Single nucleotide polymorphisms in PDCD6 gene are associated with the development of cervical squamous cell carcinoma Bin ZhouPeng BaiLin Zhang Original Article 02 November 2014 Pages: 1 - 8
Detection of inherited mutations for hereditary cancer using target enrichment and next generation sequencing Yanfang GuanHong HuXin Yi Original Article 24 August 2014 Pages: 9 - 18
Mitochondrial membrane potential and reactive oxygen species in cancer stem cells Bei-bei ZhangDao-gang WangChao Xuan Review 30 September 2014 Pages: 19 - 23
Down-regulation of malignant potential by alpha linolenic acid in human and mouse colon cancer cells John P. ChamberlandHyun-Seuk Moon Short Communication 22 October 2014 Pages: 25 - 30
Desmoid tumour in familial adenomatous polyposis patients: responses to treatments Thibault DesurmontJérémie H. LefèvreYann Parc Original Article 15 October 2014 Pages: 31 - 39
APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes Marialuisa QuadriAnnalisa VetroGuglielmina N. Ranzani Original Article 27 August 2014 Pages: 41 - 49
The impact of risk-reducing gynaecological surgery in premenopausal women at high risk of endometrial and ovarian cancer due to Lynch syndrome Ramona MoldovanSianan KeatingTara Clancy Original Article 24 October 2014 Pages: 51 - 60
Mismatch repair deficient-crypts in non-neoplastic colonic mucosa in Lynch syndrome: insights from an illustrative case Jinru ShiaZsofia K. StadlerDavid S. Klimstra Short Communication 31 August 2014 Pages: 61 - 68
Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing Ashton A. ConnorHagit Katzov-EckertJordan Lerner-Ellis Original Article 08 November 2014 Pages: 69 - 75
MLH1 promotor hypermethylation does not rule out a diagnosis of Lynch syndrome: a case report Victoria M. RaymondArden M. MorrisJoel K. Greenson Short Communication 12 September 2014 Pages: 77 - 80
Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women Beata SmolarzMarianna MakowskaHanna Romanowicz Original Article Open access 19 August 2014 Pages: 81 - 88
Gastric cancer in three relatives of a patient with a biallelic IL12RB1 mutation Ingrid P. VogelaarRachel S. van der PostEncarna Gómez García Short Communication 03 December 2014 Pages: 89 - 94
Familial and sporadic pancreatic cancer share the same molecular pathogenesis Alexis L. NorrisNicholas J. RobertsJames R. Eshleman Original Article 21 September 2014 Pages: 95 - 103
Long-term outcomes of risk-reducing surgery in unaffected women at increased familial risk of breast and/or ovarian cancer Louise HeinigerPhyllis N. ButowMelanie A. Price Original Article 05 October 2014 Pages: 105 - 115
Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability Jacopo BerrinoFranco BerrinoSiranoush Manoukian Original Article 06 November 2014 Pages: 117 - 128
Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations Lise B. AhlbornAne Y. SteffensenThomas V. O. Hansen Original Article 26 August 2014 Pages: 129 - 133
Population-based genetic risk prediction and stratification for ovarian cancer: views from women at high risk Belinda RahmanSusanne F. MeiselAnne Lanceley Original Article Open access 13 November 2014 Pages: 135 - 144
Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe Natalia BogdanovaAlexandr V. TogoThilo Dörk Short Communication 03 September 2014 Pages: 145 - 149
Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome Kirsty MannJill MageeIngrid Winship Short Communication 07 October 2014 Pages: 151 - 155
Vestibular schwannoma in a patient with neurofibromatosis type 1: clinical report and literature review Aamira HuqMaira KentwellIngrid Winship Original Article 02 November 2014 Pages: 157 - 160
Further evidence for pathogenicity of the TP53 tetramerization domain mutation p.Arg342Pro in Li–Fraumeni syndrome Anna EtzoldJulia C. SchröderDanuta Galetzka Original Article 17 September 2014 Pages: 161 - 165
Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals Shanna L. GustafsonVictoria M. RaymondJessica N. Everett Original Article 23 September 2014 Pages: 167 - 174
18th annual meeting: Collaborative Group of the Americas on Inherited Colorectal Cancer (CGA-ICC) Abstracts 16 November 2014 Pages: 175 - 209