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Molecular Biology and Evolution|February 21, 2014
On detecting incomplete soft or hard selective sweeps using haplotype structureAnna Ferrer-Admetlla, Mason Liang, Thorfinn Korneliussen, et al.Plos One|August 23, 2012
SNP calling, genotype calling, and sample allele frequency estimation from New-Generation Sequencing dataRasmus Nielsen, Thorfinn Korneliussen, Anders Albrechtsen, et al.Elife|December 20, 2022
Modeling the spatiotemporal spread of beneficial alleles using ancient genomesRasa A Muktupavela, Martin Petr, Laure Ségurel, et al.European Journal of Human Genetics : EJHG|January 23, 2014
Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish populationShengting Li, Soren Besenbacher, Yingrui Li, et al.BMC Bioinformatics|June 14, 2011
Estimation of allele frequency and association mapping using next-generation sequencing dataSu Yeon Kim, Kirk E Lohmueller, Anders Albrechtsen, et al.Cell|March 23, 2019
Human Disease Variation in the Light of Population GenomicsAna Prohaska, Fernando Racimo, Andrew J Schork, et al.Plos Genetics|October 25, 2011
Natural selection affects multiple aspects of genetic variation at putatively neutral sites across the human genomeKirk E Lohmueller, Anders Albrechtsen, Yingrui Li, et al.Nature|April 30, 2025
Picuris Pueblo oral history and genomics reveal continuity in US SouthwestThomaz Pinotti, Michael A Adler, Richard Mermejo, et al.American Journal of Human Genetics|December 3, 2013
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetesKirk E Lohmueller, Thomas Sparsø, Qibin Li, et al.Communications Biology|August 27, 2020
Ancient Jomon genome sequence analysis sheds light on migration patterns of early East Asian populationsTakashi Gakuhari, Shigeki Nakagome, Simon Rasmussen, et al.Pageof 2