Wendy K. Chung

Orcid: 0000-0003-3438-5685

According to our database1, Wendy K. Chung authored at least 9 papers between 2015 and 2024.

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

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
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Links

On csauthors.net:

Bibliography

2024
Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.
J. Am. Medical Informatics Assoc., January, 2024

2023
SHINE: protein language model-based pathogenicity prediction for short inframe insertion and deletion variants.
Briefings Bioinform., January, 2023

2022
Predicting functional effect of missense variants using graph attention neural networks.
Nat. Mac. Intell., November, 2022

Deep learning for rare disease: A scoping review.
J. Biomed. Informatics, 2022

2019
ORE identifies extreme expression effects enriched for rare variants.
Bioinform., 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

User engagement with web-based genomics education videos and implications for designing scalable patient education materials.
Proceedings of the AMIA 2019, 2019

Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants.
Proceedings of the AMIA 2019, 2019

2015
CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
J. Am. Medical Informatics Assoc., 2015


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