Nicholas J. Schork

Orcid: 0000-0003-0920-5013

According to our database1, Nicholas J. Schork authored at least 17 papers between 1999 and 2023.

Collaborative distances:

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2023
A time-series analysis of blood-based biomarkers within a 25-year longitudinal dolphin cohort.
PLoS Comput. Biol., February, 2023

2020
Optimizing Aggregated N-Of-1 Trial Designs for Predictive Biomarker Validation: Statistical Methods and Theoretical Findings.
Frontiers Digit. Health, 2020

Editorial: Creating Evidence From Real World Patient Digital Data.
Frontiers Comput. Sci., 2020

2019
Artificial intelligence and machine learning in clinical development: a translational perspective.
npj Digit. Medicine, 2019

Rare variant phasing using paired tumor: normal sequence data.
BMC Bioinform., 2019

2018
A loop-counting method for covariate-corrected low-rank biclustering of gene-expression and genome-wide association study data.
PLoS Comput. Biol., 2018

2017
Cell type discovery and representation in the era of high-content single cell phenotyping.
BMC Bioinform., 2017

Production of a Preliminary Quality Control Pipeline for Single Nuclei RNA-Seq and Its Application in the Analysis of Cell Type Diversity of Post-Mortem Human Brain Neocortex.
Proceedings of the Biocomputing 2017: Proceedings of the Pacific Symposium, 2017

2016
The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.
NeuroImage, 2016

2015
Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies.
BMC Bioinform., 2015

2011
An Application and Empirical Comparison of Statistical Analysis Methods for Associating Rare Variants to a Complex Phenotype.
Proceedings of the Biocomputing 2011: Proceedings of the Pacific Symposium, 2011

2010
A Covering Method for Detecting Genetic Associations between Rare Variants and Common Phenotypes.
PLoS Comput. Biol., 2010

The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era.
Health Informatics J., 2010

2009
Prestige centrality-based functional outlier detection in gene expression analysis.
Bioinform., 2009

2008
Predicting functional regulatory polymorphisms.
Bioinform., 2008

2007
Accurate prediction of deleterious protein kinase polymorphisms.
Bioinform., 2007

1999
Whole genome association studies in humans (abstract).
Proceedings of the Third Annual International Conference on Research in Computational Molecular Biology, 1999


  Loading...