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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

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

4. ALDH18A1‐related hereditary spastic paraplegia and developmental and epileptic encephalopathy with spike‐wave activation in sleep: Expanding the clinical phenotype

5. Pattern matching under DTW distance

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

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

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

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

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

15. Mapsembler, targeted and micro assembly of large NGS datasets on a desktop computer

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

17. Lossless filter for multiple repeats with bounded edit distance

18. Optimal neighborhood indexing for protein similarity search

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

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

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

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

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

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

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

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

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

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

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

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. 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

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

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

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

38. Commet: comparing and combining multiple metagenomic datasets

39. Read Mapping on de Bruijn graph

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

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

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

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

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

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

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

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

48. Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

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

50. RAD51B in Familial Breast Cancer.

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