Ausgabe 1/2014
Inhalt (21 Artikel)
Patient-reported disease knowledge and educational needs in Lynch syndrome: findings of an interactive multidisciplinary patient conference
Sarah A Bannon, Maureen Mork, Eduardo Vilar, Susan K Peterson, Karen Lu, Patrick M Lynch, Miguel A Rodriguez-Bigas, YiQian Nancy You
Plasma homocysteine levels and genetic polymorphisms in folate metablism are associated with breast cancer risk in chinese women
Xiayu Wu, Tianning Zou, Neng Cao, Juan Ni, Weijiang Xu, Tao Zhou, Xu Wang
Familial testicular germ cell tumor: no associated syndromic pattern identified
Christine M Mueller, Larissa A Korde, Mary L McMaster, June A Peters, Gennady Bratslavsky, Rissah J Watkins, Alex Ling, Christian P Kratz, Eric A Wulfsberg, Philip S Rosenberg, Mark H Greene
Gastric adenomas in familial adenomatous polyposis are common, but subtle, and have a benign course
Saowanee Ngamruengphong, Lisa A Boardman, Russell I Heigh, Murli Krishna, Maegan E Roberts, Douglas L Riegert-Johnson
Neurofibromatosis type I with breast cancer: not only for women!
Kuntegowdanahalli Chinnagiriyappa Lakshmaiah, Anil N Kumar, Samit Purohit, Belathur Kalegowda Viveka, Kamalakannan Rahul Rajan, Mohammed Abdul Lateef Zameer, Prabhu Namitha, Monika Lamba Saini, Hatem A Azim Jr, Kamal S Saini
Dupuytren’s disease and the risk of malignant neoplasms
Andrzej Żyluk, Katarzyna Paszkowska-Szczur, Satish Gupta, Rodney J Scott, Jan Lubiński, Tadeusz Dębniak
Colorectal cancer and self-reported tooth agenesis
Noralane M Lindor, Aung Ko Win, Steven Gallinger, Darshana Daftary, Stephen N Thibodeau, Renato Silva, Ariadne Letra
Long-term satisfaction and quality of life following risk reducing surgery in BRCA1/2 mutation carriers
Gillian W Hooker, Lesley King, Lauren VanHusen, Kristi Graves, Beth N Peshkin, Claudine Isaacs, Kathryn L Taylor, Elizabeth Poggi, Marc D Schwartz
A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland
Aneta Bąk, Hanna Janiszewska, Anna Junkiert-Czarnecka, Marta Heise, Maria Pilarska-Deltow, Ryszard Laskowski, Magdalena Pasińska, Olga Haus
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Medellín, Colombia
Julián Esteban Londoño Hernández, Marcia Llacuachaqui, Gonzalo Vásquez Palacio, Juan David Figueroa, Jorge Madrid, Mauricio Lema, Robert Royer, Song Li, Garrett Larson, Jeffrey N Weitzel, Steven A Narod
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry
Eli Marie Grindedal, Harald Aarset, Inga Bjørnevoll, Elin Røyset, Lovise Mæhle, Astrid Stormorken, Cecilie Heramb, Heidi Medvik, Pål Møller, Wenche Sjursen
The role of Wnt signaling pathway in carcinogenesis and implications for anticancer therapeutics
Asfandyar Sheikh, Asfandyar Khan Niazi, Muhammad Zafar Ahmed, Bushra Iqbal, Syed Muhammad Saad Anwer, Hira Hussain Khan
Familial cancer among consecutive uterine cancer patients in Sweden
Gerasimos Tzortzatos, Ofra Wersäll, Kristina Gemzell Danielsson, Annika Lindblom, Emma Tham, Miriam Mints
Expanding the genetic basis of copy number variation in familial breast cancer
Amy L Masson, Bente A Talseth-Palmer, Tiffany-Jane Evans, Desma M Grice, Garry N Hannan, Rodney J Scott
Sequence-based detection of mutations in cadherin 1 to determine the prevalence of germline mutations in patients with invasive lobular carcinoma of the breast
Allyson L Valente, Seth Rummel, Craig D Shriver, Rachel E Ellsworth
Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome
Karol Krzystolik, Anna Jakubowska, Jacek Gronwald, Maciej R Krawczyński, Monika Drobek-Słowik, Leszek Sagan, Leszek Cyryłowski, Wojciech Lubiński, Jan Lubiński, Cezary Cybulski
Genetic screening analysis of patients with hereditary diffuse gastric cancer from northern and northeastern Brazil
Caroline Aquino Moreira-Nunes, Mariceli Baia Leão Barros, Bárbara do Nascimento Borges, Raquel Carvalho Montenegro, Leticia Martins Lamarão, Helem Ferreira Ribeiro, Amanda Braga Bona, Paulo Pimentel Assumpção, Juan Antonio Rey, Giovanny Rebouças Pinto, Rommel Rodriguez Burbano
Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada
Taila Hartley, Luca Cavallone, Nelly Sabbaghian, Rachel Silva-Smith, Nancy Hamel, Olga Aleynikova, Erika Smith, Valerie Hastings, Pedro Pinto, Marc Tischkowitz, Eva Tomiak, William D Foulkes
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom
Mark Harland, Anne E Cust, Celia Badenas, Yu-Mei Chang, Elizabeth A Holland, Paula Aguilera, Joanne F Aitken, Bruce K Armstrong, Jennifer H Barrett, Cristina Carrera, May Chan, Joanne Gascoyne, Graham G Giles, Chantelle Agha-Hamilton, John L Hopper, Mark A Jenkins, Peter A Kanetsky, Richard F Kefford, Isabel Kolm, Johanna Lowery, Josep Malvehy, Zighereda Ogbah, Joan-Anton Puig-Butille, Jordi Orihuela-Segalés, Juliette A Randerson-Moor, Helen Schmid, Claire F Taylor, Linda Whitaker, D Timothy Bishop, Graham J Mann, Julia A Newton-Bishop, Susana Puig
TP53 p.R337H prevalence in a series of Brazilian hereditary breast cancer families
Nathalia M Cury, Victor EF Ferraz, Wilson A Silva Jr
Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma
Ewout P Boesaard, Ingrid P Vogelaar, Peter Bult, Carla AP Wauters, J Han JM van Krieken, Marjolijn JL Ligtenberg, Rachel S van der Post, Nicoline Hoogerbrugge