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13 results for Faust,+Ulrike

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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
Author / Creator: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 ; Hübbel, Verena ; Nürnberg, 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. ; Hahnen, Eric
Publisher:United States: John Wiley & Sons, Inc
Journal title:Cancer medicine (Malden, MA), 2018-04, Vol.7 (4), p.1349-1358
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ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways—lessons from breast cancer patients
Author / Creator:Sachsenweger, Juliane ; Jansche, Rebecca ; Merk, Tatjana ; Heitmeir, Benedikt ; Deniz, Miriam ; Faust, Ulrike ; Roggia, Cristiana ; Tzschach, Andreas ; Schroeder, Christopher ; Riess, Angelika ; Pospiech, Helmut ; Peltoketo, Hellevi ; Pylkäs, Katri ; Winqvist, Robert ; Wiesmüller, Lisa
Publisher:London: Springer Nature B.V
Journal title:Cell death & disease, 2023-05, Vol.14 (5), p.328
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Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
Author / Creator:Sepahi, Ilnaz ; Faust, Ulrike ; Sturm, Marc ; Bosse, Kristin ; Kehrer, Martin ; Heinrich, Tilman ; Grundman-Hauser, Kathrin ; Bauer, Peter ; Ossowski, Stephan ; Susak, Hana ; Varon, Raymonda ; Schröck, Evelin ; Niederacher, Dieter ; Auber, Bernd ; Sutter, Christian ; Arnold, Norbert ; Hahnen, Eric ; Dworniczak, Bernd ; Wang-Gorke, Shan ; Gehrig, Andrea ; Weber, Bernhard H. F. ; Engel, Christoph ; Lemke, Johannes R. ; Hartkopf, Andreas ; Nguyen, Huu Phuc ; Riess, Olaf ; Schroeder, Christopher
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2019-08, Vol.19 (1), p.787-787, Article 787
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Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome
Author / Creator:Witt, Dennis ; Faust, Ulrike ; Strobl‐Wildemann, Gertrud ; Sturm, Marc ; Buchert, Rebecca ; Zuleger, Theresia ; Admard, Jakob ; Casadei, Nicolas ; Ossowski, Stephan ; Haack, Tobias B. ; Rieß, Olaf ; Schroeder, Christopher
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2023-06, Vol.11 (6), p.e2151-n/a
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Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data
Author / Creator:Demidov, German ; Park, Joohyun ; Armeanu‐Ebinger, Sorin ; Roggia, Cristiana ; Faust, Ulrike ; Cordts, Isabell ; Blandfort, Maria ; Haack, Tobias B. ; Schroeder, Christopher ; Ossowski, Stephan
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2021-12, Vol.9 (12), p.e1807-n/a
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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
Author / Creator:Hakkaart, Christopher ; Pearson, John F. ; Marquart, Louise ; Wiggins, George A. R. ; Barnes, Daniel R. ; Robinson, Bridget A. ; Andrulis, Irene L. ; Arun, Banu K. ; Balmaña, Judith ; Barkardottir, Rosa B. ; Berger, Lieke ; Boonen, Susanne E. ; Borde, Julika ; Buys, Saundra S. ; Caligo, Maria A. ; Campbell, Ian ; Chung, Wendy K. ; Claes, Kathleen B. M. ; Collonge-Rame, Marie-Agnès ; Cook, Jackie ; Couch, Fergus J. ; de la Hoya, Miguel ; de Putter, Robin ; Dhawan, Mallika ; Diez, Orland ; Ding, Yuan Chun ; Domchek, Susan M. ; Donaldson, Alan ; Easton, Douglas F. ; Ehrencrona, Hans ; Engel, Christoph ; Evans, D. Gareth ; Faust, Ulrike ; Feliubadaló, Lidia ; Fostira, Florentia ; Garber, Judy ; Gayther, Simon A. ; Gehrig, Andrea ; Godwin, Andrew K. ; Goldgar, David E. ; Greene, Mark H. ; Hahnen, Eric ; Hamann, Ute ; Hansen, Thomas V. O. ; Hentschel, Julia ; Herold, Natalie ; Isaacs, Claudine ; Izquierdo, Angel ; Janavicius, Ramunas ; Karlan, Beth Y. ; Kemp, Zoe ; Kirk, Judy ; Konstantopoulou, Irene ; Koudijs, Marco ; Kwong, Ava ; Laitman, Yael ; Lasset, Christine ; Lazaro, Conxi ; Leslie, Goska ; Mai, Phuong L. ; Mari, Véronique ; Martens, John W. M. ; McGuffog, Lesley ; Mebirouk, Noura ; Meindl, Alfons ; Miller, Austin ; Moserle, Lidia ; Mouret-Fourme, Emmanuelle ; Musgrave, Hannah ; Neuhausen, Susan L. ; Nevanlinna, Heli ; Yie, Joanne Ngeow Yuen ; Olah, Edith ; Olopade, Olufunmilayo I. ; Osorio, Ana ; Park, Sue K. ; Parsons, Michael T. ; Pedersen, Inge Sokilde ; Peixoto, Ana ; Perez-Segura, Pedro ; Pocza, Timea ; Radice, Paolo ; Rossing, Maria ; Schmutzler, Rita K. ; Shah, Payal D. ; Side, Lucy E. ; Singer, Christian F. ; Steinemann, Doris ; Stoppa-Lyonnet, Dominique ; Teo, Soo Hwang ; Thull, Darcy L. ; Toland, Amanda E. ; Trainer, Alison H. ; Vega, Ana ; Viel, Alessandra ; Walker, Lisa ; Weitzel, Jeffrey N. ; Chenevix-Trench, Georgia ; Spurdle, Amanda B. ; Walker, Logan C.
Publisher:London: Nature Publishing Group UK
Journal title:Communications biology, 2022-10, Vol.5 (1), p.1061-1061, Article 1061
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First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implicati...
Author / Creator:Löffler, Markus W. ; Steinhilber, Julia ; Hilke, Franz J. ; Haen, Sebastian P. ; Bösmüller, Hans ; Montes-Mojarro, Ivonne-Aidee ; Bonzheim, Irina ; Stäbler, Antje ; Faust, Ulrike ; Grasshoff, Ute ; Königsrainer, Ingmar ; Rammensee, Hans-Georg ; Kanz, Lothar ; Königsrainer, Alfred ; Beckert, Stefan ; Riess, Olaf ; Schroeder, Christopher
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2018-08, Vol.19 (1), p.144-7, Article 144
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Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer
Author / Creator: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 ; Engel, Christoph
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2016-07, Vol.53 (7), p.465-471
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Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients
Author / Creator:Schroeder, Christopher ; Faust, Ulrike ; Krauße, Luisa ; Liebmann, Alexandra ; Abele, Michael ; Demidov, German ; Schütz, Leon ; Kelemen, Olga ; Pohle, Alexandra ; Gauß, Silja ; Sturm, Marc ; Roggia, Cristiana ; Streiter, Monika ; Buchert, Rebecca ; Armenau-Ebinger, Sorin ; Nann, Dominik ; Beschorner, Rudi ; Handgretinger, Rupert ; Ebinger, Martin ; Lang, Peter ; Holzer, Ursula ; Skokowa, Julia ; Ossowski, Stephan ; Haack, Tobias B ; Mau-Holzmann, Ulrike A ; Dufke, Andreas ; Riess, Olaf ; Brecht, Ines B
Publisher:Leiden: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2023-10, Vol.31 (10), p.1139-1146
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HBOC multi-gene panel testing: comparison of two sequencing centers
Author / Creator:Schroeder, Christopher ; Faust, Ulrike ; Sturm, Marc ; Hackmann, Karl ; Grundmann, Kathrin ; Harmuth, Florian ; Bosse, Kristin ; Kehrer, Martin ; Benkert, Tanja ; Klink, Barbara ; Mackenroth, Luisa ; Betcheva-Krajcir, Elitza ; Wimberger, Pauline ; Kast, Karin ; Heilig, Mechthilde ; Nguyen, Huu Phuc ; Riess, Olaf ; Schröck, Evelin ; Bauer, Peter ; Rump, Andreas
Publisher:New York: Springer US
Journal title:Breast cancer research and treatment, 2015-07, Vol.152 (1), p.129-136
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Prevalence of BRCA1/2 germline mutations in 21401 families with breast and ovarian cancer
Author / Creator: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 ; Engel, Christoph
Journal title:Journal of medical genetics, 2016-07, Vol.53 (7), p.465-471
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Gene panel testing of 5589 BRCA 1/2 ‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer
Author / Creator: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 ; Hübbel, Verena ; Nürnberg, 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. ; Hahnen, Eric
Journal title:Cancer medicine (Malden, MA), 2018-04, Vol.7 (4), p.1349-1358
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer
Author / Creator:Ferreira, Manuel A. ; Andrulis, Irene L. ; Anton-Culver, Hoda ; Aronson, Kristan J. ; Barnes, Daniel R. ; Beckmann, Matthias W. ; Behrens, Sabine ; Bermisheva, Marina ; Bogdanova, Natalia V. ; Bojesen, Stig E. ; Bolla, Manjeet K. ; Brauch, Hiltrud ; Campa, Daniele ; Campbell, Ian ; Canzian, Federico ; Carter, Jonathan ; Castelao, Jose E. ; Chang-Claude, Jenny ; Couch, Fergus J. ; Cox, Angela ; Cross, Simon S. ; de la Hoya, Miguel ; Dennis, Joe ; Devilee, Peter ; Dörk, Thilo ; Ejlertsen, Bent ; Engel, Christoph ; Eriksson, Mikael ; Fletcher, Olivia ; Flyger, Henrik ; Frost, Debra ; Gabrielson, Marike ; Gapstur, Susan M. ; Garber, Judy ; García-Sáenz, José A. ; Giles, Graham G. ; Glendon, Gord ; Godwin, Andrew K. ; González-Neira, Anna ; Gronwald, Jacek ; Guénel, Pascal ; Hall, Per ; Hamann, Ute ; He, Wei ; Hulick, Peter J. ; Humphreys, Keith ; Isaacs, Claudine ; Jakimovska, Milena ; Jakubowska, Anna ; James, Paul A. ; John, Esther M. ; Johnson, Nichola ; Karlan, Beth Y. ; Khusnutdinova, Elza ; Kiiski, Johanna I. ; Jones, Michael E. ; Konstantopoulou, Irene ; Laitman, Yael ; Lambrechts, Diether ; Lazaro, Conxi ; Lindström, Sara ; Manoochehri, Mehdi ; Margolin, Sara ; McGuffog, Lesley ; Michailidou, Kyriaki ; Montagna, Marco ; Moreno, Fernando ; Moserle, Lidia ; Nevelsteen, Ines ; Nussbaum, Robert L. ; Offit, Kenneth ; Olah, Edith ; Olopade, Olufunmilayo I. ; Osorio, Ana ; Park-Simon, Tjoung-Won ; Pedersen, Inge Sokilde ; Peixoto, Ana ; Peterlongo, Paolo ; Poppe, Bruce ; Presneau, Nadege ; Risch, Harvey A. ; Saloustros, Emmanouil ; Sanden, Kristin ; Simard, Jacques ; Singer, Christian F. ; Soucy, Penny ; Spinelli, John J. ; Spurdle, Amanda B. ; Taylor, Jack A. ; Thöne, Kathrin ; Toland, Amanda E. ; Tung, Nadine ; Vachon, Celine M. ; van Asperen, Christi J. ; van Rensburg, Elizabeth J. ; Weitzel, Jeffrey N. ; Winqvist, Robert ; Yannoukakos, Drakoulis ; Zheng, Wei ; Beesley, Jonathan
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2019-04, Vol.10 (1), p.1741-18, Article 1741
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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

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ABRAXAS1 orchestrates BRCA1 activities to counter genome destabilizing repair pathways—lessons from breast cancer patients

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Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women

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Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome

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Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data

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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

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First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extremely rare diseases with probable further implicati...

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Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer

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Clinical trio genome sequencing facilitates the interpretation of variants in cancer predisposition genes in paediatric tumour patients

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HBOC multi-gene panel testing: comparison of two sequencing centers

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Prevalence of BRCA1/2 germline mutations in 21401 families with breast and ovarian cancer

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Gene panel testing of 5589 BRCA 1/2 ‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer

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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

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