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Author Details
Full Name
Peggy L Peissig
Affiliation
Center for Precision Medicine Research, Marshfield Clinic Research Institute
ORCID
Career Start Year
1996
Papers
117
H Index
33
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37196047
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm.
PLoS One
2023
34991173
Ambiguous and Incomplete: Natural Language Processing Reveals Problematic Reporting Styles in Thyroid Ultrasound Reports.
Methods Inf Med
2022
35446370
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases.
JAMA Oncol
2022
35090449
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Med Inform Decis Mak
2022
34086673
Novel EDGE encoding method enhances ability to identify genetic interactions.
PLoS Genet
2021
33850243
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
NPJ Digit Med
2021
30414857
Novel locus for atopic dermatitis in African Americans and replication in European Americans.
J Allergy Clin Immunol
2019
31415684
Preliminary outcomes of preemptive warfarin pharmacogenetic testing at a large rural healthcare center.
Am J Health Syst Pharm
2019
31259012
Machine Learning Assisted Discovery of Novel Predictive Lab Tests Using Electronic Health Record Data.
AMIA Jt Summits Transl Sci Proc
2019
31258966
Comorbidity Characterization Among eMERGE Institutions: A Pilot Evaluation with the Johns Hopkins Adjusted Clinical Groups® System.
AMIA Jt Summits Transl Sci Proc
2019
31249589
A <i>Trans</i>-Ethnic Genome-Wide Association Study of Uterine Fibroids.
Front Genet
2019
31190122
Parathyroid hormone independently predicts fracture, vascular events, and death in patients with stage 3 and 4 chronic kidney disease.
Osteoporos Int
2019
30988330
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network.
Sci Rep
2019
30864329
Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network.
Pac Symp Biocomput
2019
31028874
Machine learning for phenotyping opioid overdose events.
J Biomed Inform
2019
31160809
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2019
30459343
Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling.
Genes Immun
2019
30547447
A Machine-Learning-Based Drug Repurposing Approach Using Baseline Regularization.
Methods Mol Biol
2019
30590574
Pharmacogenomic clinical decision support design and multi-site process outcomes analysis in the eMERGE Network.
J Am Med Inform Assoc
2019
27981563
Comparison of Outcomes Following a Switch From a Brand to an Authorized Versus Independent Generic Drug.
Clin Pharmacol Ther
2018
29888059
Using Machine Learning Algorithms to Predict Risk for Development of Calciphylaxis in Patients with Chronic Kidney Disease.
AMIA Jt Summits Transl Sci Proc
2018
30124903
A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.
J Am Med Inform Assoc
2018
30232743
Authors' Reply to Courtney Suggs and Colleagues' Comment on: "Mixed Approach Retrospective Analyses of Suicide and Suicidal Ideation for Brand Compared with Generic Central Nervous System Drugs".
Drug Saf
2018
29876376
MCIndoor20000: A fully-labeled image dataset to advance indoor objects detection.
Data Brief
2018
30166544
A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers.
Nat Commun
2018
31355361
Temporal Poisson Square Root Graphical Models.
Proc Mach Learn Res
2018
30815167
Improving breast cancer risk prediction by using demographic risk factors, abnormality features on mammograms and genetic variants.
AMIA Annu Symp Proc
2018
29703846
LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins.
Circulation
2018
29549330
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29549329
Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29706685
Quantifying predictive capability of electronic health records for the most harmful breast cancer.
Proc SPIE Int Soc Opt Eng
2018
29273807
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Nat Genet
2018
29196989
Mixed Approach Retrospective Analyses of Suicide and Suicidal Ideation for Brand Compared with Generic Central Nervous System Drugs.
Drug Saf
2018
29092097
Brand vs generic adverse event reporting patterns: An authorized generic-controlled evaluation of cardiovascular medications.
J Clin Pharm Ther
2018
27497800
Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals.
J Am Med Inform Assoc
2017
28222112
Genome-wide study of resistant hypertension identified from electronic health records.
PLoS One
2017
28152215
Comparison of Generic-to-Brand Switchback Rates Between Generic and Authorized Generic Drugs.
Pharmacotherapy
2017
28146470
Rare and low-frequency coding variants alter human adult height.
Nature
2017
28416512
Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes.
Circ Cardiovasc Genet
2017
29755826
Pharmacovigilance via Baseline Regularization with Large-Scale Longitudinal Observational Data.
KDD
2017
29079728
PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.
Nat Commun
2017
29222076
Adverse Drug Event Discovery Using Biomedical Literature: A Big Data Neural Network Adventure.
JMIR Med Inform
2017
28903894
Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.
JMIR Med Inform
2017
28641219
Comparison of brand versus generic antiepileptic drug adverse event reporting rates in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS).
Epilepsy Res
2017
28933038
Methodological Considerations for Comparison of Brand Versus Generic Versus Authorized Generic Adverse Event Reports in the US Food and Drug Administration Adverse Event Reporting System (FAERS).
Clin Drug Investig
2017
27611488
Identification of Four Novel Loci in Asthma in European American and African American Populations.
Am J Respir Crit Care Med
2017
27899403
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.
Circ Res
2017
27026615
PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability.
J Am Med Inform Assoc
2016
28316874
Computational Drug Repositioning Using Continuous Self-Controlled Case Series.
KDD
2016
28392671
Baseline Regularization for Computational Drug Repositioning with Longitudinal Observational Data.
IJCAI (U S)
2016
1 - 50 of 117
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Cornell University
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James G Linneman
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