The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes Nabil AmaraJolyane Blouin-BougieRéjean Landry Original Article 03 September 2015 Pages: 1 - 17
Screening of HELQ in breast and ovarian cancer families Liisa M. PelttariLaura KinnunenHeli Nevanlinna Original Article 08 September 2015 Pages: 19 - 23
Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned Bich-Thu DuongRavi SavarirayanIngrid Winship Original Article 15 August 2015 Pages: 25 - 29
Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients Daniel Robert QuastRalph SchneiderGabriela Möslein Original Article 15 August 2015 Pages: 31 - 40
Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer? Bar ChikmanTima DavidsonRon Lavy Original Article 10 September 2015 Pages: 41 - 47
Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects Camelia Abdel-MalakHossam DarwishRami Elshazli Original Article 28 August 2015 Pages: 49 - 56
First report of somatic mosaicism for mutations in STK11 in four patients with Peutz–Jeghers syndrome Victoria McKayDiane CairnsLynn Greenhalgh Short Communication 19 September 2015 Pages: 57 - 61
Genetic testing for Lynch syndrome: family communication and motivation Celine H. M. LeenenMariska den HeijerAnja Wagner Original Article Open access 07 October 2015 Pages: 63 - 73
Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study Minori MatsumotoTakeshi NakajimaYutaka Saito Original Article 08 October 2015 Pages: 75 - 83
Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary Janos PappMarietta Eva KovacsEdith Olah Original Article Open access 07 October 2015 Pages: 85 - 97
Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives Junyi WangBin ZhangDangui Yan Original Article 09 August 2015 Pages: 99 - 104
Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry Kris Ann P. SchultzAnne HarrisD. Ashley Hill Original Article 20 August 2015 Pages: 105 - 110
The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer Sofia MaiaMarta CardosoManuel R. Teixeira Original Article 20 August 2015 Pages: 111 - 121
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism Laura GiganteIrene PaganiniLaura Papi Short Communication 05 September 2015 Pages: 123 - 126
Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas Ernst NäfDominik LaubscherGabor Matyas Short Communication Open access 05 September 2015 Pages: 127 - 132
Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome Francesco TonelliCarlo BiaginiMaria Luisa Brandi Short Communication 22 September 2015 Pages: 133 - 138
Germline TERT promoter mutations are rare in familial melanoma Mark HarlandMia PetljakD. Timothy Bishop Original Article Open access 03 October 2015 Pages: 139 - 144
Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis Jian ZhaoXiaoyi HuangJianming Zheng Original Article 01 October 2015 Pages: 145 - 153