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

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

3. Correction: Polygenic risk modeling for prediction of epithelial ovarian cancer risk

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

5. 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.

6. Permanent Magnet Penning Trap

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

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

11. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

12. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

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

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

15. Publisher Correction: Shared heritability and functional enrichment across six solid cancers.

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

17. Shared heritability and functional enrichment across six solid cancers.

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

19. Geometric scalings for the electrostatically driven helical plasma state

20. Properties of the electrostatically driven helical plasma state

21. Electrostatically driven helical plasma state

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

23. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

24. Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

25. Immune Cell Associations with Cancer Risk

27. Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

28. An efficient mixed-precision, hybrid CPU-GPU implementation of a fully implicit particle-in-cell algorithm

29. An Energy- and Charge-conserving, Implicit, Electrostatic Particle-in-Cell Algorithm

30. Functional Variants at the 11q13 Risk Locus for Breast Cancer Regulate Cyclin D1 Expression through Long-Range Enhancers

31. Laminar Plasma Dynamos

32. No Interactions Between Previously Associated 2-Hour Glucose Gene Variants and Physical Activity or BMI on 2-Hour Glucose Levels

33. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.

36. Non-coding RNAs underlie genetic predisposition to breast cancer

37. Chromatin interactome mapping at 139 independent breast cancer risk signals

39. Table S1 from A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

40. Online Supplementary Materials from A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

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

42. RNF168 regulates R-loop resolution and genomic stability in BRCA1/2-deficient tumors

45. Exome array analysis identifies ETFB as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients

48. Ontology Database System and Triggers

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

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