Ausgabe 1/2017
Inhalt (20 Artikel)
How does genetic risk information for Lynch syndrome translate to risk management behaviours?
Emma Steel, Andrew Robbins, Mark Jenkins, Louisa Flander, Clara Gaff, Louise Keogh
Anxiety and depression symptoms among women attending group-based patient education courses for hereditary breast and ovarian cancer
Wenche Listøl, Hildegunn Høberg-Vetti, Geir Egil Eide, Cathrine Bjorvatn
Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines
Marcia Cruz-Correa, Julyann Pérez-Mayoral, Julie Dutil, Miguel Echenique, Rafael Mosquera, Keila Rivera-Román, Sharee Umpierre, Segundo Rodriguez-Quilichini, Maria Gonzalez-Pons, Myrta I. Olivera, Sherly Pardo
Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer
Tomasz Huzarski, Barbara Górecka-Szyld, Jowita Huzarska, Grażyna Psut-Muszyńska, Grażyna Wilk, Robert Sibilski, Cezary Cybulski, Beata Kozak-Klonowska, Monika Siołek, Ewa Kilar, Dorota Czudowska, Hanna Janiszewska, Dariusz Godlewski, Andrzej Mackiewicz, Joanna Jarkiewicz-Tretyn, Jadwiga Szabo-Moskal, Jacek Gronwald, Jan Lubiński, Steven A. Narod, T Byrski, T Dębniak, A Tołoczko-Grabarek, O Oszurek, M Michalak, H Rogowska-Droś, E Szatkowska, R Kulus, W Kwiecień, L Szyiński, I Winiarska, P Kasprzak, L Tomiak-Rówińska, M Kosterska-Spalska, T Dróżdż, P Sosnowski
The genetic basis of colonic adenomatous polyposis syndromes
Bente A. Talseth-Palmer
A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinoma
Caroline Kientz, Marie-Odile Joly, Laurence Faivre, Alix Clemenson, Sophie Dalac, Côme Lepage, Caroline Chapusot, Caroline Jacquot, Renaud Schiappa, Marine Lebrun
Hereditary and non-hereditary branches of family eligible for BRCA test: cancers in other sites
M. Digennaro, D. Sambiasi, S. Tommasi, B. Pilato, S. Diotaiuti, A. Kardhashi, G. Trojano, A. Tufaro, A. V. Paradiso
ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis
Yan Jiang, Chen-Yang Zhao, Li-Chun Cheng, Bing Xu, Hui-Yi Lv
Hereditary pancreatic cancer: related syndromes and clinical perspective
Sergio Carrera, Aintzane Sancho, Eider Azkona, Josune Azkuna, Guillermo Lopez-Vivanco
Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1
Charu Kaiwar, Sarah K. Macklin, Jennifer M. Gass, Jessica Jackson, Eric W. Klee, Stephanie L. Hines, John A. Stauffer, Paldeep S. Atwal
Preoperative genetic testing impacts surgical decision making in BRCA mutation carriers with breast cancer: a retrospective cohort analysis
Siddhartha Yadav, Ashley Reeves, Sarah Campian, Amy Sufka, Dana Zakalik
Hereditary gynaecologic cancers in Nepal: a proposed model of care to serve high risk populations in developing countries
Hanoon P. Pokharel, Neville F. Hacker, Lesley Andrews
Evaluation of psychosocial aspects in participants of cancer genetic counseling
Leivy Patricia González-Ramírez, Reyna Martínez-Arriaga, Erendira Camacho-Cárdenas, Azucena Del Toro-Valero, Antonio Oceguera-Villanueva, Livia Zagamé, Aída Araceli Silva-García, Adrián Daneri-Navarro
Motivators and barriers of tamoxifen use as risk-reducing medication amongst women at increased breast cancer risk: a systematic literature review
B. Meiser, W. K. T. Wong, M. Peate, C. Julian-Reynier, J. Kirk, G. Mitchell
The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation
Agnieszka Strumidło, Sylwia Skiba, Rodney J. Scott, Jan Lubiński
Emotional impact on the results of BRCA1 and BRCA2 genetic test: an observational retrospective study
Sara Mella, Barbara Muzzatti, Riccardo Dolcetti, Maria Antonietta Annunziata
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
Toni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, Heikki Järvinen, Laura Renkonen-Sinisalo, Inge Bernstein, Elke Holinski-Feder, Paola Sala, Annika Lindblom, Finlay Macrae, Ignacio Blanco, Rolf Sijmons, Jacqueline Jeffries, Hans Vasen, John Burn, Sigve Nakken, Eivind Hovig, Einar Andreas Rødland, Kukatharmini Tharmaratnam, Wouter H. de Vos tot Nederveen Cappel, James Hill, Juul Wijnen, Mark Jenkins, Maurizio Genuardi, Kate Green, Fiona Lalloo, Lone Sunde, Miriam Mints, Lucio Bertario, Marta Pineda, Matilde Navarro, Monika Morak, Ian M. Frayling, John-Paul Plazzer, Julian R. Sampson, Gabriel Capella, Gabriela Möslein, Jukka-Pekka Mecklin, Pål Møller
Clinical and genetic characterization of hereditary breast cancer in a Chinese population
Wenjing Jian, Kang Shao, Qi Qin, Xiaohong Wang, Shufen Song, Xianming Wang
RETRACTED ARTICLE: The BRCA2 variant c.68-7 T>A is associated with breast cancer
Pål Møller, Eivind Hovig
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS)
Sukanya Horpaopan, Jutta Kirfel, Sophia Peters, Michael Kloth, Robert Hüneburg, Janine Altmüller, Dmitriy Drichel, Margarete Odenthal, Glen Kristiansen, Christian Strassburg, Jacob Nattermann, Per Hoffmann, Peter Nürnberg, Reinhard Büttner, Holger Thiele, Philip Kahl, Isabel Spier, Stefan Aretz