Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations Jacopo AzzolliniMilena MarianiSiranoush Manoukian Letter to the Editor Open access 05 July 2017 Pages: 317 - 319
Family history influences the tumor characteristics and prognosis of breast cancers developing during postmenopausal hormone therapy Rainer FagerholmMaria FaltinovaCarl Blomqvist Original Article 10 October 2017 Pages: 321 - 331
Cancer risk management in Tasmanian women with BRCA1 and BRCA2 mutations Stephanie KeartonKaren WillsJo Burke Original Article 16 October 2017 Pages: 333 - 344
Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine Aleksander MyszkaTu Nguyen-DumontMelissa C. Southey Original Article Open access 19 October 2017 Pages: 345 - 349
Information and support needs of young women regarding breast cancer risk and genetic testing: adapting effective interventions for a novel population Suzanne C. O’NeillChalanda EvansKenneth P. Tercyak Original Article 09 November 2017 Pages: 351 - 360
Evaluation of current prediction models for Lynch syndrome: updating the PREMM5 model to identify PMS2 mutation carriers A. GoverdeM. C. W. SpaanderA. Wagner Original Article Open access 20 September 2017 Pages: 361 - 370
Evaluation of an online family history tool for identifying hereditary and familial colorectal cancer F. G. J. KallenbergC. M. AalfsE. Dekker Original Article Open access 21 September 2017 Pages: 371 - 380
Ectopic, retroperitoneal adrenocortical carcinoma in the setting of Lynch syndrome Jesse P. WrightKathleen W. MontgomeryKamran Idrees Short Communication 22 September 2017 Pages: 381 - 385
Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing Barbara Luísa SoaresAyslan Castro BrantMiguel Angelo Martins Moreira Original Article 20 September 2017 Pages: 387 - 394
Universal determination of microsatellite instability using BAT26 as a single marker in an Argentine colorectal cancer cohort María Laura GonzálezNatalia Causada-CaloCarlos Vaccaro Original Article 11 November 2017 Pages: 395 - 402
Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge Henry T. LynchStephen LanspaJoan Bailey-Wilson Review 25 October 2017 Pages: 403 - 414
Excluding Lynch syndrome in a female patient with metachronous DNA mismatch repair deficient colon- and ovarian cancer Stijn CrobachAnne M. L. JansenHans Morreau Short Communication Open access 09 November 2017 Pages: 415 - 420
An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review Julian DaniellJohn-Paul PlazzerFinlay Macrae Review 12 September 2017 Pages: 421 - 427
Germline mutations in lung cancer and personalized medicine Francesco CettaAlessandra RenieriElisa Frullanti Letter to the Editor 15 September 2017 Pages: 429 - 430
Penetrance of a rare familial mutation predisposing to papillary thyroid cancer Donika SaporitoPamela BrockRebecca Nagy Short Communication 12 October 2017 Pages: 431 - 434
Germline variant in MSX1 identified in a Dutch family with clustering of Barrett’s esophagus and esophageal adenocarcinoma A. M. J. van NistelrooijR. van MarionB. P. L. Wijnhoven Original Article Open access 13 November 2017 Pages: 435 - 440
Genotype phenotype correlation in Asian Indian von Hippel–Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma Nilesh LomteSanjeet KumarNalini S. Shah Original Article 09 November 2017 Pages: 441 - 449
Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics Gaëlle ColletNathalie ParodiThierry Frebourg Original Article 27 October 2017 Pages: 451 - 457
Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis Xia HaoLingzi XiaBaosen Zhou Review 10 November 2017 Pages: 459 - 468
Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries Anne BrédartJean‑Luc KopRita Schmutlzer Correction 25 October 2017 Pages: 469 - 469