Balancing the burden and benefits of colonoscopy in Lynch Syndrome Finlay Macrae EditorialNotes 15 September 2023 Pages: 399 - 401
Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayed Elsa L. S. A. van LiereImke L. JacobsDewkoemar Ramsoekh Original article Open access 12 May 2023 Pages: 403 - 411
Endoscopic and chemopreventive management of familial adenomatous polyposis syndrome J. K. StoneN. A. MehtaC. N. Bernstein Review 29 April 2023 Pages: 413 - 422
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report Romy WalkerMark ClendenningDaniel D. Buchanan Brief Report Open access 15 June 2023 Pages: 423 - 428
Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study Anne Marie JelsigThomas van Overeem HansenJohn Gásdal Karstensen Original Article Open access 24 June 2023 Pages: 429 - 436
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Rachel HodanLinda Rodgers-FoucheOn behalf of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Review 21 June 2023 Pages: 437 - 448
Prevalence and genetic spectrum associated with hereditary colorectal cancer syndromes, the need to improve cancer risk awareness, and family cascade testing in Vietnam Huu-Thinh NguyenY-Thanh LuHung-Sang Tang Original Article 30 July 2023 Pages: 449 - 458
PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer Renata L. SandovalMiki HoriguchiMatthew B. Yurgelun Original Article 12 August 2023 Pages: 459 - 465
Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center Teresa S. ChaiKanhua YinKevin S. Hughes Original article 24 June 2023 Pages: 467 - 474
Unusual phenotypes in patients with a pathogenic germline variant in DICER1 Kateryna VengerMiriam ElbrachtUdo Kontny Short Communication Open access 31 July 2021 Pages: 475 - 480
In deep bioinformatic characterization of a novel fumarate hydratase variant FH c.199T > G; (p.Tyr67Asp) in hereditary leiomyomatosis and renal cell carcinoma Anisse ChamiThalía Rodrigues de Souza ZózimoLetícia da Conceição Braga Short Communication 15 June 2023 Pages: 481 - 486
Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis Maria Apellaniz-RuizNelly SabbaghianWilliam D. Foulkes Brief Report Open access 30 May 2023 Pages: 487 - 493
Willingness of individuals with Li-Fraumeni syndrome to participate in a cancer prevention trial: a survey study Farina J. StrueweSarah SchottChristian P. Kratz Letter to the editor Open access 23 June 2023 Pages: 495 - 497
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1 Mathilda WildingJane FlemingYemima Berman Original Article 19 June 2023 Pages: 499 - 511
Germline whole genome sequencing in adults with multiple primary tumors Yiming WangQiliang DingRaymond H. Kim Original Article 22 July 2023 Pages: 513 - 520
Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variant Corrine FillmanArravinth AnantharajahBryson W Katona Original Article 04 August 2023 Pages: 521 - 526
