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Murray H. Brilliant
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2020 – today
- 2022
- [j4]Arezoo Movaghar, David Page, Murray H. Brilliant, Marsha Mailick:
Advancing artificial intelligence-assisted pre-screening for fragile X syndrome. BMC Medical Informatics Decis. Mak. 22(1): 152 (2022) - 2021
- [j3]Ning Shang
, Atlas Khan, Fernanda Polubriaginof, Francesca Zanoni, Karla Mehl, David Fasel, Paul E. Drawz, Robert J. Carroll, Joshua C. Denny
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies. npj Digit. Medicine 4 (2021)
2010 – 2019
- 2018
- [j2]Xiayuan Huang
Applying family analyses to electronic health records to facilitate genetic research. Bioinform. 34(4): 635-642 (2018) - 2016
- [j1]Ruowang Li, Scott M. Dudek, Dokyoon Kim, Molly A. Hall, Yukiko Bradford, Peggy L. Peissig, Murray H. Brilliant, James G. Linneman, Catherine A. McCarty
Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network. BioData Min. 9: 18 (2016) - [c3]Anna Okula Basile, John R. Wallace, Peggy L. Peissig, Catherine A. McCarty, Murray H. Brilliant, Marylyn D. Ritchie:
Knowledge Driven Binning and PheWAS Analysis in Marshfield Personalized Medicine Research Project Using BioBin. PSB 2016: 249-260 - [c2]Dokyoon Kim, Anastasia Lucas, Joseph Glessner, Shefali S. Verma, Yukiko Bradford, Ruowang Li, Alex T. Frase, Hakon Hakonarson, Peggy L. Peissig, Murray H. Brilliant, Marylyn D. Ritchie:
Biofilter as a Functional Annotation Pipeline for Common and Rare Copy Number Burden. PSB 2016: 357-368 - 2014
- [c1]Shefali S. Verma, Peggy L. Peissig, Deanna S. Cross, Carol Waudby, Murray H. Brilliant, Catherine A. McCarty
Benefits of Accurate Imputations in GWAS. EvoApplications 2014: 877-889
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