Author details

Full Name

Ruowang Li

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37038201	Automated quantitative trait locus analysis (AutoQTL).	BioData Min	2023
37443040	ChatGPT and large language models in academia: opportunities and challenges.	BioData Min	2023
36541009	Risk prediction: Methods, Challenges, and Opportunities.	Pac Symp Biocomput	2023
33420026	Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.	Nat Commun	2021
33936514	Statistical Impact of Sample Size and Imbalance on Multivariate Analysis <i>in silico</i> and A Case Study in the UK Biobank.	AMIA Annu Symp Proc	2021
32235907	Electronic health records and polygenic risk scores for predicting disease risk.	Nat Rev Genet	2020
31797639	Robust-ODAL: Learning from heterogeneous health systems without sharing patient-level data.	Pac Symp Biocomput	2020
31329892	Integration of genetic and clinical information to improve imputation of data missing from electronic health records.	J Am Med Inform Assoc	2019
29795408	Integration of genetic and functional genomics data to uncover chemotherapeutic induced cytotoxicity.	Pharmacogenomics J	2019
29713383	Collective feature selection to identify crucial epistatic variants.	BioData Min	2018
28040685	Using knowledge-driven genomic interactions for multi-omics data analysis: metadimensional models for predicting clinical outcomes in ovarian carcinoma.	J Am Med Inform Assoc	2017
28612644	Methods to analyze big data in pharmacogenomics research.	Pharmacogenomics	2017
27168765	Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network.	BioData Min	2016
26776200	BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN.	Pac Symp Biocomput	2016
26048077	Predicting censored survival data based on the interactions between meta-dimensional omics data in breast cancer.	J Biomed Inform	2015
25592572	Binning somatic mutations based on biological knowledge for predicting survival: an application in renal cell carcinoma.	Pac Symp Biocomput	2015
25582081	Methods of integrating data to uncover genotype-phenotype interactions.	Nat Rev Genet	2015
25214892	Knowledge-driven genomic interactions: an application in ovarian cancer.	BioData Min	2014
24359638	ATHENA: Identifying interactions between different levels of genomic data associated with cancer clinical outcomes using grammatical evolution neural network.	BioData Min	2013
22196727	Mbd3/NURD complex regulates expression of 5-hydroxymethylcytosine marked genes in embryonic stem cells.	Cell	2011
21183072	Paternally induced transgenerational environmental reprogramming of metabolic gene expression in mammals.	Cell	2010
19522486	Stability study of PbSe semiconductor nanocrystals over concentration, size, atmosphere, and light exposure.	Langmuir	2009