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Casey Ta

11PUBLICATIONS

83CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Bioinformatic methods developmentCorpus linguisticsDeep learningEpigenetics (incl. genome methylation and epigenomics)

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Publications (11)

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|Mar 23, 2026

Interpretable Fine-tuned Large Language Models Facilitate Making Genetic Test Decisions for Rare Diseases.

Quan M Nguyen, Fangyi Chen, Cong Liu

|Oct 27, 2025

Implementing integrated genomic risk assessments for breast cancer: lessons learned from the Electronic Medical Records and Genomics study.

Cong Liu, Katherine D Crew, Jennifer Morse

|Jul 10, 2025

Announcing the Biomedical Data Translator: Initial Public Release.

Karamarie Fecho, Gwênlyn Glusman, Sergio E Baranzini

|Nov 21, 2024

Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders.

Fangyi Chen, Priyanka Ahimaz, Quan M Nguyen

|Nov 09, 2024

Mini-mental status examination phenotyping for Alzheimer's disease patients using both structured and narrative electronic health record features.

Betina Idnay, Gongbo Zhang, Fangyi Chen

|Dec 04, 2023

Phenotype-Driven Molecular Genetic Test Recommendation for Diagnosing Pediatric Rare Disorders.

Fangyi Chen, Priyanka Ahimaz, Kai Wang

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Frequent Collaborators

8 joint publications

Chunhua Weng

5 joint publications

Cong Liu

3 joint publications

Karthik Natarajan

3 joint publications

Fangyi Chen

2 joint publications

Jason Zucker

2 joint publications

Jae Hyun Kim

2 joint publications

Gongbo Zhang

2 joint publications

Wendy K Chung

2 joint publications

Kai Wang

2 joint publications

Junghwan Lee

Frequent Collaborators

8 joint publications

Chunhua Weng

5 joint publications

Cong Liu

3 joint publications

Karthik Natarajan

3 joint publications

Fangyi Chen

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