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1. A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship

5. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

6. Mendelian randomisation study of smoking exposure in relation to breast cancer risk.

7. CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers.

8. Measuring the burden of direct-to-consumer genetic testing on clinical genetics services.

11. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

12. Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9)

13. Development and validation of a targeted gene sequencing panel for application to disparate cancers

14. Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy

15. Homologous recombination DNA repair defects in PALB2-associated breast cancers

16. Homologous recombination DNA repair defects in PALB2-associated breast cancers

17. Impact of direct-to-consumer genetic testing on Australian clinical genetics services.

18. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

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

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

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

22. A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.

23. Homologous recombination DNA repair defects in PALB2-associated breast cancers.

24. Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9).

25. A novel approach for offering additional findings to patients: Separating this decision from diagnostic testing.

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

27. Homologous recombination DNA repair defects in PALB2-associated breast cancers (vol 5, 23, 2019)

28. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

29. Polygenic risk scores for prediction of breast cancer and breast cancer subtypes

30. Heritable DNA methylation marks associated with susceptibility to breast cancer /631/67/69 /631/337/176/1988 /692/699/67/1347 /692/308/2056 /45 /45/61 article.

31. Phenotype assessment and pilot observational study of intranasal bevacizumab in hereditary haemorrhagic telangiectasia (HHT).

32. Absence of renal phenotype in hereditary haemorrhagic telangiectasia

33. RAD51B in familial breast cancer.

34. Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment

39. Hereditary haemorhagic telangiectasia, an australian cohort: Clinical and investigative features.

40. A Model for Peer Experiential and Reciprocal Supervision (PEERS) for Genetic Counselors: Development and Preliminary Evaluation Within Clinical Practice

44. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

45. Impact of direct-to-consumer genetic testing on Australian clinical genetics services.

46. Living with Hereditary Haemorrhagic Telangiectasia: stigma, coping with unpredictable symptoms, and self-advocacy.

47. A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.

48. Absence of renal phenotype in hereditary haemorrhagic telangiectasia.

49. A rapid scoring tool to assess mutation probability in patients with inherited cardiac disorders.

50. Cohort study of Gorlin syndrome with emphasis on standardised phenotyping and quality of life assessment.

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