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FAVOR: functional annotation of variants online resource and annotator for variation across the human genome., , , , , , , , , and 14 other author(s). Nucleic Acids Res., 51 (D1): 1300-1311 (January 2023)Usability of a novel clinician interface for genetic results., , , , , , , , and . J. Biomed. Informatics, 45 (5): 950-957 (2012)Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates., , , , , , , , , and 1 other author(s). Appl. Clin. Inform., 07 (02): 461-476 (2016)Building the foundation for genomics in precision medicine, and . Nature, 526 (7573): 336--342 (Oct 14, 2015)A Novel Clinician Interface to Improve Access to Up-to-date Genetic Results., , , , , , , , , and . AMIA, AMIA, (2013)The Clinical Pharmacogenetics Implementation Consortium (CPIC) Term Standardization for Clinical Pharmacogenetic Test Results: Alleles and Phenotypes., , , , , , , , , and 2 other author(s). CRI, AMIA, (2016)Genomic considerations for FHIR®; eMERGE implementation lessons., , , , , , , , , and 16 other author(s). J. Biomed. Informatics, (2021)Lessons Learned in the Implementation of Novel IT Infrastructure to Communicate Genetic Variant Updates., , , , , , , , , and . AMIA, AMIA, (2012)