Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk Rajneesh KaurBettina MeiserPaul A. James Original Article 24 September 2018 Pages: 147 - 152
Electronically ascertained extended pedigrees in breast cancer genetic counseling V. StefansdottirH. SkirtonJ. J. Jonsson Original Article 24 September 2018 Pages: 153 - 160
Ovarian small cell carcinoma in one of a pair of monozygous twins Somayyeh FahiminiyaNelly SabbaghianWilliam D. Foulkes Letter to the Editor 04 October 2018 Pages: 161 - 163
Massive juvenile polyposis of the stomach in a family with SMAD4 gene mutation Maurizio Ponz de LeonMonica PedroniLuca Reggiani Bonetti Original Article 08 September 2018 Pages: 165 - 172
Germline mutation p.N363K in POLE is associated with an increased risk of colorectal cancer and giant cell glioblastoma P. Vande PerreA. SiegfriedR. Guimbaud Short Communication 27 October 2018 Pages: 173 - 178
NTHL1-associate polyposis: first Australian case report Alexandra GrovesMargaret GleesonAllan D. Spigelman Short Communication 11 March 2019 Pages: 179 - 182
Risk of multiple colorectal cancer development depends on age and subgroup in individuals with hereditary predisposition Lars J. LindbergWia Wegen-HaitsmaMef Nilbert Original Article 09 October 2018 Pages: 183 - 191
A squamous cell carcinoma in a young woman with Lynch syndrome F. AdanM. B. CrijnsM. W. Bekkenk Short Communication 17 December 2018 Pages: 193 - 196
Monoallelic MUTYH carrier status is not associated with increased breast cancer risk in a multigene panel cohort Kelly FulkHolly LaDucaKory Jasperson Original Article 23 December 2018 Pages: 197 - 201
Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis Erin G. SutcliffeAmanda Bartenbaker ThompsonBenjamin D. Solomon Original Article 02 January 2019 Pages: 203 - 209
Recent advances in Lynch syndrome Leah H. BillerSapna SyngalMatthew B. Yurgelun Review 09 January 2019 Pages: 211 - 219
Interest in, willingness-to-pay for and willingness-to-recommend genetic testing for prostate cancer among affected men after radical prostatectomy Marcel MayerKatharina SeligKathleen Herkommer Original Article 18 September 2018 Pages: 221 - 230
Genetic counselling of young women with breast cancer for Li–Fraumeni syndrome: a nationwide survey on the experiences and attitudes of genetics professionals J. J. BakhuizenM. E. VelthuizenM. G. Ausems Original Article Open access 20 September 2018 Pages: 231 - 239
Referral frequency, attrition rate, and outcomes of germline testing in patients with pancreatic adenocarcinoma Evan J. WalkerJulia CarnevaleAndrew H. Ko Original Article 28 September 2018 Pages: 241 - 251
Cleft lip/palate and hereditary diffuse gastric cancer: report of a family harboring a CDH1 c.687 + 1G > A germline mutation and review of the literature Florian ObermairMelanie RammerGerald Webersinke Original Article 10 October 2018 Pages: 253 - 260
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome Shahid Mahmood BaigAmbrin FatimaHai Yan Short Communication 26 November 2018 Pages: 261 - 265
Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018) Mijke VisserNienke van der StoepNelleke Gruis Review 18 January 2019 Pages: 267 - 271
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort J. J. BakhuizenF. B. HogervorstM. G. Ausems Original Article 03 January 2019 Pages: 273 - 280
Boosting care and knowledge about hereditary cancer: European Reference Network on Genetic Tumour Risk Syndromes Janet R. VosLisette GiepmansERN GENTURIS Short Communication Open access 09 October 2018 Pages: 281 - 284
Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed methods approach Kelly ReumkensChristine E. M. de Die-SmuldersLiesbeth A. D. M. van Osch Original Article Open access 17 January 2019 Pages: 285 - 291