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1. Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease

4. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

5. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

6. Evidence for an ancient BRCA1 pathogenic variant in inherited breast cancer patients from Senegal

7. Data from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

8. Supplementary Methods, Tables 1-3, Figure 1 from Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

11. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

13. Familial hematological malignancies: new IDH2 mutation

14. The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

16. Mutational analysis of JAK2, CBL, RUNX1, and NPM1 genes in familial aggregation of hematological malignancies

18. Association and Performance of Polygenic Risk Scores for Breast Cancer Among French Women Presenting or Not a Familial Predisposition to the Disease

21. A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers

22. Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

24. Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study

25. Variation in breast cancer risk with mutation position, smoking, alcohol, and chest X-ray history, in the French National BRCA1/2 carrier cohort (GENEPSO)

26. Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers

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

29. Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer

32. Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants

33. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

34. Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome

37. Prédispositions héréditaires au cancer colorectal

39. Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk

40. Additional file 1: of Novel BRCA2 pathogenic variant c.5219 T > G; p.(Leu1740Ter) in a consanguineous Senegalese family with hereditary breast cancer

42. Breast cancer risk in BRCA1 and BRCA2 mutation carriers and polyglutamine repeat length in the AIB1 gene

43. Typical medullary breast carcinomas have a basal/myoepithelial phenotype

45. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

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

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

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