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2. Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

3. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

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

5. Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.

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. Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers

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. Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers

13. Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

14. Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

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

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

19. MLL2 mutation detection in 86 patients with Kabuki syndrome: A genotype-phenotype study

20. MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study

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

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

23. Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats

24. MLL2mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study

26. Men with metastatic prostate cancer carrying a pathogenic germline variant in breast cancer genes: disclosure of genetic test results to relatives.

27. The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2.

28. Contraceptives and cancer risks in BRCA1/2 pathogenic variant carriers: a systematic review and meta-analysis.

29. Survival of BRCA1/BRCA2-associated pT1 breast cancer patients, a cohort study.

30. The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant.

31. Lack of genotype-phenotype correlation in basal cell nevus syndrome: A Dutch multicenter retrospective cohort study.

32. Genetic counseling of patients with ovarian carcinoma: acceptance, timing, and psychological wellbeing.

33. Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition.

34. Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers.

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

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

37. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.

38. TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort.

39. 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.

40. Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers.

41. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

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

43. Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.

44. Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners.

45. Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

46. Germline BRCA1/2 mutation testing is indicated in every patient with epithelial ovarian cancer: A systematic review.

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

48. Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility.

49. Deleterious Germline BLM Mutations and the Risk for Early-onset Colorectal Cancer.

50. Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer.

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