Search

Your search keyword '"Bubien V"' showing total 34 results

Search Constraints

Start Over You searched for: Author "Bubien V" Remove constraint Author: "Bubien V"
34 results on '"Bubien V"'

Search Results

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

5. 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).

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

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

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

10. Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

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

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

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

14. Increased incidence of pathogenic variants in ATMin the context of testing for breast and ovarian cancer predisposition

15. Abstract P5-09-07: Risk reducing strategy in germline BRCA mutated patients with locally advanced breast cancer. Establishing mastectomy as a preventing procedure of local recurrence

16. Abstract P5-16-23: Rapid germline BRCA screening for locally advanced breast cancer changes surgical procedure after neoadjuvant chemotherapy

17. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

18. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

19. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

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

21. Le risque cumulé de cancers est élevé dans la maladie de Cowden

22. Classification of PTEN germline non-truncating variants: a new approach to interpretation.

23. Familial uveal melanoma and other tumors in 25 families with monoallelic germline MBD4 variants.

24. Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.

25. PTEN alterations in sporadic and BRCA1-associated triple negative breast carcinomas.

26. Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

27. TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing.

28. Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.

29. Ovarian Clear Cell Carcinoma in Cowden Syndrome.

30. Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: A proof of principle study.

31. Insertion of Alu elements at a PTEN hotspot in Cowden syndrome.

32. Long clinical benefit achieved in two patients with malignant paraganglioma treated by metronomic cyclophosphamide.

33. [Hereditary ovarian carcinomas: clinico-biological features and treatment].

34. High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome.

Catalog

Books, media, physical & digital resources