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Large language models facilitate the generation of electronic health record phenotyping algorithms.
- Published in:
- Journal of the American Medical Informatics Association, 2024, v. 31, n. 9, p. 1994, doi. 10.1093/jamia/ocae072
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- Article
Benchmarking computational variant effect predictors by their ability to infer human traits.
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- Genome Biology, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s13059-024-03314-7
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- Article
The electrophysiologic effects of KCNQ1 extend beyond expression of I<sub>Ks</sub>: evidence from genetic and pharmacologic block.
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- Cardiovascular Research, 2024, v. 120, n. 7, p. 735, doi. 10.1093/cvr/cvae042
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- Article
Clinical associations with a polygenic predisposition to benign lower white blood cell counts.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47804-5
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- Article
Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity.
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- JAMA Network Open, 2024, v. 7, n. 3, p. e243821, doi. 10.1001/jamanetworkopen.2024.3821
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- Article
Recurrence After Atrial Fibrillation Ablation and Investigational Biomarkers of Cardiac Remodeling.
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- Journal of the American Heart Association, 2024, v. 13, n. 6, p. 1, doi. 10.1161/JAHA.123.031029
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- Article
Machine Learning Prediction of Treatment Response to Inhaled Corticosteroids in Asthma.
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- Journal of Personalized Medicine, 2024, v. 14, n. 3, p. 246, doi. 10.3390/jpm14030246
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- Article
Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer's disease with real-world clinical validation.
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- NPJ Digital Medicine, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s41746-024-01038-3
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- Publication type:
- Article
Antipsychotics and the QTc Interval During Delirium in the Intensive Care Unit: A Secondary Analysis of a Randomized Clinical Trial.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 1, p. e2352034, doi. 10.1001/jamanetworkopen.2023.52034
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- Article
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
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- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01284-w
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- Publication type:
- Article
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics.
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- Bioinformatics, 2023, v. 39, n. 11, p. 1, doi. 10.1093/bioinformatics/btad655
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- Article
Correction: Hypertension genetic risk score is associated with burden of coronary heart disease among patients referred for coronary angiography.
- Published in:
- 2023
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- Correction Notice
Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41185-x
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- Publication type:
- Article
Association of Longitudinal Activity Measures and Diabetes Risk: An Analysis From the National Institutes of Health All of Us Research Program.
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- Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 5, p. 1101, doi. 10.1210/clinem/dgac695
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- Publication type:
- Article
Daily Step Counts Before and After the COVID-19 Pandemic Among All of Us Research Participants.
- Published in:
- JAMA Network Open, 2023, v. 6, n. 3, p. e233526, doi. 10.1001/jamanetworkopen.2023.3526
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- Publication type:
- Article
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
- Published in:
- European Heart Journal, 2022, v. 43, n. 45, p. 4707, doi. 10.1093/eurheartj/ehac322
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- Article
Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update.
- Published in:
- Clinical Pharmacology & Therapeutics, 2022, v. 112, n. 5, p. 959, doi. 10.1002/cpt.2526
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- Article
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27751-1
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- Publication type:
- Article
Loperamide Induced Recurrent Torsades de Pointes: A Case Report.
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- Journal of Pharmacy Practice, 2022, v. 35, n. 5, p. 791, doi. 10.1177/08971900211004832
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- Article
A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
- Published in:
- 2022
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- Publication type:
- journal article
Frequency of benign neutropenia among Black versus White individuals undergoing a bone marrow assessment.
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- Journal of Cellular & Molecular Medicine, 2022, v. 26, n. 13, p. 3628, doi. 10.1111/jcmm.17346
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- Article
Genetic Determinants of Body Mass Index and Fasting Glucose Are Mediators of Grade 1 Diastolic Dysfunction.
- Published in:
- 2022
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- Publication type:
- journal article
The 3D mutational constraint on amino acid sites in the human proteome.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30936-x
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- Publication type:
- Article
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin‐Associated Musculoskeletal Symptoms.
- Published in:
- Clinical Pharmacology & Therapeutics, 2022, v. 111, n. 5, p. 1007, doi. 10.1002/cpt.2557
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- Publication type:
- Article
Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel Na V 1.5.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 4, p. 2225, doi. 10.3390/ijms23042225
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- Publication type:
- Article
Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27751-1
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- Publication type:
- Article
Phenome-Wide Association Studies.
- Published in:
- JAMA: Journal of the American Medical Association, 2022, v. 327, n. 1, p. 75, doi. 10.1001/jama.2021.20356
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- Publication type:
- Article
Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance study.
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- European Heart Journal, 2021, v. 42, n. 38, p. 3915, doi. 10.1093/eurheartj/ehab362
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- Publication type:
- Article
Deep learning analysis of electrocardiogram for risk prediction of drug-induced arrhythmias and diagnosis of long QT syndrome.
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- European Heart Journal, 2021, v. 42, n. 38, p. 3948, doi. 10.1093/eurheartj/ehab588
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- Article
The Case for Expanding the FDA Box Warning on Clopidogrel to CYP2C19 Intermediate Metabolizers.
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- Clinical Pharmacology & Therapeutics, 2021, v. 110, n. 4, p. 860, doi. 10.1002/cpt.2215
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- Publication type:
- Article
Heart failure clinical care analysis uncovers risk reduction opportunities for preserved ejection fraction subtype.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97831-1
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- Publication type:
- Article
Recurrent Pregnancy Loss and Concealed Long-QT Syndrome.
- Published in:
- 2021
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- Publication type:
- journal article
Machine Learning Challenges in Pharmacogenomic Research.
- Published in:
- Clinical Pharmacology & Therapeutics, 2021, v. 110, n. 3, p. 552, doi. 10.1002/cpt.2329
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- Publication type:
- Article
Genome‐Wide Approach to Measure Variant‐Based Heritability of Drug Outcome Phenotypes.
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- Clinical Pharmacology & Therapeutics, 2021, v. 110, n. 3, p. 714, doi. 10.1002/cpt.2323
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- Publication type:
- Article
2-Hydroxybenzylamine (2-HOBA) to prevent early recurrence of atrial fibrillation after catheter ablation: protocol for a randomized controlled trial including detection of AF using a wearable device.
- Published in:
- 2021
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- Publication type:
- journal article
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
- Published in:
- 2021
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- Publication type:
- journal article
Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height.
- Published in:
- 2021
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- Publication type:
- journal article
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
- Published in:
- 2021
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- Publication type:
- journal article
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis.
- Published in:
- Lupus, 2021, v. 30, n. 8, p. 1264, doi. 10.1177/09612033211014952
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- Publication type:
- Article
High-throughput framework for genetic analyses of adverse drug reactions using electronic health records.
- Published in:
- PLoS Genetics, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pgen.1009593
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- Publication type:
- Article
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
- Published in:
- 2020
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- Publication type:
- journal article
Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis.
- Published in:
- Arthritis & Rheumatology, 2020, v. 72, n. 9, p. 1483, doi. 10.1002/art.41291
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- Article
Understanding the use of observational and randomized data in cardiovascular medicine.
- Published in:
- European Heart Journal, 2020, v. 41, n. 27, p. 2571, doi. 10.1093/eurheartj/ehaa020
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- Publication type:
- Article
A Bayesian method to estimate variant-induced disease penetrance.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 6, p. 1, doi. 10.1371/journal.pgen.1008862
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- Article
Leveraging Human Genetics to Identify Safety Signals Prior to Drug Marketing Approval and Clinical Use.
- Published in:
- 2020
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- Publication type:
- journal article
Development of a System for Postmarketing Population Pharmacokinetic and Pharmacodynamic Studies Using Real‐World Data From Electronic Health Records.
- Published in:
- Clinical Pharmacology & Therapeutics, 2020, v. 107, n. 4, p. 934, doi. 10.1002/cpt.1787
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- Publication type:
- Article
Atropine-induced sinus tachycardia protects against exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.
- Published in:
- 2020
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- Publication type:
- journal article
Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease.
- Published in:
- 2020
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- Publication type:
- journal article
John A. Oates: A Founding Father of Clinical Pharmacology.
- Published in:
- Clinical Pharmacology & Therapeutics, 2019, v. 106, n. 6, p. 1155, doi. 10.1002/cpt.1614
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- Publication type:
- Article
Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease.
- Published in:
- 2019
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- Publication type:
- journal article