Iftikhar J. Kullo

According to our database1, Iftikhar J. Kullo authored at least 22 papers between 2010 and 2020.

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Bibliography

2020
Integrating pharmacogenomics into the electronic health record by implementing genomic indicators.
J. Am. Medical Informatics Assoc., 2020

2019
Making work visible for electronic phenotype implementation: Lessons learned from the eMERGE network.
J. Biomed. Informatics, 2019

Facilitating phenotype transfer using a common data model.
J. Biomed. Informatics, 2019

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43, 870 individuals from the eMERGE network.
Proceedings of the Biocomputing 2019: Proceedings of the Pacific Symposium, 2019

Usability Evaluation of a Clinical Decision Support Tool for Management of Peripheral Artery Disease Patients.
Proceedings of the AMIA 2019, 2019

2018
Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
J. Am. Medical Informatics Assoc., 2018

Natural language processing of clinical notes for identification of critical limb ischemia.
Int. J. Medical Informatics, 2018

Leveraging the Electronic Health Record to Create an Automated Real-time Prognostic Tool for Peripheral Arterial Disease.
Proceedings of the AMIA 2018, 2018

2017
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
BioData Min., 2017

Mortality Prognostic Model for Peripheral Arterial Disease.
Proceedings of the Summit on Clinical Research Informatics, 2017

Surveillance of Peripheral Arterial Disease Cases Using Natural Language Processing of Clinical Notes.
Proceedings of the Summit on Clinical Research Informatics, 2017

Guideline Based Recommended Therapies in PAD Patients Identified by NLP: A Quality Assessment Project.
Proceedings of the AMIA 2017, 2017

Development & Implementation of a Clinical Decision Support Tool for Familial Hypercholesterolemia.
Proceedings of the AMIA 2017, 2017

2016
Identifying peripheral arterial disease cases using natural language processing of clinical notes.
Proceedings of the 2016 IEEE-EMBS International Conference on Biomedical and Health Informatics, 2016

2015

Public Implementation Resources for Genomic Medicine.
Proceedings of the AMIA 2015, 2015

Exploring Gaps of Family History Documentation in EHR for Precision Medicine - A Case Study of Familial Hypercholesterolemia Ascertainment.
Proceedings of the AMIA 2015, 2015

2014

2012
Gene expression profiling of peripheral blood mononuclear cells in the setting of peripheral arterial disease.
J. Clin. Bioinform., 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

2010
An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records.
J. Biomed. Informatics, 2010

Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease.
J. Am. Medical Informatics Assoc., 2010


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