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5. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

7. MUTYH-Associated Polyposis

9. Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

10. A mosaic PIK3CA variant in a young adult with diffuse gastric cancer: case report

11. Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database (Genetics in Medicine, (2020), 22, 1, (15-25), 10.1038/s41436-019-0596-9)

12. GENOTYPE-PHENOTYPE ASSOCIATIONS PROVIDE A RATIONAL TO IDENTIFY POTENTIALLY ACTIONABLE VUS

17. Recommendations to improve identification of hereditary and familial colorectal cancer in Europe

18. Peutz-Jeghers syndrome: a systematic review and recommendations for management

19. Analysis in the Prospective Lynch Syndrome Database identifies sarcoma as part of the Lynch syndrome tumor spectrum

21. Guidelines for the clinical management of familial adenomatous polyposis (FAP)

22. Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutation

27. Dye chromoendoscopy leads to a higher adenoma detection in the duodenum and stomach in patients with familial adenomatous polyposis

30. A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

33. No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies

35. Aktuelle Empfehlungen des „Deutschen Konsortiums Familiärer Darmkrebs“ zur Überwachung der kolonischen und extrakolonischen Tumorrisiken bei Patienten mit Lynch-Syndrom

40. Genomic and transcriptomic heterogeneity of colorectal tumors arising in Lynch Syndrome

44. Chromoendoskopie versus konventionelle Endoskopie im oberen Gastrointestinaltrakt bei Patienten mit familiärer adenomatöser Polyposis (ChroPol-I)

48. Langzeitergebnisse der chemopräventiven rektalen Sulindac-Therapie gegen Rektum-Adenome bei kolektomierten FAP-Patienten unter Berücksichtigung des Einfluss der APC- oder MUTYH-Gen Mutation

49. Die prophylaktische totale Gastrektomie bei der Behandlung hereditärer tumor-assoziierter Syndrome

50. Deciphering the Colon Cancer Genes-Report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010

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