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1. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing

4. Neptune: an environment for the delivery of genomic medicine

7. Positive impact of genetic counseling assistants on genetic counseling efficiency, patient volume, and cost in a cancer genetics clinic

8. Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

9. Scheduled and Breakthrough Opioid Use for Cancer Pain in an Inpatient Setting at a Tertiary Cancer Hospital

11. A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort

14. Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

19. Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs

21. List of Contributors

22. Contributors

24. Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US

25. Correction to: Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants

34. Understanding the Patient Experience of Receiving Clinically Actionable Genetic Results from the MyCode Community Health Initiative, a Population-Based Genomic Screening Initiative

35. Creativity in Assessment of Library Instruction.

39. Combination Therapy of Physical Activity and Dexamethasone for Cancer-Related Fatigue: A Phase II Randomized Double-Blind Controlled Trial

41. Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer

42. Do research participants share genomic screening results with family members?

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