Characterization of BRCA1 and BRCA2 variants found in a Norwegian breast or ovarian cancer cohort Elisabeth JarhelleHilde Monica Frostad Riise StenslandMarijke Van Ghelue Original Article 05 August 2016 Pages: 1 - 16
Community attitudes towards a Jewish community BRCA1/2 testing program Nicole CousensRajneesh KaurLesley Andrews Original Article 01 August 2016 Pages: 17 - 28
Frequency of germline PALB2 mutations among women with epithelial ovarian cancer Joanne KotsopoulosVictoria SopikMohammad R. Akbari Original Article 08 September 2016 Pages: 29 - 34
Do women change their breast cancer mammogram screening behaviour after BRCA1/2 testing? Geneviève LaroucheJocelyne ChiquetteMichel Dorval Short Communication 23 August 2016 Pages: 35 - 40
BRCA testing within the Department of Veterans Affairs: concordance with clinical practice guidelines Danielle S. ChunBrygida BerseJulie A. Lynch Original Article 02 September 2016 Pages: 41 - 49
Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling Patrick R. BenusiglioMarina Di MariaOlivier Caron Original Article 13 September 2016 Pages: 51 - 56
First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome H. Ziada-BouchaarK. SifiN. Abadi Original Article 28 July 2016 Pages: 57 - 66
A novel germline POLE mutation causes an early onset cancer prone syndrome mimicking constitutional mismatch repair deficiency Katharina WimmerAndreas BeilkenChristian P. Kratz Original Article Open access 29 August 2016 Pages: 67 - 71
Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression Verónica CabreiraCarla PintoManuel R. Teixeira Original Article 31 August 2016 Pages: 73 - 81
Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer Afaf ElsaidRami ElshazliCamelia Abdel-Malak Original Article 08 September 2016 Pages: 83 - 90
Pancreas-sparing total duodenectomy for Spigelman stage IV duodenal polyposis associated with familial adenomatous polyposis: experience of 10 cases at a single institution Yuichiro WatanabeHideyuki IshidaHideki Ishikawa Original Article 21 September 2016 Pages: 91 - 98
Exploring clinicians’ attitudes about using aspirin for risk reduction in people with Lynch Syndrome with no personal diagnosis of colorectal cancer Yanni ChenMichelle PeateGillian Mitchell Original Article 27 September 2016 Pages: 99 - 109
Dilemmas in the management of screen-detected lesions in patients at high risk for pancreatic cancer Isaura S. IbrahimBert A. BonsingHans F. A. Vasen Short Communication Open access 12 July 2016 Pages: 111 - 115
Hereditary leiomyomatosis and renal cell cancer syndrome: identification and clinical characterization of a novel mutation in the FH gene in a Colombian family Carolina Arenas ValenciaMartha Lucia Rodríguez LópezClara Eugenia Arteaga Díaz Original Article 26 August 2016 Pages: 117 - 122
Calculating the optimal surveillance for head and neck paraganglioma in SDHB-mutation carriers Karin EijkelenkampThamara E. OsingaAnouk N. A. van der Horst-Schrivers Original Article Open access 29 August 2016 Pages: 123 - 130
Nevoid basal cell carcinoma syndrome caused by splicing mutations in the PTCH1 gene Chise KatoKentaro FujiiToshiyuki Miyashita Original Article 25 August 2016 Pages: 131 - 138
Genetically diagnosed Birt–Hogg–Dubé syndrome and familial cerebral cavernous malformations in the same individual: a case report James WhitworthBrian Stausbøl-GrønAnne-Bine Skytte Short Communication Open access 08 October 2016 Pages: 139 - 142
Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance Ingrid C.A.W. KoningsFemme HarinckOn behalf of the Dutch research group on pancreatic cancer surveillance in high-risk individuals Original Article Open access 14 September 2016 Pages: 143 - 151
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases Walid Sabri HamadouSawsen BesbesZohra Soua Original Article 12 September 2016 Pages: 153 - 157
Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program David J. HermelWendy C. McKinnonMarc S. Greenblatt Original Article 11 July 2016 Pages: 159 - 166