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3. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

4. Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature Communications, (2021), 12, 1, (1078), 10.1038/s41467-020-20496-3).

5. Erratum: Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (Nature communications (2021) 12 1 (1078)).

6. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.

7. A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.

8. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores.

9. Association of genomic domains in BRCA1 and BRCA2 with prostate cancer risk and aggressiveness.

10. Cancer risks associated with germline PALB2 pathogenic variants: An international study of 524 families.

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

12. Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome

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

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

15. Common genomic variants are associated with incidence and clinicopathogenic features in familial breast cancer.

16. Clinical studies on subtle chromosomal rearrangements: experiences in the UK

17. Rare variants in XRCC2 as breast cancer susceptibility alleles

18. A role for common genomic variants in the assessment of familial breast cancer.

19. Moving toward personalized medicine: Treatment-focused genetic testing of women newly diagnosed with ovarian cancer.

20. Rare variants in XRCC2 as breast cancer susceptibility alleles

21. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity

22. Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.

23. A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation

24. An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome

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