Hereditary Breast and Ovarian Cancer Service in Sparsely Populated Western Pomerania

por Felbor, Ute, Bülow, Robin, Schmutzler, Rita K., Rath, Matthias
Publicado 2022

Activating Somatic FGFR2 Mutations in Breast Cancer

por Reintjes, Nadine, Li, Yun, Becker, Alexandra, Rohmann, Edyta, Schmutzler, Rita, Wollnik, Bernd
Publicado 2013

Long-term survival of a BRCA2 mutation carrier following second ovarian cancer relapse using PARPi therapy: A case report

por Bredow, Kathrin, Blümcke, Britta, Schneider, Stephanie, Püsken, Michael, Schmutzler, Rita, Rhiem, Kerstin
Publicado 2022

“You Always Have It in the Back of Your Mind”—Feelings, Coping, and Support Needs of Women with Pathogenic Variants in Moderate-Risk Genes for Hereditary Breast Cancer Attending Ge...

por Stracke, Claudia, Lemmen, Clarissa, Rhiem, Kerstin, Schmutzler, Rita, Kautz-Freimuth, Sibylle, Stock, Stephanie
Publicado 2022

Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics

por Ernst, Corinna, Hahnen, Eric, Engel, Christoph, Nothnagel, Michael, Weber, Jonas, Schmutzler, Rita K., Hauke, Jan
Publicado 2018

Decision Aids for Preventive Treatment Alternatives for BRCA1/2 Mutation Carriers: a Systematic Review

por Krassuski, Lisa Marlene, Kautz-Freimuth, Sibylle, Vennedey, Vera, Rhiem, Kerstin, Schmutzler, Rita K., Stock, Stephanie
Publicado 2021

Psychological factors and the uptake of preventative measures in BRCA1/2 pathogenic variant carriers: results of a prospective cohort study

por Dick, Julia, Tüchler, Anja, Brédart, Anne, Vitinius, Frank, Wassermann, Kirsten, Rhiem, Kerstin, Schmutzler, Rita K.
Publicado 2022

Non-small cell neuroendocrine carcinoma of the ovary in a BRCA2-germline mutation carrier: A case report and brief review of the literature

por Herold, Natalie, Wappenschmidt, Barbara, Markiefka, Birgid, Keupp, Katharina, Kröber, Sandra, Hahnen, Eric, Schmutzler, Rita, Rhiem, Kerstin
Publicado 2018

Evaluation of two evidence-based decision aids for female BRCA1/2 mutation carriers in Germany: study protocol for a randomised controlled parallel-group trial

por Kautz-Freimuth, Sibylle, Redaèlli, Marcus, Isselhard, Anna, Shukri, Arim, Vodermaier, Andrea, Rhiem, Kerstin, Schmutzler, Rita, Stock, Stephanie
Publicado 2022

Satisfaction and Quality of Life of Healthy and Unilateral Diseased BRCA1/2 Pathogenic Variant Carriers after Risk-Reducing Mastectomy and Reconstruction Using the BREAST-Q Questio...

por Herold, Natalie, Hellmich, Martin, Lichtenheldt, Frank, Ataseven, Beyhan, Hillebrand, Vanessa, Wappenschmidt, Barbara, Schmutzler, Rita Katharina, Rhiem, Kerstin
Publicado 2022

TP53-binding protein variants and breast cancer risk: a case-control study

por Frank, Bernd, Hemminki, Kari, Bermejo, Justo Lorenzo, Klaes, Rüdiger, Bugert, Peter, Wappenschmidt, Barbara, Schmutzler, Rita K, Burwinkel, Barbara
Publicado 2005

Effectiveness of evidence-based decision aids for women with pathogenic BRCA1 or BRCA2 variants in the german health care context: results from a randomized controlled trial

por Kautz-Freimuth, Sibylle, Redaèlli, Marcus, Shukri, Arim, Kentenich, Hannah, Simic, Dusan, Mildenberger, Vanessa, Schmutzler, Rita, Rhiem, Kerstin, Stock, Stephanie
Publicado 2023

Olaparib for metastatic breast cancer in a patient with a germline PALB2 variant

por Kuemmel, Sherko, Harrach, Hakima, Schmutzler, Rita K., Kostara, Athina, Ziegler-Löhr, Katja, Dyson, Mark H., Chiari, Ouafaa, Reinisch, Mattea
Publicado 2020

Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study

por Burwinkel, Barbara, Shanmugam, Kalai S, Hemminki, Kari, Meindl, Alfons, Schmutzler, Rita K, Sutter, Christian, Wappenschmidt, Barbara, Kiechle, Marion, Bartram, Claus R, Frank, Bernd
Publicado 2006

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

por Frank, Bernd, Hemminki, Kari, Meindl, Alfons, Wappenschmidt, Barbara, Sutter, Christian, Kiechle, Marion, Bugert, Peter, Schmutzler, Rita K, Bartram, Claus R, Burwinkel, Barbara
Publicado 2007

Patient-Centered Care in Breast Cancer Genetic Clinics

por Brédart, Anne, Anota, Amélie, Dick, Julia, Kuboth, Violetta, Lareyre, Olivier, De Pauw, Antoine, Cano, Alejandra, Stoppa-Lyonnet, Dominique, Schmutzler, Rita, Dolbeault, Sylvie, Kop, Jean-Luc
Publicado 2018

Psychosocial problems in women attending French, German and Spanish genetics clinics before and after targeted or multigene testing results: an observational prospective study

por Brédart, Anne, Kop, Jean-Luc, Dick, Julia, Cano, Alejandra, De Pauw, Antoine, Anota, Amélie, Brunet, Joan, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita, Dolbeault, Sylvie
Publicado 2019

Assessment of psychosocial difficulties by genetic clinicians and distress in women at high risk of breast cancer: a prospective study

por Brédart, Anne, Kop, Jean-Luc, Tüchler, Anja, De Pauw, Antoine, Cano, Alejandra, Dick, Julia, Rhiem, Kerstin, Devilee, Peter, Schmutzler, Rita, Stoppa-Lyonnet, Dominique, Dolbeault, Sylvie
Publicado 2022

Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction

por Wappenschmidt, Barbara, Becker, Alexandra A., Hauke, Jan, Weber, Ute, Engert, Stefanie, Köhler, Juliane, Kast, Karin, Arnold, Norbert, Rhiem, Kerstin, Hahnen, Eric, Meindl, Alfons, Schmutzler, Rita K.
Publicado 2012

Nurse-led decision coaching by specialized nurses for healthy BRCA1/2 gene mutation carriers - adaptation and pilot testing of a curriculum for nurses: a qualitative study

por Berger-Höger, Birte, Vitinius, Frank, Fischer, Hannah, Beifus, Karolina, Köberlein-Neu, Juliane, Isselhard, Anna, Töpper, Maren, Wiedemann, Regina, Rhiem, Kerstin, Schmutzler, Rita, Stock, Stephanie, Steckelberg, Anke
Publicado 2022