Iftikhar J. Kullo
Orcid: 0000-0002-6524-3471
According to our database1,
Iftikhar J. Kullo
authored at least 28 papers
between 2010 and 2024.
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Bibliography
2024
Effect of clinical decision support for severe hypercholesterolemia on low-density lipoprotein cholesterol levels.
npj Digit. Medicine, 2024
2023
J. Am. Medical Informatics Assoc., February, 2023
2022
Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions.
BMC Medical Informatics Decis. Mak., 2022
2021
Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies.
npj Digit. Medicine, 2021
J. Biomed. Informatics, 2021
Patient Perspectives on 'FH Family Share, ' a Tool to Increase Uptake of Cascade Testing for Familial Hypercholesterolemia.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
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
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
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
Proceedings of the MEDINFO 2015: eHealth-enabled Health, 2015
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
A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project.
Proceedings of the AMIA 2014, 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