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List of works by David S Carrell

A Robust e-Epidemiology Tool in Phenotyping Heart Failure with Differentiation for Preserved and Reduced Ejection Fraction: the Electronic Medical Records and Genomics (eMERGE) Network

scientific article

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

scientific article published in Nature Communications

An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.

scientific article

Assessment of a combined testing strategy for detection of antibodies to human herpesvirus 8 (HHV-8) in persons with Kaposi's sarcoma, persons with asymptomatic HHV-8 infection, and persons at low risk for HHV-8 infection

scientific article

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

scientific article published on January 2016

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

scientific article published on 01 January 2020

C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease

scientific article published on June 2013

Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40.

scientific article

Clinical documentation of patient-reported medical cannabis use in primary care: Toward scalable extraction using natural language processing methods

scientific article published on 01 January 2022

Coding variants in TREM2 increase risk for Alzheimer's disease

scientific article

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

scientific article

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

scientific article published on 24 July 2017

Facilitating phenotype transfer using a common data model

scientific article published on 17 July 2019

GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease

scientific article

Genetic studies of plasma analytes identify novel potential biomarkers for several complex traits.

scientific article

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

scientific article

Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers

scientific article published on 28 February 2017

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

scientific article

Identifying and classifying opioid-related overdoses: A validation study

scientific article published on 24 April 2019

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

scientific article

Measuring problem prescription opioid use among patients receiving long-term opioid analgesic treatment: development and evaluation of an algorithm for use in EHR and claims data

scientific article published on 28 April 2020

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

scientific article

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

scientific article

Natural history of genital herpes simplex virus type 1 infection

scientific article

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

scientific article published on 28 November 2016

Parkinson disease is not associated with C9ORF72 repeat expansions

scientific article published on 30 October 2012

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

scientific article

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

scientific article

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

scientific article

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

scientific article

Polymerase chain reaction for detection of herpes simplex virus (HSV) DNA on mucosal surfaces: comparison with HSV isolation in cell culture

scientific article published on 31 October 2003

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

scientific article

Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease

scientific article

Role of ABCA7 loss-of-function variant in Alzheimer's disease: a replication study in European-Americans

scientific article

SORL1 variants across Alzheimer's disease European American cohorts

scientific article published on 21 September 2016

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

scientific article

TREM2 is associated with increased risk for Alzheimer's disease in African Americans

scientific article published on 10 April 2015

The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers

scientific article

The machine giveth and the machine taketh away: a parrot attack on clinical text deidentified with hiding in plain sight

scientific article published on 01 December 2019

The phenotypic legacy of admixture between modern humans and Neandertals

scientific article

Two-day regimen of acyclovir for treatment of recurrent genital herpes simplex virus type 2 infection

scientific article published on 20 February 2002

Using natural language processing of clinical text to enhance identification of opioid-related overdoses in electronic health records data

scientific article published on 19 June 2019

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

scientific article

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