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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

American journal of human genetics, 2010-04, Vol.86 (4), p.560-572

2010

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Epidemiology of atrial fibrillation in the All of Us Research Program

PloS one, 2022-03, Vol.17 (3), p.e0265498

2022

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Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey

Journal of personalized medicine, 2018-07, Vol.8 (3), p.24

2018

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Examining sociodemographic correlates of opioid use, misuse, and use disorders in the All of Us Research Program

PloS one, 2023-08, Vol.18 (8), p.e0290416-e0290416

2023

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Exome Sequencing Implicates an Increased Burden of Rare Potassium Channel Variants in the Risk of Drug-Induced Long QT Interval Syndrome

Journal of the American College of Cardiology, 2014-04, Vol.63 (14), p.1430-1437

2014

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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

American journal of human genetics, 2011-10, Vol.89 (4), p.529-542

2011

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Measuring social determinants of health in the All of Us Research Program

Scientific reports, 2024-04, Vol.14 (1), p.8815-8815, Article 8815

2024

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Geographic Variation in Obesity at the State Level in the All of Us Research Program

Preventing chronic disease, 2021-12, Vol.18, p.E104-E104, Article 210094

2021

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Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record

Pharmacogenomics, 2012-03, Vol.13 (4), p.407-418

2012

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Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions

BMC medical informatics and decision making, 2022-01, Vol.22 (1), p.23-23, Article 23

2022

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Modulators of normal electrocardiographic intervals identified in a large electronic medical record

Heart rhythm, 2011-02, Vol.8 (2), p.271-277

2011

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Building evidence and measuring clinical outcomes for genomic medicine

The Lancet (British edition), 2019-08, Vol.394 (10198), p.604-610

2019

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Phenotype risk scores identify patients with unrecognized Mendelian disease patterns

Science (American Association for the Advancement of Science), 2018-03, Vol.359 (6381), p.1233-1239

2018

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Genome- and Phenome-Wide Analyses of Cardiac Conduction Identifies Markers of Arrhythmia Risk

Circulation (New York, N.Y.), 2013-04, Vol.127 (13), p.1377-1385

2013

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Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program

Journal of the American Medical Informatics Association : JAMIA, 2021-03, Vol.28 (4), p.695-703

2021

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Identification of Genomic Predictors of Atrioventricular Conduction: Using Electronic Medical Records as a Tool for Genome Science

Circulation (New York, N.Y.), 2010-11, Vol.122 (20), p.2016-2021

2010

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Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single‐Patient Data Meta‐Analysis in More Than 15,000 Individuals

Clinical pharmacology and therapeutics, 2019-06, Vol.105 (6), p.1477-1491

2019

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Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort

Scientific reports, 2022-11, Vol.12 (1), p.19797-19797, Article 19797

2022

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Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine Disorders

The journal of clinical endocrinology and metabolism, 2018-06, Vol.103 (6), p.2234-2243

2018

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Hypertension prevalence in the All of Us Research Program among groups traditionally underrepresented in medical research

Scientific reports, 2021-06, Vol.11 (1), p.12849-12849, Article 12849

2021

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Achieving a Representative Sample of Asian Americans in Biomedical Research Through Community-Based Approaches: Comparing Demographic Data in the All of Us Research Program With the American Community Survey

Journal of transcultural nursing, 2023-01, Vol.34 (1), p.59-67

2023

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Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy

Circulation. Cardiovascular genetics, 2013-08, Vol.6 (4), p.317

2013

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Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin

Journal of the American Medical Informatics Association : JAMIA, 2011-07, Vol.18 (4), p.387-391

2011

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Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record

Epidemiology of atrial fibrillation in the All of Us Research Program

Physician-Reported Benefits and Barriers to Clinical Implementation of Genomic Medicine: A Multi-Site IGNITE-Network Survey

Examining sociodemographic correlates of opioid use, misuse, and use disorders in the All of Us Research Program

Exome Sequencing Implicates an Increased Burden of Rare Potassium Channel Variants in the Risk of Drug-Induced Long QT Interval Syndrome

Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Measuring social determinants of health in the All of Us Research Program

Genome-wide study of resistant hypertension identified from electronic health records

Interactions between genetic variation and cellular environment in skeletal muscle gene expression

Geographic Variation in Obesity at the State Level in the All of Us Research Program

Predicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record

Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions

Modulators of normal electrocardiographic intervals identified in a large electronic medical record

Building evidence and measuring clinical outcomes for genomic medicine

Phenotype risk scores identify patients with unrecognized Mendelian disease patterns

Genome- and Phenome-Wide Analyses of Cardiac Conduction Identifies Markers of Arrhythmia Risk

Comparison of family health history in surveys vs electronic health record data mapped to the observational medical outcomes partnership data model in the All of Us Research Program

Identification of Genomic Predictors of Atrioventricular Conduction: Using Electronic Medical Records as a Tool for Genome Science

Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single‐Patient Data Meta‐Analysis in More Than 15,000 Individuals

Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort

Rare Variants in the Gene ALPL That Cause Hypophosphatasia Are Strongly Associated With Ovarian and Uterine Disorders

Hypertension prevalence in the All of Us Research Program among groups traditionally underrepresented in medical research

Achieving a Representative Sample of Asian Americans in Biomedical Research Through Community-Based Approaches: Comparing Demographic Data in the All of Us Research Program With the American Community Survey

Whole exome sequencing identifies a causal RBM20 mutation in a large pedigree with familial dilated cardiomyopathy

Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin

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