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36 results on '"Chanock, Stephen J"'

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1. Inflated expectations: Rare-variant association analysis using public controls

2. Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies.

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

5. Genetic variation in POT1 and risk of thyroid subsequent malignant neoplasm: A report from the Childhood Cancer Survivor Study

6. Body Mass Index Genetic Risk Score and Endometrial Cancer Risk

7. Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.

8. Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults

9. Correction: Vitamin D Metabolic Pathway Genes and Pancreatic Cancer Risk

10. Genetic Variation in the TP53 Pathway and Bladder Cancer Risk. A Comprehensive Analysis

11. Application of Multi-SNP Approaches Bayesian LASSO and AUC-RF to Detect Main Effects of Inflammatory-Gene Variants Associated with Bladder Cancer Risk

12. An Absolute Risk Model to Identify Individuals at Elevated Risk for Pancreatic Cancer in the General Population

14. Genetic Variants in Epidermal Growth Factor Receptor Pathway Genes and Risk of Esophageal Squamous Cell Carcinoma and Gastric Cancer in a Chinese Population

15. Common Single Nucleotide Polymorphisms in Genes Related to Immune Function and Risk of Papillary Thyroid Cancer

16. A Genome-Wide Scan for Breast Cancer Risk Haplotypes among African American Women

18. Socioeconomic and Nutritional Factors Account for the Association of Gastric Cancer with Amerindian Ancestry in a Latin American Admixed Population

19. Genome-Wide Association Study of Circulating Estradiol, Testosterone, and Sex Hormone-Binding Globulin in Postmenopausal Women

20. Single Nucleotide Polymorphisms in the PRDX3 and RPS19 and Risk of HPV Persistence and Cervical Precancer/Cancer

21. Large-Scale Pathway-Based Analysis of Bladder Cancer Genome-Wide Association Data from Five Studies of European Background

22. Variation in Effects of Non-Hodgkin Lymphoma Risk Factors According to the Human Leukocyte Antigen (HLA)-DRB1*01:01 Allele and Ancestral Haplotype 8.1

23. Genome-Wide Association Study of Relative Telomere Length

24. Characterizing Associations and SNP-Environment Interactions for GWAS-Identified Prostate Cancer Risk Markers—Results from BPC3

27. Common Genetic Variants and Risk for HPV Persistence and Progression to Cervical Cancer

29. Phase I Metabolic Genes and Risk of Lung Cancer: Multiple Polymorphisms and mRNA Expression

30. Common Gene Variants in the Tumor Necrosis Factor (TNF) and TNF Receptor Superfamilies and NF-kB Transcription Factors and Non-Hodgkin Lymphoma Risk

31. Genetic Variation in the TP53 Pathway and Bladder Cancer Risk. A Comprehensive Analysis.

32. Common Genetic Variants in miR-1206 (8q24.2) and miR-612 (11q13.3) Affect Biogenesis of Mature miRNA Forms.

33. Genetic Admixture and Population Substructure in Guanacaste Costa Rica.

34. Common Gene Variants in the Tumor Necrosis Factor (TNF) and TNF Receptor Superfamilies and NF-κB Transcription Factors and Non-Hodgκin Lymphoma Risκ.

35. Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus.

36. MicroRNA related polymorphisms and breast cancer risk.

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