Dana C. Crawford

Orcid: 0000-0002-6437-6248

According to our database1, Dana C. Crawford authored at least 35 papers between 2010 and 2021.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

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Online presence:

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Bibliography

2021
Computational Challenges and Artificial Intelligence in Precision Medicine.
Proceedings of the Biocomputing 2021: Proceedings of the Pacific Symposium, 2021

2020
Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return ofResearch Results at a Cleveland Public Hospital.
Proceedings of the Pacific Symposium on Biocomputing 2020, 2020

Session Introduction.
Proceedings of the Pacific Symposium on Biocomputing 2020, 2020

2019
Session introduction.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

2018
Local ancestry transitions modify snp-trait associations.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

Session Introduction.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

Integrating community-level data resources for precision medicine research.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018

2017
Session Introduction.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

Development and Performance of Text-Mining Algorithms to Extract Socioeconomic Status from De-Identified Electronic Health Records.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record.
Proceedings of the Summit on Clinical Research Informatics, 2017

2016
The detection and characterization of pleiotropy: discovery, progress, and promise.
Briefings Bioinform., 2016

The Challenges in Using Electronic Health Records for Pharmacogenomics and Precision Medicine Research.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Testing Population-Specific Quantitative Trait Associations for Clinical Outcome Relevance in a Biorepository Linked to Electronic Health Records: LPA and Myocardial Infarction in African Americans.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Kidney Disease Genetics and the Importance of Diversity in Precision Medicine.
Proceedings of the Biocomputing 2016: Proceedings of the Pacific Symposium, 2016

Searching in the Dark: Phenotyping Diabetic Retinopathy in a De-Identified Electronic Medical Record Sample of African Americans.
Proceedings of the Summit on Clinical Research Informatics, 2016

Drug-drug Interaction Profiles of Medication Regimens Extracted from a De-identified Electronic Medical Records System.
Proceedings of the Summit on Clinical Research Informatics, 2016

2015
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.
BioData Min., 2015

The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study.
BioData Min., 2015

Mitochondrial Variation and the Risk of Age-Related Macular Degeneration Across Diverse Populations.
Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015

Identification of Gene-Gene and Gene-Environment Interactions Within the Fibrinogen Gene Cluster for Fibrinogen Levels in Three Ethnically Diverse Populations.
Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015

Measures of Exposure Impact Genetic Association Studies: An Example in Vitamin K Levels and VKORC1.
Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015

2014
Extraction of echocardiographic data from the electronic medical record is a rapid and efficient method for study of cardiac structure and function.
J. Clin. Bioinform., 2014

SecureMA: protecting participant privacy in genetic association meta-analysis.
Bioinform., 2014

Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies.
BioData Min., 2014

Session introduction.
Proceedings of the Biocomputing 2014: Proceedings of the Pacific Symposium, 2014

Utilization of an EMR-Biorepository to Identify the Genetic Predictors of Calcineurin-Inhibitor Toxicity in Heart Transplant Recipients.
Proceedings of the Biocomputing 2014: Proceedings of the Pacific Symposium, 2014

Development of a Data-Mining Algorithm to Identify Ages at Reproductive Milestones in Electronic Medical Records.
Proceedings of the Biocomputing 2014: Proceedings of the Pacific Symposium, 2014

Replication of SCN5A Associations with Electrocardiographic Traits in African Americans from Clinical and Epidemiologic Studies.
Proceedings of the Applications of Evolutionary Computation - 17th European Conference, 2014

2013
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.
Bioinform., 2013

2012
Visually integrating and exploring high throughput Phenome-Wide Association Study (PheWAS) results using PheWAS-View.
BioData Min., 2012

Using PheWAS to Assess Pleiotropy of Genetic Risk Scores for Rheumatoid Arthritis and Coronary Artery Disease in the eMERGE Network.
Proceedings of the AMIA 2012, 2012

2011
Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin.
J. Am. Medical Informatics Assoc., 2011

Visual Integration of Results from a Large Dna Biobank (Biovu) Using Synthesis-View.
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011

2010
PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.
Bioinform., 2010

Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis.
BioData Min., 2010


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