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1. No Association Between Pharmacogenomics Variants and Hospital and Emergency Department Utilization: A Mayo Clinic Biobank Retrospective Study

2. Association of mitochondrial DNA copy number with self-rated health status

3. Pathway to Ascertain the Role of Pharmacogenomics in Healthcare Utilization Outcomes [Response to Letter]

4. CYP2D6 phenotypes are associated with adverse outcomes related to opioid medications

5. Increased risk of hospitalization for ultrarapid metabolizers of cytochrome P450 2D6

6. Health behaviors and quality of life predictors for risk of hospitalization in an electronic health record-linked biobank

7. Evidence of Gene-Environment Interactions between Common Breast Cancer Susceptibility Loci and Established Environmental Risk Factors

8. PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2

9. Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: A combined case-control study

10. Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

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

12. Body mass index and breast cancer survival: a Mendelian randomization analysis

13. Comprehensive and Integrated Genomic Characterization of Adult Soft Tissue Sarcomas

14. Abstract OT3-02-01: Development of cell-free nucleic acid-based tests for early detection of breast cancer: The STRIVE study

15. RAD51B in familial breast cancer

16. Abstract P1-05-20: Comparing the frequency and types of genetic aberrations between older and younger women with metastatic breast cancer at the University of North Carolina at Chapel Hill

17. Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair EDITORIAL COMMENT

18. SNP-SNP interaction analysis of NF-kappa B signaling pathway on breast cancer survival

19. Identification of novel genetic markers of breast cancer survival

20. Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

26. Different cellular p16(INK4a) localisation may signal different survival outcomes in head and neck cancer.

27. A novel automated mammographic density measure and breast cancer risk.

29. Prepregnancy exposure to cigarette smoking and subsequent risk of postmenopausal breast cancer.

30. High-folate diets and breast cancer survival in a prospective cohort study.

33. Perception of genetic risk among genetic counselors.

35. Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

36. Association analysis identifies 65 new breast cancer risk loci

37. Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

38. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

41. Block Nystagmus

42. Accurate variant detection across non-amplified and whole genome amplified DNA using targeted next generation sequencing

43. Bilateral macular hole formation secondary to sclopetaria caused by shockwaves transmitted by a posterior vector: case report

45. Race/ethnicity and disease severity in IgA nephropathy

46. Automated discovery of drug treatment patterns for endocrine therapy of breast cancer within an electronic medical record.

47. Cellular Redistribution Of Taurine In Osmotically Swollen Rat Hippocampus

49. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

50. DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

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