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1. Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making

2. Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

3. 'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations

4. Prophylactic total pancreatectomy in individuals at high risk of pancreatic ductal adenocarcinoma (PROPAN): systematic review and shared decision-making programme using decision tables

5. The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

6. Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

7. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

8. Online decision support for persons having a genetic predisposition to cancer and their partners during reproductive decision-making

9. The development of an online decision aid to support persons having a genetic predisposition to cancer and their partners during reproductive decision-making: a usability and pilot study

10. Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study

11. The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With BRCA1 or BRCA2 Mutations

12. Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

13. Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility

14. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

15. Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88

16. Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

17. Factors associated with cancer worries in individuals participating in annual pancreatic cancer surveillance

18. Assessing associations between the AURKAHMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

19. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

20. Pancreatic Cancer-Associated Gene Polymorphisms in a Nation-Wide Cohort of P16-Leiden Germline Mutation Carriers; a Case-Control Study Medical Genetics

21. Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers

22. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

23. Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

24. Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

25. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

26. Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

27. A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers

28. Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

29. Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

30. Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

31. Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

32. Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

33. Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer

34. Point mutations throughout the GL13 gene cause Greig cephalopolysyndactyly syndrome

35. Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

36. Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008

37. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis

40. Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008.

42. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

43. Large- and medium-sized arterial aneurysms in two patients with SMAD4-related juvenile polyposis syndrome.

44. The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?

45. Patients' experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study.

46. Surgical Oncologists and Nurses in Breast Cancer Care are Ready to Provide Pre-Test Genetic Counseling.

47. Development of ileal adenomas after ileal pouch-anal anastomosis versus end ileostomy in patients with familial adenomatous polyposis.

48. [Guidelines on genetic testing in psychiatry: an overview].

49. [Genetic risk of mental illness: what do we know and how do we communicate this?]

50. Clinical value of a screening tool for tumor predisposition syndromes in childhood cancer patients (TuPS): a prospective, observational, multi-center study.

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