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SMART precision cancer medicine: a FHIR-based app to provide genomic information at the point of care., , , , , , , , , and 2 other author(s). J. Am. Medical Informatics Assoc., 23 (4): 701-710 (2016)Classifying non-small cell lung cancer types and transcriptomic subtypes using convolutional neural networks., , , , , , and . J. Am. Medical Informatics Assoc., 27 (5): 757-769 (2020)High-throughput multimodal automated phenotyping (MAP) with application to PheWAS., , , , , , , , , and 9 other author(s). J. Am. Medical Informatics Assoc., 26 (11): 1255-1262 (2019)PGAGENE: integrating quantitative gene-specific results from the NHLBI Programs for Genomic Applications., , and . Bioinform., 19 (6): 778-779 (2003)Comparing expression profiles of genes with similar promoter regions., , and . Bioinform., 18 (12): 1576-1584 (2002)Construction of extra-large scale screening tools for risks of severe mental illnesses using real world healthcare data., , , , , , and . CoRR, (2022)Quantifying the relationship between co-expression, co-regulation and gene function., , and . BMC Bioinform., (2004)Reproducible and Shareable Quantifications of Pathogenicity., , , and . PSB, page 231-242. (2016)Human Genome Variation: Linking Genotypes to Clinical Phenotypes - Session Introduction., , and . Pacific Symposium on Biocomputing, page 3-5. (2001)Strategies for maintaining patient privacy in i2b2., , , , and . JAMIA, 18 (Supplement): 103-108 (2011)