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Clinical relevance of KRAS mutation detection in metastatic colorectal cancer treated by Cetuximab plus chemotherapy
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Published in British journal of cancer (23.04.2007)
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High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease
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Published in Molecular psychiatry (01.09.2012)
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De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease
Rovelet-Lecrux, A, Charbonnier, C, Wallon, D, Nicolas, G, Seaman, M N J, Pottier, C, Breusegem, S Y, Mathur, P P, Jenardhanan, P, Le Guennec, K, Mukadam, A S, Quenez, O, Coutant, S, Rousseau, S, Richard, A-C, Boland, A, Deleuze, J-F, Frebourg, T, Hannequin, D, Campion, D
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17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression
Le Guennec, K, Quenez, O, Nicolas, G, Wallon, D, Rousseau, S, Richard, A-C, Alexander, J, Paschou, P, Charbonnier, C, Bellenguez, C, Grenier-Boley, B, Lechner, D, Bihoreau, M-T, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Martinaud, O, Kalev, O, Mehrabian, S, Traykov, L, Ströbel, T, Le Ber, I, Caroppo, P, Epelbaum, S, Jonveaux, T, Pasquier, F, Rollin-Sillaire, A, Génin, E, Guyant-Maréchal, L, Kovacs, G G, Lambert, J-C, Hannequin, D, Campion, D, Rovelet-Lecrux, A
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LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
S. Hacein-Bey-Abina, Von Kalle, C., Schmidt, M., McCormack, M. P., Wulffraat, N., Leboulch, P., Lim, A., Osborne, C. S., Pawliuk, R., Morillon, E., Sorensen, R., Forster, A., Fraser, P., Cohen, J. I., G. de Saint Basile, Alexander, I., Wintergerst, U., Frebourg, T., Aurias, A., Stoppa-Lyonnet, D., Romana, S., Radford-Weiss, I., Gross, F., Valensi, F., Delabesse, E., Macintyre, E., Sigaux, F., Soulier, J., Leiva, L. E., Wissler, M., Prinz, C., Rabbitts, T. H., Le Deist, F., Fischer, A., Cavazzana-Calvo, M.
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Raux, G, Guyant-Maréchal, L, Martin, C, Bou, J, Penet, C, Brice, A, Hannequin, D, Frebourg, T, Campion, D
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Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome
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Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations
Le Caignec, C, Boceno, M, Saugier-Veber, P, Jacquemont, S, Joubert, M, David, A, Frebourg, T, Rival, J M
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A cryopyrin-associated periodic syndrome with joint destruction
Lequerré, T., Vittecoq, O., Saugier-Veber, P., Goldenberg, A., Patoz, P., Frébourg, T., Le Loët, X.
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BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing
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A new genotoxicity assay based on p53 target gene induction
Zerdoumi, Y., Kasper, E., Soubigou, F., Adriouch, S., Bougeard, G., Frebourg, T., Flaman, J-M.
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P53 germline mutations in childhood cancers and cancer risk for carrier individuals
CHOMPRET, A, BRUGIERES, L, FREBOURG, T, LEMERLE, J, BONAÏTI-PELLIE, C, FEUNTEUN, J, RONSIN, M, GARDES, M, DESSARPS-FREICHEY, F, ABEL, A, HUA, D, LIGOT, L, DONDON, M.-G, BRESSAC-DE PAILLERETS, B
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TP53 mutations predict disease control in metastatic colorectal cancer treated with cetuximab-based chemotherapy
ODEN-GANGLOFF, A, DI FIORE, F, LE PESSOT, F, SABOURIN, J.-C, TUECH, J.-J, MICHEL, P, FREBOURG, T, BIBEAU, F, LAMY, A, BOUGEARD, G, CHARBONNIER, F, BLANCHARD, F, TOUGERON, D, YCHOU, M, BOISSIERE, F
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Unusual Phenotypic Alteration of β Amyloid Precursor Protein (β APP) Maturation by a New Val-715 → Met β APP-770 Mutation Responsible for Probable Early-Onset Alzheimer's Disease
Ancolio, K., Dumanchin, C., Barelli, H., Warter, J. M., Brice, A., Campion, D., Frébourg, T., Checler, F.
Published in Proceedings of the National Academy of Sciences - PNAS (30.03.1999)
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Molecular profiling of bladder tumors based on the detection of FGFR3 and TP53 mutations
Lamy, A, Gobet, F, Laurent, M, Blanchard, F, Varin, C, Moulin, C, Andreou, A, Frebourg, T, Pfister, C
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