Authors:
Auroy, S
Avril, MF
Chompret, A
Pham, D
Goldstein, AM
Bianchi-Scarra, G
Frebourg, T
Joly, P
Spatz, A
Rubino, C
Demenais, F
Bressac-de Paillerets, B
Citation: S. Auroy et al., Sporadic multiple primary melanoma cases: CDKN2A germline mutations with afounder effect, GENE CHROM, 32(3), 2001, pp. 195-202
Authors:
Avril, MF
Chompret, A
Verne-Fourment, L
Terrier-Lacombe, MJ
Spatz, A
Fizazi, K
Bressac-de Paillerets, B
Demenais, F
Theodore, C
Citation: Mf. Avril et al., Association between germ cell tumours, large numbers of naevi, atypical naevi and melanoma, MELANOMA RE, 11(2), 2001, pp. 117-122
Authors:
Briollais, L
Chompret, A
Guilloud-Bataille, M
Bressac-de Paillerets, B
Avril, MF
Demenais, F
Citation: L. Briollais et al., Patterns of familial aggregation of three melanoma risk factors: great number of naevi, light phototype and high degree of sun exposure, INT J EPID, 29(3), 2000, pp. 408-415
Authors:
Soufir, N
Bressac-de Paillerets, B
Desjardins, L
Levy, C
Bombled, J
Gorin, I
Schlienger, P
Stoppa-Lyonnet, D
Citation: N. Soufir et al., Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes, BR J CANC, 82(4), 2000, pp. 818-822
Authors:
Dieumegard, B
Grandjouan, S
Sabourin, JC
Le Bihan, ML
Lefrere, I",Bellefqih,"Pignon, JP
Rougier, P
Lasser, P
Benard, J
Couturier, D
Bressac-de Paillerets, B
Citation: B. Dieumegard et al., Extensive molecular screening for hereditary non-polyposis colorectal cancer, BR J CANC, 82(4), 2000, pp. 871-880
Authors:
Chompret, A
Brugieres, L
Ronsin, M
Gardes, M
Dessarps-Freichey, F
Abel, A
Hua, D
Ligot, L
Dondon, MG
Bressac-de Paillerets, B
Frebourg, T
Lemerle, J
Bonaiti-Pellie, C
Feunteun, J
Citation: A. Chompret et al., p53 germline mutations in childhood cancers and cancer risk for carrier individuals, BR J CANC, 82(12), 2000, pp. 1932-1937
Authors:
Mazoyer, S
Leary, J
Kirk, J
Fleischmann, E
Wagner, T
Claes, K
Messiaen, L
Foulkes, W
Desrochers, M
Simard, J
Phelan, CM
Kwan, E
Narod, SA
Vahteristo, P
Nevanlinna, H
Durando, X
Bignon, YJ
Peyrat, JP
Bonnardel, C
Sinilnikova, OM
Puget, N
Lenoir, GM
Mazoyer, S
Audoynaud, C
Goldgar, D
Maugard, C
Caux, V
Gad, S
Stoppa-Lyonnet, D
Nogues, C
Lidereau, R
Machavoine, C
Bressac-de Paillerets, B
Kuschel, B
Betz, B
Niederacher, D
Beckmann, MW
Hamann, U
Gayther, SA
Ponder, BAP
Robinson, M
Taylor, GR
Bishop, T
Catteau, A
Solomon, E
Cohen, B
Steel, M
Collins, N
Stratton, M
van der Looij, M
Olah, E
Miller, NJ
Barton, DE
Sverdlov, RS
Friedman, E
Radice, P
Montagna, M
Sensi, E
Caligo, M
van Eijk, R
Devilee, P
van der Luijt, R
Heimdal, K
Moller, P
Borg, A
Diez, O
Cortes, J
Domenech, M
Baiget, M
Osorio, A
Benitez, J
Borg, A
Maillet, P
Sappino, AP
Ozdag, H
Ozcelik, T
Ozturk, M
Rohlfs, EM
Boyd, J
McDermott, D
Offit, K
Unger, M
Nathanson, K
Weber, BL
Sellers, TA
Hampton, E
Couch, FJ
Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212