Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families Jazlyn ReadJudith SymmonsNicholas K. Hayward Original Article 23 April 2016 Pages: 651 - 663
Chemoprevention of familial adenomatous polyposis Patrick M. Lynch Original Article 15 April 2016 Pages: 467 - 475
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome Tiziana CavalliFrancesco GiudiciFrancesco Tonelli Original Article 12 April 2016 Pages: 645 - 649
Familial adenomatous polyposis in pediatrics: natural history, emerging surveillance and management protocols, chemopreventive strategies, and areas of ongoing debate Seth SepterCaitlin E. LawsonThomas Attard Original Article 07 April 2016 Pages: 477 - 485
Recent discoveries in the molecular genetics of Lynch syndrome C. Richard Boland Original Article 02 April 2016 Pages: 395 - 403
Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency Maureen E. MorkEster BorrasEduardo Vilar Short Communication 26 March 2016 Pages: 587 - 591
MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation Aurélia NguyenGaelle BougeardNatacha Entz-Werle Short Communication 26 March 2016 Pages: 571 - 577
Lynch syndrome in South America: past, present and future Carlos A. VaccaroCarlos SarrocaJames Church Original Article 23 March 2016 Pages: 437 - 445
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry Hans F. A. VasenMary E. VelthuizenJuul T. Wijnen Original Article Open access 14 March 2016 Pages: 429 - 435
Genetic counseling and cascade genetic testing in Lynch syndrome Heather Hampel Original Article 11 March 2016 Pages: 423 - 427
Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer Aryana S. JacobsMarc D. SchwartzBeth N. Peshkin Original Article 11 March 2016 Pages: 529 - 539
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome Aysel AhadovaMagnus von Knebel DoeberitzMatthias Kloor Original Article 09 March 2016 Pages: 579 - 586
Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes Noralane M. LindorJohn HopperJames Dowty Original Article Open access 09 March 2016 Pages: 367 - 370
Evaluation of TP53 Pro72Arg and MDM2 SNP285–SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations Francesca PontiSerena CorsiniLuca Sangiorgi Original Article 08 March 2016 Pages: 635 - 643
No evidence of increased breast cancer risk for proven noncarriers from BRCA1 and BRCA2 families Henriette Roed NielsenJanne PetersenAnne-Bine Skytte Original Article 07 March 2016 Pages: 523 - 528
Decentralized colonoscopic surveillance with high patient compliance prevents hereditary and familial colorectal cancer Olle SjöströmLars LindholmBeatrice Melin Original Article Open access 02 March 2016 Pages: 543 - 551
Evolution of cancer risk assessment and counseling related to psychological, financial and legal implications Carrie Snyder Original Article 26 February 2016 Pages: 493 - 496
MEN 2A-related cutaneous lichen amyloidosis: report of three kindred and systematic literature review of clinical, biochemical and molecular characteristics Jessica Oliboni ScapineliLucieli CeolinAna Luiza Maia Original Article 26 February 2016 Pages: 625 - 633
Difference in CXCR4 expression between sporadic and VHL-related hemangioblastoma Roeliene C. KruizingaDenise M. S. van MarionAnnemiek M. E. Walenkamp Original Article Open access 26 February 2016 Pages: 607 - 616
Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India Manjunath GoroshiTushar BandgarNalini S. Shah Original Article 23 February 2016 Pages: 617 - 624
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study Mary B. DalySusan MontgomeryKaren Ruth Original Article Open access 20 February 2016 Pages: 697 - 706
Familial atypical multiple mole melanoma (FAMMM) syndrome: history, genetics, and heterogeneity Henry T. LynchTrudy G. Shaw Original Article 18 February 2016 Pages: 487 - 491
Colonoscopy and chromoscopy in hereditary colorectal cancer syndromes Erin Jenkins WesslingStephen J. Lanspa Original Article 18 February 2016 Pages: 453 - 455
Finding the needle in a haystack: identification of cases of Lynch syndrome with MLH1 epimutation Megan P. Hitchins Original Article 17 February 2016 Pages: 413 - 422
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers Z. GhorbanoghliM. H. NieuwenhuisJ. T. Wijnen Original Article Open access 15 February 2016 Pages: 563 - 570
High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine Zoran GatalicaSemir VranicSandeep Reddy Original Article Open access 13 February 2016 Pages: 405 - 412
Müllerian intra-abdominal carcinomatosis in hereditary breast ovarian cancer syndrome: implications for risk-reducing surgery Murray Joseph CaseyAgnes B. Colanta Original Article 13 February 2016 Pages: 371 - 384
Update on Lynch syndrome genomics Päivi Peltomäki Original Article Open access 12 February 2016 Pages: 385 - 393
Hereditary cancer syndromes: utilizing DNA repair deficiency as therapeutic target Gaurav GoyalTiffany FanPeter Todd Silberstein Original Article Open access 12 February 2016 Pages: 359 - 366
Evaluation of laboratory perspectives on hereditary cancer panels Jessica StollScott M. WeissmanKristen J. Vogel Postula Original Article 11 February 2016 Pages: 689 - 696
Controversies in the surgery of patients with familial adenomatous polyposis and Lynch syndrome James M. Church Original Article 11 February 2016 Pages: 447 - 451
Modeling the dyadic effects of parenting, stress, and coping on parent–child communication in families tested for hereditary breast-ovarian cancer risk Jada G. HamiltonDarren MaysKenneth P. Tercyak Original Article 05 February 2016 Pages: 513 - 522
Rapid detection of germline mutations for hereditary gastrointestinal polyposis/cancers using HaloPlex target enrichment and high-throughput sequencing technologies Masakazu KohdaKensuke KumamotoYasushi Okazaki Original Article 02 February 2016 Pages: 553 - 562
A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma Borum SagongYoung Joon SeoIn Seok Moon Original Article 01 February 2016 Pages: 601 - 606
Migrant breast cancer patients and their participation in genetic counseling: results from a registry-based study J. E. BaarsA. M. van DulmenM. G. E. M. Ausems Original Article Open access 01 February 2016 Pages: 163 - 171
BRCA1/BRCA2 founder mutations and cancer risks: impact in the western Danish population Henriette Roed NielsenMef NilbertChristina Therkildsen Original Article 01 February 2016 Pages: 507 - 512
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosis Renaud SabatierElise LavitPatrice Viens Original Article 01 February 2016 Pages: 497 - 506
Constitutional MLH1 methylation presenting with colonic polyposis syndrome and not Lynch syndrome Trilokesh D. KidambiAmie BlancoJonathan P. Terdiman Short Communication 18 January 2016 Pages: 275 - 280
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis Isabel SpierMartin KerickStefan Aretz Original Article 16 January 2016 Pages: 281 - 288
CDH1 germline mutations and hereditary lobular breast cancer Giovanni CorsoMattia IntraViviana Galimberti REVIEW 13 January 2016 Pages: 215 - 219
Developing and assessing the utility of a You-Tube based clinical genetics video channel for families affected by inherited tumours G. E. JonesJ. H. SingletaryJ. G. Barwell Letter to the Editor 11 January 2016 Pages: 351 - 355
Germline BAP1 mutations misreported as somatic based on tumor-only testing Mohamed H. Abdel-RahmanKaran RaiColleen M. Cebulla Short Communication 09 January 2016 Pages: 327 - 330
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety Erica SermijnLiesbeth DelesieJacques De Grève Original Article Open access 09 January 2016 Pages: 155 - 162
Relationship of immunohistochemistry, copy number aberrations and epigenetic disorders with BRCAness pattern in hereditary and sporadic breast cancer Rosa Murria EstalSarai Palanca SuelaPascual Bolufer Gilabert Original Article 02 January 2016 Pages: 193 - 200
Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment Leigh A. BaumgartKristen J. Vogel PostulaWilliam A. Knaus Original Article 28 December 2015 Pages: 331 - 339
Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect Ingrid P. VogelaarMarjolijn J. L. LigtenbergNicoline Hoogerbrugge Original Article Open access 23 December 2015 Pages: 289 - 296
Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis Nicolás Casellas-CabreraYaritza Díaz-AlgorriMarcia Cruz-Correa Original Article 21 December 2015 Pages: 267 - 274
Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer Kirsten F. L. DoumaEvelien DekkerCora M. Aalfs Original Article Open access 19 December 2015 Pages: 231 - 240
Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients Keiko TakiYuri SatoMasami Arai Short Communication 18 December 2015 Pages: 261 - 265
