

5

Software and database for the analysis of mutations in the human LDL receptor gene.

Varret M, Rabès JP, Collod-Béroud G, Junien C, Boileau C, Béroud C. Varret M, et al. Among authors: beroud c. Nucleic Acids Res. 1997 Jan 1;25(1):172-80. doi: 10.1093/nar/25.1.172. Nucleic Acids Res. 1997. PMID: 9016531 Free PMC article.

6

Marfan Database (third edition): new mutations and new routines for the software.

Collod-Béroud G, Béroud C, Ades L, Black C, Boxer M, Brock DJ, Holman KJ, de Paepe A, Francke U, Grau U, Hayward C, Klein HG, Liu W, Nuytinck L, Peltonen L, Alvarez Perez AB, Rantamäki T, Junien C, Boileau C. Collod-Béroud G, et al. Among authors: beroud c. Nucleic Acids Res. 1998 Jan 1;26(1):229-3. doi: 10.1093/nar/26.1.229. Nucleic Acids Res. 1998. PMID: 9399842 Free PMC article.

7

[Von Hippel-Lindau disease: a hereditary disease that impacts multiple tissues].

Richard S, Giraud S, Hammel P, Beroud C, Joly D, Olschwang S, Resche F. Richard S, et al. Among authors: beroud c. Presse Med. 1998 Jun 20;27(22):1112-20. Presse Med. 1998. PMID: 9767816 Review. French. No abstract available.

8

Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC.

Gallou C, Joly D, Méjean A, Staroz F, Martin N, Tarlet G, Orfanelli MT, Bouvier R, Droz D, Chrétien Y, Maréchal JM, Richard S, Junien C, Béroud C. Gallou C, et al. Among authors: beroud c. Hum Mutat. 1999;13(6):464-75. doi: 10.1002/(SICI)1098-1004(1999)13:6<464::AID-HUMU6>3.0.CO;2-A. Hum Mutat. 1999. PMID: 10408776

9

UMD (Universal mutation database): a generic software to build and analyze locus-specific databases.

Béroud C, Collod-Béroud G, Boileau C, Soussi T, Junien C. Béroud C, et al. Hum Mutat. 2000;15(1):86-94. doi: 10.1002/(SICI)1098-1004(200001)15:1<86::AID-HUMU16>3.0.CO;2-4. Hum Mutat. 2000. PMID: 10612827

10

Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.

Wautot V, Vercherat C, Lespinasse J, Chambe B, Lenoir GM, Zhang CX, Porchet N, Cordier M, Béroud C, Calender A. Wautot V, et al. Among authors: beroud c. Hum Mutat. 2002 Jul;20(1):35-47. doi: 10.1002/humu.10092. Hum Mutat. 2002. PMID: 12112656

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