Katherine P. Liao

Orcid: 0000-0002-4797-3200

According to our database1, Katherine P. Liao authored at least 26 papers between 2012 and 2024.

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

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2024
LATTE: Label-efficient incident phenotyping from longitudinal electronic health records.
Patterns, January, 2024

Centralized Interactive Phenomics Resource: an integrated online phenomics knowledgebase for health data users.
J. Am. Medical Informatics Assoc., 2024

2023
Semi-supervised calibration of noisy event risk (SCANER) with electronic health records.
J. Biomed. Informatics, August, 2023

Framework of the Centralized Interactive Phenomics Resource (CIPHER) standard for electronic health data-based phenomics knowledgebase.
J. Am. Medical Informatics Assoc., April, 2023

Multimodal representation learning for predicting molecule-disease relations.
Bioinform., February, 2023

2022
Multiview Incomplete Knowledge Graph Integration with application to cross-institutional EHR data harmonization.
J. Biomed. Informatics, 2022

Scalable relevance ranking algorithm via semantic similarity assessment improves efficiency of medical chart review.
J. Biomed. Informatics, 2022

Binary acronym disambiguation in clinical notes from electronic health records with an application in computational phenotyping.
Int. J. Medical Informatics, 2022

Knowledge-Driven Online Multimodal Automated Phenotyping System.
Proceedings of the AMIA 2022, 2022

2021
Clinical knowledge extraction via sparse embedding regression (KESER) with multi-center large scale electronic health record data.
npj Digit. Medicine, 2021

ATLAS: an automated association test using probabilistically linked health records with application to genetic studies.
J. Am. Medical Informatics Assoc., 2021

2019
EXTraction of EMR numerical data: an efficient and generalizable tool to EXTEND clinical research.
BMC Medical Informatics Decis. Mak., 2019

Automated grouping of medical codes via multiview banded spectral clustering.
J. Biomed. Informatics, 2019

Feature extraction for phenotyping from semantic and knowledge resources.
J. Biomed. Informatics, 2019

High-throughput multimodal automated phenotyping (MAP) with application to PheWAS.
J. Am. Medical Informatics Assoc., 2019

2018
Enabling phenotypic big data with PheNorm.
J. Am. Medical Informatics Assoc., 2018

PheProb: probabilistic phenotyping using diagnosis codes to improve power for genetic association studies.
J. Am. Medical Informatics Assoc., 2018

High-Throughput Multimodal Automated Phenotyping (MAP) Incorporating Natural Language Processing with Application to PheWAS.
Proceedings of the AMIA 2018, 2018

2017
Surrogate-assisted feature extraction for high-throughput phenotyping.
J. Am. Medical Informatics Assoc., 2017

High-throughput Phenotyping via Denoised Normal Mixture Transformation.
Proceedings of the AMIA 2017, 2017

Improving EHR Chart Review Efficiency via Semantic Similarity Assessment.
Proceedings of the AMIA 2017, 2017

2015
Toward high-throughput phenotyping: unbiased automated feature extraction and selection from knowledge sources.
J. Am. Medical Informatics Assoc., 2015

Demonstrating the Advantages of Applying Data Mining Techniques on Time-Dependent Electronic Medical Records.
Proceedings of the AMIA 2015, 2015

2014
PheWAS and Genetics Define Subphenotypes in Drug Response.
Proceedings of the AMIA 2014, 2014

2012
Portability of an algorithm to identify rheumatoid arthritis in electronic health records.
J. Am. Medical Informatics Assoc., 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


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