Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis von Hotz, Alrun, Oji, Vinzenz, Bourrat, Emmanuelle, Jonca, Nathalie, Mazereeuw-Hautier, Juliette, Betz, Regina C, Blume-Peytavi, Ulrike, Stieler, Karola, Morice-Picard, Fanny, Schönbuchner, Ines, Markus, Susanne, Schlipf, Nina, Fischer, Judith

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Tazarotene 0.015% Cream as a Potential Topical Agent for Management of Ichthyosis in Dorfman-Chanarin Syndrome von Niculescu, Luana, Ruini, Cristel, Srour, Jerome, Salzer, Suzanna, Schönbuchner, Ines, von Braunmühl, Tanja, Ruzicka, Thomas, Hohenleutner, Ulrich, Giehl, Kathrin A, Fischer, Judith, Wollenberg, Andreas

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Erythrodermia Congenitalis Ichthyosiformis Bullosa of Brocq von Sander, Dorothea, Schröder, Josef, Schönbuchner, Ines, Schreml, Julia, Karrer, Sigrid, Berneburg, Mark, Schreml, Stephan

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers von Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans Mw, Nelen, Marcel R, Ausems, Margreet Gem, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J

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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis von Hotz, Alrun, Oji, Vmzenz, Bourrat, Emmanuelle, Jonca, Nathalie, Mazereeuw-Hautier, Juliette, Betz, Regina C, Blume-Peytavi, Ulrike, Stieler, Karola, Morice-Picard, Fanny, Schoenbuchner, Ines, Markus, Susanne, Schlipf, Nina, Fischer, Judith

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Gross rearrangements in BRCA1 but not BRCA2 play a notable role in predisposition to breast and ovarian cancer in high-risk families of German origin von Preisler-Adams, Sabine, Schönbuchner, Ines, Fiebig, Britta, Welling, Brigitte, Dworniczak, Bernd, Weber, Bernhard H.F.

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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 Couch, Fergus J, Nevanlinna, Heli, Robson, Mark, Sherman, Mark, Ejlertsen, Bent, Osorio, Ana, Durán, Mercedes, Benítez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Papi, Laura, Ottini, Laura, Bernard, Loris, Verheus, Martijn, Meijers-Heijboer, Hanne EJ, Nelen, Marcel R, Kets, C Marleen, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Jones, J Louise, Izatt, Louise, Adlard, Julian, Cook, Jackie, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Meindl, Alfons, Arnold, Norbert, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Schäfer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Cornelis, François, Mazoyer, Sylvie, Muller, Danièle, Coupier, Isabelle, Kientz, Caroline, Longy, Michel, Caldes, Trinidad, de la Hoya, Miguel, Aittomäki, Kristiina, Blanco, Ignacio, Soucy, Penny, Montagna, Marco, Tognazzo, Silvia, D'Andrea, Emma, Rebbeck, Tim, Olopade, Olufunmilayo, Weitzel, Jeffrey N, Ganz, Patricia A, Wang, Xianshu, Fredericksen, Zachary, Lindor, Noralane M, Szabo, Csilla, Sakr, Rita, Singer, Christian F, Tea, Muy-Kheng, Greene, Mark H, Imyanitov, Evgeny, O'Malley, Frances P, Glendon, Gordon, Toland, Amanda E, Gerdes, Anne-Marie, Kruse, Torben A, Jensen, Uffe Birk, Skytte, Anne-Bine, Soller, Maria, Henriksson, Karin, Stenmark-Askmalm, Marie, Karlsson, Per, Ding, Yuan Chun, Neuhausen, Susan L, Beattie, Mary, Moysich, Kirsten B, Karlan, Beth Y, Gross, Jenny, John, Esther M, Southey, Melissa C, Hopper, John L, Terry, Mary Beth, Goldgar, David, Andrulis, Irene L, Antoniou, Antonis C, GEMO Study Collaborators, HEBON, kConFab Investigators, Ontario Cancer Genetics Network, SWE-BRCA

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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 Couch, Fergus J, Eccles, Diana, Nevanlinna, Heli, Robson, Mark, Sherman, Mark, Ejlertsen, Bent, Osorio, Ana, Munoz-Repeto, Ivan, Peterlongo, Paolo, Manoukian, Siranoush, Papi, Laura, Ottini, Laura, Bernard, Loris, Verheus, Martijn, Meijers-Heijboer, Hanne E. J, Nelen, Marcel R, Kets, C. Marleen, Tilanus-Linthorst, Madeleine M. A, van der Luijt, Rob B, van Os, Theo, Rookus, Matti, Jones, J. Louise, Izatt, Louise, Adlard, Julian, Cook, Jackie, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew K, Schmutzler, Rita K, Rhiem, Kerstin, Meindl, Alfons, Arnold, Norbert, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Cornelis, Francois, Mazoyer, Sylvie, Leone, Melanie, Hardouin, Agnes, Pujol, Pascal, Coupier, Isabelle, Kientz, Caroline, Longy, Michel, Caldes, Trinidad, de la Hoya, Miguel, Aittomäki, Kristiina, Blanco, Ignacio, Barkardottir, Rosa B, Soucy, Penny, Montagna, Marco, Tognazzo, Silvia, D'Andrea, Emma, Rebbeck, Tim, Olopade, Olufunmilayo I, Weitzel, Jeffrey N, Ganz, Patricia A, Wang, Xianshu, Fredericksen, Zachary, Lindor, Noralane M, Szabo, Csilla, Sakr, Rita, Singer, Christian F, Tea, Muy-Kheng, Greene, Mark H, Imyanitov, Evgeny, O'Malley, Frances P, Ozcelik, Hilmi, Glendon, Gordon, Toland, Amanda E, Gerdes, Anne-Marie, Kruse, Torben A, Jensen, Uffe Birk, Skytte, Anne-Bine, Soller, Maria, Henriksson, Karin, Arver, Brita, Stenmark-Askmalm, Marie, Karlsson, Per, Ding, Yuan Chun, Neuhausen, Susan L, Beattie, Mary, Moysich, Kirsten B, Karlan, Beth Y, Gross, Jenny, John, Esther M, Southey, Melissa C, Hopper, John L, Terry, Mary Beth, Goldgar, David, Andrulis, Irene L, Antoniou, Antonis C

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Gesetzliche Grundlagen und Handlungsempfehlungen in der Humangenetischen Beratung von Holzhauser, Ivana, Schönbuchner, Ines

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