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American Journal of Human Genetics|July 30, 2025
Rare-variant association studies: When are aggregation tests more powerful than single-variant tests?Debraj Bose, Christian Fuchsberger, Michael BoehnkeGenetic Epidemiology|September 15, 2019
Combining sequence data from multiple studies: Impact of analysis strategies on rare variant calling and association resultsZhongsheng Chen, Michael Boehnke, Christian FuchsbergerBioinformatics (Oxford, England)|September 12, 2018
emeraLD: rapid linkage disequilibrium estimation with massive datasetsCorbin Quick, Christian Fuchsberger, Daniel Taliun, et al.Bioinformatics (Oxford, England)|January 29, 2008
Jenti: an efficient tool for mining complex inbred genealogiesMario Falchi, Christian FuchsbergerGenetic Epidemiology|June 29, 2017
Improving power for rare-variant tests by integrating external controlsSeunggeun Lee, Sehee Kim, Christian FuchsbergerPlos Genetics|April 24, 2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseLoukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, et al.American Journal of Human Genetics|January 21, 2014
A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cellJennifer R Kulzer, Michael L Stitzel, Mario A Morken, et al.Genetic Epidemiology|June 11, 2020
Sequencing and imputation in GWAS: Cost-effective strategies to increase power and genomic coverage across diverse populationsCorbin Quick, Pramod Anugu, Solomon Musani, et al.Genetic Epidemiology|February 14, 2006
Haplotype association analysis for late onset diseases using nuclear family dataChun Li, Michael BoehnkeGenetic Epidemiology|June 9, 2020
Power loss due to testing association between covariate-adjusted traits and genetic variantsPranav Yajnik, Michael BoehnkePageof 47