ClinGen--the Clinical Genome Resource | New England Journal of Medicine | 2015 | 635 |
Biological interpretation of genome-wide association studies using predicted gene functions | Nature Communications | 2015 | 489 |
Digital inequalities and why they matter | Information, Communication and Society | 2015 | 379 |
Building the foundation for genomics in precision medicine | Nature | 2015 | 290 |
Actionable exomic incidental findings in 6503 participants: challenges of variant classification | Genome Research | 2015 | 252 |
Development of phenotype algorithms using electronic medical records and incorporating natural language processing | BMJ, The | 2015 | 159 |
Choosing wisely: prevalence and correlates of low-value health care services in the United States | Journal of General Internal Medicine | 2015 | 155 |
Prenatal antidepressant exposure is associated with risk for attention-deficit hyperactivity disorder but not autism spectrum disorder in a large health system | Molecular Psychiatry | 2015 | 137 |
Global implementation of genomic medicine: We are not alone | Science Translational Medicine | 2015 | 112 |
Toward high-throughput phenotyping: unbiased automated feature extraction and selection from knowledge sources | Journal of the American Medical Informatics Association: JAMIA | 2015 | 95 |
Colonoscopy is associated with a reduced risk for colon cancer and mortality in patients with inflammatory bowel diseases | Clinical Gastroenterology and Hepatology | 2015 | 80 |
Validation of electronic health record phenotyping of bipolar disorder cases and controls | American Journal of Psychiatry | 2015 | 79 |
TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits | PLoS ONE | 2015 | 77 |
Vitamin D and the development of allergic disease: how important is it? | Clinical and Experimental Allergy | 2015 | 74 |
Problem list completeness in electronic health records: A multi-site study and assessment of success factors | International Journal of Medical Informatics | 2015 | 69 |
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels | Human Molecular Genetics | 2015 | 68 |
Returning a Research Participant's Genomic Results to Relatives: Analysis and Recommendations | Journal of Law, Medicine and Ethics | 2015 | 67 |
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record | Journal of the American Medical Informatics Association: JAMIA | 2015 | 63 |
The Empirical Foundations of Teledermatology: A Review of the Research Evidence | Telemedicine Journal and E-Health | 2015 | 57 |
Methods to Develop an Electronic Medical Record Phenotype Algorithm to Compare the Risk of Coronary Artery Disease across 3 Chronic Disease Cohorts | PLoS ONE | 2015 | 57 |
Patient engagement with a mobile web-based telemonitoring system for heart failure self-management: a pilot study | JMIR MHealth and UHealth | 2015 | 56 |
A respiratory chain controlled signal transduction cascade in the mitochondrial intermembrane space mediates hydrogen peroxide signaling | Proceedings of the National Academy of Sciences of the United States of America | 2015 | 47 |
Automatic identification of methotrexate-induced liver toxicity in patients with rheumatoid arthritis from the electronic medical record | Journal of the American Medical Informatics Association: JAMIA | 2015 | 47 |
Mouse and human CRKL is dosage sensitive for cardiac outflow tract formation | American Journal of Human Genetics | 2015 | 47 |
Improving transgender health by building safe clinical environments that promote existing resilience: Results from a qualitative analysis of providers | BMC Pediatrics | 2015 | 46 |