BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer Estelle JamardBertrand VolardSophie Krieger Short Communication 25 October 2016 Pages: 167 - 171
Risk algorithms that include pathology adjustment for HER2 amplification need to make further downward adjustments in likelihood scores D. G. EvansE. R. WoodwardF. Lalloo Original Article Open access 31 October 2016 Pages: 173 - 179
Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe Natalia BogdanovaKatja PfeiferThilo Dörk Short Communication 10 November 2016 Pages: 181 - 186
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer Martin P. NilssonChristof WinterNiklas Loman Original Article Open access 24 January 2017 Pages: 187 - 193
Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing Anna RohlinEva RambechMargareta Nordling Original Article Open access 30 September 2016 Pages: 195 - 203
Pain evaluation during gynaecological surveillance in women with Lynch syndrome Jorien Helder-WoolderinkGeertruida de BockMarian Mourits Original Article Open access 27 October 2016 Pages: 205 - 210
Attenuated polyposis of the large bowel: a morphologic and molecular approach Maurizio Ponz de LeonMonica PedroniLuca Reggiani Bonetti Original Article 25 October 2016 Pages: 211 - 220
Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome Eva WieldersElly Delzenne-GoetteHein te Riele Original Article 21 November 2016 Pages: 221 - 229
Cancer screening behaviors and risk perceptions among family members of colorectal cancer patients with unexplained mismatch repair deficiency Lior H. KatzShailesh AdvaniSusan K. Peterson Original Article 10 November 2016 Pages: 231 - 237
Colonoscopy in Lynch syndrome: the need for a new quality score Jurjen J. BoonstraWouter H. de Vos tot Nederveen CappelHans F. A. Vasen Letter to the Editor 09 November 2016 Pages: 239 - 241
TP53 and CDKN1A mutation analysis in families with Li–Fraumeni and Li–Fraumeni like syndromes Raissa Coelho AndradeAnna Claudia Evangelista dos SantosFernando Regla Vargas Original Article 06 October 2016 Pages: 243 - 248
Cystic parathyroid glands in MEN1: A rare entity? Tiziana CavalliFrancesco GiudiciFrancesco Tonelli Original Article 20 October 2016 Pages: 249 - 256
Uptake of genetic counseling, genetic testing and surveillance in hereditary malignant melanoma (CDKN2A) in Norway Trine LevinLovise Mæhle Original Article Open access 01 November 2016 Pages: 257 - 265
A case of multiple gastrointestinal stromal tumors caused by a germline KIT gene mutation (p.Leu576Pro) Rita Vale RodriguesFilipa SantosAntónio Dias Pereira Short Communication 22 October 2016 Pages: 267 - 270
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands Charlotte J. DommeringLidewij HennemanHanne Meijers-Heijboer Original Article Open access 08 November 2016 Pages: 271 - 277
Four generations of SDHB-related disease: complexities in management U. SrirangalingamM. LeCainK. Metcalfe Original Article Open access 28 November 2016 Pages: 279 - 282
All in the family? Analyzing the impact of family history in addition to genotype on medullary thyroid carcinoma aggressiveness in MEN2A patients Kristin L. LongCarol EtzelElizabeth G. Grubbs Original Article 18 November 2016 Pages: 283 - 289
DICER1 mutation and tumors associated with a familial tumor predisposition syndrome: practical considerations Eduardo J. Bardón-CanchoAna Haro-DíazCarmen Garrido-Colino Short Communication 09 November 2016 Pages: 291 - 294
Recurrent TP53 missense mutation in cancer patients of Arab descent Aviad ZickLuna KadouriTamar Peretz Original Article 19 November 2016 Pages: 295 - 301
Double germline mutations in APC and BRCA2 in an individual with a pancreatic tumor Caroline GoehringerChristian SutterUte Moog Original Article 12 November 2016 Pages: 303 - 309