1. The incidence of PALB2 c.3113G>A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia

   • Zhi L. Teo
   • Sarah D. Sawyer
   • Melissa C. Southey

   Letter to the Editor 08 March 2013 Pages: 587 - 595

   

2. Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer

   • Shaheen Alanee
   • Sohela Shah
   • Kenneth Offit

   Original Article 09 March 2013 Pages: 597 - 600

   

3. Is the psychological impact of genetic testing moderated by support and sharing of test results to family and friends?

   • Julie Lapointe
   • Michel Dorval
   • Claire Julian-Reynier

   Original Article 09 March 2013 Pages: 601 - 610

   

4. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome

   • Katsunori Fujii
   • Hirofumi Ohashi
   • Toshiyuki Miyashita

   Original Article 12 March 2013 Pages: 611 - 614

   

5. Interest of individuals from BRCA families to participate in research studies focused on male BRCA carriers

   • Tuya Pal
   • Susan Vadaparampil
   • Kelly Metcalfe

   Original Article 16 March 2013 Pages: 615 - 619

6. Factors affecting the decision to undergo risk-reducing salpingo-oophorectomy among women with BRCA gene mutation

   • Dongwon Kim
   • Eunyoung Kang
   • Sung-Won Kim

   Original Article 16 March 2013 Pages: 621 - 628

   

7. Do individuals with a family history of colorectal cancer adhere to medical recommendations for the prevention of colorectal cancer?

   • Karen Bronner
   • Ilse Mesters
   • Revital Kariv

   Original Article 02 April 2013 Pages: 629 - 637

   

8. Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study

   • Katja Aktan-Collan
   • Helena Kääriäinen
   • Ari Haukkala

   Original Article 20 March 2013 Pages: 639 - 646

   

9. Case report: metachronous central nervous system desmoid tumours and thyroid carcinoma in a young familial adenomatous polyposis patient

   • G. I. Butel-Simoes
   • A. D. Spigelman

   Original Article 21 April 2013 Pages: 647 - 649

10. Self administered screening for hereditary cancers in conjunction with mammography and ultrasound

    • Charles H. McDonnell
    • David J. Seidenwurm
    • Kristie A. Bobolis

    Original Article 13 April 2013 Pages: 651 - 656

    

11. Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia

    • Jie Zhu
    • Liang Cui
    • Jiang-Ping Gao

    Original Article 11 June 2013 Pages: 657 - 667

    

12. Extracolonic cancer risk in patients with serrated polyposis syndrome and their first-degree relatives

    • Yark Hazewinkel
    • Johannes B. Reitsma
    • Evelien Dekker

    Original Article 17 April 2013 Pages: 669 - 673

13. Can we test for hereditary cancer at 18 years when we start surveillance at 25? Patient reported outcomes

    • Aisha S. Sie
    • Judith B. Prins
    • Nicoline Hoogerbrugge

    Original Article 21 April 2013 Pages: 675 - 682

    

14. Underestimated survival predictions of the prognostic tools Adjuvant! Online and PREDICT in BRCA1-associated breast cancer patients

    • Grigorijs Plakhins
    • Arvids Irmejs
    • Janis Gardovskis

    Original Article 03 May 2013 Pages: 683 - 689

    

15. Association of the BRCA1 promoter polymorphism rs11655505 with the risk of familial breast and/or ovarian cancer

    • Beata Bielinska
    • Pawel Gaj
    • Janusz A. Siedlecki

    Original Article 09 May 2013 Pages: 691 - 698

16. “High rate of recurrent adenomatosis during endoscopic surveillance after duodenectomy in patients with familial adenomatous polyposis”

    • Yasser A. Alderlieste
    • Barbara A. Bastiaansen
    • Evelien Dekker

    Original Article 10 May 2013 Pages: 699 - 706

    

17. Chemoprevention in Lynch syndrome

    • John Burn
    • John C. Mathers
    • D. Tim Bishop

    Original Paper 24 July 2013 Pages: 707 - 718

    

18. Phenotypic heterogeneity of hereditary gynecologic cancers: a report from the Creighton hereditary cancer registry

    • Murray Joseph Casey
    • Chhanda Bewtra
    • Patrice Watson

    Original Article 12 May 2013 Pages: 719 - 740

    

19. Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity

    • M. P. Farrell
    • D. J. Hughes
    • D. J. Gallagher

    Original Article 28 May 2013 Pages: 741 - 747

    

20. Rectal cancers in patients with familial adenomatous polyposis

    • Jennifer Liang
    • James M. Church

    Original Article 16 May 2013 Pages: 749 - 754

    

21. Polymorphisms in arachidonic acid metabolism-related genes and the risk and prognosis of colorectal cancer

    • Shuying Li
    • Xiaojuan Zhao
    • Yashuang Zhao

    Original Article 29 May 2013 Pages: 755 - 765

    

22. Novel and recurrent BRCA1/BRCA2 mutations in early onset and familial breast and ovarian cancer detected in the Program of Genetic Counseling in Cancer of Valencian Community (eastern Spain). Relationship of family phenotypes with mutation prevalence

    • Inmaculada de Juan Jiménez
    • Zaida García Casado
    • Pascual Bolufer Gilabert

    Short Communication 12 March 2013 Pages: 767 - 777

23. The Proceedings of the Collaborative Group of the Americas on Inherited Colorectal Cancer Sheraton Boston Hotel, Boston, Massachusetts, October 27–29, 2012

    Abstracts 01 May 2013 Pages: 779 - 809