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 21 papers between 2006 and 2018.

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

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

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
An Integrative Pipeline for Multi-Modal Discovery of Disease Relationships.
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

Matching Cancer Genomes to Established Cell Lines for Personalized Oncology.
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

Content-based microarray search using differential expression profiles.
BMC Bioinform., 2010

2009
Ontology-driven indexing of public datasets for translational bioinformatics.
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


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