The IL-10 promoter haplotype and cancer risk: evidence from a meta-analysis Kui ZhangLushun ZhangLin Zhang Review Article 29 May 2012 Pages: 313 - 319
French experts report on MUTYH-associated polyposis (MAP) Bruno BuecherCatherine BonaïtiJean-Christophe Saurin Original Article 27 April 2012 Pages: 321 - 328
Common MUTYH mutations and colorectal cancer risk in multiethnic populations Flavio LejbkowiczIlana CohenGad Rennert Original Article 28 February 2012 Pages: 329 - 335
A prospective study of bowel preparation for colonoscopy with polyethylene glycol-electrolyte solution versus sodium phosphate in Lynch syndrome: a randomized trial Maria W. J. van Vugt van PinxterenMariëtte C. A. van KouwenFokko M. Nagengast Original Article Open access 23 February 2012 Pages: 337 - 341
Adequacy of family history taking in ovarian cancer patients: a population-based study Anne M. van AltenaSandra van AarleJoanne A. de Hullu Original Article Open access 03 March 2012 Pages: 343 - 349
Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases Izabela BrozekMagdalena RatajskaJanusz Limon Original Article Open access 01 March 2012 Pages: 351 - 354
Molecular characterization of parathyroid tumors from two patients with hereditary colorectal cancer syndromes Adam AndreassonLuqman SulaimanC. Christofer Juhlin Original Article 01 March 2012 Pages: 355 - 362
Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance Irma KluijtRolf H. SijmonsAnemieke Cats Original Article 03 March 2012 Pages: 363 - 369
The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees’ outcome Ulla PlattenJohanna RantalaBrita Arver Original Article Open access 08 March 2012 Pages: 371 - 379
Mutation screening of RAD51C in high-risk breast and ovarian cancer families Wenping LuXianshu WangFergus J. Couch Original Article 04 April 2012 Pages: 381 - 385
Nephron sparing surgery in von Hippel-Lindau associated renal cell carcinoma; clinicopathological long-term follow-up C. A. JilgHartmut P. H. NeumannW. Schultze-Seemann Original Article 17 March 2012 Pages: 387 - 394
Uroepithelial and kidney carcinoma in Lynch syndrome Markku AarnioMatti SäilyJukka-Pekka Mecklin Original Article 04 April 2012 Pages: 395 - 401
The consequences of risk reducing salpingo-oophorectomy: the case for a coordinated approach to long-term follow up post surgical menopause Carmel PezaroPaul JamesGillian Mitchell Original Article 03 April 2012 Pages: 403 - 410
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome Giovanni PontiLorenza PastorinoStefania Seidenari Original Article 08 May 2012 Pages: 411 - 418
A multidisciplinary clinic for individualizing management of patients at increased risk for breast and gynecologic cancer Natalie J. EngelPatricia GordonKristin K. Zorn Original Article 27 May 2012 Pages: 419 - 427
Breast cancer risk factors differ between Asian and white women with BRCA1/2 mutations Monique A. de BruinAva KwongAllison W. Kurian Original Article 26 May 2012 Pages: 429 - 439
Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry Mala PandeChongjuan WeiMarsha L. Frazier Original Article 20 June 2012 Pages: 441 - 447
Closing the loop: an interactive action-research conference format for delivering updated medical information while eliciting Latina patient/family experiences and psychosocial needs post-genetic cancer risk assessment Deborah J. MacDonaldJulia DeriKathleen R. Blazer Original Article 08 June 2012 Pages: 449 - 458
Microsatellite instability testing in Korean patients with colorectal cancer Jung Ryul OhDuck-Woo KimJae-Gahb Park Original Article 06 June 2012 Pages: 459 - 466
Causes of death of mutation carriers in Finnish Lynch syndrome families Kirsi PylvänäinenTuula LehtinenJukka-Pekka Mecklin Original Article 09 June 2012 Pages: 467 - 471
Breast and ovarian cancer risk management in a French cohort of 158 women carrying a BRCA1 or BRCA2 germline mutation: patient choices and outcome Pascale ThisAnne de la RochefordièreDominique Stoppa-Lyonnet Original Article 19 June 2012 Pages: 473 - 482
Germline mutations in BRIP1 and PALB2 in Jewish high cancer risk families Irene CatucciRoni MilgromPaolo Peterlongo Original Article 13 June 2012 Pages: 483 - 491
Outcomes of a systems-level intervention offering breast cancer risk assessments to low-income underserved women Darren MaysMcKane E. SharffKenneth P. Tercyak Original Article 19 June 2012 Pages: 493 - 502
High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis Rania Abdelmaksoud-DammakImen Miladi-AbdennadherRaja Mokdad-Gargouri Original Article 29 June 2012 Pages: 503 - 508
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome Michael P. FarrellDavid J. HughesPeter A. Daly Original Article 07 July 2012 Pages: 509 - 518
Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian families Miklós TanyiJudit OlaszLászló Damjanovich Short Communication 01 March 2012 Pages: 519 - 524
Analysis of a Finnish family confirms RHBDF2 mutations as the underlying factor in tylosis with esophageal cancer Silva SaarinenPia VahteristoLauri A. Aaltonen Short Communication 26 May 2012 Pages: 525 - 528
Hepatoblastoma in two siblings and familial adenomatous polyposis: causal nexus or coincidence? Christina EversHarald GasparUte Moog Short Communication 13 June 2012 Pages: 529 - 533
Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma Karin A. W. WadtAnne-Marie GerdesMette K. Andersen Short Communication 21 June 2012 Pages: 535 - 537
The evolution of personalized cancer genetic counseling in the era of personalized medicine Hetal S. VigCatharine Wang Letter to the Editor 15 March 2012 Pages: 539 - 544