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Connection

Mark Hoffman to Genetic Testing

This is a "connection" page, showing publications Mark Hoffman has written about Genetic Testing.

 
Connection Strength
  
 
 
1.012
  
  1. Fowler SA, Saunders CJ, Hoffman MA. Variation among Consent Forms for Clinical Whole Exome Sequencing. J Genet Couns. 2018 02; 27(1):104-114.
    View in: PubMed
    Score: 0.559
  2. Hoffman MA. The genome-enabled electronic medical record. J Biomed Inform. 2007 Feb; 40(1):44-6.
    View in: PubMed
    Score: 0.255
  3. Hoffman MA, Williams MS. Electronic medical records and personalized medicine. Hum Genet. 2011 Jul; 130(1):33-9.
    View in: PubMed
    Score: 0.091
  4. Deshmukh VG, Hoffman MA, Arnoldi C, Bray BE, Mitchell JA. Efficiency of CYP2C9 genetic test representation for automated pharmacogenetic decision support. Methods Inf Med. 2009; 48(3):282-90.
    View in: PubMed
    Score: 0.079
  5. Yu PP, Hoffman MA, Hayes DF. Biomarkers and oncology: the path forward to a learning health system. Arch Pathol Lab Med. 2015 Apr; 139(4):451-6.
    View in: PubMed
    Score: 0.029
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.