Ning Shang

Orcid: 0000-0001-7040-5204

Affiliations:
  • Columbia University, New York, NY, USA


According to our database1, Ning Shang authored at least 22 papers between 2014 and 2023.

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

Timeline

Legend:

Book  In proceedings  Article  PhD thesis  Dataset  Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
Characterizing variability of electronic health record-driven phenotype definitions.
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

Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies.
npj Digit. Medicine, 2021

Similarity-based health risk prediction using Domain Fusion and electronic health records data.
J. Biomed. Informatics, 2021

Evaluation of Criteria2Query: Towards Augmented Intelligence for Cohort Identification.
Proceedings of the MEDINFO 2021: One World, One Health - Global Partnership for Digital Innovation, 2021

2020
Adapting electronic health records-derived phenotypes to claims data: Lessons learned in using limited clinical data for phenotyping.
J. Biomed. Informatics, 2020

A graph-based method for reconstructing entities from coordination ellipsis in medical text.
J. Am. Medical Informatics Assoc., 2020

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

Ensembles of natural language processing systems for portable phenotyping solutions.
J. Biomed. Informatics, 2019

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

Criteria2Query: a natural language interface to clinical databases for cohort definition.
J. Am. Medical Informatics Assoc., 2019

2018
A conceptual framework for evaluating data suitability for observational studies.
J. Am. Medical Informatics Assoc., 2018

The representativeness of eligible patients in type 2 diabetes trials: a case study using GIST 2.0.
J. Am. Medical Informatics Assoc., 2018

A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments.
J. Am. Medical Informatics Assoc., 2018

Effect of vocabulary mapping for conditions on phenotype cohorts.
J. Am. Medical Informatics Assoc., 2018

Low Screening Rates for Diabetes Mellitus Among Family Members of Affected Relatives.
Proceedings of the AMIA 2018, 2018

2016
The Applicability of an EHR Phenotype for Cohort Identification.
Proceedings of the Summit on Clinical Research Informatics, 2016

A Method for Enhancing the Portability of Electronic Phenotyping Algorithms: An eMERGE Pilot Study.
Proceedings of the AMIA 2016, 2016

Classification-by-Analogy: Using Vector Representations of Implicit Relationships to Identify Plausibly Causal Drug/Side-effect Relationships.
Proceedings of the AMIA 2016, 2016

2015
A Framework for Assessing Clinical Data Suitability for Observational Study.
Proceedings of the AMIA 2015, 2015

2014
Identifying Plausible Adverse Drug Reactions Using Knowledge Extracted from the Literature.
Proceedings of the AMIA 2014, 2014


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