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22 results on '"O'Connell, Shona"'

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1. A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

2. The impact of coding germline variants on contralateral breast cancer risk and survival

3. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

4. Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset

5. Additional file 1 of A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

6. A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

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

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

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

10. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

11. Publisher correction : Homologous recombination DNA repair defects in PALB2-associated breast cancers

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

13. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

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

15. Annexin A1 expression in a pooled breast cancer series: Association with tumor subtypes and prognosis

16. Annexin A1 expression in a pooled breast cancer series: Association with tumor subtypes and prognosis

17. Targeted Prostate Cancer Screening in BRCA1 and BRCA2 Mutation Carriers: Results from the Initial Screening Round of the IMPACT Study

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

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

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

21. A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome.

22. TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.

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