Joshua C. Denny American professor of biomedical informatics
Denny, Joshua Charles
VIAF ID: 160180893 (Personal)
Permalink: http://viaf.org/viaf/160180893
Preferred Forms
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
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| Evaluation of a novel terminology to categorize clinical document section headers and a related clinical note section tagger, 2007: |
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| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization |
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| Genetic determinants of variability in warfarin response after the dose-titration phase. |
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| Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium |
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| Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network |
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| Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting |
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| Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia |
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| Genetics of rheumatoid arthritis contributes to biology and drug discovery |
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| Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk |
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| Genome-Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol |
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| Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults. |
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| Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity |
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| A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough |
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| Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy |
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| Genome-wide study of resistant hypertension identified from electronic health records |
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| Genotype and risk of major bleeding during warfarin treatment |
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| Harnessing next-generation informatics for personalizing medicine: a report from AMIA's 2014 Health Policy Invitational Meeting. |
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| High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE |
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| A hybrid system for temporal information extraction from clinical text |
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| Hypertension is a modifiable risk factor for osteonecrosis in acute lymphoblastic leukemia |
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| Identification of unique venous thromboembolism-susceptibility variants in African-Americans. |
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| Identifying genetically driven clinical phenotypes using linear mixed models |
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| Identifying lupus patients in electronic health records: Development and validation of machine learning algorithms and application of rule-based algorithms |
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| Identifying Metastases-related Information from Pathology Reports of Lung Cancer Patients |
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| Identifying potential drugs that induce QT prolongation using electronic medical records |
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| Identifying UMLS concepts from ECG Impressions using KnowledgeMap. |
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| The IGNITE network: a model for genomic medicine implementation and research |
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| The influence of big (clinical) data and genomics on precision medicine and drug development. |
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| An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies. |
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| The KnowledgeMap project: development of a concept-based medical school curriculum database |
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| A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease |
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| A Modular Architecture for Electronic Health Record-Driven Phenotyping |
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| A multi-institution evaluation of clinical profile anonymization |
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| A multi-stage genome-wide association study of uterine fibroids in African Americans |
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| A natural language processing algorithm to define a venous thromboembolism phenotype |
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| A New Tool to Identify Key Biomedical Concepts in Text Documents, with Special Application to Curriculum Content |
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| The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementation |
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| A Phenome-Wide Association Study Identifies a Novel Asthma Risk Locus Near TERC. |
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| A phenome-wide association study to discover pleiotropic effects of , , and |
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| A Phenome-Wide Association Study Uncovers a Role for Autoimmunity in the Development of Chronic Obstructive Pulmonary Disease. |
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| A Phenome-wide Mendelian Randomisation study on genetically determined serum urate levels in UK Biobank cohort |
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| The phenotypic legacy of admixture between modern humans and Neandertals |
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| A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies |
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| The polygenic architecture of left ventricular mass mirrors the clinical epidemiology |
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| A polymorphism in HLA-G modifies statin benefit in asthma |
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| A prognostic model based on readily available clinical data enriched a pre-emptive pharmacogenetic testing program. |
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| A prototype application for real-time recognition and disambiguation of clinical abbreviations |
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| A Prototype for Executable and Portable Electronic Clinical Quality Measures Using the KNIME Analytics Platform. |
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| SJS/TEN 2017: Building Multidisciplinary Networks to Drive Science and Translation |
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| SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function |
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| A Standards-based Semantic Metadata Repository to Support EHR-driven Phenotype Authoring and Execution |
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| A stepwise approach to implementing pharmacogenetic testing in the primary care setting |
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| STRATEGIES FOR EQUITABLE PHARMACOGENOMIC-GUIDED WARFARIN DOSING AMONG EUROPEAN AND AFRICAN AMERICAN INDIVIDUALS IN A CLINICAL POPULATION |
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| A study of active learning methods for named entity recognition in clinical text |
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| A study of machine-learning-based approaches to extract clinical entities and their assertions from discharge summaries. |
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| A study of transportability of an existing smoking status detection module across institutions. |
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| A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers |
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| Syntactic parsing of clinical text: guideline and corpus development with handling ill-formed sentences |
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| Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease |
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| Teaching evidence-based medicine: Impact on students' literature use and inpatient clinical documentation. |
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| A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project |
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| Trans-ethnic association study of blood pressure determinants in over 750,000 individuals |
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| Transcription factor ETV1 is essential for rapid conduction in the heart |
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| TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits |
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| Type 2 diabetes risk forecasting from EMR data using machine learning. |
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| Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling |
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| The use of a DNA biobank linked to electronic medical records to characterize pharmacogenomic predictors of tacrolimus dose requirement in kidney transplant recipients |
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| Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study |
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| Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects |
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| Using Human 'Experiments of Nature' to Predict Drug Safety Issues: An Example with PCSK9 Inhibitors |
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| Using natural language processing to provide personalized learning opportunities from trainee clinical notes. |
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| Using systems approaches to address challenges for clinical implementation of pharmacogenomics |
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| Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA) |
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| Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients |
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| Validating drug repurposing signals using electronic health records: a case study of metformin associated with reduced cancer mortality |
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| Validation and enhancement of a computable medication indication resource (MEDI) using a large practice-based dataset |
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| Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network |
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| The Vanderbilt Experience with Electronic Health Records |
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| Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies |
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| প্রত্যুত্তর |
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