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1. A Likelihood Ratio Approach for Utilizing Case-Control Data in the Clinical Classification of Rare Sequence Variants: Application to BRCA1 and BRCA2

3. Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2

4. Pattern matching under DTW distance

5. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

6. Critical Assessment of Metagenome Interpretation: the second round of challenges

7. Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival

8. FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women

9. Rare germline copy number variants (CNVs) and breast cancer risk

10. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis.

11. 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.

12. PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

13. Pleiotropy-guided transcriptome imputation from normal and tumor tissues identifies candidate susceptibility genes for breast and ovarian cancer.

14. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

15. Toward perfect reads: self-correction of short reads via mapping on de Bruijn graphs

16. Two truncating variants in FANCC and breast cancer risk.

17. Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

19. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

20. Polygenic risk modeling for prediction of epithelial ovarian cancer risk

21. Breast cancer risks associated with missense variants in breast cancer susceptibility genes

22. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

23. A resource-frugal probabilistic dictionary and applications in bioinformatics

24. Fast and scalable minimal perfect hashing for massive key sets

25. Rare germline copy number variants (CNVs) and breast cancer risk

26. A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

27. The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

28. Critical Assessment of Metagenome Interpretation—a benchmark of metagenomics software

29. Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

30. Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

31. Mendelian randomisation study of smoking exposure in relation to breast cancer risk

32. A resource-frugal probabilistic dictionary and applications in (meta)genomics

33. Multiple Comparative Metagenomics using Multiset k-mer Counting

34. Genomic evidence for global ocean plankton biogeography shaped by large-scale current systems

35. Commet: comparing and combining multiple metagenomic datasets

36. Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases

37. BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

38. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

39. Read Mapping on de Bruijn graph

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

41. A Discrete Logarithm-based Approach to Compute Low-Weight Multiples of Binary Polynomials

42. Protein truncating variants in FANCM and risk for ER-negative/triple negative breast cancer

43. Fine‐scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

44. Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

45. Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.

46. An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

47. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

48. Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

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

50. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

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