Béroud C - Search Results

1

BRCA Share: A Collection of Clinical BRCA Gene Variants.

Béroud C, Letovsky SI, Braastad CD, Caputo SM, Beaudoux O, Bignon YJ, Bressac-De Paillerets B, Bronner M, Buell CM, Collod-Béroud G, Coulet F, Derive N, Divincenzo C, Elzinga CD, Garrec C, Houdayer C, Karbassi I, Lizard S, Love A, Muller D, Nagan N, Nery CR, Rai G, Revillion F, Salgado D, Sévenet N, Sinilnikova O, Sobol H, Stoppa-Lyonnet D, Toulas C, Trautman E, Vaur D, Vilquin P, Weymouth KS, Willis A; Laboratory Corporation of America Variant Classification Group; Quest Diagnostics Variant Classification Group; UNICANCER Genetic Group BRCA Laboratory Network; Eisenberg M, Strom CM. Béroud C, et al. Hum Mutat. 2016 Dec;37(12):1318-1328. doi: 10.1002/humu.23113. Epub 2016 Sep 28. Hum Mutat. 2016. PMID: 27633797 Free article.

2

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.

3

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

4

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

5

p53 website and analysis of p53 gene mutations in human cancer: forging a link between epidemiology and carcinogenesis.

Soussi T, Dehouche K, Béroud C. Soussi T, et al. Among authors: beroud c. Hum Mutat. 2000;15(1):105-13. doi: 10.1002/(SICI)1098-1004(200001)15:1<105::AID-HUMU19>3.0.CO;2-G. Hum Mutat. 2000. PMID: 10612830

6

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

7

The UMD-LDLR database: additions to the software and 490 new entries to the database.

Villéger L, Abifadel M, Allard D, Rabès JP, Thiart R, Kotze MJ, Béroud C, Junien C, Boileau C, Varret M. Villéger L, et al. Among authors: beroud c. Hum Mutat. 2002 Aug;20(2):81-7. doi: 10.1002/humu.10102. Hum Mutat. 2002. PMID: 12124988 Review.

8

The UMD-p53 database: new mutations and analysis tools.

Béroud C, Soussi T. Béroud C, et al. Hum Mutat. 2003 Mar;21(3):176-81. doi: 10.1002/humu.10187. Hum Mutat. 2003. PMID: 12619103 Review.

9

Significance of TP53 mutations in human cancer: a critical analysis of mutations at CpG dinucleotides.

Soussi T, Béroud C. Soussi T, et al. Among authors: beroud c. Hum Mutat. 2003 Mar;21(3):192-200. doi: 10.1002/humu.10189. Hum Mutat. 2003. PMID: 12619105 Review.

10

Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.

Collod-Béroud G, Le Bourdelles S, Ades L, Ala-Kokko L, Booms P, Boxer M, Child A, Comeglio P, De Paepe A, Hyland JC, Holman K, Kaitila I, Loeys B, Matyas G, Nuytinck L, Peltonen L, Rantamaki T, Robinson P, Steinmann B, Junien C, Béroud C, Boileau C. Collod-Béroud G, et al. Among authors: beroud c. Hum Mutat. 2003 Sep;22(3):199-208. doi: 10.1002/humu.10249. Hum Mutat. 2003. PMID: 12938084 Review.

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