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Robert C Green, M.D.

Co-Author

This page shows the publications co-authored by Robert Green and Jason Vassy.
Connection Strength

3.170
  1. How to know when physicians are ready for genomic medicine. Sci Transl Med. 2015 May 13; 7(287):287fs19.
    View in: PubMed
    Score: 0.634
  2. A one-page summary report of genome sequencing for the healthy adult. Public Health Genomics. 2015; 18(2):123-9.
    View in: PubMed
    Score: 0.621
  3. Effect of Pharmacogenetic Testing for Statin Myopathy Risk vs Usual Care on Blood Cholesterol: A Randomized Clinical Trial. JAMA Netw Open. 2020 12 01; 3(12):e2027092.
    View in: PubMed
    Score: 0.233
  4. Reconciling Opportunistic and Population Screening in Clinical Genomics. Mayo Clin Proc. 2019 01; 94(1):103-109.
    View in: PubMed
    Score: 0.204
  5. How Primary Care Providers Talk to Patients about Genome Sequencing Results: Risk, Rationale, and Recommendation. J Gen Intern Med. 2018 06; 33(6):877-885.
    View in: PubMed
    Score: 0.191
  6. The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial. Ann Intern Med. 2017 08 01; 167(3):159-169.
    View in: PubMed
    Score: 0.184
  7. Prescription medication changes following direct-to-consumer personal genomic testing: findings from the Impact of Personal Genomics (PGen) Study. Genet Med. 2017 05; 19(5):537-545.
    View in: PubMed
    Score: 0.174
  8. 'Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project. Per Med. 2015; 12(1):23-32.
    View in: PubMed
    Score: 0.155
  9. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 2014 Mar 20; 15:85.
    View in: PubMed
    Score: 0.146
  10. Genomic medicine in primary care: barriers and assets. Postgrad Med J. 2013 Nov; 89(1057):615-6.
    View in: PubMed
    Score: 0.143
  11. Genetic susceptibility testing for chronic disease and intention for behavior change in healthy young adults. J Community Genet. 2013 Apr; 4(2):263-71.
    View in: PubMed
    Score: 0.136
  12. Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 May; 21(5):1261-1262.
    View in: PubMed
    Score: 0.052
  13. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019 05; 21(5):1100-1110.
    View in: PubMed
    Score: 0.050
  14. Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial. Genet Med. 2018 12; 20(12):1544-1553.
    View in: PubMed
    Score: 0.048
  15. When bins blur: Patient perspectives on categories of results from clinical whole genome sequencing. AJOB Empir Bioeth. 2017 Apr-Jun; 8(2):82-88.
    View in: PubMed
    Score: 0.045
  16. Patients' perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project. Per Med. 2016 Jan 01; 13(1):13-20.
    View in: PubMed
    Score: 0.041
  17. Are physicians prepared for whole genome sequencing? a qualitative analysis. Clin Genet. 2016 Feb; 89(2):228-34.
    View in: PubMed
    Score: 0.040
  18. A systematic approach to the reporting of medically relevant findings from whole genome sequencing. BMC Med Genet. 2014 Dec 14; 15:134.
    View in: PubMed
    Score: 0.039
  19. Personalized genetic risk counseling to motivate diabetes prevention: a randomized trial. Diabetes Care. 2013 Jan; 36(1):13-9.
    View in: PubMed
    Score: 0.033
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.