Henry R. Kranzler
According to our database1,
Henry R. Kranzler
authored at least 10 papers
between 2012 and 2022.
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Bibliography
2022
BioData Min., 2022
2020
Identifying Clinical Risk Factors for Opioid Use Disorder using a Distributed Algorithm to Combine Real-World Data from a Large Clinical Data Research Network.
Proceedings of the AMIA 2020, 2020
2017
Collaborative phenotype inference from comorbid substance use disorders and genotypes.
Proceedings of the 2017 IEEE International Conference on Bioinformatics and Biomedicine, 2017
2014
Multiview Comodeling to Improve Subtyping and Genetic Association of Complex Diseases.
IEEE J. Biomed. Health Informatics, 2014
BMC Bioinform., 2014
Identifying heritable composite traits from multivariate phenotypes and genome-wide SNPs.
Proceedings of the 2014 IEEE International Conference on Bioinformatics and Biomedicine, 2014
2013
Quadratic optimization to identify highly heritable quantitative traits from complex phenotypic features.
Proceedings of the 19th ACM SIGKDD International Conference on Knowledge Discovery and Data Mining, 2013
Multi-view biclustering for genotype-phenotype association studies of complex diseases.
Proceedings of the 2013 IEEE International Conference on Bioinformatics and Biomedicine, 2013
2012
Bioinform., 2012
A multi-objective program for quantitative subtyping of clinically relevant phenotypes.
Proceedings of the 2012 IEEE International Conference on Bioinformatics and Biomedicine, 2012