1. Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort

   • Elisabeth Jarhelle
   • Hilde Monica Frostad Riise Stensland
   • Marijke Van Ghelue

   Original Article 05 August 2016 Pages: 1 - 16

   

2. Community attitudes towards a Jewish community BRCA1/2 testing program

   • Nicole Cousens
   • Rajneesh Kaur
   • Lesley Andrews

   Original Article 01 August 2016 Pages: 17 - 28

3. Frequency of germline PALB2 mutations among women with epithelial ovarian cancer

   • Joanne Kotsopoulos
   • Victoria Sopik
   • Mohammad R. Akbari

   Original Article 08 September 2016 Pages: 29 - 34

4. Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing?

   • Geneviève Larouche
   • Jocelyne Chiquette
   • Michel Dorval

   Short Communication 23 August 2016 Pages: 35 - 40

   

5. BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelines

   • Danielle S. Chun
   • Brygida Berse
   • Julie A. Lynch

   Original Article 02 September 2016 Pages: 41 - 49

   

6. Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling

   • Patrick R. Benusiglio
   • Marina Di Maria
   • Olivier Caron

   Original Article 13 September 2016 Pages: 51 - 56

7. First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome

   • H. Ziada-Bouchaar
   • K. Sifi
   • N. Abadi

   Original Article 28 July 2016 Pages: 57 - 66

   

8. A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency

   • Katharina Wimmer
   • Andreas Beilken
   • Christian P. Kratz

   Original Article Open access 29 August 2016 Pages: 67 - 71

   

9. Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression

   • Verónica Cabreira
   • Carla Pinto
   • Manuel R. Teixeira

   Original Article 31 August 2016 Pages: 73 - 81

   

10. Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer

    • Afaf Elsaid
    • Rami Elshazli
    • Camelia Abdel-Malak

    Original Article 08 September 2016 Pages: 83 - 90

11. Pancreas-sparing total duodenectomy for Spigelman stage IV duodenal polyposis associated with familial adenomatous polyposis: experience of 10 cases at a single institution

    • Yuichiro Watanabe
    • Hideyuki Ishida
    • Hideki Ishikawa

    Original Article 21 September 2016 Pages: 91 - 98

    

12. Exploring clinicians’ attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer

    • Yanni Chen
    • Michelle Peate
    • Gillian Mitchell

    Original Article 27 September 2016 Pages: 99 - 109

    

13. Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer

    • Isaura S. Ibrahim
    • Bert A. Bonsing
    • Hans F. A. Vasen

    Short Communication Open access 12 July 2016 Pages: 111 - 115

    

14. Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian family

    • Carolina Arenas Valencia
    • Martha Lucia Rodríguez López
    • Clara Eugenia Arteaga Díaz

    Original Article 26 August 2016 Pages: 117 - 122

    

15. Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers

    • Karin Eijkelenkamp
    • Thamara E. Osinga
    • Anouk N. A. van der Horst-Schrivers

    Original Article Open access 29 August 2016 Pages: 123 - 130

    

16. Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene

    • Chise Kato
    • Kentaro Fujii
    • Toshiyuki Miyashita

    Original Article 25 August 2016 Pages: 131 - 138

    

17. Genetically diagnosed Birt–Hogg–Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report

    • James Whitworth
    • Brian Stausbøl-Grøn
    • Anne-Bine Skytte

    Short Communication Open access 08 October 2016 Pages: 139 - 142

    

18. Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance

    • Ingrid C.A.W. Konings
    • Femme Harinck
    • On behalf of the Dutch research group on pancreatic cancer surveillance in high-risk individuals

    Original Article Open access 14 September 2016 Pages: 143 - 151

    

19. Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases

    • Walid Sabri Hamadou
    • Sawsen Besbes
    • Zohra Soua

    Original Article 12 September 2016 Pages: 153 - 157

20. Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program

    • David J. Hermel
    • Wendy C. McKinnon
    • Marc S. Greenblatt

    Original Article 11 July 2016 Pages: 159 - 166