1. Single nucleotide polymorphisms in PDCD6 gene are associated with the development of cervical squamous cell carcinoma

   • Bin Zhou
   • Peng Bai
   • Lin Zhang

   Original Article 02 November 2014 Pages: 1 - 8

   

2. Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing

   • Yanfang Guan
   • Hong Hu
   • Xin Yi

   Original Article 24 August 2014 Pages: 9 - 18

   

3. Mitochondrial membrane potential and reactive oxygen species in cancer stem cells

   • Bei-bei Zhang
   • Dao-gang Wang
   • Chao Xuan

   Review 30 September 2014 Pages: 19 - 23

   

4. Down-regulation of malignant potential by alpha linolenic acid in human and mouse colon cancer cells

   • John P. Chamberland
   • Hyun-Seuk Moon

   Short Communication 22 October 2014 Pages: 25 - 30

   

5. Desmoid tumour in familial adenomatous polyposis patients: responses to treatments

   • Thibault Desurmont
   • Jérémie H. Lefèvre
   • Yann Parc

   Original Article 15 October 2014 Pages: 31 - 39

   

6. APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes

   • Marialuisa Quadri
   • Annalisa Vetro
   • Guglielmina N. Ranzani

   Original Article 27 August 2014 Pages: 41 - 49

   

7. The impact of risk-reducing gynaecological surgery in premenopausal women at high risk of endometrial and ovarian cancer due to Lynch syndrome

   • Ramona Moldovan
   • Sianan Keating
   • Tara Clancy

   Original Article 24 October 2014 Pages: 51 - 60

   

8. Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case

   • Jinru Shia
   • Zsofia K. Stadler
   • David S. Klimstra

   Short Communication 31 August 2014 Pages: 61 - 68

   

9. Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing

   • Ashton A. Connor
   • Hagit Katzov-Eckert
   • Jordan Lerner-Ellis

   Original Article 08 November 2014 Pages: 69 - 75

   

10. MLH1 promotor hypermethylation does not rule out a diagnosis of Lynch syndrome: a case report

    • Victoria M. Raymond
    • Arden M. Morris
    • Joel K. Greenson

    Short Communication 12 September 2014 Pages: 77 - 80

    

11. Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women

    • Beata Smolarz
    • Marianna Makowska
    • Hanna Romanowicz

    Original Article Open access 19 August 2014 Pages: 81 - 88

12. Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation

    • Ingrid P. Vogelaar
    • Rachel S. van der Post
    • Encarna Gómez García

    Short Communication 03 December 2014 Pages: 89 - 94

    

13. Familial and sporadic pancreatic cancer share the same molecular pathogenesis

    • Alexis L. Norris
    • Nicholas J. Roberts
    • James R. Eshleman

    Original Article 21 September 2014 Pages: 95 - 103

    

14. Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer

    • Louise Heiniger
    • Phyllis N. Butow
    • Melanie A. Price

    Original Article 05 October 2014 Pages: 105 - 115

    

15. Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability

    • Jacopo Berrino
    • Franco Berrino
    • Siranoush Manoukian

    Original Article 06 November 2014 Pages: 117 - 128

    

16. Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations

    • Lise B. Ahlborn
    • Ane Y. Steffensen
    • Thomas V. O. Hansen

    Original Article 26 August 2014 Pages: 129 - 133

    

17. Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk

    • Belinda Rahman
    • Susanne F. Meisel
    • Anne Lanceley

    Original Article Open access 13 November 2014 Pages: 135 - 144

18. Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

    • Natalia Bogdanova
    • Alexandr V. Togo
    • Thilo Dörk

    Short Communication 03 September 2014 Pages: 145 - 149

19. Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome

    • Kirsty Mann
    • Jill Magee
    • Ingrid Winship

    Short Communication 07 October 2014 Pages: 151 - 155

    

20. Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review

    • Aamira Huq
    • Maira Kentwell
    • Ingrid Winship

    Original Article 02 November 2014 Pages: 157 - 160

21. Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li–Fraumeni syndrome

    • Anna Etzold
    • Julia C. Schröder
    • Danuta Galetzka

    Original Article 17 September 2014 Pages: 161 - 165

    

22. Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals

    • Shanna L. Gustafson
    • Victoria M. Raymond
    • Jessica N. Everett

    Original Article 23 September 2014 Pages: 167 - 174

    

23. 18th annual meeting: Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC)

    Abstracts 16 November 2014 Pages: 175 - 209