1. Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk

   • Rajneesh Kaur
   • Bettina Meiser
   • Paul A. James

   Original Article 24 September 2018 Pages: 147 - 152

   

2. Electronically ascertained extended pedigrees in breast cancer genetic counseling

   • V. Stefansdottir
   • H. Skirton
   • J. J. Jonsson

   Original Article 24 September 2018 Pages: 153 - 160

   

3. Ovarian small cell carcinoma in one of a pair of monozygous twins

   • Somayyeh Fahiminiya
   • Nelly Sabbaghian
   • William D. Foulkes

   Letter to the Editor 04 October 2018 Pages: 161 - 163

   

4. Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation

   • Maurizio Ponz de Leon
   • Monica Pedroni
   • Luca Reggiani Bonetti

   Original Article 08 September 2018 Pages: 165 - 172

   

5. Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma

   • P. Vande Perre
   • A. Siegfried
   • R. Guimbaud

   Short Communication 27 October 2018 Pages: 173 - 178

   

6. NTHL1-associate polyposis: first Australian case report

   • Alexandra Groves
   • Margaret Gleeson
   • Allan D. Spigelman

   Short Communication 11 March 2019 Pages: 179 - 182

7. Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition

   • Lars J. Lindberg
   • Wia Wegen-Haitsma
   • Mef Nilbert

   Original Article 09 October 2018 Pages: 183 - 191

   

8. A squamous cell carcinoma in a young woman with Lynch syndrome

   • F. Adan
   • M. B. Crijns
   • M. W. Bekkenk

   Short Communication 17 December 2018 Pages: 193 - 196

   

9. Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort

   • Kelly Fulk
   • Holly LaDuca
   • Kory Jasperson

   Original Article 23 December 2018 Pages: 197 - 201

10. Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis

    • Erin G. Sutcliffe
    • Amanda Bartenbaker Thompson
    • Benjamin D. Solomon

    Original Article 02 January 2019 Pages: 203 - 209

    

11. Recent advances in Lynch syndrome

    • Leah H. Biller
    • Sapna Syngal
    • Matthew B. Yurgelun

    Review 09 January 2019 Pages: 211 - 219

12. Interest in, willingness-to-pay for and willingness-to-recommend genetic testing for prostate cancer among affected men after radical prostatectomy

    • Marcel Mayer
    • Katharina Selig
    • Kathleen Herkommer

    Original Article 18 September 2018 Pages: 221 - 230

    

13. Genetic counselling of young women with breast cancer for Li–Fraumeni syndrome: a nationwide survey on the experiences and attitudes of genetics professionals

    • J. J. Bakhuizen
    • M. E. Velthuizen
    • M. G. Ausems

    Original Article Open access 20 September 2018 Pages: 231 - 239

14. Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma

    • Evan J. Walker
    • Julia Carnevale
    • Andrew H. Ko

    Original Article 28 September 2018 Pages: 241 - 251

    

15. Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature

    • Florian Obermair
    • Melanie Rammer
    • Gerald Webersinke

    Original Article 10 October 2018 Pages: 253 - 260

    

16. Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome

    • Shahid Mahmood Baig
    • Ambrin Fatima
    • Hai Yan

    Short Communication 26 November 2018 Pages: 261 - 265

    

17. Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018)

    • Mijke Visser
    • Nienke van der Stoep
    • Nelleke Gruis

    Review 18 January 2019 Pages: 267 - 271

18. TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort

    • J. J. Bakhuizen
    • F. B. Hogervorst
    • M. G. Ausems

    Original Article 03 January 2019 Pages: 273 - 280

    

19. Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes

    • Janet R. Vos
    • Lisette Giepmans
    • ERN GENTURIS

    Short Communication Open access 09 October 2018 Pages: 281 - 284

20. Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed methods approach

    • Kelly Reumkens
    • Christine E. M. de Die-Smulders
    • Liesbeth A. D. M. van Osch

    Original Article Open access 17 January 2019 Pages: 285 - 291