A relative survival regression model using B-spline functions to model non-proportional hazards von Giorgi, Roch, Abrahamowicz, Michal, Quantin, Catherine, Bolard, Philippe, Esteve, Jacques, Gouvernet, Joanny, Faivre, Jean

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Modelling time-dependent hazard ratios in relative survival: Application to colon cancer von Bolard, P, Quantin, C, Esteve, J, Faivre, J, Abrahamowicz, M

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Étude de relations de mutation entre unités fonctionnelles d'un centre hospitalier par l'analyse structurale de réseaux von Dellinger, A, Bolard, P

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Modeling of High-cost Patient Distribution within Renal Failure Diagnosis Related Group von Quantin, C., Sauleau, E., Bolard, P., Mousson, C., Kerkri, M., Lecomte, P.Brunet, Moreau, T., Dusserre, L.

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Comparison of Cox's and relative survival models when estimating the effects of prognostic factors on disease-specific mortality: a simulation study under proportional excess hazar... von Teuff, Gwenaël Le, Abrahamowicz, Michal, Bolard, Philippe, Quantin, Catherine

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Interval cancers in a community-based programme of colorectal cancer screening with faecal occult blood test von Tazi, M A, Faivre, J, Lejeune, C, Bolard, P, Phelip, J-M, Benhamiche, A-M

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Modelling time-dependent hazard ratios in relative survival von Bolard, P, Quantin, C, Esteve, J, Faivre, J, Abrahamowicz, M

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Complete Human and Rat Ex Vivo Spermatogenesis from Fresh or Frozen Testicular Tissue von Perrard, Marie-Hélène, Sereni, Nicolas, Schluth-Bolard, Caroline, Blondet, Antonine, D Estaing, Sandrine Giscard, Plotton, Ingrid, Morel-Journel, Nicolas, Lejeune, Hervé, David, Laurent, Durand, Philippe

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Performance of semiconductor sequencing platform for non‐invasive prenatal genetic screening for fetal aneuploidy: results from a multicenter prospective cohort study in a clinical... von El Khattabi, L. Allach, Brun, S., Gueguen, P., Chatron, N., Guichoux, E., Schutz, S., Nectoux, J., Sorlin, A., Quere, M., Boudjarane, J., Tsatsaris, V., Mandelbrot, L., Schluth‐Bolard, C., Dupont, J. M., Rooryck, C., Cormier, Alexandre, Ferec, Claude, Da Foncesca Pipoli, Juliana, Letourneur, Franck, Bonnet, Céline, Jonveaux, Philippe, Bardel, Claire, Lagarde, Arnaud, Badens, Catherine, Levy, Nicolas, Duboc, Véronique, Paquis‐Fluckinger, Véronique, Boureau‐Wirth, Amandine, Bannwarth, Sylvie, Arveiler, Benoît, Lacombe, Didier, Goossens, Michel, Vidaud, Michel, Massardier, Jérôme, Saliou, Anne‐Hélène, Sanlaville, Damien

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Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders von Yammine, T, Reynaud, N, Lejeune, H, Diguet, F, Rollat-Farnier, P A, Labalme, A, Plotton, I, Farra, C, Sanlaville, D, Chouery, E, Schluth-Bolard, C

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Interstitial 12p13.1 deletion involving GRIN2B in three patients with intellectual disability von Dimassi, Sarra, Andrieux, Joris, Labalme, Audrey, Lesca, Gaétan, Cordier, Marie-Pierre, Boute, Odile, Neut, Dorothée, Edery, Patrick, Sanlaville, Damien, Schluth-Bolard, Caroline

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Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome von Dery, Tania, Chatron, Nicolas, Alqahtani, Amerh, Pugeat, Michel, Till, Marianne, Edery, Patrick, Sanlaville, Damien, Schluth-Bolard, Caroline, Nicolino, Marc, Lesca, Gaetan, Putoux, Audrey

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A Case of Trisomy 13 Mosaicism Presenting with a Severe Aortic Root Dilatation and Marfanoid Habitus due to an Unpredictable Cytogenetic Mechanism von Monin, Pauline, Reynaud, Nicolas, Hanna, Nadine, Dupuis-Girod, Sophie, Till, Marianne, Arnaud, Pauline, Labalme, Audrey, Alix, Eudeline, Poizat-Amar, Coline, Faoucher, Marie, Ravella, Lucie, Debost, Bernard, Obadia, Jean-François, Zech, Jean-Christophe, Boileau, Catherine, Sanlaville, Damien, Edery, Patrick, Putoux, Audrey, Schluth-Bolard, Caroline

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Direct visualization of the highly polymorphic RNU2 locus in proximity to the BRCA1 gene von Tessereau, Chloé, Buisson, Monique, Monnet, Nastasia, Imbert, Marine, Barjhoux, Laure, Schluth-Bolard, Caroline, Sanlaville, Damien, Conseiller, Emmanuel, Ceppi, Maurizio, Sinilnikova, Olga M, Mazoyer, Sylvie

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ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder von Carapito, Raphael, Ivanova, Ekaterina L., Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine, Tran Mau-Them, Frédéric, Jean-Marçais, Nolwenn, Hiatt, Susan M., Cooper, Gregory M., Tvrdik, Tatiana, Muir, Alison M., Dimartino, Clémantine, Chopra, Maya, Amiel, Jeanne, Gordon, Christopher T., Dutreux, Fabien, Garde, Aurore, Thauvin-Robinet, Christel, Wang, Xia, Leduc, Magalie S., Phillips, Meredith, Crawford, Heather P., Kukolich, Mary K., Hunt, David, Harrison, Victoria, Kharbanda, Mira, Smigiel, Robert, Gold, Nina, Hung, Christina Y., Viskochil, David H., Dugan, Sarah L., Bayrak-Toydemir, Pinar, Joly-Helas, Géraldine, Guerrot, Anne-Marie, Schluth-Bolard, Caroline, Rio, Marlène, Wentzensen, Ingrid M., McWalter, Kirsty, Schnur, Rhonda E., Lewis, Andrea M., Lalani, Seema R., Mensah-Bonsu, Noël, Céraline, Jocelyn, Sun, Zijie, Ploski, Rafal, Bacino, Carlos A., Mefford, Heather C., Faivre, Laurence, Bodamer, Olaf, Chelly, Jamel, Isidor, Bertrand, Bahram, Seiamak

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HBB loss of heterozygosity in the hemopoietic lineage gives rise to an unusual sickle-cell trait phenotype von Joly, Philippe, Schluth-Bolard, Caroline, Lacan, Philippe, Barro, Claire, Pissard, Serge, Labalme, Audrey, Sanlaville, Damien, Badens, Catherine

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6q22.1 deletion is associated with epilepsy and abnormal movements von Schluth-Bolard, C, Flamand-Roze, E, Masurel, A, Olivier-Faivre, L, Callier, P, Charles, P, Keren, B, Guillot, N, Labalme, A, Sanlaville, D, Mochel, F, Des Portes, V, Lesca, G

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PD-0405: Determination of reference levels for quality assurance of flattening filter free beams von Vanetti, E, Clivio, A, Belosi, M.F, Cozzi, L, Nicolini, G, Bolard, G, Fenoglietto, P, Krauss, H, Fogliata, A

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Three new cases of asparagine synthetase deficiency: Confirmation of a poor neurological outcome and a new molecular mechanism von Faoucher, M, Putoux, A, Francannet, C, Poulat, A.L, Chatron, N, Aquaviva, C, Labalme, A, Schluth-Bolard, C, Till, M, Saban, C, Desportes, V, Sanlaville, D, Edery, P, Lesca, G

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Mapping of chromosomal balanced rearrangements by whole-genome sequencing identifies genes involved in epilepsy von Masson, J, Diguet, F, Rollat-Farnier, P.A, Mazoyer, S, Lesca, G, Kremer, V, Flori, E, Portnoï, M.F, Siffroi, J.P, Valence, S, Till, M, Edery, P, Sanlaville, D, Schluth-Bolard, C

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