Rare Mutations in XRCC2 Increase the Risk of Breast Cancer von Park, D.J., Lesueur, F., Nguyen-Dumont, T., Pertesi, M., Odefrey, F., Hammet, F., Neuhausen, S.L., John, E.M., Andrulis, I.L., Terry, M.B., Daly, M., Buys, S., Le Calvez-Kelm, F., Lonie, A., Pope, B.J., Tsimiklis, H., Voegele, C., Hilbers, F.M., Hoogerbrugge, N., Barroso, A., Osorio, A., Giles, G.G., Devilee, P., Benitez, J., Hopper, J.L., Tavtigian, S.V., Goldgar, D.E., Southey, M.C.

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Multigene testing of moderate-risk genes: be mindful of the missense von Young, E L, Feng, B J, Stark, A W, Damiola, F, Durand, G, Forey, N, Francy, T C, Gammon, A, Kohlmann, W K, Kaphingst, K A, McKay-Chopin, S, Nguyen-Dumont, T, Oliver, J, Paquette, A M, Pertesi, M, Robinot, N, Rosenthal, J S, Vallee, M, Voegele, C, Hopper, J L, Southey, M C, Andrulis, I L, John, E M, Hashibe, M, Gertz, J, Le Calvez-Kelm, F, Lesueur, F, Goldgar, D E, Tavtigian, S V

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Circulating concentrations of insulin‐like growth factor‐I, insulin‐like growth factor‐binding protein‐3, genetic polymorphisms and mammographic density in premenopausal Mexican wo... von Rinaldi, S., Biessy, C., Hernandez, M., Lesueur, F., dos‐Santos‐Silva, I., Rice, M.S., Lajous, M., Lopez‐Ridaura, R., Torres‐Mejía, G., Romieu, I.

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Perceptions of Inclusive Education in Mexico City: An Exploratory Study von Lavin, Carlos E., Francis, Grace L., Mason, Linda H., LeSueur, Robert F.

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Detection of BRCA1/2 mutations in breast cancer patients from Thailand and Pakistan von Ahmad, J, Le Calvez-Kelm, F, Daud, S, Voegele, C, Vallée, M, Ahmad, A, Kakar, N, McKay, JD, Gaborieau, V, Léoné, M, Sinilnikova, O, Sangrajrang, S, Tavtigian, SV, Lesueur, F

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A sample storage management system for biobanks von Voegele, C., Alteyrac, L., Caboux, E., Smans, M., Lesueur, F., Le Calvez-Kelm, F., Hainaut, P.

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39 The Search for Rare Variants That Contribute to Cancer Susceptibility von Lesueur, F, Bertolotto, C, Park, D.J, Demenais, F, Ballotti, R, Bressac-de Paillerets, B, Southey, M.C, Goldgar, D.E, Tavtitgian, S.V

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Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma von Avril, M-F, Bahadoran, P, Cabaret, O, Caron, O, de la Fouchardière, A, Demenais, F, Desjardins, L, Frébourg, T, Hammel, P, Leccia, M-T, Lesueur, F, Mahé, E, Martin, L, Maubec, E, Remenieras, A, Richard, S, Robert, C, Soufir, N, Stoppa-Lyonnet, D, Thomas, L, Vabres, P, Bressac-de Paillerets, B

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The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma von 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

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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer von BENUSIGLIO, P. R, PHAROAH, P. D, PONDER, B. A. J, SMITH, P. L, LESUEUR, F, CONROY, D, LUBEN, R. N, DEW, G, JORDAN, C, DUNNING, A, EASTON, D. F

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3.2-O7Women’s mental health in the perinatal period according to migrant status: the French nationally representative ELFE birth cohort study von El-Khoury Lesueur, F, Melchior, M

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3.2-O7; Women’s mental health in the perinatal period according to migrant status: the French nationally representative ELFE birth cohort study von El-Khoury Lesueur, F, Melchior, M

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Germline Homozygous Mutations at Codon 804 in the RET Protooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients von Lesueur, F., Cebrian, A., Cranston, A., Leyland, J., Faid, T. M., Clements, M. R., Robledo, M., Whittaker, J., Ponder, B. A. J.

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Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer von McKay, J D, Thompson, D, Lesueur, F, Stankov, K, Pastore, A, Watfah, C, Strolz, S, Riccabona, G, Moncayo, R, Romeo, G, Goldgar, D E

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Unexpected pregnancy, experience of sexual violence and contraception among women who use cannabis or other illegal substance in the Great Paris Region: Data from the 2016 Health B... von Embersin-Kyprianou, C., Yermachenko, A., Massari, El-Khoury-Lesueur, F., Melchior, M.

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Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population von Lesueur, F, Song, H, Ahmed, S, Luccarini, C, Jordan, C, Luben, R, Easton, D F, Dunning, A M, Pharoah, P D, Ponder, B A J

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Genetic heterogeneity in familial nonmedullary thyroid carcinoma : Exclusion of linkage to RET, MNG1 and TCO in 56 families von LESUEUR, F, STARK, M, TOCCO, T, AYADI, H, DELISLE, M. J, GOLDGAR, D. E, SCHLUMBERGER, M, ROMEO, G, CANZIAN, F

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Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes von Chaudru, Valérie, Lo, M. T., Lesueur, F., Marian, C., Mohamdi, H., Laud, K., Barrois, M., Chompret, A., Avril, M. F., Demenais, F., Paillerets, B. Bressac-de

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The role of prenatal social support in social inequalities with regard to maternal postpartum depression according to migrant status: J Affect Disord von Nakamura, A., El-Khoury Lesueur, F., Sutter-Dallay, Anne-Laure, Franck, J. E., Thierry, X., Melchior, M., van Der Waerden, J.

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Circulating plasma phospholipid fatty acids and risk of pancreatic cancer in a large European cohort von Matejcic, M., Lesueur, F., Biessy, C., Renault, A.L., Mebirouk, N., Yammine, S., Keski‐Rahkonen, P., Li, K., Hémon, B., Weiderpass, E., Rebours, V., Boutron‐Ruault, M.C., Carbonnel, F., Kaaks, R., Katzke, V., Kuhn, T., Boeing, H., Trichopoulou, A., Palli, D., Agnoli, C., Panico, S., Tumino, R., Sacerdote, C., Quirós, J.R., Duell, E.J., Porta, M., Sánchez, M.J., Chirlaque, M.D., Barricarte, A., Amiano, P., Ye, W., Peeters, P.H., Khaw, K.T., Perez‐Cornago, A., Key, T.J., Bueno‐de‐Mesquita, H.B., Riboli, E., Vineis, P., Romieu, I., Gunter, M.J., Chajès, V.

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