Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis Renaud SabatierElise LavitPatrice Viens Original Article 01 February 2016 Pages: 497 - 506
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population Henriette Roed NielsenMef NilbertChristina Therkildsen Original Article 01 February 2016 Pages: 507 - 512
Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk Jada G. HamiltonDarren MaysKenneth P. Tercyak Original Article 05 February 2016 Pages: 513 - 522
No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families Henriette Roed NielsenJanne PetersenAnne-Bine Skytte Original Article 07 March 2016 Pages: 523 - 528
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer Aryana S. JacobsMarc D. SchwartzBeth N. Peshkin Original Article 11 March 2016 Pages: 529 - 539
Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer Olle SjöströmLars LindholmBeatrice Melin Original Article Open access 02 March 2016 Pages: 543 - 551
Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies Masakazu KohdaKensuke KumamotoYasushi Okazaki Original Article 02 February 2016 Pages: 553 - 562
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers Z. GhorbanoghliM. H. NieuwenhuisJ. T. Wijnen Original Article Open access 15 February 2016 Pages: 563 - 570
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation Aurélia NguyenGaelle BougeardNatacha Entz-Werle Short Communication 26 March 2016 Pages: 571 - 577
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome Aysel AhadovaMagnus von Knebel DoeberitzMatthias Kloor Original Article 09 March 2016 Pages: 579 - 586
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency Maureen E. MorkEster BorrasEduardo Vilar Short Communication 26 March 2016 Pages: 587 - 591
Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes Sara E. DobbinsPeter BroderickRichard S. Houlston Original Article Open access 29 June 2016 Pages: 593 - 599
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma Borum SagongYoung Joon SeoIn Seok Moon Original Article 01 February 2016 Pages: 601 - 606
Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma Roeliene C. KruizingaDenise M. S. van MarionAnnemiek M. E. Walenkamp Original Article Open access 26 February 2016 Pages: 607 - 616
Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India Manjunath GoroshiTushar BandgarNalini S. Shah Original Article 23 February 2016 Pages: 617 - 624
MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics Jessica Oliboni ScapineliLucieli CeolinAna Luiza Maia Original Article 26 February 2016 Pages: 625 - 633
Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations Francesca PontiSerena CorsiniLuca Sangiorgi Original Article 08 March 2016 Pages: 635 - 643
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome Tiziana CavalliFrancesco GiudiciFrancesco Tonelli Original Article 12 April 2016 Pages: 645 - 649
Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families Jazlyn ReadJudith SymmonsNicholas K. Hayward Original Article 23 April 2016 Pages: 651 - 663
An investigation of the factors effecting high-risk individuals’ decision-making about prophylactic total gastrectomy and surveillance for hereditary diffuse gastric cancer (HDGC) Nina HallowellShirlene BadgerJulia Lawton Original Article 02 June 2016 Pages: 665 - 676
Occurrence of renal cell carcinoma and hematologic malignancies (predominantly lymphoid) in individuals and in families Janice P. DutcherPeter H. WiernikRangaswamy Chintapatla Original Article 22 June 2016 Pages: 677 - 687
Evaluation of laboratory perspectives on hereditary cancer panels Jessica StollScott M. WeissmanKristen J. Vogel Postula Original Article 11 February 2016 Pages: 689 - 696
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study Mary B. DalySusan MontgomeryKaren Ruth Original Article Open access 20 February 2016 Pages: 697 - 706
A model for patient-direct screening and referral for familial cancer risk Kristin B. NiendorfMelissa A. GellerRobert D. Madoff Original Article 27 June 2016 Pages: 707 - 716