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Anzahl der Publikationen: 10
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
Borde, Julika; Laitman, Yael; Bluemcke, Britta; Niederacher, Dieter; Weber-Lassalle, Konstantin; Sutter, Christian; Rump, Andreas; Arnold, Norbert; Wang-Gohrke, Shan; Horvath, Judit; Gehrig, Andrea; Schmidt, Gunnar; Dutrannoy, Veronique; Ramser, Juliane; Hentschel, Julia; Meindl, Alfons; Schroeder, Christopher; Wappenschmidt, Barbara; Engel, Christoph; Kuchenbaecker, Karoline; Schmutzler, Rita K.; Friedman, Eitan; Hahnen, Eric und Ernst, Corinna
(2022):
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers.
In: BMC Cancer, Bd. 22, Nr. 1, 706
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
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 
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
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
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]
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
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
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