Found: 142
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Systematic replication of smoking disease associations using survey responses and EHR data in the All of Us Research Program.
- Published in:
- Journal of the American Medical Informatics Association, 2024, v. 31, n. 1, p. 139, doi. 10.1093/jamia/ocad205
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- Article
Data-driven science and diversity in the All of Us Research Program.
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- Science Translational Medicine, 2023, v. 15, n. 726, p. 1, doi. 10.1126/scitranslmed.ade9214
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- Article
Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-41185-x
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- Publication type:
- Article
Phenotype Risk Score but Not Genetic Risk Score Aids in Identifying Individuals With Systemic Lupus Erythematosus in the Electronic Health Record.
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- Arthritis & Rheumatology, 2023, v. 75, n. 9, p. 1532, doi. 10.1002/art.42544
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- Article
Population genetic testing and SERPINA1 sequencing identifies unidentified alpha-1 antitrypsin deficiency alleles and gene-environment interaction with hepatitis C infection.
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- PLoS ONE, 2023, v. 18, n. 8, p. 1, doi. 10.1371/journal.pone.0286469
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- Article
Drug‐Induced Liver Injury with Commonly Used Antibiotics in the All of Us Research Program.
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- Clinical Pharmacology & Therapeutics, 2023, v. 114, n. 2, p. 404, doi. 10.1002/cpt.2930
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- Article
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
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- PLoS ONE, 2023, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0283553
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- Article
Impact of COVID-19 on the All of Us Research Program.
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- American Journal of Epidemiology, 2023, v. 192, n. 1, p. 11, doi. 10.1093/aje/kwac169
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- Article
Genetically predicted sex hormone levels and health outcomes: phenome-wide Mendelian randomization investigation.
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- International Journal of Epidemiology, 2022, v. 51, n. 6, p. 1931, doi. 10.1093/ije/dyac036
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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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- Article
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30678-w
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- Article
Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach.
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- BMC Genomics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12864-022-08600-x
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- Article
Cox regression is robust to inaccurate EHR-extracted event time: an application to EHR-based GWAS.
- Published in:
- Bioinformatics, 2022, v. 38, n. 8, p. 2297, doi. 10.1093/bioinformatics/btac086
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- Publication type:
- Article
Antibodies to Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in All of Us Research Program Participants, 2 January to 18 March 2020.
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- Clinical Infectious Diseases, 2022, v. 74, n. 4, p. 584, doi. 10.1093/cid/ciab519
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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.
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- JAMA: Journal of the American Medical Association, 2022, v. 327, n. 1, p. 75, doi. 10.1001/jama.2021.20356
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- Article
The U.S. National Library of Medicine's impact on precision and genomic medicine.
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- Information Services & Use, 2022, v. 42, n. 1, p. 71, doi. 10.3233/ISU-210144
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- Article
DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions.
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- 2021
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- Publication type:
- journal article
PheWAS-ME: a web-app for interactive exploration of multimorbidity patterns in PheWAS.
- Published in:
- Bioinformatics, 2021, v. 37, n. 12, p. 1778, doi. 10.1093/bioinformatics/btaa870
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- Publication type:
- Article
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes.
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- JAMA Network Open, 2021, v. 4, n. 6, p. e2112820, doi. 10.1001/jamanetworkopen.2021.12820
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- Article
Meeting the challenge: Health information technology's essential role in achieving precision medicine.
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- 2021
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- Publication type:
- journal 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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- Article
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
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- NPJ Digital Medicine, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s41746-021-00428-1
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- Publication type:
- Article
Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-020-00854-2
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- Publication type:
- Article
Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome.
- Published in:
- 2021
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- Publication type:
- journal article
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.
- Published in:
- PLoS Genetics, 2020, v. 16, n. 11, p. 1, doi. 10.1371/journal.pgen.1009077
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- Publication type:
- Article
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records.
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- 2020
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- Publication type:
- journal article
Diversity and inclusion for the All of Us research program: A scoping review.
- Published in:
- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0234962
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- Article
Leveraging Human Genetics to Identify Safety Signals Prior to Drug Marketing Approval and Clinical Use.
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- 2020
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- Publication type:
- journal article
Evaluating the Utility of Polygenic Risk Scores in Identifying High-Risk Individuals for Eight Common Cancers.
- Published in:
- JNCI Cancer Spectrum, 2020, v. 4, n. 3, p. 1, doi. 10.1093/jncics/pkaa021
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- Article
Development of a System for Postmarketing Population Pharmacokinetic and Pharmacodynamic Studies Using Real‐World Data From Electronic Health Records.
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- Clinical Pharmacology & Therapeutics, 2020, v. 107, n. 4, p. 934, doi. 10.1002/cpt.1787
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- Article
medExtractR: A targeted, customizable approach to medication extraction from electronic health records.
- Published in:
- 2020
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- Publication type:
- journal article
A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies.
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- 2020
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- Publication type:
- journal article
Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease.
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- 2019
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- Publication type:
- journal article
Cox regression increases power to detect genotype-phenotype associations in genomic studies using the electronic health record.
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- BMC Genomics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12864-019-6192-1
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- Article
Cost-aware active learning for named entity recognition in clinical text.
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- 2019
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- Publication type:
- journal article
Genetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study.
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- 2019
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- journal article
Phenome-wide Mendelian-randomization study of genetically determined vitamin D on multiple health outcomes using the UK Biobank study.
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- 2019
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- journal article
Genome‐Wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol.
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- Clinical Pharmacology & Therapeutics, 2019, v. 106, n. 3, p. 623, doi. 10.1002/cpt.1439
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- Article
A Decision-Theoretic Approach to Panel-Based, Preemptive Genotyping.
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- MDM Policy & Practice, 2019, v. 4, n. 2, p. N.PAG, doi. 10.1177/2381468319864337
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- Publication type:
- Article
Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA).
- Published in:
- PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0212112
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- Article
Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36745-x
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- Article
Phenome-Wide Association Studies Uncover a Novel Association of Increased Atrial Fibrillation in Male Patients With Systemic Lupus Erythematosus.
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- 2018
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- Publication type:
- journal article
Reply to Ward and Colleagues' Comment on "Using Human Experiments of Nature to Predict Drug Safety Issues: An Example with PCSK9 Inhibitors".
- Published in:
- 2018
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- Publication type:
- letter
Evaluating statistical approaches to leverage large clinical datasets for uncovering therapeutic and adverse medication effects.
- Published in:
- Bioinformatics, 2018, v. 34, n. 17, p. 2988, doi. 10.1093/bioinformatics/bty306
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- Publication type:
- Article
Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records.
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- 2018
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- Publication type:
- journal article
PregOMICS—Leveraging systems biology and bioinformatics for drug repurposing in maternal‐child health.
- Published in:
- American Journal of Reproductive Immunology, 2018, v. 80, n. 2, p. 1, doi. 10.1111/aji.12971
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- Article
A Phenome-Wide Association Study Uncovers a Role for Autoimmunity in the Development of Chronic Obstructive Pulmonary Disease.
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- American Journal of Respiratory Cell & Molecular Biology, 2018, v. 58, n. 6, p. 777, doi. 10.1165/rcmb.2017-0409le
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- Publication type:
- Article
Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects.
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- Clinical Pharmacology & Therapeutics, 2018, v. 103, n. 5, p. 778, doi. 10.1002/cpt.1048
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- Article
Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome.
- Published in:
- Clinical Pharmacology & Therapeutics, 2018, v. 103, n. 5, p. 787, doi. 10.1002/cpt.1035
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- Article