Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Robert C Green, M.D.

Co-Author

This page shows the publications co-authored by Robert Green and Joel Krier.
Connection Strength

2.623
  1. Genomic sequencing in clinical practice: applications, challenges, and opportunities. Dialogues Clin Neurosci. 2016 09; 18(3):299-312.
    View in: PubMed
    Score: 0.696
  2. Management of Incidental Findings in Clinical Genomic Sequencing. Curr Protoc Hum Genet. 2015 Oct 06; 87:9.23.1-9.23.16.
    View in: PubMed
    Score: 0.653
  3. Management of incidental findings in clinical genomic sequencing. Curr Protoc Hum Genet. 2013; Chapter 9:Unit9.23.
    View in: PubMed
    Score: 0.540
  4. Reclassification of genetic-based risk predictions as GWAS data accumulate. Genome Med. 2016 Feb 17; 8(1):20.
    View in: PubMed
    Score: 0.168
  5. A one-page summary report of genome sequencing for the healthy adult. Public Health Genomics. 2015; 18(2):123-9.
    View in: PubMed
    Score: 0.156
  6. 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
  7. 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
  8. An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery. NPJ Genom Med. 2018; 3:21.
    View in: PubMed
    Score: 0.050
  9. Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report. Cold Spring Harb Mol Case Stud. 2018 08; 4(4).
    View in: PubMed
    Score: 0.050
  10. The BabySeq project: implementing genomic sequencing in newborns. BMC Pediatr. 2018 07 09; 18(1):225.
    View in: PubMed
    Score: 0.049
  11. 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: 0.046
  12. 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
  13. Summarizing polygenic risks for complex diseases in a clinical whole-genome report. Genet Med. 2015 Jul; 17(7):536-44.
    View in: PubMed
    Score: 0.038
  14. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine. Trials. 2014 Mar 20; 15:85.
    View in: PubMed
    Score: 0.037
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.