Contralateral Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers von Graeser, Monika K, Engel, Christoph, Rhiem, Kerstin, Gadzicki, Dorothea, Bick, Ulrich, Kast, Karin, Froster, Ursula G, Schlehe, Bettina, Bechtold, Astrid, Arnold, Norbert, Preisler-Adams, Sabine, Nestle-Kraemling, Carolin, Zaino, Mohammad, Loeffler, Markus, Kiechle, Marion, Meindl, Alfons, Varga, Dominic, Schmutzler, Rita K

Volltext

Clinical delineation of the PACS1-related syndrome-Report on 19 patients von Schuurs-Hoeijmakers, Janneke H. M., Landsverk, Megan L., Foulds, Nicola, Kukolich, Mary K., Gavrilova, Ralitza H., Greville-Heygate, Stephanie, Hanson-Kahn, Andrea, Bernstein, Jonathan A., Glass, Jennifer, Chitayat, David, Burrow, Thomas A., Husami, Ammar, Collins, Kathleen, Wusik, Katie, van der Aa, Nathalie, Kooy, Frank, Brown, Kate Tatton, Gadzicki, Dorothea, Kini, Usha, Alvarez, Sara, Fernández-Jaén, Alberto, McGehee, Frank, Selby, Katherine, Tarailo-Graovac, Maja, Van Allen, Margot, van Karnebeek, Clara D. M., Stavropoulos, Dimitri J., Marshall, Christian R., Merico, Daniele, Gregor, Anne, Zweier, Christiane, Hopkin, Robert J., Chu, Yoyo Wing-Yiu, Chung, Brian Hon-Yin, de Vries, Bert B. A., Devriendt, Koenraad, Hurles, Matthew E., Brunner, Han G.

Volltext

Breast cancer susceptibility: current knowledge and implications for genetic counselling von RIPPERGER, Tim, GADZICKI, Dorothea, MEINDL, Alfons, SCHIEGELBERGER, Brigitte

Volltext

The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort s... von Rhiem, Kerstin, Engel, Christoph, Graeser, Monika, Zachariae, Silke, Kast, Karin, Kiechle, Marion, Ditsch, Nina, Janni, Wolfgang, Mundhenke, Christoph, Golatta, Michael, Varga, Dominic, Preisler-Adams, Sabine, Heinrich, Tilman, Bick, Ulrich, Gadzicki, Dorothea, Briest, Susanne, Meindl, Alfons, Schmutzler, Rita K

Volltext

Evaluating the performance of the breast cancer genetic risk models BOADICEA, IBIS, BRCAPRO and Claus for predicting BRCA1/2 mutation carrier probabilities: a study based on 7352 f... von Fischer, Christine, Kuchenbäcker, Karoline, Engel, Christoph, Zachariae, Silke, Rhiem, Kerstin, Meindl, Alfons, Rahner, Nils, Dikow, Nicola, Plendl, Hansjörg, Debatin, Irmgard, Grimm, Tiemo, Gadzicki, Dorothea, Flöttmann, Ricarda, Horvath, Judit, Schröck, Evelin, Stock, Friedrich, Schäfer, Dieter, Schwaab, Ira, Kartsonaki, Christiana, Mavaddat, Nasim, Schlegelberger, Brigitte, Antoniou, Antonis C, Schmutzler, Rita

Volltext

Diagnostic accuracy of methods for the detection of BRCA1 and BRCA2 mutations : a systematic review von GERHARDUS, Ansgar, SCHLEBERGER, Henriette, SCHLEGELBERGER, Brigitte, GADZICKI, Dorothea

Volltext

BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk von Spurdle, Amanda B, Whiley, Phillip J, Thompson, Bryony, Feng, Bingjian, Healey, Sue, Brown, Melissa A, Pettigrew, Christopher, Van Asperen, Christi J, Ausems, Margreet G E M, Kattentidt-Mouravieva, Anna A, van den Ouweland, Ans M W, Belgium UV Consortium, Dutch, Lindblom, Annika, Pigg, Maritta H, Schmutzler, Rita K, Engel, Christoph, Meindl, Alfons, Caputo, Sandrine, Sinilnikova, Olga M, Lidereau, Rosette, Couch, Fergus J, Guidugli, Lucia, Hansen, Thomas van Overeem, Thomassen, Mads, Eccles, Diana M, Tucker, Kathy, Benitez, Javier, Domchek, Susan M, Toland, Amanda E, Van Rensburg, Elizabeth J, Wappenschmidt, Barbara, Borg, Åke, Vreeswijk, Maaike P G, Goldgar, David E

Volltext

No evidence for breast cancer susceptibility associated with variants of BRD7, a component of p53 and BRCA1 pathways von Penkert, Judith, Schlegelberger, Brigitte, Steinemann, Doris, Gadzicki, Dorothea

Volltext

Recurrent involvement of heterochromatic regions in multiple myeloma—A multicolor FISH study von Lange, Kathrin, Gadzicki, Dorothea, Schlegelberger, Brigitte, Göhring, Gudrun

Volltext

Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany von Gadzicki, Dorothea, Evans, D. Gareth, Harris, Hilary, Julian-Reynier, Claire, Nippert, Irmgard, Schmidtke, Jörg, Tibben, Aad, van Asperen, Christi J., Schlegelberger, Brigitte

Volltext

Comprehensive genetic and functional characterization of IPH-926: a novel CDH1-null tumour cell line from human lobular breast cancer von Christgen, Matthias, Bruchhardt, Henriette, Hadamitzky, Catarina, Rudolph, Cornelia, Steinemann, Doris, Gadzicki, Dorothea, Hasemeier, Britta, Römermann, Daniel, Focken, Tim, Krech, Till, Ballmaier, Matthias, Schlegelberger, Brigitte, Kreipe, Hans, Lehmann, Ulrich

Volltext

Low‐risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients von Hemminki, Kari, Müller‐Myhsok, Bertram, Lichtner, Peter, Engel, Christoph, Chen, Bowang, Burwinkel, Barbara, Försti, Asta, Sutter, Christian, Wappenschmidt, Barbara, Hellebrand, Heide, Illig, Thomas, Arnold, Norbert, Niederacher, Dieter, Dworniczak, Bernd, Deissler, Helmut, Kast, Karin, Gadzicki, Dorothea, Meitinger, Thomas, Wichmann, H.‐Erich, Kiechle, Marion, Bartram, Claus R., Schmutzler, Rita K., Meindl, Alfons

Volltext

Association of death receptor 4 variant (683A>C) with ovarian cancer risk in BRCA1 mutation carriers von Dick, Michelle G., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Varon-Mateeva, Raymonda, Sutter, Christian, Niederacher, Dieter, Deissler, Helmut, Preisler-Adams, Sabine, Kast, Karin, Schäfer, Dieter, Gadzicki, Dorothea, Heinritz, Wolfram, Wappenschmidt, Barbara, Schmutzler, Rita K.

Volltext

Standardised fluorescence in situ hybridisation in cytological and histological specimens von WILKENS, Ludwig, GERR, Heidrun, GADZICKI, Dorothea, KREIPE, Hans, SCHLEGELBERGER, Brigitte

Volltext

Clinical delineation of the PACS1-related Syndrome-Report on 19 Patients von Schuurs-Hoeijmakers, Janneke H.M, Landsverk, Megan L, Foulds, Nicola, Kukolich, Mary K, Gavrilova, Ralitza H, Greville-Heygate, Stephanie, Hanson-Kahn, Andrea, Bernstein, Jonathan A, Glass, Jennifer, Chitayat, David, Burrow, Thomas A, Husami, Ammar, Collins, Kathleen, Wusik, Katie, van der Aa, Nathalie, Kooy, Frank, Brown, Kate Tatton, Gadzicki, Dorothea, Kini, Usha, Alvarez, Sara, Fernández-Jaén, Alberto, McGehee, Frank, Selby, Katherine, Tarailo-Graovac, Maja, Van Allen, Margot, van Karnebeek, Clara D.M, Stavropoulos, Dimitri J, Marshall, Christian R, Merico, Daniele, Gregor, Anne, Zweier, Christiane, Hopkin, Robert J, Chu, Yoyo Wing-Yiu, Chung, Brian Hon-Yin, de Vries, Bert B.A, Devriendt, Koenraad, Hurles, Matthew E, Brunner, Han G

Volltext

Comprehensive genetic and functional characterization of IPH-926 : a novel CDHI-null tumour cell line from human lobular breast cancer von CHRISTGEN, Matthias, BRUCHHARDT, Henriette, BALLMAIER, Matthias, SCHLEGELBERGER, Brigitte, KREIPE, Hans, LEHMANN, Ulrich, HADAMITZKY, Catarina, RUDOLPH, Cornelia, STEINEMANN, Doris, GADZICKI, Dorothea, HASEMEIER, Britta, RÖMERMANN, Daniel, FOCKEN, Tim, KRECH, Till

Volltext

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene von Gadzicki, Dorothea, Müller-Vahl, Kirsten R., Heller, Daniela, Ossege, Sebastian, Nöthen, Markus M., Hebebrand, Johannes, Stuhrmann, Manfred

Volltext

Novel CHD7 mutations contributing to the mutation spectrum in patients with CHARGE syndrome von Wessels, Kathrin, Bohnhorst, Bettina, Luhmer, Ingrid, Morlot, Susanne, Bohring, Axel, Jonasson, Jon, Epplen, Jörg T, Gadzicki, Dorothea, Glaser, Stefanie, Göhring, Gudrun, Mälzer, Madeleine, Hein, Anke, Arslan-Kirchner, Mine, Stuhrmann, Manfred, Schmidtke, Jörg, Pabst, Brigitte

Volltext

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers von Antoniou, Antonis C, Soucy, Penny, Beesley, Jonathan, McGuffog, Lesley, Lee, Andrew, Healey, Sue, Lindblom, Annika, Arver, Brita, Karlsson, Per, Nathanson, Kate, Domchek, Susan, Rebbeck, Tim, Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, ZÅowowcka-PerÅowska, Elżbieta, Osorio, Ana, Andrñs, Raquel, Hamann, Ute, Verhoef, Senno, Wijnen, Juul, Gómez Garcia, Encarna B, Ligtenberg, Marjolijn J, Kriege, Mieke, Ausems, Margreet GEM, Oosterwijk, Jan C, Fineberg, Elena, Lalloo, Fiona, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Douglas, Fiona, Brewer, Carole, Hodgson, Shirley, Morrison, Patrick J, Walker, Lisa, Rogers, Mark T, Donaldson, Alan, Dorkins, Huw, Godwin, Andrew K, Bove, Betsy, Stoppa-Lyonnet, Dominique, Houdayer, Claude, Buecher, Bruno, de Pauw, Antoine, Mazoyer, Sylvie, Bressac- de Paillerets, Brigitte, Caron, Olivier, Frenay, Marc, Ferrer, Sandra Fert, Mortemousque, Isabelle, Daly, Mary, Southey, Melissa, Goldgar, David, Kaulich, Daphne Geschwantler, Nielsen, Finn C, Barkardottir, Rosa B, Kirchhoff, Tomas, Joseph, Vijai, Piedmonte, Marion, Cohn, David, Fiorica, James, Oliani, Cristina, Tihomirova, Laima, Blanco, Ignacio, Valle, J Del, Gayther, Simon A, Teo, Soo-Hwang, Ganz, Patricia A, Beattie, Mary S, Wappenschmidt, Barbara, Ditsch, Nina, Heidemann, Simone, Preisler-Adams, Sabine, Gadzicki, Dorothea, Varon-Mateeva, Raymonda, Gehrig, Andrea, Caldes, Trinidad, Nevanlinna, Heli, Muranen, Taru A, Lespñrance, Bernard, Spurdle, Amanda B, Neuhausen, Susan L, Ding, Yuan C, Pankratz, Vernon S, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Papi, Laura, Ottini, Laura, Radice, Paolo, Loud, Jennifer T, Andrulis, Irene L, Ozcelik, Hilmi, Glendon, Gord, Thomassen, Mads, Kruse, Torben A, Chenevix-Trench, Georgia, Couch, Fergus J, Simard, Jacques

Volltext

Common Variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 Are Associated with Breast Cancer Risk for BRCA1 and/or BRCA2 Mutation Carriers von Antoniou, Antonis C, Kuchenbaecker, Karoline B, Soucy, Penny, Beesley, Jonathan, McGuffog, Lesley, Barrowdale, Daniel, Sinilnikova, Olga M, Caligo, Maria A, Arver, Brita, Karlsson, Per, Domchek, Susan, Rebbeck, Tim, Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Osorio, Ana, Andrés, Raquel, Benítez, Javier, Hamann, Ute, Hogervorst, Frans B, van Os, Theo A, Meijers-Heijboer, Hanne EJ, Peock, Susan, Frost, Debra, Platte, Radka, Fineberg, Elena, Lalloo, Fiona, Eeles, Ros, Adlard, Julian, Cook, Jackie, Brewer, Carole, Hodgson, Shirley, Morrison, Patrick J, Donaldson, Alan, Dorkins, Huw, Stoppa-Lyonnet, Dominique, de Pauw, Antoine, Mazoyer, Sylvie, Calender, Alain, Bressac- de Paillerets, Brigitte, Caron, Olivier, Sobol, Hagay, Frenay, Marc, Prieur, Fabienne, Ferrer, Sandra Fert, Mortemousque, Isabelle, Southey, Melissa, Fink-Retter, Anneliese, Kaulich, Daphne Geschwantler, Nielsen, Finn C, Barkardottir, Rosa B, Gaudet, Mia, Joseph, Vijai, Piedmonte, Marion, Kirk, Judy, Hurteau, Jean, Byron, John, Montagna, Marco, Tihomirova, Laima, Blanco, Ignacio, Lazaro, Conxi, Teulé, Alex, Valle, J Del, Teo, Soo-Hwang, Ganz, Patricia A, Beattie, Mary S, Wappenschmidt, Barbara, Ditsch, Nina, Heidemann, Simone, Niederacher, Dieter, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Deissler, Helmut, Gehrig, Andrea, Caldes, Trinidad, de la Hoya, Miguel, Spurdle, Amanda B, Wang, Xianshu, Fredericksen, Zachary, Lindor, Noralane M, Peterlongo, Paolo, Peissel, Bernard, Bonanni, Bernardo, Bernard, Loris, Papi, Laura, Greene, Mark H, Loud, Jennifer T, Ozcelik, Hilmi, Mulligan, Anna Marie, Glendon, Gord, Gerdes, Anne-Marie, Skytte, Anne-Bine, Kruse, Torben A, Simard, Jacques, Easton, Douglas F, Walker, Lisa, Jacobs, Chris, Evans, D Gareth, Lee, Andrew

Volltext