Desmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis Fábio Guilherme CamposCarlos Augusto Real MartinezIvan Cecconello Original Article 06 December 2014 Pages: 211 - 219
Comparison of proctocolectomy and ileal pouch-anal anastomosis to colectomy and ileorectal anastomosis in familial adenomatous polyposis L. KoskenvuoH. MustonenA. Lepistö Original Article 11 December 2014 Pages: 221 - 227
A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2 Mingkun XieYating LiJin Wu Original Article 03 January 2015 Pages: 229 - 239
Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer Iikki DonnerTuula KiviluotoPia Vahteristo Original Article 10 January 2015 Pages: 241 - 246
High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations Astrid A. OutIvonne J. H. M. van MinderhoutFrederik J. Hes Original Article Open access 21 January 2015 Pages: 247 - 257
Defective DNA mismatch repair activity is common in sebaceous neoplasms, and may be an ineffective approach to screen for Lynch syndrome Anu R. LambaAngela Y. MooreC. Richard Boland Original Article 01 February 2015 Pages: 259 - 264
Health professionals’ evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer Kirsten F. L. DoumaBettina MeiserKathy Tucker Original Article 13 November 2014 Pages: 265 - 272
Impact of BRCA1/2 mutation on young women’s 5-year parenthood rates: a prospective comparative study (GENEPSO-PS cohort) Julien ManciniEmmanuelle Mouret-FourmeClaire Julian-Reynier Original Article 31 December 2014 Pages: 273 - 279
The effect of oral 3,3′-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriers Dina NikitinaMarcia LlacuachaquiJoanne Kotsopoulos Short Communication 23 January 2015 Pages: 281 - 286
Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features Paul A. JamesSarah SawyerGillian Mitchell Original Article 13 February 2015 Pages: 287 - 295
Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers Chongjuan WeiBo PengChristopher I. Amos Original Article 26 February 2015 Pages: 297 - 306
Erratum to: Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers Chongjuan WeiBo PengChristopher I. Amos Erratum 28 March 2015 Pages: 307 - 307
First-Line sunitinib in patients with renal cell carcinoma (RCC) in von Hippel–Lindau (VHL) disease: clinical outcome and patterns of radiological response Anna RomaMarco MaruzzoVittorina Zagonel Original Article 13 November 2014 Pages: 309 - 316
Parental age and Neurofibromatosis Type 1: a report from the NF1 Patient Registry Initiative Qian LiuNancy ZoellnerKimberly J. Johnson Original Article 10 December 2014 Pages: 317 - 324
The roles of AXIN2 in tumorigenesis and epigenetic regulation Shuang LiChunpeng WangXin Liu Review Article 13 December 2014 Pages: 325 - 331
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers Mariana Fitarelli-KiehlJuliana GiacomazziPatricia Ashton-Prolla Short Communication 07 January 2015 Pages: 333 - 336
Germline RAD51B truncating mutation in a family with cutaneous melanoma Karin A. W. WadtLauren G. AoudeAnne-Marie Gerdes Original Article 20 January 2015 Pages: 337 - 340