Congenital Toxoplasma Infection: Monthly Prenatal Screening Decreases Transmission Rate and Improves Clinical Outcome at Age 3 Years von Wallon, M., Peyron, F., Cornu, C., Vinault, S., Abrahamowicz, M., Kopp, C. Bonithon, Binquet, C.

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The epigenetic control of transposable elements and imprinted genes in newborns is affected by the mode of conception: ART versus spontaneous conception without underlying infertil... von Choux, C, Binquet, C, Carmignac, V, Bruno, C, Chapusot, C, Barberet, J, Lamotte, M, Sagot, P, Bourc'his, D, Fauque, P

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Do assisted reproductive technologies and in vitro embryo culture influence the epigenetic control of imprinted genes and transposable elements in children? von Barberet, J, Binquet, C, Guilleman, M, Doukani, A, Choux, C, Bruno, C, Bourredjem, A, Chapusot, C, Bourc’his, D, Duffourd, Y, Fauque, P

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MEN1 Disease Occurring Before 21 Years Old: A 160-Patient Cohort Study From the Groupe d'étude des Tumeurs Endocrines von Goudet, P, Dalac, A, Le Bras, M, Cardot-Bauters, C, Niccoli, P, Lévy-Bohbot, N, du Boullay, H, Bertagna, X, Ruszniewski, P, Borson-Chazot, F, Vergès, B, Sadoul, J. L, Ménégaux, F, Tabarin, A, Kühn, J. M, d'Anella, P, Chabre, O, Christin-Maitre, S, Cadiot, G, Binquet, C, Delemer, B

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Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature von Delanne, J., Nambot, S., Chassagne, A., Putois, O., Pelissier, A., Peyron, C., Gautier, E., Thevenon, J., Cretin, E., Bruel, A.L., Goussot, V., Ghiringhelli, F., Boidot, R., Tran Mau-Them, F., Philippe, C., Vitobello, A., Demougeot, L., Vernin, C., Lapointe, A.S., Bardou, M., Luu, M., Binquet, C., Lejeune, C., Joly, L., Juif, C., Baurand, A., Sawka, C., Bertolone, G., Duffourd, Y., Sanlaville, D., Pujol, P., Geneviève, D., Houdayer, F., Thauvin-Robinet, C., Faivre, L.

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OP10.09: Prenatal exome sequencing: a powerful tool to improve description of prenatal features related to genetic disorders von Bourgon, N., Them, F. Tran Mau, Bruel, A., Safraou, H., Denomme‐Pichon, A., Rousseau, T., Vitobello, A., Philippe, C., Binquet, C., Duffour, Y., Faivre, L., Thauvin, C.

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EP06.12: Prospective reanalysis of unsolved prenatal exome sequencing: diagnostic yield and contribution of postnatal/post‐mortem findings von Bourgon, N., Them, F. Tran Mau, Safraou, H., Bruel, A., Denomme‐Pichon, A., Vitobello, A., Binquet, C., Duffour, Y., Faivre, L., Thauvin, C.

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Effect of Mutation Type and Location on Clinical Outcome in 1,013 Probands with Marfan Syndrome or Related Phenotypes and FBN1 Mutations: An International Study von Faivre, L., Collod-Beroud, G., Loeys, B.L., Child, A., Binquet, C., Gautier, E., Callewaert, B., Arbustini, E., Mayer, K., Arslan-Kirchner, M., Kiotsekoglou, A., Comeglio, P., Marziliano, N., Dietz, H.C., Halliday, D., Beroud, C., Bonithon-Kopp, C., Claustres, M., Muti, C., Plauchu, H., Robinson, P.N., Adès, L.C., Biggin, A., Benetts, B., Brett, M., Holman, K.J., De Backer, J., Coucke, P., Francke, U., De Paepe, A., Jondeau, G., Boileau, C.

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Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting von Soilly, A L, Robert-Viard, C, Besse, C, Bruel, A L, Gerard, B, Boland, A, Piton, A, Duffourd, Y, Muller, J, Poë, C, Jouan, T, El Doueiri, S, Faivre, L, Bacq-Daian, D, Isidor, B, Genevieve, D, Odent, S, Philip, N, Doco-Fenzy, M, Lacombe, D, Asensio, M L, Deleuze, J F, Binquet, C, Thauvin-Robinet, C, Lejeune, C

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Effectiveness, safety, and cost–utility of a knee brace in medial knee osteoarthritis: the ERGONOMIE randomized controlled trial von Gueugnon, M., Fournel, I., Soilly, A.-L., Diaz, A., Baulot, E., Bussière, C., Casillas, J.M., Cherasse, A., Conrozier, T., Loeuille, D., Maillefert, J.-F., Mazalovic, K., Timsit, M., Wendling, D., Ramon, A., Binquet, C., Morisset, C., Ornetti, P.

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Diagnosis of postoperative pancreatic fistula von Facy, O., Chalumeau, C., Poussier, M., Binquet, C., Rat, P., Ortega-Deballon, P.

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Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study von Thevenon, J, Bourredjem, A, Faivre, L, Cardot-Bauters, C, Calender, A, Le Bras, M, Giraud, S, Niccoli, P, Odou, M F, Borson-Chazot, F, Barlier, A, Lombard-Bohas, C, Clauser, E, Tabarin, A, Pasmant, E, Chabre, O, Castermans, E, Ruszniewski, P, Bertherat, J, Delemer, B, Christin-Maitre, S, Beckers, A, Guilhem, I, Rohmer, V, Goichot, B, Caron, P, Baudin, E, Chanson, P, Groussin, L, Du Boullay, H, Weryha, G, Lecomte, P, Schillo, F, Bihan, H, Archambeaud, F, Kerlan, V, Bourcigaux, N, Kuhn, J M, Vergès, B, Rodier, M, Renard, M, Sadoul, J L, Binquet, C, Goudet, P

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Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management von Avila, M., Dyment, D.A., Sagen, J.V., St-Onge, J., Moog, U., Chung, B.H.Y., Mo, S., Mansour, S., Albanese, A., Garcia, S., Martin, D.O., Lopez, A.A., Claudi, T., König, R., White, S.M., Sawyer, S.L., Bernstein, J.A., Slattery, L., Jobling, R.K., Yoon, G., Curry, C.J., Merrer, M.L., Luyer, B.L., Héron, D., Mathieu-Dramard, M., Bitoun, P., Odent, S., Amiel, J., Kuentz, P., Thevenon, J., Laville, M., Reznik, Y., Fagour, C., Nunes, M.-L., Delesalle, D., Manouvrier, S., Lascols, O., Huet, F., Binquet, C., Faivre, L., Rivière, J.-B., Vigouroux, C., Njølstad, P.R., Innes, A.M., Thauvin-Robinet, C.

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Coûts de la sclérose en plaques en France von Fromont, A., Lehanneur, M.-N., Rollot, F., Weill, A., Clerc, L., Bonithon Kopp, C., Binquet, C., Moreau, T.

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Histologically Proven Bronchial Neuroendocrine Tumors in MEN1: A GTE 51-Case Cohort Study von Lecomte, P., Binquet, C., Le Bras, M., Tabarin, A., Cardot-Bauters, C., Borson-Chazot, F., Lombard-Bohas, C., Baudin, E., Delemer, B., Klein, M., Vergès, B., Aparicio, T., Cosson, E., Beckers, A., Caron, Ph, Chabre, O., Chanson, Ph, Du Boullay, H., Guilhem, I., Niccoli, P., Rohmer, V., Guigay, J., Vulpoi, C., Scoazec, J. Y., Goudet, P.

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The montrachet study von Creuzot, C., Bron, A., Binquet, C.

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Incidence de l’endophtalmie après injection intravitréenne : peut-on se passer de l’antibioprophylaxie ? von Ramel, J.-C., Bron, A.-M., Isaico, R., Meillon, C., Binquet, C., Creuzot-Garcher, C.

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Retinal vascular network: Changes with aging and systemic vascular disease (cardiac and cerebral) von Arnould, L, Guenancia, C, Binquet, C, Delcourt, C, Chiquet, C, Daien, V, Cottin, Y, Bron, A M, Acar, N, Creuzot-Garcher, C

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The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening von Thauvin-Robinet, C, Munck, A, Huet, F, Génin, E, Bellis, G, Gautier, E, Audrézet, M-P, Férec, C, Lalau, G, Georges, M Des, Claustres, M, Bienvenu, T, Gérard, B, Boisseau, P, Cabet-Bey, F, Feldmann, D, Clavel, C, Bieth, E, Iron, A, Simon-Bouy, B, Costa, C, Medina, R, Leclerc, J, Hubert, D, Nové-Josserand, R, Sermet-Gaudelus, I, Rault, G, Flori, J, Leroy, S, Wizla, N, Bellon, G, Haloun, A, Perez-Martin, S, d’Acremont, G, Corvol, H, Clément, A, Houssin, E, Binquet, C, Bonithon-Kopp, C, Alberti-Boulmé, C, Morris, M A, Faivre, L, Goossens, M, Roussey, M

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The new Ghent criteria for Marfan syndrome: what do they change? von Faivre, L, Collod-Beroud, G, Adès, L, Arbustini, E, Child, A, Callewaert, BL, Loeys, B, Binquet, C, Gautier, E, Mayer, K, Arslan-Kirchner, M, Grasso, M, Beroud, C, Hamroun, D, Bonithon-Kopp, C, Plauchu, H, Robinson, PN, De Backer, J, Coucke, P, Francke, U, Bouchot, O, Wolf, JE, Stheneur, C, Hanna, N, Detaint, D, De Paepe, A, Boileau, C, Jondeau, G

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