1. Detection of false positive mutations in BRCA gene by next generation sequencing

   • Moushumi Suryavanshi
   • Dushyant Kumar
   • Anurag Mehta

   Original Article 15 November 2016 Pages: 311 - 317

   

2. Outcomes of retesting BRCA negative patients using multigene panels

   • Siddhartha Yadav
   • Ashley Reeves
   • Dana Zakalik

   Original Article 22 November 2016 Pages: 319 - 328

   

3. Novel and reported pathogenic variants in exon 11 of BRCA2 gene in a cohort of Sri Lankan young breast cancer patients

   • Sumadee De Silva
   • Kamani Hemamala Tennekoon
   • Lakshika Jayasekara

   Original Article 30 December 2016 Pages: 329 - 338

   

4. The association between prognosis of breast cancer and first-degree family history of breast or ovarian cancer: a systematic review and meta-analysis

   • Jun-Long Song
   • Chuang Chen
   • Sheng-Rong Sun

   REVIEW 07 February 2017 Pages: 339 - 349

   

5. Correlation between germline mutations in MMR genes and microsatellite instability in ovarian cancer specimens

   • Mohammad R. Akbari
   • Shiyu Zhang
   • Tuya Pal

   Original Article 07 February 2017 Pages: 351 - 355

6. Identification of MSH2 inversion of exons 1–7 in clinical evaluation of families with suspected Lynch syndrome

   • Maureen E. Mork
   • Andrea Rodriguez
   • Eduardo Vilar

   Short Communication 21 December 2016 Pages: 357 - 361

   

7. Gastric tumours in FAP

   • Sarah-Jane Walton
   • Ian M. Frayling
   • Andrew Latchford

   Original Article 07 March 2017 Pages: 363 - 369

   

8. Gastric cancer in FAP: a concerning rise in incidence

   • Gautam Mankaney
   • Pamela Leone
   • Carol A. Burke

   Short Communication 09 February 2017 Pages: 371 - 376

9. Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives

   • Jessica Ezzell Hunter
   • Kathleen A. Arnold
   • Katrina A. B. Goddard

   Original Article 07 February 2017 Pages: 377 - 387

   

10. Identification of a rare germline NBN gene mutation by whole exome sequencing in a lung-cancer survivor from a large family with various types of cancer

    • Makia J. Marafie
    • Mohammed Dashti
    • Fahd Al-Mulla

    Original Article 14 November 2016 Pages: 389 - 394

    

11. The hereditary nature of small cell carcinoma of the ovary, hypercalcemic type: two new familial cases

    • Leora Witkowski
    • Nancy Donini
    • William D. Foulkes

    Short Communication Open access 19 November 2016 Pages: 395 - 399

    

12. Embryonal rhabdomyosarcoma in a patient with a heterozygous frameshift variant in the DICER1 gene and additional manifestations of the DICER1 syndrome

    • Julia Fremerey
    • Stefan Balzer
    • Michaela Kuhlen

    Short Communication 28 November 2016 Pages: 401 - 405

    

13. ATM mutations for surgeons

    • Sara A. Mansfield
    • Robert Pilarski
    • Doreen M. Agnese

    Short Communication 17 December 2016 Pages: 407 - 410

14. Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study

    • Maryam Mahmoodi
    • Tu Nguyen-Dumont
    • Ingrid Winship

    Original Article 06 January 2017 Pages: 411 - 416

15. A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case report

    • Hu Tan
    • Xianda Wei
    • Lingqian Wu

    Short Communication 09 February 2017 Pages: 417 - 422

    

16. Psychosocial morbidity in TP53 mutation carriers: is whole-body cancer screening beneficial?

    • Kate A. McBride
    • Mandy L. Ballinger
    • Gillian Mitchell

    Original Article 25 January 2017 Pages: 423 - 432

    

17. Baseline results from the UK SIGNIFY study: a whole-body MRI screening study in TP53 mutation carriers and matched controls

    • Sibel Saya
    • Emma Killick
    • Rosalind A. Eeles

    Original Article Open access 16 January 2017 Pages: 433 - 440

18. Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia

    • Candice Feben
    • Careni Spencer
    • Amanda Krause

    Original Article 09 February 2017 Pages: 441 - 446

    

19. Supporting disclosure of genetic information to family members: professional practice and timelines in cancer genetics

    • Benjamin Derbez
    • Antoine de Pauw
    • Sandrine de Montgolfier

    Original Article 14 March 2017 Pages: 447 - 457

    

20. Patients with negative multi-gene panel testing: a back to the future paradox?

    • Steven M. Sorscher

    Letter to the Editor 03 March 2017 Pages: 459 - 459