Auflistung nach Autor "Faust, Ulrike E. A."

Anzeige der Dokumente 1-15 von 15

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

Roggia, Cristiana; Schroeder, Christopher; Riess, Angelika; Faust, Ulrike E. A. (2023)
Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Faust, Ulrike E. A.; Wagner, Philipp Georg (2020)
Characterisation of novel uveal melanoma cell lines under serum-free conditions

Bartz-Schmidt, Karl U.; Süsskind, Daniela; Schrader, Merle; Henke-Fahle, Sigrid; Bauer, Peter; Faust, Ulrike E. A.; Gauss, Silja (2013)
Combined genetic and splicing analysis of BRCA1 c.[594-2A > C; 641A > G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms

Faust, Ulrike E. A. (2016)
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

Faust, Ulrike E. A. (2020)
First case report of malignant peritoneal mesothelioma and oral verrucous carcinoma in a patient with a germline PTEN mutation: a combination of extreme rare diseases with probable further implications

Montes-Mojarro, Ivonne A.; Bonzheim, Irina; Stäbler, Antje Ulrike; Grasshoff, Ute; Rammensee, Hans-Georg; Kanz, Lothar; Beckert, Stefan; Löffler, Markus W.; Steinhilber, Julia Perdika; Hilke, Franz Joachim; Haen, Sebastian P.; Faust, Ulrike E. A.; Königsrainer, Ingmar; Königsrainer, Alfred; Rieß, Olaf; Schroeder, Christopher; Bösmüller, Hans (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

Faust, Ulrike E. A. (2018)
Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Brauch, Hiltrud; Faust, Ulrike E. A.; Nguyen, Huu Phuc (2019)
Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approaches

Roggia, Cristiana; Gschwind, Axel; Seibel-Kelemen, Olga; Hertler, Sonja; Liebmann, Alexandra; Bonzheim, Irina; Hartkopf, Andreas; Bitzer, Michael; Brecht, Ines B.; Ruhm, Kristina; Ossowski, Stephan; Schroeder, Christopher; Armeanu-Ebinger, Sorin; Faust, Ulrike E. A.; Haack, Tobias; Neumann, Manuela Claudia; Forschner, Andrea Lydia; Malek, Nisar Peter; Möller, Yvonne; Löwenheim, Hubert Martin; Riess, Olaf (2023)
HBOC multi-gene panel testing: comparison of two sequencing centers

Schroeder, Christopher; Faust, Ulrike E. A.; Sturm, Marc; Grundmann-Hauser, Kathrin; Harmuth, Florian; Bosse, Kristin; Kehrer, Martin; Benkert, Tanja; Heilig, Mechthilde; Nguyen, Huu Phuc; Rieß, Olaf; Bauer, Peter (2015)
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women

Sepahi, Ilnaz; Sturm, Marc; Bosse, Kristin; Kehrer, Martin; Heinrich, Tilman; Grundmann-Hauser, Kathrin; Bauer, Peter; Ossowski, Stephan; Hartkopf, Andreas; Faust, Ulrike E. A.; Rieß, Olaf; Schroeder, Christopher (2019)
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Faust, Ulrike E. A.; Heinrich, Tilman (2019)
Performance of Breast Cancer Polygenic Risk Scores in 760 Female CHEK2 Germline Mutation Carriers

Faust, Ulrike E. A. (2021)
Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer

Faust, Ulrike E. A. (2016)
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia

Pogoda, Michaela; Hilke, Franz Joachim; Lohmann, Ebba; Sturm, Marc; Lenz, Florian; Matthes, Jakob; Muyas, Francesc; Ossowski, Stephan; Faust, Ulrike E. A.; Sepahi, Ilnaz; Casadei, Nicolas; Poths, Sven; Rieß, Olaf; Schroeder, Christopher; Grundmann-Hauser, Kathrin (2019)

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Auflistung nach Autor "Faust, Ulrike E. A."

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