Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer Y. C. LeeM. Bresselfor the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) Original Article Open access 11 March 2017 Pages: 461 - 469
Prevalence of two BRCA1 mutations, 5382insC and 300T > G, in ovarian cancer patients from Ukraine I. GorodetskaS. SergaI. Kozeretska Original Article 11 March 2017 Pages: 471 - 476
Molecular characterization and clinical interpretation of BRCA1/BRCA2 variants in families from Murcia (south-eastern Spain) with hereditary breast and ovarian cancer: clinical–pathological features in BRCA carriers and non-carriers Xavier Gabaldó Barrios Mª Desamparados Sarabia MeseguerFrancisco Ruiz Espejo Original Article 05 May 2017 Pages: 477 - 489
Loss of MSH2 and MSH6 due to heterozygous germline defects in MSH3 and MSH6 Monika MorakSarah KäsbauerElke Holinski-Feder Original Article 20 May 2017 Pages: 491 - 500
Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria Maribel González-AcostaJesús del ValleGabriel Capellá Original Article 01 April 2017 Pages: 501 - 507
General practitioner attitudes towards prescribing aspirin to carriers of Lynch Syndrome: findings from a national survey Samuel G. SmithRobbie FoyJack Cuzick Original Article Open access 22 April 2017 Pages: 509 - 516
Genetic polymorphisms of NFκB1-94ins/delATTG and NFκBIA-881A/G genes in Egyptian patients with colorectal cancer Mohamed Ragab YoussefZeinab Ibraheim AttiaAhmad Settin Original Article 07 April 2017 Pages: 517 - 524
Universal screening for microsatellite instability in colorectal cancer in the clinical genomics era: new recommendations, methods, and considerations Jaclyn F. HechtmanSumit MiddhaJinru Shia Letter to the Editor 12 April 2017 Pages: 525 - 529
High-risk individuals’ perceptions of reproductive genetic testing for CDH1 mutations Nina HallowellShirlene BadgerJulia Lawton Short Communication 15 February 2017 Pages: 531 - 535
Lower gastrointestinal neuroendocrine neoplasms associated with hereditary cancer syndromes: a case series Trilokesh D. KidambiChristina PedleyJonathan P. Terdiman Original Article 10 March 2017 Pages: 537 - 543
Inherited DNA repair gene mutations detected by tumor next generation sequencing in urinary tract cancers Sumati GuptaSamantha GreenbergWendy Kohlmann Short Communication 18 March 2017 Pages: 545 - 550
A case of contralateral breast cancer and skin cancer associated with NBN heterozygous pathogenic variant c.698_701delAACA Jennifer GassJessica JacksonPaldeep S. Atwal Short Communication 03 April 2017 Pages: 551 - 553
A Peutz–Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report Jy-Ming ChiangTse-Ching Chen Short Communication 08 April 2017 Pages: 555 - 560
A new POT1 germline mutation—expanding the spectrum of POT1-associated cancers Tremika Le-Shan WilsonNamita HattangadyTobias Else Original Article 07 April 2017 Pages: 561 - 566
A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families Patricia LlovetFrancisco J. IllanaVanesa García-Barberán Original Article 01 June 2017 Pages: 567 - 575
Identification of novel potential genetic predictors of urothelial bladder carcinoma susceptibility in Pakistani population Syeda Hafiza Benish AliKashif Sardar BangashRaheel Qamar Original Article 06 April 2017 Pages: 577 - 594
Placing negative multi-gene panel results into clinical context David J. HermelWendy C. McKinnonMarc S. Greenblatt Letter to the Editor 28 April 2017 Pages: 595 - 595
All in the family? Communication of cancer survivors with their families Deborah J. BowenJennifer L. HayWylie Burke Original Article 03 April 2017 Pages: 597 - 603
Importance of updating family cancer history in childhood cancer survivors Selena RussoMeera WarbyRichard J. Cohn Letter to the Editor 12 April 2017 Pages: 605 - 610
Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes Elisabeth A. RosenthalJohn Michael O. RanolaBrian H. Shirts Original Article 22 May 2017 Pages: 611 - 620
