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2. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

3. Correction: Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes

4. Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes

5. Targeted long-read sequencing of the Ewing sarcoma 6p25.1 susceptibility locus identifies germline-somatic interactions with EWSR1-FLI1 binding

6. Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome

7. Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

8. Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

9. Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for 13 Cancer Types

10. Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types.

11. Characterization of Large Structural Genetic Mosaicism in Human Autosomes

12. A genome-wide association study of marginal zone lymphoma shows association to the HLA region.

13. Sex specific associations in genome wide association analysis of renal cell carcinoma

14. Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

15. Genome-wide Association Study Identifies Five Susceptibility Loci for Follicular Lymphoma outside the HLA Region

16. Data from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

17. Supplementary Table 3 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

18. Supplementary Table 1 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

19. Supplementary Table 6 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

20. Supplementary Table 5 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

21. Supplementary Figures 1 - 11 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

22. Supplementary Table 2 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

23. Supplementary Table 4 from A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma

24. Mutations in the HPV16 genome induced by APOBEC3 are associated with viral clearance

25. Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations

26. Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

27. Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations

28. Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women

29. Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes

30. Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia

32. Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry

35. Genetic variants in fas signaling pathway genes and risk of gastric cancer

37. Genetic variants in DNA repair pathway genes and risk of esophageal squamous cell carcinoma and gastric adenocarcinoma in a Chinese population

39. Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies

40. Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer

41. The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

42. A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3

45. Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

46. Association of HPV35 with cervical carcinogenesis among women of African ancestry: Evidence of viral‐host interaction with implications for disease intervention

47. Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women

48. Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia

50. Genome-Wide Association Study Identifies an Immune-Related Etiology for Severe Aplastic Anemia

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