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275 results on '"Lesueur F"'

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1. Identification of new breast cancer predisposition genes via whole exome sequencing

3. Recommandations pour le diagnostic de prédisposition génétique au mélanome cutané et pour la prise en charge des personnes à risque

4. First international workshop of the ATM and Cancer Risk Group (4–5 December 2019)

5. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

8. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

9. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

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

11. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

12. The role of prenatal social support in social inequalities with regard to maternal postpartum depression according to migrant status

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

21. A transcriptome-wide association study among 97,898 women to identify candidate susceptibility genes for epithelial ovarian cancer risk

22. Circulating plasma phospholipid fatty acids and risk of pancreatic cancer in a large European cohort

23. Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families

24. Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148

25. Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

26. Circulating plasma phospholipid fatty acids and risk of pancreatic cancer in a large European cohort

29. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

30. Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

31. Erratum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma (Nature (2011) 480:94-98 doi:10.1038/nature10539)

32. Rare Mutations in XRCC2 Increase the Risk of Breast Cancer

33. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma†

34. No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

36. The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma

37. The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

39. Circulating concentrations of insulin-like growth factor-I, insulin-like growth factor-binding protein-3, genetic polymorphisms and mammographic density in premenopausal Mexican women: Results from the ESMaestras cohort

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