Christoph Lange
Orcid: 0000-0003-2620-1030Affiliations:
- Harvard School of Public Health, Department of Biostatistics, Cambridge, MA, USA
- University of Bonn, Institute for Genomic Mathematics, Germany
- German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany
According to our database1,
Christoph Lange
authored at least 16 papers
between 2006 and 2024.
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Bibliography
2024
BMC Bioinform., December, 2024
Prediction of disease-free survival for precision medicine using cooperative learning on multi-omic data.
Briefings Bioinform., 2024
2023
A comparison between similarity matrices for principal component analysis to assess population stratification in sequenced genetic data sets.
Briefings Bioinform., January, 2023
2022
Unsupervised outlier detection applied to SARS-CoV-2 nucleotide sequences can identify sequences of common variants and other variants of interest.
BMC Bioinform., December, 2022
2021
A fast and efficient smoothing approach to Lasso regression and an application in statistical genetics: polygenic risk scores for chronic obstructive pulmonary disease (COPD).
Stat. Comput., 2021
A unifying framework for rare variant association testing in family-based designs, including higher criticism approaches, SKATs, and burden tests.
Bioinform., 2021
2019
Local and Global Stratification Analysis in Whole Genome Sequencing (WGS) Studies Using LocStra.
Proceedings of the Computational Advances in Bio and Medical Sciences, 2019
2017
Bioinform., 2017
2016
Utilizing the Jaccard index to reveal population stratification in sequencing data: a simulation study and an application to the 1000 Genomes Project.
Bioinform., 2016
2014
On the simultaneous association analysis of large genomic regions: a massive multi-locus association test.
Bioinform., 2014
2012
Handling the data management needs of high-throughput sequencing data: SpeedGene, a compression algorithm for the efficient storage of genetic data.
BMC Bioinform., 2012
'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate.
Bioinform., 2012
2011
Quantitative trait prediction based on genetic marker-array data, a simulation study.
Bioinform., 2011
2008
2006
P<sup>2</sup>BAT: a massive parallel implementation of PBAT for genome-wide association studies in R.
Bioinform., 2006