Rong Chen
Affiliations:- Stanford University School of Medicine, Stanford, USA
- Lucile Packard Children's Hospital, Palo Alto, USA
According to our database1,
Rong Chen
authored at least 25 papers
between 2006 and 2021.
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Bibliography
2021
Applying Bayesian hyperparameter optimization towards accurate and efficient topic modeling in clinical notes.
Proceedings of the 9th IEEE International Conference on Healthcare Informatics, 2021
The Real-World Trend Analysis of Cancer Drugs Empowered by Natural Language Processing.
Proceedings of the AMIA 2021, American Medical Informatics Association Annual Symposium, San Diego, CA, USA, October 30, 2021, 2021
2020
DxTree: a visual analytics tool for hierarchical representation of disease cohort counts for clinical trials.
Proceedings of the AMIA 2020, 2020
2018
Systematic analyses of drugs and disease indications in RepurposeDB reveal pharmacological, biological and epidemiological factors influencing drug repositioning.
Briefings Bioinform., 2018
Loss-of-function of neuroplasticity-related genes confers risk for human neurodevelopmental disorders.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018
Automated disease cohort selection using word embeddings from Electronic Health Records.
Proceedings of the Biocomputing 2018: Proceedings of the Pacific Symposium, 2018
2017
Identify Cancer Driver Genes Through Shared Mendelian Disease Pathogenic Variants and Cancer Somatic Mutations.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017
2016
Integrating 400 million variants from 80, 000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts.
BMC Bioinform., 2016
Comparative analyses of population-scale phenomic data in electronic medical records reveal race-specific disease networks.
Bioinform., 2016
DIVAS: a centralized genetic variant repository representing 150 000 individuals from multiple disease cohorts.
Bioinform., 2016
2015
Proceedings of the Biocomputing 2015: Proceedings of the Pacific Symposium, 2015
2013
Systematic Identification of Risk Factors for Alzheimer's Disease Through Shared Genetic Architecture and Electronic Medical Records.
Proceedings of the Biocomputing 2013: Proceedings of the Pacific Symposium, 2013
2012
Integrative Approach to Pain Genetics Identifies Pain Sensitivity Loci across Diseases.
PLoS Comput. Biol., 2012
Clinical utility of sequence-based genotype compared with that derivable from genotyping arrays.
J. Am. Medical Informatics Assoc., 2012
Data-driven integration of epidemiological and toxicological data to select candidate interacting genes and environmental factors in association with disease.
Bioinform., 2012
2011
ProfileChaser: searching microarray repositories based on genome-wide patterns of differential expression.
Bioinform., 2011
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011
The Reference Human Genome Demonstrates High Risk of Type 1 Diabetes and Other Disorders.
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011
2010
Network-Based Elucidation of Human Disease Similarities Reveals Common Functional Modules Enriched for Pluripotent Drug Targets.
PLoS Comput. Biol., 2010
Differentially Expressed RNA from Public Microarray Data Identifies Serum Protein Biomarkers for Cross-Organ Transplant Rejection and Other Conditions.
PLoS Comput. Biol., 2010
BMC Bioinform., 2010
2009
BMC Bioinform., 2009
2008
GeneChaser: Identifying all biological and clinical conditions in which genes of interest are differentially expressed.
BMC Bioinform., 2008
2007
Methodologies for Extracting Functional Pharmacogenomic Experiments from International Repository.
Proceedings of the AMIA 2007, 2007
2006
Finding Disease-Related Genomic Experiments Within an International Repository: First Steps in Translational Bioinformatics.
Proceedings of the AMIA 2006, 2006