Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin Ana KrivokucaVita Setrajcic DragosSrdjan Novakovic Original Article 06 July 2017 Pages: 179 - 185
Discovery of mutations in homologous recombination genes in African-American women with breast cancer Yuan Chun DingAaron W. AdamsonSusan L. Neuhausen Original Article 02 September 2017 Pages: 187 - 195
Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing Masood AlqahtaniCaitlin EdwardsBarry Iacopetta Original Article 22 June 2017 Pages: 197 - 203
Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland Daniel R. EvansJane S. GreenMichael O. Woods Short Communication 28 June 2017 Pages: 205 - 208
A new hereditary colorectal cancer network in the Middle East and eastern mediterranean countries to improve care for high-risk families Zeinab GhorbanoghliCarol JabariHans Vasen Short Communication Open access 06 July 2017 Pages: 209 - 212
Erratum to: A new hereditary colorectal cancer network in the Middle East and eastern Mediterranean countries to improve care for high-risk families Zeinab GhorbanoghliCarol JabariHans Vasen Erratum 27 July 2017 Pages: 213 - 213
A germline missense mutation in exon 3 of the MSH2 gene in a Lynch syndrome family: correlation with phenotype and localization assay Francesca BianchiElena MaccaroniRossana Berardi Original Article 07 August 2017 Pages: 215 - 224
Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations Tao WangZsofia K. StadlerJinru Shia Short Communication 17 August 2017 Pages: 225 - 228
Dental anomalies in pediatric patients with familial adenomatous polyposis Seth SepterBrenda BohatyLynn Roosa Friesen Original Article 08 September 2017 Pages: 229 - 234
The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes Thomas P. SlavinSusan L. NeuhausenClinical Cancer Genomics Community Research Network (CCGCRN) Original Article 08 July 2017 Pages: 235 - 245
Remarkable effects of imatinib in a family with young onset gastrointestinal stromal tumors and cutaneous hyperpigmentation associated with a germline KIT-Trp557Arg mutation: case report and literature overview S. FaragL. E. van der KolkN. Steeghs Short Communication 14 July 2017 Pages: 247 - 253
Pancreatic adenocarcinoma with a germline PTEN p.Arg234Gln mutation Sunao UemuraHiroyuki MatsubayashiKen Yamaguchi Short Communication 28 July 2017 Pages: 255 - 259
Mutational analysis of the RB1 gene and the inheritance patterns of retinoblastoma in Jordan Yacoub A. YousefAbdelghani TbakhiMustafa Mehyar Original Article 12 August 2017 Pages: 261 - 268
p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers Gabriel S. MacedoIgor Araujo VieiraPatricia Ashton-Prolla Original Article 29 July 2017 Pages: 269 - 274
Pancreatic neuroendocrine tumor in a patient with a TSC1 variant: case report and review of the literature Parisa MortajiKatherine T. MorrisShawnia Ryan Review 08 September 2017 Pages: 275 - 280
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations Bruno BuecherAntoine De PauwLisa Golmard Short Communication 17 August 2017 Pages: 281 - 285
Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic Jasmina BojadzievaBehrang AminiLouise C. Strong Original Article 07 October 2017 Pages: 287 - 294
A comparison of cosegregation analysis methods for the clinical setting John Michael O. RañolaQuanhui LiuBrian H. Shirts Original Article 10 July 2017 Pages: 295 - 302
Issues related to family history of cancer at the end of life: a palliative care providers’ survey Catherine GonthierSylvie PelletierMichel Dorval Short Communication 03 July 2017 Pages: 303 - 307
Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing Rhodé M. BijlsmaHester WesselsAnnelien L. Bredenoord Original Article Open access 29 August 2017 Pages: 309 - 316