Leonhard Med, a trusted research environment for processing sensitive research data von Okoniewski, Michal J., Wiegand, Anna, Schmid, Diana Coman, Bolliger, Christian, Bovino, Cristian, Belluco, Mattia, Wüst, Thomas, Byrde, Olivier, Maffioletti, Sergio, Rinn, Bernd

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Massively parallel flow computation with application to fluid mixing von Byrde, Olivier

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Parallel incompressible flow simulations: from chemical mixers to solar racing cars von Sawley, Mark L, Byrde, Olivier, Cobut, David

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High Frequency of Germline SUFU Mutations in Children With Desmoplastic/Nodular Medulloblastoma Younger Than 3 Years of Age von Brugières, Laurence, Remenieras, Audrey, Pierron, Gaëlle, Varlet, Pascale, Forget, Sébastien, Byrde, Véronique, Bombled, Johny, Puget, Stéphanie, Caron, Olivier, Dufour, Christelle, Delattre, Olivier, Bressac-de Paillerets, Brigitte, Grill, Jacques

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CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study von Benusiglio, Patrick R, Malka, David, Rouleau, Etienne, De Pauw, Antoine, Buecher, Bruno, Noguès, Catherine, Fourme, Emmanuelle, Colas, Chrystelle, Coulet, Florence, Warcoin, Mathilde, Grandjouan, Sophie, Sezeur, Alain, Laurent-Puig, Pierre, Molière, Diane, Tlemsani, Camille, Di Maria, Marina, Byrde, Veronique, Delaloge, Suzette, Blayau, Martine, Caron, Olivier

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Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer von Gaudet, Mia M, Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, Segrè, Ayellet V, McGee, Kate, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M, Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, Frenay, Marc, GEMO Study Collaborators, Hogervorst, Frans B L, Rookus, Matti A, Collée, J Margriet, Hoogerbrugge, Nicoline, van Roozendaal, Kees E P, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V, Caldés, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Peterlongo, Paolo, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Rennert, Gad, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, D'Andrea, Emma, Friedman, Eitan, Laitman, Yael, Borg, Ake, Beattie, Mary, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Hopper, John L, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Overeem Hansen, Thomas V, Nielsen, Finn C, Greene, Mark H, Greene, Mark I, Mai, Phuong L, Osorio, Ana, Durán, Mercedes, Andres, Raquel, Benítez, Javier, Weitzel, Jeffrey N, Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Walker, Lisa

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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... von Mulligan, Anna Marie, Couch, Fergus J, Barrowdale, Daniel, Domchek, Susan M, Eccles, Diana, Nevanlinna, Heli, Ramus, Susan J, Robson, Mark, Sherman, Mark, Spurdle, Amanda B, Wappenschmidt, Barbara, Lee, Andrew, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M, Janavicius, Ramunas, Hansen, Thomas vO, Nielsen, Finn C, Ejlertsen, Bent, Osorio, Ana, Muñoz-Repeto, Iván, Durán, Mercedes, Godino, Javier, Pertesi, Maroulio, Benítez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Pasini, Barbara, Papi, Laura, Ottini, Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Hamann, Ute, Verheus, Martijn, Meijers-Heijboer, Hanne E J, Wijnen, Juul, Gómez García, Encarna B, Nelen, Marcel R, Kets, C Marleen, Seynaeve, Caroline, Tilanus-Linthorst, Madeleine M A, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Frost, Debra, Jones, J Louise, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Donaldson, Alan, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Fiebig, Britta, Heinritz, Wolfram, Schäfer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Fassy-Colcombet, Marion, Cornelis, François, Mazoyer, Sylvie, Léoné, Mélanie, Boutry-Kryza, Nadia, Hardouin, Agnès, Berthet, Pascaline, Muller, Danièle, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal

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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers von Wang, Xianshu, Pankratz, V. Shane, Fredericksen, Zachary, Tarrell, Robert, Karaus, Mary, McGuffog, Lesley, Pharaoh, Paul D.P., Ponder, Bruce A.J., Dunning, Alison M., Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Houdayer, Claude, Hogervorst, Frans B.L., Hooning, Maartje J., Ligtenberg, Marjolijn J., Spurdle, Amanda, Chenevix-Trench, Georgia, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Catherina, Fink, Anneliese, Szabo, Csilla I., Zikan, Michal, Foretova, Lenka, Claes, Kathleen, Thomas, Gilles, Hoover, Robert N., Hunter, David J., Chanock, Stephen J., Easton, Douglas F., Antoniou, Antonis C., Couch, Fergus J.

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The rs2910164:G>C SNP in the MIR146A gene is not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers von Garcia, Amandine I., Cox, David G., Barjhoux, Laure, Verny-Pierre, Carole, Barnes, Daniel, Antoniou, Antonis C., Stoppa-Lyonnet, Dominique, Sinilnikova, Olga M., Mazoyer, Sylvie

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High Frequency of Germline S UFU Mutations in Children With Desmoplastic/Nodular Medulloblastoma Younger Than 3 Years of Age von BRUGIERES, Laurence, REMENIERAS, Audrey, DELATTRE, Olivier, BRESSAC-DE PAILLERETS, Brigitte, GRILL, Jacques, PIERRON, Gaëlle, VARLET, Pascale, FORGET, Sébastien, BYRDE, Véronique, BOMBLED, Johny, PUGET, Stéphanie, CARON, Olivier, DUFOUR, Christelle

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Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers von SPURDLE, Amanda B, MARQUART, Louise, GSCHWANTLER-KAULICH, Daphne, BLUM, Joanne L, TUNG, Nadine, WEITZEL, Jeff, LYNCH, Henry, GARBER, Judy, EASTON, Douglas F, PEOCK, Susan, COOK, Margaret, OLIVER, Clare T, MCGUFFOG, Lesley, FROST, Debra, CONROY, Don, GARETH EVANS, D, LALLOO, Fiona, EELES, Ros, IZATT, Louise, DAVIDSON, Rosemarie, CHU, Carol, ECCLES, Diana, SELKIRK, Christina G, HEALEY, Sue, DALY, Mary, ISAACS, Claudine, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BUECHER, Bruno, BELOTTI, Muriel, MAZOYER, Sylvie, BARJHOUX, Laure, VERNY-PIERRE, Carole, LASSET, Christine, SINILNIKOVA, Olga, DREYFUS, Hélène, PUJOL, Pascal, COLLONGE-RAME, Marie-Agnès, ROOKUS, Matti A, VERHOEF, Senno, KRIEGE, Mieke, HOOGERBRUGGE, Nicoline, AUSEMS, Margreet G. E. M, VAN OS, Theo A, WIJNEN, Juul, FEI WAN, DEVILEE, Peter, MEIJERS-HEIJBOER, Hanne E. J, BLOK, Marinus J, HEIKKINEN, Tuomas, NEVANLINNA, Heli, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BYRSKI, Tomasz, DUROCHER, Francine, XIAOQING CHEN, BEESLEY, Jonathan, SINGER, Christian F, DRESSLER, Anne-Catharine

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