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List of works by Jennifer A Pacheco

A Machine Learning Algorithm for Identifying Atopic Dermatitis in Adults from Electronic Health Records

scientific article published on 01 August 2017

A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids.

scientific article published on 12 June 2019

A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments

scientific article published on 01 November 2018

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

scientific article published on 12 September 2013

A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough

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A multi-institution evaluation of clinical profile anonymization

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A rigorous algorithm to detect and clean inaccurate adult height records within EHR systems.

scientific article published on 19 February 2014

A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers

scientific article published in Nature Communications

Accuracy of phenotyping chronic rhinosinusitis in the electronic health record.

scientific article published on March 2014

Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans

scientific article

Adverse events after surgery for nonmalignant colon polyps are common and associated with increased length of stay and costs.

scientific article published on 29 January 2016

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans

scientific article published on March 2017

Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

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Cortical thickness is influenced by regionally specific genetic factors

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Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical Data

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Desiderata for computable representations of electronic health records-driven phenotype algorithms

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Desiderata for the development of next-generation electronic health record phenotype libraries

scientific article published on 01 September 2021

Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems

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Design patterns for the development of electronic health record-driven phenotype extraction algorithms

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Electronic medical records for genetic research: results of the eMERGE consortium

scientific article published on April 2011

Elevated incidence of fractures in women with invasive breast cancer.

scientific article published on 21 August 2015

Factors Associated With Long-Term Weight Loss Following Bariatric Surgery Using 2 Methods for Repeated Measures Analysis

scientific article published on 18 June 2015

Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans

scientific article published on 28 March 2013

Genetic and environmental contributions to regional cortical surface area in humans: a magnetic resonance imaging twin study

scientific article published on 4 March 2011

Genetic and environmental influences on the size of specific brain regions in midlife: the VETSA MRI study

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Genetic patterns of correlation among subcortical volumes in humans: results from a magnetic resonance imaging twin study

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Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network

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Genetic variation in the HLA region is associated with susceptibility to herpes zoster

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

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High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE

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Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)

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Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus

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Investigating the Genetic Architecture of the PR Interval Using Clinical Phenotypes

scientific article published on April 2017

LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data

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Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

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Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network

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Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies

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PheKB: a catalog and workflow for creating electronic phenotype algorithms for transportability

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Portability of an algorithm to identify rheumatoid arthritis in electronic health records.

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Predicting the location of entorhinal cortex from MRI.

scientific article published on 16 April 2009

Probing the Virtual Proteome to Identify Novel Disease Biomarkers

scientific article published on 01 November 2018

Prototype Development: Context-Driven Dynamic XML Ophthalmologic Data Capture Application.

scientific article published on 13 September 2017

Regional white matter volume differences in nondemented aging and Alzheimer's disease

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Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies

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Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

scientific article published on 14 July 2016

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data

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The power of genetic diversity in genome-wide association studies of lipids

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

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Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study

scientific article published on 19 November 2011

Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network

scientific article published on 26 March 2013

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

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rs4771122 Predicts Multiple Measures of Long-Term Weight Loss After Bariatric Surgery

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