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Anzahl der Publikationen: 18
Zeitschriftenartikel
Rolfes, Muriel; Borde, Julika; Möllenhoff, Kathrin; Kayali, Mohamad; Ernst, Corinna; Gehrig, Andrea; Sutter, Christian; Ramser, Juliane; Niederacher, Dieter; Horvath, Judit; Arnold, Norbert; Meindl, Alfons; Auber, Bernd; Rump, Andreas; Wang-Gohrke, Shan; Ritter, Julia; Hentschel, Julia; Thiele, Holger; Altmüller, Janine; Nürnberg, Peter; Rhiem, Kerstin; Engel, Christoph; Wappenschmidt, Barbara; Schmutzler, Rita K.; Hahnen, Eric und Hauke, Jan
(2022):
Prevalence of Cancer Predisposition Germline Variants in Male Breast Cancer Patients: Results of the German Consortium for Hereditary Breast and Ovarian Cancer.
In: Cancers, Bd. 14, Nr. 13, 3292
Schouten, Philip C.; Richters, Lisa; Vis, Daniel J.; Kommoss, Stefan; Dijk, Ewald van; Ernst, Corinna; Kluin, Roelof J. C.; Marme, Frederik; Lips, Esther H.; Schmidt, Sandra; Scheerman, Esther; Prieske, Katharina; Deurzen, Carolien H. M. van; Burges, Alexander; Ewing-Graham, Patricia C.; Dietrich, Dimo; Jager, Agnes; De Gregorio, Nikolaus; Hauke, Jan; Du Bois, Andreas; Nederlof, Petra M.; Wessels, Lodewyk F.; Hahnen, Eric; Harter, Philipp; Linn, Sabine C. und Schmutzler, Rita K.
(2021):
Ovarian Cancer-Specific BRCA-like Copy-Number Aberration Classifiers Detect Mutations Associated with Homologous Recombination Deficiency in the AGO-TR1 Trial.
In: Clinical Cancer Research, Bd. 27, Nr. 23: S. 6559-6569
Borde, Julika; Ernst, Corinna; Wappenschmidt, Barbara; Niederacher, Dieter; Weber-Lassalle, Konstantin; Schmidt, Gunnar; Hauke, Jan; Quante, Anne S.; Weber-Lassalle, Nana; Horvath, Judit; Pohl-Rescigno, Esther; Arnold, Norbert; Rump, Andreas; Gehrig, Andrea; Hentschel, Julia; Faust, Ulrike; Dutrannoy, Veronique; Meindl, Alfons; Kuzyakova, Maria; Wang-Gohrke, Shan; Weber, Bernhard H. F.; Sutter, Christian; Volk, Alexander E.; Giannakopoulou, Olga; Lee, Andrew; Engel, Christoph; Schmidt, Marjanka K.; Antoniou, Antonis C.; Schmutzler, Rita K.; Kuchenbaecker, Karoline und Hahnen, Eric
(2021):
Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers.
In: Jnci-Journal of the National Cancer Institute, Bd. 113, Nr. 7, djaa203: S. 893-899
Hauke, Jan 
ORCID: https://orcid.org/0000-0001-8236-4075; Harter, Philipp; Ernst, Corinna ORCID: https://orcid.org/0000-0001-7756-8815; Burges, Alexander; Schmidt, Sandra; Reuss, Alexander; Borde, Julika; De Gregorio, Nikolaus; Dietrich, Dimo; El-Balat, Ahmed; Kayali, Mohamad; Gevensleben, Heidrun; Hilpert, Felix; Altmüller, Janine; Heimbach, André; Meier, Werner; Schoemig-Markiefka, Birgid; Thiele, Holger; Kimmig, Rainer; Nürnberg, Peter; Kast, Karin; Richters, Lisa; Sehouli, Jalid; Schmutzler, Rita K und Hahnen, Eric ORCID: https://orcid.org/0000-0002-1152-8367
(2020):
Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883).
In: Journal of Medical Genetics, Bd. 59, Nr. 3: S. 248-252
ORCID: https://orcid.org/0000-0001-8236-4075; Harter, Philipp; Ernst, Corinna ORCID: https://orcid.org/0000-0001-7756-8815; Burges, Alexander; Schmidt, Sandra; Reuss, Alexander; Borde, Julika; De Gregorio, Nikolaus; Dietrich, Dimo; El-Balat, Ahmed; Kayali, Mohamad; Gevensleben, Heidrun; Hilpert, Felix; Altmüller, Janine; Heimbach, André; Meier, Werner; Schoemig-Markiefka, Birgid; Thiele, Holger; Kimmig, Rainer; Nürnberg, Peter; Kast, Karin; Richters, Lisa; Sehouli, Jalid; Schmutzler, Rita K und Hahnen, Eric ORCID: https://orcid.org/0000-0002-1152-8367
(2020):
Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883).
In: Journal of Medical Genetics, Bd. 59, Nr. 3: S. 248-252
Wappenschmidt, Barbara; Hauke, Jan; Faust, Ulrike; Niederacher, Dieter; Wiesmueler, Lisa; Schmidt, Gunnar; Gross, Evi; Gehrig, Andrea; Sutter, Christian; Ramser, Juliane; Rump, Andreas; Arnold, Norbert und Meindl, Alfons
(2020):
Criteria of the German Consortium for Hereditary Breast and Ovarian Cancer for the Classification of Germline Sequence Variants in Risk Genes for Hereditary Breast and Ovarian Cancer.
In: Geburtshilfe und Frauenheilkunde, Bd. 80, Nr. 4: S. 410-429
Patel, Vivek L.; Busch, Evan L.; Friebel, Tara M.; Cronin, Angel; Leslie, Goska; McGuffog, Lesley; Adlard, Julian; Agata, Simona; Agnarsson, Bjarni A.; Ahmed, Munaza; Aittomaki, Kristiina; Alducci, Elisa; Andrulis, Irene L.; Arason, Adalgeir; Arnold, Norbert; Artioli, Grazia; Arver, Brita; Auber, Bernd; Azzollini, Jacopo; Balmana, Judith; Barkardottir, Rosa B.; Barnes, Daniel R.; Barroso, Alicia; Barrowdale, Daniel; Belotti, Muriel; Benitez, Javier; Bertelsen, Brigitte; Blok, Marinus J.; Bodrogi, Istvan; Bonadona, Valerie; Bonanni, Bernardo; Bondavalli, Davide; Boonen, Susanne E.; Borde, Julika; Borg, Ake; Bradbury, Angela R.; Brady, Angela; Brewer, Carole; Brunet, Joan; Buecher, Bruno; Buys, Saundra S.; Cabezas-Camarero, Santiago; Caldes, Trinidad; Caliebe, Almuth; Caligo, Maria A.; Calvello, Mariarosaria; Campbell, Ian G.; Carnevali, Ileana; Carrasco, Estela; Chan, Tsun L.; Chu, Annie T. W.; Chung, Wendy K.; Claes, Kathleen B. M.; Cook, Jackie; Cortesi, Laura; Couch, Fergus J.; Daly, Mary B.; Damante, Giuseppe; Darder, Esther; Davidson, Rosemarie; de la Hoya, Miguel; Della Puppa, Lara; Dennis, Joe; Diez, Orland; Ding, Yuan Chun; Ditsch, Nina; Domchek, Susan M.; Donaldson, Alan; Dworniczak, Bernd; Easton, Douglas F.; Eccles, Diana M.; Eeles, Rosalind A.; Ehrencrona, Hans; Ejlertsen, Bent; Engel, Christoph; Evans, D. Gareth; Faivre, Laurence; Faust, Ulrike; Feliubadalo, Lidia; Foretova, Lenka; Fostira, Florentia; Fountzilas, George; Frost, Debra; Garcia-Barberan, Vanesa; Garre, Pilar; Gauthier-Villars, Marion; Geczi, Lajos; Gehrig, Andrea; Gerdes, Anne-Marie; Gesta, Paul; Giannini, Giuseppe; Glendon, Gord; Godwin, Andrew K.; Goldgar, David E.; Greene, Mark H.; Gutierrez-Barrera, Angelica M.; Hahnen, Eric; Hamann, Ute; Hauke, Jan; Herold, Natalie; Hogervorst, Frans B. L.; Honisch, Ellen; Hopper, John L.; Hulick, Peter J.; Izatt, Louise; Jager, Agnes; James, Paul; Janavicius, Ramunas; Jensen, Uffe Birk; Jensen, Thomas Dyrso; Johannsson, Oskar Th; John, Esther M.; Joseph, Vijai; Kang, Eunyoung; Kast, Karin; Kiiski, Johanna I.; Kim, Sung-Won; Kim, Zisun; Ko, Kwang-Pil; Konstantopoulou, Irene; Kramer, Gero; Krogh, Lotte; Kruse, Torben A.; Kwong, Ava; Larsen, Mirjam; Lasset, Christine; Lautrup, Charlotte; Lazaro, Conxi; Lee, Jihyoun; Lee, Jong Won; Lee, Min Hyuk; Lemke, Johannes; Lesueur, Fabienne; Liljegren, Annelie; Lindblom, Annika; Llovet, Patricia; Lopez-Fernandez, Adria; Lopez-Perolio, Irene; Lorca, Victor; Loud, Jennifer T.; Ma, Edmond S. K.; Mai, Phuong L.; Manoukian, Siranoush; Mari, Veronique; Martin, Lynn; Matricardi, Laura; Mebirouk, Noura; Medici, Veronica; Meijers-Heijboer, Hanne E. J.; Meindl, Alfons; Mensenkamp, Arjen R.; Miller, Clare; Gomes, Denise Molina; Montagna, Marco; Mooij, Thea M.; Moserle, Lidia; Mouret-Fourme, Emmanuelle; Mulligan, Anna Marie; Nathanson, Katherine L.; Navratilova, Marie; Nevanlinna, Heli; Niederacher, Dieter; Nielsen, Finn C. Cilius; Nikitina-Zake, Liene; Offit, Kenneth; Olah, Edith; Olopade, Olufunmilayo I.; Ong, Kai-Ren; Osorio, Ana; Ott, Claus-Eric; Palli, Domenico; Park, Sue K.; Parsons, Michael T.; Pedersen, Inge Sokilde; Peissel, Bernard; Peixoto, Ana; Perez-Segura, Pedro; Peterlongo, Paolo; Petersen, Annabeth Hogh; Porteous, Mary E.; Angel Pujana, Miguel; Radice, Paolo; Ramser, Juliane; Rantala, Johanna; Rashid, Muhammad U.; Rhiem, Kerstin; Rizzolo, Piera; Robson, Mark E.; Rookus, Matti A.; Rossing, Caroline M.; Ruddy, Kathryn J.; Santos, Catarina; Saule, Claire; Scarpitta, Rosa; Schmutzler, Rita K.; Schuster, Helene; Senter, Leigha; Seynaeve, Caroline M.; Shah, Payal D.; Sharma, Priyanka; Shin, Vivian Y.; Silvestri, Valentina; Simard, Jacques; Singer, Christian F.; Skytte, Anne-Bine; Snape, Katie; Solano, Angela R.; Soucy, Penny; Southey, Melissa C.; Spurdle, Amanda B.; Steele, Linda; Steinemann, Doris; Stoppa-Lyonnet, Dominique; Stradella, Agostina; Sunde, Lone; Sutter, Christian; Tan, Yen Y.; Teixeira, Manuel R.; Teo, Soo Hwang; Thomassen, Mads; Tibiletti, Maria Grazia; Tischkowitz, Marc; Tognazzo, Silvia; Toland, Amanda E.; Tommasi, Stefania; Torres, Diana; Toss, Angela; Trainer, Alison H.; Tung, Nadine; Asperen, Christi J. van; Baan, Frederieke H. van der; Kolk, Lizet E. van der; Luijt, Rob B. van der; Hest, Liselotte P. van; Varesco, Liliana; Varon-Mateeva, Raymonda; Viel, Alessandra; Vierstrate, Jeroen; Villa, Roberta; von Wachenfeldt, Anna; Wagner, Philipp; Wang-Gohrke, Shan; Wappenschmidt, Barbara; Weitzel, Jeffrey N.; Wieme, Greet; Yadav, Siddhartha; Yannoukakos, Drakoulis; Yoon, Sook-Yee; Zanzottera, Cristina; Zorn, Kristin K.; D'Amico, Anthony V.; Freedman, Matthew L.; Pomerantz, Mark M.; Chenevix-Trench, Georgia; Antoniou, Antonis C.; Neuhausen, Susan L.; Ottini, Laura; Nielsen, Henriette Roed und Rebbeck, Timothy R.
(2020):
Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.
In: Cancer Research, Bd. 80, Nr. 3: S. 624-638
Hauke, Jan; Hahnen, Eric; Schneider, Stephanie; Reuss, Alexander; Richters, Lisa; Kommoss, Stefan; Heimbach, Andre; Marme, Frederik; Schmidt, Sandra; Prieske, Katharina; Gevensleben, Heidrun; Burges, Alexander; Borde, Julika; De Gregorio, Nikolaus; Nuernberg, Peter; El-Balat, Ahmed; Thiele, Holger; Hilpert, Felix; Altmüller, Janine; Meier, Werner; Dietrich, Dimo; Kimmig, Rainer; Schoemig-Markiefka, Birgid; Kast, Karin; Braicu, Elena Ioana; Baumann, Klaus; Jackisch, Christian; Park-Simon, Tjoung-Won; Ernst, Corinna; Hanker, Lars; Pfisterer, Jacobus; Schnelzer, Andreas; du Bois, Andreas; Schmutzler, Rita K. und Harter, Philipp
(2019):
Deleterious somatic variants in 473 consecutive individuals with ovarian cancer: results of the observational AGO-TR1 study (NCT02222883).
In: Journal of Medical Genetics, Bd. 56, Nr. 9: S. 574-580
[PDF, 705kB]
Parsons, Michael T.; Tudini, Emma; Li, Hongyan; Hahnen, Eric; Wappenschmidt, Barbara; Feliubadalo, Lidia; Aalfs, Cora M.; Agata, Simona; Aittomaki, Kristiina; Alducci, Elisa; Concepcion Alonso-Cerezo, Maria; Arnold, Norbert; Auber, Bernd; Austin, Rachel; Azzollini, Jacopo; Balmana, Judith; Barbieri, Elena; Bartram, Claus R.; Blanco, Ana; Bluemcke, Britta; Bonache, Sandra; Bonanni, Bernardo; Borg, Ake; Bortesi, Beatrice; Brunet, Joan; Bruzzone, Carla; Bucksch, Karolin; Cagnoli, Giulia; Caldes, Trinidad; Caliebe, Almuth; Caligo, Maria A.; Calvello, Mariarosaria; Capone, Gabriele L.; Caputo, Sandrine M.; Carnevali, Ileana; Carrasco, Estela; Caux-Moncoutier, Virginie; Cavalli, Pietro; Cini, Giulia; Clarke, Edward M.; Concolino, Paola; Cops, Elisa J.; Cortesi, Laura; Couch, Fergus J.; Darder, Esther; de la Hoya, Miguel; Dean, Michael; Debatin, Irmgard; Del Valle, Jesus; Delnatte, Capucine; Derive, Nicolas; Diez, Orland; Ditsch, Nina; Domchek, Susan M.; Dutrannoy, Veronique; Eccles, Diana M.; Ehrencrona, Hans; Enders, Ute; Evans, D. Gareth; Farra, Chantal; Faust, Ulrike; Felbor, Ute; Feroce, Irene; Fine, Miriam; Foulkes, William D.; Galvao, Henrique Cr; Gambino, Gaetana; Gehrig, Andrea; Gensini, Francesca; Gerdes, Anne-Marie; Germani, Aldo; Giesecke, Jutta; Gismondi, Viviana; Gomez, Carolina; Garcia, Encarna B. Gomez; Gonzalez, Sara; Grau, Elia; Grill, Sabine; Gross, Eva; Guerrieri-Gonzaga, Aliana; Guillaud-Bataille, Marine; Gutierrez-Enriquez, Sara; Haaf, Thomas; Hackmann, Karl; Hansen, Thomas Vo; Harris, Marion; Hauke, Jan; Heinrich, Tilman; Hellebrand, Heide; Herold, Karen N.; Honisch, Ellen; Horvath, Judit; Houdayer, Claude; Huebbel, Verena; Iglesias, Silvia; Izquierdo, Angel; James, Paul A.; Janssen, Linda Am; Jeschke, Udo; Kaulfuss, Silke; Keupp, Katharina; Kiechle, Marion; Koelbl, Alexandra; Krieger, Sophie; Kruse, Torben A.; Kvist, Anders; Lalloo, Fiona; Larsen, Mirjam; Lattimore, Vanessa L.; Lautrup, Charlotte; Ledig, Susanne; Leinert, Elena; Lewis, Alexandra L.; Lim, Joanna; Löffler, Markus; Lopez-Fernandez, Adria; Lucci-Cordisco, Emanuela; Maass, Nicolai; Manoukian, Siranoush; Marabelli, Monica; Matricardi, Laura; Meindl, Alfons; Michelli, Rodrigo D.; Moghadasi, Setareh; Moles-Fernandez, Alejandro; Montagna, Marco; Montalban, Gemma; Monteiro, Alvaro N.; Montes, Eva; Mori, Luigi; Moserle, Lidia; Müller, Clemens R.; Mundhenke, Christoph; Naldi, Nadia; Nathanson, Katherine L.; Navarro, Matilde; Nevanlinna, Heli; Nichols, Cassandra B.; Niederacher, Dieter; Nielsen, Henriette R.; Ong, Kai-ren; Pachter, Nicholas; Palmero, Edenir; Papi, Laura; Pedersen, Inge Sokilde; Peissel, Bernard; Perez-Segura, Pedro; Pfeifer, Katharina; Pineda, Marta; Pohl-Rescigno, Esther; Poplawski, Nicola K.; Porfirio, Berardino; Quante, Anne S.; Ramser, Juliane; Reis, Rui M.; Revillion, Francoise; Rhiem, Kerstin; Riboli, Barbara; Ritter, Julia; Rivera, Daniela; Rofes, Paula; Rump, Andreas; Salinas, Monica; Sanchez de Abajo, Ana Maria; Schmidt, Gunnar; Schönwiese, Ulrike; Seggewiss, Jochen; Solanes, Ares; Steinemann, Doris; Stiller, Mathias; Stoppa-Lyonnet, Dominique; Sullivan, Kelly J.; Susman, Rachel; Sutter, Christian; Tavtigian, Sean; Teo, Soo H.; Teule, Alex; Thomassen, Mads; Tibiletti, Maria Grazia; Tischkowitz, Marc; Tognazzo, Silvia; Toland, Amanda E.; Tornero, Eva; Torngren, Therese; Torres-Esquius, Sara; Toss, Angela; Trainer, Alison H.; Tucker, Katherine M.; van Asperen, Christi J.; van Mackelenbergh, Marion T.; Varesco, Liliana; Vargas-Parra, Gardenia; Varon, Raymonda; Vega, Ana; Velasco, Angela; Vesper, Anne-Sophie; Viel, Alessandra; Vreeswijk, Maaike P. G.; Wagner, Sebastian A.; Waha, Anke; Walker, Logan C.; Walters, Rhiannon J.; Wang-Gohrke, Shan; Weber, Bernhard H. F.; Weichert, Wilko; Wieland, Kerstin; Wiesmüller, Lisa; Witzel, Isabell; Woeckel, Achim; Woodward, Emma R.; Zachariae, Silke; Zampiga, Valentina; Zeder-Goss, Christine; Lazaro, Conxi; De Nicolo, Arcangela; Radice, Paolo; Engel, Christoph; Schmutzler, Rita K.; Goldgar, David E. und Spurdle, Amanda B.
(2019):
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification.
In: Human Mutation, Bd. 40, Nr. 9: S. 1557-1578
Weber-Lassalle, Nana; Borde, Julika; Weber-Lassalle, Konstantin; Horvath, Judit; Niederacher, Dieter; Arnold, Norbert; Kaulfuss, Silke; Ernst, Corinna; Paul, Victoria G.; Honisch, Ellen; Klaschik, Kristina; Volk, Alexander E.; Kubisch, Christian; Rapp, Steffen; Lichey, Nadine; Altmüller, Janine; Lepkes, Louisa; Pohl-Rescigno, Esther; Thiele, Holger; Nuernberg, Peter; Larsen, Mirjam; Richters, Lisa; Rhiem, Kerstin; Wappenschmidt, Barbara; Engel, Christoph; Meindl, Alfons; Schmutzler, Rita K.; Hahnen, Eric und Hauke, Jan
(2019):
Germline loss-of-function variants in the BARD1 gene are associated with early-onset familial breast cancer but not ovarian cancer.
In: Breast Cancer Research, Bd. 21, 55
Qian, Frank; Rookus, Matti A.; Leslie, Goska; Risch, Harvey A.; Greene, Mark H.; Aalfs, Cora M.; Adank, Muriel A.; Adlard, Julian; Agnarsson, Bjarni A.; Ahmed, Munaza; Aittomaki, Kristiina; Andrulis, Irene L.; Arnold, Norbert; Arun, Banu K.; Ausems, Margreet G. E. M.; Azzollini, Jacopo; Barrowdale, Daniel; Barwell, Julian; Benitez, Javier; Bialkowska, Katarzyna; Bonadona, Valerie; Borde, Julika; Borg, Ake; Bradbury, Angela R.; Brunet, Joan; Buys, Saundra S.; Caldes, Trinidad; Caligo, Maria A.; Campbell, Ian; Carter, Jonathan; Chiquette, Jocelyne; Chung, Wendy K.; Claes, Kathleen B. M.; Collee, J. Margriet; Collonge-Rame, Marie-Agnes; Couch, Fergus J.; Daly, Mary B.; Delnatte, Capucine; Diez, Orland; Domchek, Susan M.; Dorfling, Cecilia M.; Eason, Jacqueline; Easton, Douglas F.; Eeles, Ros; Engel, Christoph; Evans, D. Gareth; Faivre, Laurence; Feliubado, Lidia; Foretova, Lenka; Friedman, Eitan; Frost, Debra; Ganz, Patricia A.; Garber, Judy; Garcia-Barberan, Vanesa; Gehrig, Andrea; Glendon, Gord; Godwin, Andrew K.; Garcia, Encarna B. Gomez; Hamann, Ute; Hauke, Jan; Hopper, John L.; Hulick, Peter J.; Imyanitov, Evgeny N.; Isaacs, Claudine; Izatt, Louise; Jakubowska, Anna; Janavicius, Ramunas; John, Esther M.; Karlan, Beth Y.; Kets, Carolien M.; Laitman, Yael; Lazaro, Conxi; Leroux, Dominique; Lester, Jenny; Lesueur, Fabienne; Loud, Jennifer T.; Lubinski, Jan; Lukomska, Alicja; McGuffog, Lesley; Mebirouk, Noura; Meijers-Heijboer, Hanne E. J.; Meindl, Alfons; Miller, Austin; Montagna, Marco; Mooij, Thea M.; Mouret-Fourme, Emmanuelle; Nathanson, Katherine L.; Nehoray, Bita; Neuhausen, Susan L.; Nevanlinna, Heli; Nielsen, Finn C.; Offit, Kenneth; Olah, Edith; Ong, Kai-ren; Oosterwijk, Jan C.; Ottini, Laura; Parsons, Michael T.; Peterlongo, Paolo; Pfeiler, Georg; Pradhan, Nisha; Radice, Paolo; Ramus, Susan J.; Rantala, Johanna; Rennert, Gad; Robson, Mark; Rodriguez, Gustavo C.; Salani, Ritu; Scheuner, Maren T.; Schmutzler, Rita K.; Shah, Payal D.; Side, Lucy E.; Simard, Jacques; Singer, Christian F.; Steinemann, Doris; Stoppa-Lyonnet, Dominique; Tan, Yen Yen; Teixeira, Manuel R.; Terry, Mary Beth; Thomassen, Mads; Tischkowitz, Marc; Tognazzo, Silvia; Toland, Amanda E.; Tung, Nadine; van Asperen, Christi J.; van Engelen, Klaartje; van Rensburg, Elizabeth J.; Venat-Bouvet, Laurence; Vierstraete, Jeroen; Wagner, Gabriel; Walker, Lisa; Weitze, Jeffrey N.; Yannoukakos, Drakoulis; Antoniou, Antonis C.; Goldgar, David E.; Olopade, Olufunmilayo; Chenevix-Trench, Georgia; Rebbeck, Timothy R. und Huo, Dezheng
(2019):
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
In: British Journal of Cancer, Bd. 121, Nr. 2: S. 180-192
Dork, Thilo; Peterlongo, Paolo; Mannermaa, Arto; Bolla, Manjeet K.; Wang, Qin; Dennis, Joe; Ahearn, Thomas; Andrulis, Irene L.; Anton-Culver, Hoda; Arndt, Volker; Aronson, Kristan J.; Augustinsson, Annelie; Freeman, Laura E. Beane; Beckmann, Matthias W.; Beeghly-Fadiel, Alicia; Behrens, Sabine; Bermisheva, Marina; Blomqvist, Carl; Bogdanova, Natalia; Bojesen, Stig E.; Brauch, Hiltrud; Brenner, Hermann; Burwinkel, Barbara; Canzian, Federico; Chan, Tsun L.; Chang-Claude, Jenny; Chanock, Stephen J.; Choi, Ji-Yeob; Christiansen, Hans; Clarke, Christine L.; Couch, Fergus J.; Czene, Kamila; Daly, Mary B.; dos-Santos-Silva, Isabel; Dwek, Miriam; Eccles, Diana M.; Ekici, Arif B.; Eriksson, Mikael; Evans, D. Gareth; Fasching, Peter A.; Figueroa, Jonine; Flyger, Henrik; Fritschisl, Lin; Gabrielson, Marike; Gago-Dominguez, Manuela; Gao, Chi; Gapstur, Susan M.; Garcia-Closas, Montserrat; Garcia-Saenz, Jose A.; Gaudet, Mia M.; Giles, Graham G.; Goldberg, Mark S.; Goldgar, David E.; Guenel, Pascal; Haeberle, Lothar; Haiman, Christopher A.; Hakansson, Niclas; Hall, Per; Hamann, Ute; Hartman, Mikael; Hauke, Jan; Hein, Alexander; Hillemanns, Peter; Hogervorst, Frans B. L.; Hooning, Maartje J.; Hopper, John L.; Howell, Tony; Huo, Dezheng; Ito, Hidemi; Iwasaki, Motoki; Jakubowska, Anna; Janni, Wolfgang; John, Esther M.; Jung, Audrey; Kaaks, Rudolf; Kang, Daehee; Kapoor, Pooja Middha; Khusnutdinova, Elza; Kim, Sung-Won; Kitahara, Cari M.; Koutros, Stella; Kraft, Peter; Kristensen, Vessela N.; Kwon, Ava; Lambrechts, Diether; Le Marchand, Loic; Li, Jingmei; Lindstrom, Sara; Linet, Martha; Lo, Wing-Yee; Long, Jirong; Lophatananon, Artitaya; Lubinski, Jan; Manoochehri, Mehdi; Manoukian, Siranoush; Margolin, Sara; Martinez, Elena; Matsuo, Keitaro; Mavroudis, Dimitris; Meindl, Alfons; Menon, Usha; Milne, Roger L.; Taib, Nur Aishah Mohd; Muir, Kenneth; Mulligan, Anna Marie; Neuhausen, Susan L.; Nevanlinna, Heli; Neven, Patrick; Newman, William G.; Offit, Kenneth; Olopade, Olufunmilayo; Olshan, Andrew F.; Olson, Janet E.; Olsson, Hakan; Park, Sue K.; Park-Simon, Tjoung-Won; Peto, Julian; Plaseska-Karanfilska, Dijana; Pohl-Rescigno, Esther; Presneau, Nadege; Rack, Brigitte; Radice, Paolo; Rashid, Muhammad U.; Rennert, Gad; Rennert, Hedy S.; Romero, Atocha; Ruebner, Matthias; Saloustros, Emmanouil; Schmidt, Marjanka K.; Schmutzler, Rita K.; Schneider, Michael O.; Schoemaker, Minouk J.; Scott, Christopher; Shen, Chen-Yang; Shu, Xiao-Ou; Simard, Jacques; Slager, Susan; Smichkoska, Snezhana; Southey, Melissa C.; Spinelli, John J.; Stone, Jennifer; Surowy, Harald; Swerdlow, Anthony J.; Tamimi, Rulla M.; Tapper, William J.; Teo, Soo H.; Terry, Mary Beth; Toland, Amanda E.; Tollenaar, Rob A. E. M.; Torres, Diana; Torres-Mejia, Gabriela; Troester, Melissa A.; Truong, Therese; Tsugane, Shoichiro; Untch, Michael; Vachon, Celine M.; van den Ouweland, Ans M. W.; van Veen, Elke M.; Vijai, Joseph; Wendt, Camilla; Wolk, Alicja; Yu, Jyh-Cherng; Zheng, Wei; Ziogas, Argyrios; Ziv, Elad; Dunning, Alison M.; Pharoah, Paul D. P.; Schindler, Detlev; Devilee, Peter; Easton, Douglas F.; Balleine, Rosemary; Baxter, Robert; Braye, Stephen; Carpenter, Jane; Dahlstrom, Jane; Forbes, John; Lee, C. Soon; Marsh, Deborah; Morey, Adrienne; Pathmanathan, Nirmala; Scott, Rodney; Simpson, Peter; Spigelman, Allan; Wilcken, Nicholas; Yip, Desmond; Zeps, Nikolajs; Borresen-Dale, Anne-Lise; Alnaes, Grethe I. Grenaker; Sahlberg, Kristine K.; Ottestad, Lars; Karesen, Rolf; Schlichting, Ellen; Holmen, Marit Muri; Sauer, Toril; Haakensen, Vilde; Engebraten, Olav; Naume, Bjorn; Fossa, Alexander; Kiserud, Cecile E.; Reinertsen, Kristin; Helland, Aslaug; Riis, Margit und Geisler, Jürgen
(2019):
Two truncating variants in FANCC and breast cancer risk.
In: Scientific Reports, Bd. 9, 12524
[PDF, 986kB]
Weber-Lassalle, Konstantin; Harter, Philipp; Hauke, Jan; Ernst, Corinna; Kommoss, Stefan; Marme, Frederik; Weber-Lassalle, Nana; Prieske, Katharina; Dietrich, Dimo; Borde, Julika; Pohl-Rescigno, Esther; Reuss, Alexander; Ataseven, Beyhan; Engel, Christoph; Stingl, Julia C.; Schmutzler, Rita K. und Hahnen, Eric
(2018):
Diagnosis of Li-Fraumeni Syndrome: Differentiating TP53 germline mutations from clonal hematopoiesis Results of the observational AGO-TR1 trial.
In: Human Mutation, Bd. 39, Nr. 12: S. 2040-2046
Colombo, Mara; Lopez-Perolio, Irene; Meeks, Huong D.; Caleca, Laura; Parsons, Michael T.; Li, Hongyan; Vecchi, Giovanna de; Tudini, Emma; Foglia, Claudia; Mondini, Patrizia; Manoukian, Siranoush; Behar, Raquel; Garcia, Encarna B. Gomez; Meindl, Alfons; Montagna, Marco; Niederacher, Dieter; Schmidt, Ane Y.; Varesco, Liliana; Wappenschmidt, Barbara; Bolla, Manjeet K.; Dennis, Joe; Michailidou, Kyriaki; Wang, Qin; Aittomaki, Kristiina; Andrulis, Irene L.; Anton-Culver, Hoda; Arndt, Volker; Beckmann, Matthias W.; Beeghly-Fadel, Alicia; Benitez, Javier; Böckx, Bram; Bogdanova, Natalia V.; Bojesen, Stig E.; Bonanni, Bernardo; Brauch, Hiltrud; Brenner, Hermann; Burwinkel, Barbara; Chang-Claude, Jenny; Conroy, Don M.; Couch, Fergus J.; Cox, Angela; Cross, Simon S.; Czene, Kamila; Devilee, Peter; Dork, Thilo; Eriksson, Mikael; Fasching, Peter A.; Figueroa, Jonine; Fletcher, Olivia; Flyger, Henrik; Gabrielson, Marike; Garcia-Closas, Montserrat; Giles, Graham G.; Gonzalez-Neira, Anna; Guenel, Pascal; Haiman, Christopher A.; Hall, Per; Hamann, Ute; Hartman, Mikael; Hauke, Jan; Hollestelle, Antoinette; Hopper, John L.; Jakubowska, Anna; Jung, Audrey; Kosma, Veli-Matti; Lambrechts, Diether; Marchand, Loid le; Lindblom, Annika; Lubinski, Jan; Mannermaa, Arto; Margolin, Sara; Miao, Hui; Milne, Roger L.; Neuhausen, Susan L.; Nevanlinna, Heli; Olson, Janet E.; Peterlongo, Paolo; Peto, Julian; Pylkas, Katri; Sawyer, Elinor J.; Schmidt, Marjanka K.; Schmutzler, Rita K.; Schneeweiss, Andreas; Schömaker, Minouk J.; See, Mee Hoong; Southey, Melissa C.; Swerdlow, Anthony; Teo, Soo H.; Toland, Amanda E.; Tomlinson, Ian; Truong, Therese; Asperen, Christi J. van; Ouweland, Ans M. W. van den; Kolk, Lizet E. van der; Winqvist, Robert; Yannoukakos, Drakoulis; Zheng, Wei; Dunning, Alison M.; Easton, Douglas F.; Henderson, Alex; Hogervorst, Frans B. L.; Izatt, Louise; Offitt, Kenneth; Side, Lucy E.; Rensburg, Elizabeth J. van; McGuffog, Lesley; Antoniou, Antonis C.; Chenevix-Trench, Georgia; Spurdle, Amanda B.; Goldgar, David E.; Hoya, Miguel de la und Radice, Paolo
(2018):
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.
In: Human Mutation, Bd. 39, Nr. 5: S. 729-741
Hauke, Jan; Horvath, Judit; Gross, Eva; Gehrig, Andrea; Honisch, Ellen; Hackmann, Karl; Schmidt, Gunnar; Arnold, Norbert; Faust, Ulrike; Sutter, Christian; Hentschel, Julia; Wang-Gohrke, Shan; Smogavec, Mateja; Weber, Bernhard H. F.; Weber-Lassalle, Nana; Weber-Lassalle, Konstantin; Borde, Julika; Ernst, Corinna; Altmüller, Janine; Volk, Alexander E.; Thiele, Holger; Huebbel, Verena; Nuernberg, Peter; Keupp, Katharina; Versmold, Beatrix; Pohl, Esther; Kubisch, Christian; Grill, Sabine; Paul, Victoria; Herold, Natalie; Lichey, Nadine; Rhiem, Kerstin; Ditsch, Nina; Ruckert, Christian; Wappenschmidt, Barbara; Auber, Bernd; Rump, Andreas; Niederacher, Dieter; Haaf, Thomas; Ramser, Juliane; Dworniczak, Bernd; Engel, Christoph; Meindl, Alfons; Schmutzler, Rita K. und Hahnen, Eric
(2018):
Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer.
In: Cancer Medicine, Bd. 7, Nr. 4: S. 1349-1358
Engel, Christoph; Rhiem, Kerstin; Hahnen, Eric; Loibl, Sibylle; Weber, Karsten E.; Seiler, Sabine; Zachariae, Silke; Hauke, Jan; Wappenschmidt, Barbara; Waha, Anke; Blümcke, Britta; Kiechle, Marion; Meindl, Alfons; Niederacher, Dieter; Bartram, Claus R.; Speiser, Dorothee; Schlegelberger, Brigitte; Arnold, Norbert; Wieacker, Peter; Leinert, Elena; Gehrig, Andrea; Briest, Susanne; Kast, Karin; Riess, Olaf; Emons, Günter; Weber, Bernhard H. F.; Engel, Jutta und Schmutzler, Rita K.
(2018):
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history.
In: BMC Cancer
18:265
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Waha, Anke; Versmold, Beatrix; Kast, Karin; Kiechle, Marion; Ditsch, Nina; Meindl, Alfons; Niederacher, Dieter; Hahnen, Eric; Arnold, Norbert; Mundhenke, Christoph; Horvath, Judit; Auber, Bernd; Dikow, Nicola; Hauke, Jan; Wappenschmidt, Barbara; Riess, Olaf; Schott, Sarah; Speiser, Dorothee; Faust, Ulrike; Sutter, Christian; Rhiem, Kerstin und Schmutzler, Rita Katharina
(2017):
Konsensusempfehlung des Deutschen Konsortiums Familiärer Brust- und Eierstockkrebs zum Umgang mit Ergebnissen der Multigenanalyse.
In: Geburtshilfe und Frauenheilkunde, Bd. 77, Nr. 7: S. 733-739
Neidhardt, Guido; Hauke, Jan; Ramser, Juliane; Gross, Eva; Gehrig, Andrea; Müller, Clemens R.; Kahlert, Anne-Karin; Hackmann, Karl; Honisch, Ellen; Niederacher, Dieter; Heilmann-Heimbach, Stefanie; Franke, Andre; Lieb, Wolfgang; Thiele, Holger; Altmüller, Janine; Nürnberg, Peter; Klaschik, Kristina; Ernst, Corinna; Ditsch, Nina; Jessen, Frank; Ramirez, Alfredo; Wappenschmidt, Barbara; Engel, Christoph; Rhiem, Kerstin; Meindl, Alfons; Schmutzler, Rita K. und Hahnen, Eric
(2017):
Association Between Loss-of-Function Mutations Within the FANCM Gene and Early-Onset Familial Breast Cancer.
In: Jama Oncology, Bd. 3, Nr. 9: S. 1245-1248
Kast, Karin; Rhiem, Kerstin; Wappenschmidt, Barbara; Hahnen, Eric; Hauke, Jan; Bluemcke, Britta; Zarghooni, Verena; Herold, Natalie; Ditsch, Nina; Kiechle, Marion; Braun, Michael; Fischer, Christine; Dikow, Nicola; Schott, Sarah; Rahner, Nils; Niederacher, Dieter; Fehm, Tanja; Gehrig, Andrea; Mueller-Reible, Clemens; Arnold, Norbert; Maass, Nicolai; Borck, Guntram; de Gregorio, Nikolaus; Scholz, Caroline; Auber, Bernd; Varon-Manteeva, Raymonda; Speiser, Dorothee; Horvath, Judit; Lichey, Nadine; Wimberger, Pauline; Stark, Sylvia; Faust, Ulrike; Weber, Bernhard H. F.; Emons, Gunter; Zachariae, Silke; Meindl, Alfons; Schmutzler, Rita K. und Engel, Christoph
(2016):
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer.
In: Journal of Medical Genetics, Bd. 53, Nr. 7: S. 465-471
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