1. Balancing the burden and benefits of colonoscopy in Lynch Syndrome

   • Finlay Macrae

   EditorialNotes 15 September 2023 Pages: 399 - 401

2. Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayed

   • Elsa L. S. A. van Liere
   • Imke L. Jacobs
   • Dewkoemar Ramsoekh

   Original article Open access 12 May 2023 Pages: 403 - 411

   

3. Endoscopic and chemopreventive management of familial adenomatous polyposis syndrome

   • J. K. Stone
   • N. A. Mehta
   • C. N. Bernstein

   Review 29 April 2023 Pages: 413 - 422

4. 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 Walker
   • Mark Clendenning
   • Daniel D. Buchanan

   Brief Report Open access 15 June 2023 Pages: 423 - 428

   

5. Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study

   • Anne Marie Jelsig
   • Thomas van Overeem Hansen
   • John Gásdal Karstensen

   Original Article Open access 24 June 2023 Pages: 429 - 436

   

6. 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 Hodan
   • Linda Rodgers-Fouche
   • On behalf of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer

   Review 21 June 2023 Pages: 437 - 448

7. 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 Nguyen
   • Y-Thanh Lu
   • Hung-Sang Tang

   Original Article 30 July 2023 Pages: 449 - 458

   

8. PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer

   • Renata L. Sandoval
   • Miki Horiguchi
   • Matthew B. Yurgelun

   Original Article 12 August 2023 Pages: 459 - 465

9. Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center

   • Teresa S. Chai
   • Kanhua Yin
   • Kevin S. Hughes

   Original article 24 June 2023 Pages: 467 - 474

   

10. Unusual phenotypes in patients with a pathogenic germline variant in DICER1

    • Kateryna Venger
    • Miriam Elbracht
    • Udo Kontny

    Short Communication Open access 31 July 2021 Pages: 475 - 480

    

11. In deep bioinformatic characterization of a novel fumarate hydratase variant FH c.199T > G; (p.Tyr67Asp) in hereditary leiomyomatosis and renal cell carcinoma

    • Anisse Chami
    • Thalía Rodrigues de Souza Zózimo
    • Letícia da Conceição Braga

    Short Communication 15 June 2023 Pages: 481 - 486

    

12. Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

    • Maria Apellaniz-Ruiz
    • Nelly Sabbaghian
    • William D. Foulkes

    Brief Report Open access 30 May 2023 Pages: 487 - 493

    

13. Willingness of individuals with Li-Fraumeni syndrome to participate in a cancer prevention trial: a survey study

    • Farina J. Struewe
    • Sarah Schott
    • Christian P. Kratz

    Letter to the editor Open access 23 June 2023 Pages: 495 - 497

    

14. Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1

    • Mathilda Wilding
    • Jane Fleming
    • Yemima Berman

    Original Article 19 June 2023 Pages: 499 - 511

    

15. Germline whole genome sequencing in adults with multiple primary tumors

    • Yiming Wang
    • Qiliang Ding
    • Raymond H. Kim

    Original Article 22 July 2023 Pages: 513 - 520

16. Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variant

    • Corrine Fillman
    • Arravinth Anantharajah
    • Bryson W Katona

    Original Article 04 August 2023 Pages: 521 - 526