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Anzahl der Publikationen: 11
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
Dumont, Martine; Weber-Lassalle, Nana; Joly-Beauparlant, Charles; Ernst, Corinna; Droit, Arnaud; Feng, Bing-Jian; Dubois, Stephane; Collin-Deschesnes, Annie-Claude; Soucy, Penny; Vallee, Maxime; Fournier, Frederic; Lemacon, Audrey; Adank, Muriel A.; Allen, Jamie; Altmueller, Janine; Arnold, Norbert; Ausems, Margreet G. E. M.; Berutti, Riccardo; Bolla, Manjeet K.; Bull, Shelley; Carvalho, Sara; Cornelissen, Sten; Dufault, Michael R.; Dunning, Alison M.; Engel, Christoph; Gehrig, Andrea; Geurts-Giele, Willemina R. R.; Gieger, Christian; Green, Jessica; Hackmann, Karl; Helmy, Mohamed; Hentschel, Julia; Hogervorst, Frans B. L.; Hollestelle, Antoinette; Hooning, Maartje J.; Horvath, Judit; Ikram, M. Arfan; Kaulfuss, Silke; Keeman, Renske; Kuang, Da; Luccarini, Craig; Maier, Wolfgang; Martens, John W. M.; Niederacher, Dieter; Nurnberg, Peter; Ott, Claus-Eric; Peters, Annette; Pharoah, Paul D. P.; Ramirez, Alfredo; Ramser, Juliane; Riedel-Heller, Steffi; Schmidt, Gunnar; Shah, Mitul; Scherer, Martin; Stabler, Antje; Strom, Tim M.; Sutter, Christian; Thiele, Holger; Asperen, Christi J. van; Kolk, Lizet van der; Luijt, Rob B. van der; Volk, Alexander E.; Wagner, Michael; Waisfisz, Quinten; Wang, Qin; Wang-Gohrke, Shan; Weber, Bernhard H. F.; Devilee, Peter; Tavtigian, Sean; Bader, Gary D.; Meindl, Alfons; Goldgar, David E.; Andrulis, Irene L.; Schmutzler, Rita K.; Easton, Douglas F.; Schmidt, Marjanka K.; Hahnen, Eric und Simard, Jacques
(2022):
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry.
In: Cancers, Bd. 14, Nr. 14, 3363
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
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
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
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
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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
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