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Pedro L. Teixeira

Researcher at Vanderbilt University

Publications -  11
Citations -  521

Pedro L. Teixeira is an academic researcher from Vanderbilt University. The author has contributed to research in topics: Genome-wide association study & Odds ratio. The author has an hindex of 8, co-authored 11 publications receiving 404 citations. Previous affiliations of Pedro L. Teixeira include Vanderbilt University Medical Center.

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Combining billing codes, clinical notes, and medications from electronic health records provides superior phenotyping performance.

TL;DR: Multiple EHR components provide a more consistent and higher performance than a single one for the selected phenotypes, and are suggested for future phenotyping design in order to obtain an ideal result.
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Genetic Risk Prediction of Atrial Fibrillation.

TL;DR: Comprehensive AF genetic risk scores were associated with incident AF beyond associations for clinical AF risk factors but offered small improvements in discrimination, and was associated with stroke in age- and sex-adjusted models.
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Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals

TL;DR: Phenotyping algorithms applied to electronic health record (EHR) data enable investigators to identify large cohorts for clinical and genomic research and shows that billing codes or blood pressure readings alone yield good hypertension classification performance.
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Benchmarking ligand-based virtual High-Throughput Screening with the PubChem database.

TL;DR: This work assembles nine data sets from realistic HTS campaigns representing major families of drug target proteins for benchmarking LB-CADD methods, and builds a new cheminformatics framework BCL::ChemInfo, which is freely available for non-commercial use.
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A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.

TL;DR: Results indicate that SNPs in KCNIP4 may modulate ACEi-induced cough risk, and identify associations on chromosome 4 in an intron of KCnIP4.