A test of automated use of electronic health records to aid in diagnosis of genetic disease
Author:
Funder
U.S. National Library of Medicine
Vanderbilt University
National Institutes of Health
Vanderbilt University Medical Center
National Human Genome Research Institute
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference19 articles.
1. Can you hear us now? The impact of health-care utilization by rare disease patients in the United States;Navarrete-Opazo;Genet Med,2021
2. The collective impact of rare diseases in Western Australia: an estimate using a population-based cohort;Walker;Genet Med,2017
3. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns;Bastarache;Science,2018
4. Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder;Wendt;Mol Psychiatry,2022
5. Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease;Bastarache;J Am Med Inform Assoc,2019
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