1. Clinical and pathologic characteristics of breast cancer patients carrying the c.3481_3491del11 mutation

   • R. El Tannouri
   • E. Albuisson
   • E. Luporsi

   Original Article 17 March 2018 Pages: 1 - 8

2. Reminders of cancer risk and pain catastrophizing: relationships with cancer worry and perceived risk in women with a first-degree relative with breast cancer

   • Colette A. Whitney
   • Caroline S. Dorfman
   • Tamara J. Somers

   Original Article 20 April 2018 Pages: 9 - 18

   

3. Cholesterol profile in women with premature menopause after risk reducing salpingo-oophorectomy

   • Natalia Teixeira
   • Marian J. Mourits
   • Geertruida H. de Bock

   Original Article Open access 07 June 2018 Pages: 19 - 27

4. Capillary electrophoresis as alternative method to detect tumor genetic mutations: the model built on the founder BRCA1 c.4964_4982del19 variant

   • Maria De Bonis
   • Angelo Minucci
   • Ettore Capoluongo

   Original Article 22 June 2018 Pages: 29 - 35

   

5. The BRCA1 exon 13 duplication: clinical characteristics of 22 families in Northern Sweden

   • Christina Edwinsdotter Ardnor
   • Anna Rosén
   • Beatrice Melin

   Short Communication Open access 22 August 2018 Pages: 37 - 42

   

6. Unsolicited information letters to increase awareness of Lynch syndrome and familial colorectal cancer: reactions and attitudes

   • Helle Vendel Petersen
   • Birgitte Lidegaard Frederiksen
   • Mef Nilbert

   Original Article 12 April 2018 Pages: 43 - 51

7. Prevalence of thyroid diseases in familial adenomatous polyposis: a systematic review and meta-analysis

   • Jirat Chenbhanich
   • Amporn Atsawarungruangkit
   • Prasit Phowthongkum

   Original Article 16 April 2018 Pages: 53 - 62

   

8. Identification of a novel GREM1 duplication in a patient with multiple colon polyps

   • Danielle B. McKenna
   • Jeroen Van Den Akker
   • Bryson W. Katona

   Short Communication 26 May 2018 Pages: 63 - 66

   

9. Modified capture–recapture estimates of the number of families with Lynch syndrome in Central Ohio

   • John Michael O. Ranola
   • Rachel Pearlman
   • Brian H. Shirts

   Original Article 17 July 2018 Pages: 67 - 73

   

10. Outcome of thyroid ultrasound screening in FAP patients with a normal baseline exam

    • Marc Monachese
    • Gautam Mankaney
    • Carol A. Burke

    Original Article 12 July 2018 Pages: 75 - 82

    

11. Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Māori

    • Christopher Hakkaart
    • Lis Ellison-Loschmann
    • Parry Guilford

    Original Article Open access 27 March 2018 Pages: 83 - 90

    

12. Hemangioblastoma in Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome: a phenotypic overlap between VHL and HLRCC Syndromes

    • Eryn Dow
    • Ingrid M. Winship

    Original Article 04 April 2018 Pages: 91 - 95

    

13. Sarcoma in neurofibromatosis 2: case report and review of the literature

    • C. Linder
    • M. J. Smith
    • D. G. R. Evans

    Original Article 14 May 2018 Pages: 97 - 100

    

14. Report of a bi-allelic truncating germline mutation in TP53

    • Natasha J. Brown
    • Kanika Bhatia
    • Jordan R. Hansford

    Short Communication 08 May 2018 Pages: 101 - 104

    

15. Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer

    • Lisa Bush
    • Melyssa Aronson
    • Kory Jasperson

    Short Communication 21 May 2018 Pages: 105 - 108

    

16. Low-level parental mosaicism in an apparent de novo case of Peutz–Jeghers syndrome

    • G. I. Butel-Simoes
    • A. D. Spigelman
    • R. E. Vilain

    Original Article 14 June 2018 Pages: 109 - 112

    

17. Candidate susceptibility variants in angioimmunoblastic T-cell lymphoma

    • Iikki Donner
    • Riku Katainen
    • Lauri A. Aaltonen

    Short Communication 10 August 2018 Pages: 113 - 119

18. Physician interpretation of variants of uncertain significance

    • Sarah K. Macklin
    • Jessica L. Jackson
    • Stephanie L. Hines

    Original Article 02 May 2018 Pages: 121 - 126

19. The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice

    • Fred H Menko
    • Jacqueline A ter Stege
    • Eveline M A Bleiker

    Review 30 May 2018 Pages: 127 - 135

20. The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study

    • Kelly Reumkens
    • Marly H. E. Tummers
    • Liesbeth A. D. M. van Osch

    Original Article Open access 30 May 2018 Pages: 137 - 146