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Extensive molecular screening for hereditary non-polyposis colorectal cancer.
Published in:
2000
By:
- Dieumegard, B;
- Grandjouan, S;
- Sabourin, J-C;
- Bihan, M-L Le;
- Lefrère, I;
- Bellefqih;
- Pignon, J-P;
- Rougier, P;
- Lasser, P;
- Bénard, J;
- Couturier, D;
- Paillerets, B Bressac-de;
- Le Bihan, M L;
- Bressac-de Paillerets, B
Publication type:
journal article
Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers.
Published in:
Clinical Genetics, 2017, v. 92, n. 6, p. 606, doi. 10.1111/cge.13014
By:
- Muller, M.;
- Ferlicot, S.;
- Guillaud-Bataille, M.;
- Le Teuff, G.;
- Genestie, C.;
- Deveaux, S.;
- Slama, A.;
- Poulalhon, N.;
- Escudier, B.;
- Albiges, L.;
- Soufir, N.;
- Avril, M.-F.;
- Gardie, B.;
- Saldana, C.;
- Allory, Y.;
- Gimenez-Roqueplo, A.-P.;
- Bressac-de Paillerets, B.;
- Richard, S.;
- Benusiglio, P.R.
Publication type:
Article
Germline BAP1 mutations predispose also to multiple basal cell carcinomas.
Published in:
Clinical Genetics, 2015, v. 88, n. 3, p. 273, doi. 10.1111/cge.12472
By:
- de la Fouchardière, A.;
- Cabaret, O.;
- Savin, L.;
- Combemale, P.;
- Schvartz, H.;
- Penet, C.;
- Bonadona, V.;
- Soufir, N.;
- Bressac‐de Paillerets, B.
Publication type:
Article
Short Report Real-time PCR-based gene dosage assay for detecting BRCA1 rearrangements in breast–ovarian cancer families.
Published in:
Clinical Genetics, 2004, v. 65, n. 2, p. 131, doi. 10.1111/j.0009-9163.2004.00200.x
By:
- Barrois, M.;
- Bièche, I.;
- Mazoyer, S.;
- Champèm, M. H.;
- Bressac-de Paillerets, B.;
- Lidereau, R.
Publication type:
Article
Selective G to T mutations of p53 gene in hepatocellular carcinoma from southern Africa.
Published in:
Nature, 1991, v. 350, n. 6317, p. 429, doi. 10.1038/350429a0
By:
- Bressac, B.;
- Kew, M.
Publication type:
Article
Non-Hodgkin's lymphomas and myeloid disorders: deletions associated with t(2;5) and t(3;5) detected by FISH.
Published in:
1998
By:
- Dragon-Durey, M-A;
- Goguel, A-F;
- Leonard, C;
- Berger, R;
- Bressac-de-Paillerets, B;
- Fauvet, D;
- Bernheim, A
Publication type:
journal article
Prise en charge des formes familiales de tumeurs rares : mélanomes familiaux et primitifs multiples.
Published in:
Oncologie (Tech Science Press), 2008, v. 10, n. 6, p. 411, doi. 10.1007/s10269-008-0906-3
By:
- Avril, M.-F.;
- Bressac-de Paillerets, B.;
- Demenais, F.
Publication type:
Article
Prédisposition génétique aux cancers du sein et de l’ovaire: Diagnostic moléculaire et conséquences.
Published in:
Oncologie (Tech Science Press), 2006, v. 8, n. 3, p. 213, doi. 10.1007/s10269-006-0361-y
By:
- Delaloge, S.;
- Albiges, L.;
- Bressac -- de Paillerets, B.;
- Chompret, A.
Publication type:
Article
Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas.
Published in:
1996
By:
- Moutou, Céline;
- Bihan, Christine Le;
- Chompret, Agnès;
- Poisson, Nicole;
- Brugières, Laurence;
- Bressac, Brigitte;
- Feunteun, Jean;
- Lemerle, Jean;
- Bonaïti-Pellié, Catherine;
- Moutou, C;
- Le Bihan, C;
- Chompret, A;
- Poisson, N;
- Brugières, L;
- Bressac, B;
- Feunteun, J;
- Lemerle, J;
- Bonaïti-Pellié, C
Publication type:
journal article
The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.
Published in:
Digestive Diseases & Sciences, 2023, v. 68, n. 4, p. 1525, doi. 10.1007/s10620-022-07733-z
By:
- Baz, M.;
- Gondran-Teiller, V.;
- Bressac, B.;
- Cabaret, O.;
- Fievet, A.;
- Dimaria, M.;
- Goldbarg, V.;
- Colas, C.;
- Bonnet-Dupeyron, M. N.;
- Tinat, J.;
- Lebrun, M.;
- Mari, V.;
- Limacher, J. M.;
- Corsini, C.;
- Ginglinger, E.;
- Saurin, J. C.;
- Brahimi, A.;
- Rouzier, C.;
- Giraud, S.;
- Schuster, H.
Publication type:
Article
Subungual squamous cell carcinoma in a BAP1 germline pathogenic variant carrier.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2021, v. 35, n. 10, p. e665, doi. 10.1111/jdv.17372
By:
- Idoudi, S.;
- Bressac‐ de Paillerets, B.;
- Balme, B.;
- Bonnet‐Dupeyron, M.‐N.;
- Golmard, L.;
- Thomas, L.
Publication type:
Article
Contribution of CDKN2A/P16, P14, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma.
Published in:
Familial Cancer, 2010, v. 9, n. 4, p. 663, doi. 10.1007/s10689-010-9379-9
By:
- Buecher, B.;
- Gauthier-Villars, M.;
- Desjardins, L.;
- Lumbroso-Le Rouic, L.;
- Levy, C.;
- Pauw, A.;
- Bombled, J.;
- Tirapo, C.;
- Houdayer, C.;
- Bressac-de Paillerets, B.;
- Stoppa-Lyonnet, D.
Publication type:
Article
Prevalence of the E318 K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history.
Published in:
Pigment Cell & Melanoma Research, 2013, v. 26, n. 2, p. 259, doi. 10.1111/pcmr.12047
By:
- Ghiorzo, P.;
- Pastorino, L.;
- Queirolo, P.;
- Bruno, W.;
- Tibiletti, M. G.;
- Nasti, S.;
- Andreotti, V.;
- Paillerets, B. Bressac‐de;
- Bianchi Scarrà, G.
Publication type:
Article
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
Published in:
2008
By:
- Lesueur, F;
- de Lichy, M;
- Barrois, M;
- Durand, G;
- Bombled, J;
- Avril, M-F;
- Chompret, A;
- Boitier, F;
- Lenoir, G M;
- Bressac-de Paillerets, B;
- French Familial Melanoma Study Group;
- Baccard, Monique;
- Bachollet, Bertrand;
- Berthet, Pascaline;
- Bonadona, Valérie;
- Bonnetblanc, Jean-Marie;
- Caron, Olivier;
- Chevrant-Breton, Jacqueline;
- Cuny, Jean-François;
- Dalle, Stéphane
Publication type:
journal article
Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma.
Published in:
2007
By:
- Gad, S.;
- Lefèvre, S. H.;
- Khoo, S. K.;
- Giraud, S.;
- Vieillefond, A.;
- Vasiliu, V.;
- Ferlicot, S.;
- Molinié, V.;
- Denoux, Y.;
- Thiounn, N.;
- Chrétien, Y.;
- Méjean, A.;
- Zerbib, M.;
- Benoît, G.;
- Hervé, J. M.;
- Allègre, G.;
- Bressac-de Paillerets, B.;
- Teh, B. T.;
- Richard, S.
Publication type:
Correction Notice
Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma.
Published in:
British Journal of Cancer, 2007, v. 96, n. 2, p. 336, doi. 10.1038/sj.bjc.6603492
By:
- Gad, S.;
- Lefèvre, S. H.;
- Khoo, S. K.;
- Giraud, S.;
- Vieillefond, A.;
- Vasiliu, V.;
- Ferlicot, S.;
- Molinié, V.;
- Denoux, Y.;
- Thiounn, N.;
- Chrétien, Y.;
- Méjean, A.;
- Zerbib, M.;
- Benoît, G.;
- Hervé, J. M.;
- Allègre, G.;
- Bressac-de Paillerets, B.;
- Teh, B. T.;
- Richard, S.
Publication type:
Article
Search for germline alterations in CDKN2A/ARF and CDK4 of 42 Jewish melanoma families with or without neural system tumours.
Published in:
2005
By:
- Marian, C.;
- Scope, A.;
- Laud, K.;
- Friedman, E.;
- Pavlotsky, F.;
- Yakobson, E.;
- Bressac-de Paillerets, B.;
- Azizi, E.
Publication type:
journal article
P53 germline mutations in childhood cancers and cancer risk for carrier individuals.
Published in:
British Journal of Cancer, 2000, v. 82, n. 12, p. 1932
By:
- Chompret, A;
- Brugières, L;
- Ronsin, M;
- Gardes, M;
- Dessarps-Freichey, F;
- Abel, A;
- Hua, D;
- Ligot, L;
- Dondon, M-G;
- Paillerets, B Bressac-de;
- Frébourg, T;
- Lemerle, J;
- Bonaïti-Pellié, C;
- Feunteun, J
Publication type:
Article
Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16<sup>INK4A</sup>, P14<sup>ARF</sup> or cdk4 genes.
Published in:
British Journal of Cancer, 2000, v. 82, n. 4, p. 818, doi. 10.1054/bjoc.1999.1005
By:
- Soufir, N;
- Paillerets, B Bressac-de;
- Desjardins, L;
- Lévy, C;
- Bombled, J;
- Gorin, I;
- Schlienger, P;
- Stoppa-Lyonnet, D
Publication type:
Article
Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families.
Published in:
British Journal of Cancer, 1999, v. 80, n. 7, p. 1042, doi. 10.1038/sj.bjc.6690460
By:
- Janin, N;
- Andrieu, N;
- Ossian, K;
- Laugé, A;
- Croquette, M-F;
- Griscelli, C;
- Debré, M;
- Bressac-de-Paillerets, B;
- Aurias, A;
- Stoppa-Lyonnet, D
Publication type:
Article
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study.
Published in:
JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 20, p. 1568, doi. 10.1093/jnci/djq363
By:
- Demenais, F.;
- Mohamdi, H.;
- Chaudru, V.;
- Goldstein, A. M.;
- Newton Bishop, J. A.;
- Bishop, D. T.;
- Kanetsky, P. A.;
- Hayward, N. K.;
- Gillanders, E.;
- Elder, D. E.;
- Avril, M. F.;
- Azizi, E.;
- Van Belle, P.;
- Bergman, W.;
- Bianchi-Scarrà, G.;
- Bressac-de Paillerets, B.;
- Calista, D.;
- Carrera, C.;
- Hansson, J.;
- Harland, M.
Publication type:
Article
Genital and anorectal mucosal melanoma is associated with cutaneous melanoma in patients and in families.
Published in:
British Journal of Dermatology, 2013, v. 169, n. 3, p. 594, doi. 10.1111/bjd.12421
By:
- Cazenave, H.;
- Maubec, E.;
- Mohamdi, H.;
- Grange, F.;
- Bressac‐de Paillerets, B.;
- Demenais, F.;
- Avril, M.F.
Publication type:
Article
Novel FH mutation in a patient with cutaneous leiomyomatosis associated with cutis verticis gyrata, eruptive collagenoma and Charcot-Marie-Tooth disease M. Marque et al. Novel FH mutation.
Published in:
British Journal of Dermatology, 2010, v. 163, n. 6, p. 1337, doi. 10.1111/j.1365-2133.2010.09912.x
By:
- Marque, M.;
- Gardie, B.;
- Bressac de Paillerets, B.;
- Rustin, P.;
- Guillot, B.;
- Richard, S.;
- Bessis, D.
Publication type:
Article

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