Search

Your search keyword '"Auber B."' showing total 32 results

Search Constraints

Start Over You searched for: Author "Auber B." Remove constraint Author: "Auber B." Database OAIster Remove constraint Database: OAIster
32 results on '"Auber B."'

Search Results

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

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

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

4. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

5. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

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

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

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

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

10. Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D

11. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

12. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

13. Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

14. Rare heterozygous DHTKD1 variants in patients with amyotrophic lateral sclerosis

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

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

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

18. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

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

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

21. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.

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

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

24. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

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

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

27. Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

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

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

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

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

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

Catalog

Books, media, physical & digital resources