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Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants, , , , and . The American Journal of Human Genetics, 92 (6): 841 - 853 (2013)Automated Identification of Families in Electronic Health Records to Support Clinical Research., , , , , , , , , and 3 other author(s). CRI, AMIA, (2017)Copy number variation genotyping using family information., , , , , , and . BMC Bioinform., (2013)On the frequency of copy number variants., , , , and . Bioinform., 24 (20): 2350-2355 (2008)Discovering Influential Variables: A General Computer Intensive Method for Common Genetic Disorders., , , , and . Handbook of Statistical Bioinformatics, Springer, (2011)QRank: a novel quantile regression tool for eQTL discovery., , , , , and . Bioinform., 33 (14): 2123-2130 (2017)Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies., , , , , , , , , and 23 other author(s). npj Digit. Medicine, (2021)Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies., , , , , , , , , and 4 other author(s). npj Digit. Medicine, (2021)