Henry R. Kranzler

According to our database1, Henry R. Kranzler authored at least 10 papers between 2012 and 2022.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2022
Novel digital approaches to the assessment of problematic opioid use.
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

Ttn as a likely causal gene for QTL of alcohol preference on mouse chromosome 2.
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
M<sup>3</sup>: an improved SNP calling algorithm for Illumina BeadArray data.
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


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