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 Matthew Lebo.
Connection Strength

1.820
  1. "Big Data" Gets Personal. Sci Transl Med. 2016 Jan 20; 8(322):322fs3-3fs3.
    View in: PubMed
    Score: 0.648
  2. Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization. Am J Hum Genet. 2021 12 02; 108(12):2224-2237.
    View in: PubMed
    Score: 0.242
  3. A framework for automated gene selection in genomic applications. Genet Med. 2021 10; 23(10):1993-1997.
    View in: PubMed
    Score: 0.235
  4. Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project. Genet Med. 2021 07; 23(7):1372-1375.
    View in: PubMed
    Score: 0.058
  5. Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestry. Transfusion. 2020 06; 60(6):1294-1307.
    View in: PubMed
    Score: 0.055
  6. Automated typing of red blood cell and platelet antigens from whole exome sequences. Transfusion. 2019 10; 59(10):3253-3263.
    View in: PubMed
    Score: 0.052
  7. Analyzing and Reanalyzing the Genome: Findings from the MedSeq Project. Am J Hum Genet. 2019 07 03; 105(1):177-188.
    View in: PubMed
    Score: 0.051
  8. Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. Am J Hum Genet. 2019 01 03; 104(1):76-93.
    View in: PubMed
    Score: 0.050
  9. A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga. Transfusion. 2019 03; 59(3):908-915.
    View in: PubMed
    Score: 0.050
  10. 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: 0.048
  11. Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study. Lancet Haematol. 2018 Jun; 5(6):e241-e251.
    View in: PubMed
    Score: 0.048
  12. A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients. Circ Cardiovasc Genet. 2017 Oct; 10(5).
    View in: PubMed
    Score: 0.046
  13. 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: 0.045
  14. A curated gene list for reporting results of newborn genomic sequencing. Genet Med. 2017 07; 19(7):809-818.
    View in: PubMed
    Score: 0.043
  15. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. Am J Hum Genet. 2016 07 07; 99(1):247.
    View in: PubMed
    Score: 0.042
  16. Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium. Am J Hum Genet. 2016 06 02; 98(6):1067-1076.
    View in: PubMed
    Score: 0.041
  17. 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: 0.038
  18. Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy. Am J Hum Genet. 2011 Feb 11; 88(2):183-92.
    View in: PubMed
    Score: 0.029
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.