Ausgabe 4/2015
Inhalt (21 Artikel)
Psychological distress related to BRCA testing in ovarian cancer patients
Merete Bjørnslett, Alv A. Dahl, Øystein Sørebø, Anne Dørum
BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study
Inmaculada de Juan, Sarai Palanca, Asunción Domenech, Lidia Feliubadaló, Ángel Segura, Ana Osorio, Isabel Chirivella, Miguel de la Hoya, Ana Beatriz Sánchez, Mar Infante, Isabel Tena, Orland Díez, Zaida Garcia-Casado, Ana Vega, Àlex Teulé, Alicia Barroso, Pedro Pérez, Mercedes Durán, Estela Carrasco, Mª José Juan-Fita, Rosa Murria, Marta Llop, Eva Barragan, Ángel Izquierdo, Javier Benítez, Trinidad Caldés, Dolores Salas, Pascual Bolufer
BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review
Claudio Spinelli, Silvia Strambi, Lorenzo Piccini, Leonardo Rossi, Paolo Aretini, Adelaide Caligo
Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK
Dhivya Chandrasekaran, Usha Menon, Gareth Evans, Robin Crawford, Ertan Saridogan, Chris Jacobs, Marc Tischkowitz, Elly Brockbank, Jatinder Kalsi, Davor Jurkovic, Ranjit Manchanda
Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis
N. N. Basu, S. Ingham, J. Hodson, F. Lalloo, M. Bulman, A. Howell, D. G. Evans
The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy
Jessica E. van der Aa, Jacob P. Hoogendam, Els S. F. Butter, Margreet G. E. M. Ausems, René H. M. Verheijen, Ronald P. Zweemer
Childhood cancers in families with and without Lynch syndrome
John A. Heath, Jeanette C. Reece, Daniel D. Buchanan, Graham Casey, Carol A. Durno, Steven Gallinger, Robert W. Haile, Polly A. Newcomb, John D. Potter, Stephen N. Thibodeau, Loïc Le Marchand, Noralane M. Lindor, John L. Hopper, Mark A. Jenkins, Aung Ko Win
Survival in familial colorectal cancer: a Danish cohort study
Charlotte Kvist Lautrup, Ellen M. Mikkelsen, Timothy L. Lash, Niels Katballe, Lone Sunde
A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case–control study
Süleyman Bayram, Yakup Ülger, Ahmet Taner Sümbül, Berrin Yalınbaş Kaya, Ahmet Rencüzoğulları, Ahmet Genç, Yusuf Sevgiler, Onur Bozkurt, Eyyüp Rencüzoğulları
Massive gastric polyposis associated with a germline SMAD4 gene mutation
Eline Soer, Wouter H. de Vos tot Nederveen Cappel, Marjolijn J. L. Ligtenberg, Freek Moll, Robert G. Pierik, Juda Vecht, Hans F. A. Vasen, Antoine Flierman
Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene
Aung Ko Win, Jeanette C. Reece, Daniel D. Buchanan, Mark Clendenning, Joanne P. Young, Sean P. Cleary, Hyeja Kim, Michelle Cotterchio, James G. Dowty, Robert J. MacInnis, Katherine M. Tucker, Ingrid M. Winship, Finlay A. Macrae, Terrilea Burnett, Loïc Le Marchand, Graham Casey, Robert W. Haile, Polly A. Newcomb, Stephen N. Thibodeau, Noralane M. Lindor, John L. Hopper, Steven Gallinger, Mark A. Jenkins
Genotype–phenotype analysis of von Hippel–Lindau syndrome in fifteen Indian families
Narendranath Vikkath, Sindhu Valiyaveedan, Sheela Nampoothiri, Natasha Radhakrishnan, Gopal S. Pillai, Vasantha Nair, Ginil Kumar Pooleri, Georgie Mathew, Krishnakumar N. Menon, Prasanth S. Ariyannur, Ashok B. Pillai
Birt–Hogg–Dubé syndrome and intracranial vascular pathologies
Rahul Kapoor, Alexander I. Evins, Diala Steitieh, Antonio Bernardo, Philip E. Stieg
Follicular variant of papillary thyroid cancer in Alström syndrome
M. Papadakis, A. Meyer, F. Schuster, N. Weyerbrock, C. Corinth, C. Dotzenrath
Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis
Maria João Bugalho, Ana Luísa Silva, Rita Domingues
High accuracy of family history of melanoma in Danish melanoma cases
Karin A. W. Wadt, Krzysztof T. Drzewiecki, Anne-Marie Gerdes
Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene
Thereasa Rich, Michelle Jackson, Alejandro Roman-Gonzalez, Komal Shah, Gilbert J. Cote, Camilo Jimenez
POLE mutations in families predisposed to cutaneous melanoma
Lauren G. Aoude, Ellen Heitzer, Peter Johansson, Michael Gartside, Karin Wadt, Antonia L. Pritchard, Jane M. Palmer, Judith Symmons, Anne-Marie Gerdes, Grant W. Montgomery, Nicholas G. Martin, Ian Tomlinson, Stephen Kearsey, Nicholas K. Hayward
Prevalence and detection of psychosocial problems in cancer genetic counseling
W. Eijzenga, E. M. A. Bleiker, D. E. E. Hahn, L. E. Van der Kolk, G. N. Sidharta, N. K. Aaronson
Supporting families with Cancer: A patient centred survivorship model of care
Emily Victoria Craft, Caron Billington, Rory O’Sullivan, Wendy Watson, Nicola Suter-Giorgini, Joanne Singletary, Elizabeth King, Matthew Perfirgines, Annette Cashmore, Julian Barwell
Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines
Rebecca K. Marcus, Jennifer L. Geurts, Jessica A. Grzybowski, Kiran K. Turaga, T. Clark Gamblin, Kimberly A. Strong, Fabian M. Johnston