Integration of genetic and clinical information to improve imputation of data missing from electronic health records

Por Li, Ruowang, Chen, Yong, Moore, Jason H
Publicado no J Am Med Inform Assoc (2019)

ATHENA: Identifying interactions between different levels of genomic data associated with cancer clinical outcomes using grammatical evolution neural network

Por Kim, Dokyoon, Li, Ruowang, Dudek, Scott M, Ritchie, Marylyn D
Publicado em 2013

Predicting censored survival data based on the interactions between meta-dimensional omics data in breast cancer

Por Kim, Dokyoon, Li, Ruowang, Dudek, Scott M., Ritchie, Marylyn D.
Publicado no J Biomed Inform (2015)

BINNING SOMATIC MUTATIONS BASED ON BIOLOGICAL KNOWLEDGE FOR PREDICTING SURVIVAL: AN APPLICATION IN RENAL CELL CARCINOMA

Por Kim, Dokyoon, Li, Ruowang, Dudek, Scott M., Wallace, John R., Ritchie, Marylyn D.
Publicado no Pac Symp Biocomput (2015)

Using knowledge-driven genomic interactions for multi-omics data analysis: metadimensional models for predicting clinical outcomes in ovarian carcinoma

Por Kim, Dokyoon, Li, Ruowang, Lucas, Anastasia, Verma, Shefali S, Dudek, Scott M, Ritchie, Marylyn D
Publicado no J Am Med Inform Assoc (2017)

Robust-ODAL: Learning from heterogeneous health systems without sharing patient-level data

Por Tong, Jiayi, Duan, Rui, Li, Ruowang, Scheuemie, Martijn J., Moore, Jason H., Chen, Yong
Publicado no Pac Symp Biocomput (2020)

Knowledge-driven genomic interactions: an application in ovarian cancer

Por Kim, Dokyoon, Li, Ruowang, Dudek, Scott M, Frase, Alex T, Pendergrass, Sarah A, Ritchie, Marylyn D
Publicado em 2014

A regression framework to uncover pleiotropy in large-scale electronic health record data

Por Li, Ruowang, Duan, Rui, Kember, Rachel L, Rader, Daniel J, Damrauer, Scott M, Moore, Jason H, Chen, Yong
Publicado no J Am Med Inform Assoc (2019)

Mbd3/NURD complex regulates expression of 5-hydroxymethylcytosine marked genes in embryonic stem cells

Por Yildirim, Ozlem, Li, Ruowang, Hung, Jui-Hung, Chen, Poshen B., Dong, Xianjun, Ee, Ly-sha, Weng, Zhiping, Rando, Oliver J., Fazzio, Thomas G.
Publicado em 2011

BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN

Por KIM, DOKYOON, LUCAS, ANASTASIA, GLESSNER, JOSEPH, VERMA, SHEFALI S., BRADFORD, YUKI, LI, RUOWANG, FRASE, ALEX T., HAKONARSON, HAKON, PEISSIG, PEGGY, BRILLIANT, MURRAY, RITCHIE, MARYLYN D.
Publicado no Pac Symp Biocomput (2016)

Collective feature selection to identify crucial epistatic variants

Por Verma, Shefali S., Lucas, Anastasia, Zhang, Xinyuan, Veturi, Yogasudha, Dudek, Scott, Li, Binglan, Li, Ruowang, Urbanowicz, Ryan, Moore, Jason H., Kim, Dokyoon, Ritchie, Marylyn D.
Publicado no BioData Min (2018)

Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network

Por Li, Ruowang, Dudek, Scott M., Kim, Dokyoon, Hall, Molly A., Bradford, Yuki, Peissig, Peggy L., Brilliant, Murray H., Linneman, James G., McCarty, Catherine A., Bao, Le, Ritchie, Marylyn D.
Publicado no BioData Min (2016)

Paternally-induced transgenerational environmental reprogramming of metabolic gene expression in mammals

Por Carone, Benjamin R., Fauquier, Lucas, Habib, Naomi, Shea, Jeremy M., Hart, Caroline E., Li, Ruowang, Bock, Christoph, Li, Chengjian, Zamore, Phillip D., Meissner, Alexander, Weng, Zhiping, Hofmann, Hans A., Friedman, Nir, Rando, Oliver J.
Publicado em 2010

Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics

Por Li, Ruowang, Duan, Rui, Zhang, Xinyuan, Lumley, Thomas, Pendergrass, Sarah, Bauer, Christopher, Hakonarson, Hakon, Carrell, David S., Smoller, Jordan W., Wei, Wei-Qi, Carroll, Robert, Velez Edwards, Digna R., Wiesner, Georgia, Sleiman, Patrick, Denny, Josh C., Mosley, Jonathan D., Ritchie, Marylyn D., Chen, Yong, Moore, Jason H.
Publicado no Nat Commun (2021)