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Genome Research|August 21, 2020
Detection of simple and complex de novo mutations with multiple reference sequencesKiran V Garimella, Zamin Iqbal, Michael A Krause, et al.Nature Genetics|August 6, 2002
Human genome sequence variation and the influence of gene history, mutation and recombinationDavid E Reich, Stephen F Schaffner, Mark J Daly, et al.Bioinformatics (Oxford, England)|April 4, 2019
HLA*LA-HLA typing from linearly projected graph alignmentsAlexander T Dilthey, Alexander J Mentzer, Raphael Carapito, et al.Plos 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.Medrxiv : the Preprint Server for Health Sciences|February 23, 2026
Genome-wide analysis implicates inner ear development in Ménière's diseaseZhuozheng Shi, Ravi Mandla, Jingjing Li, et al.American Journal of Human Genetics|June 16, 2026
Genome-wide analysis implicates inner ear development in Ménière diseaseZhuozheng Shi, Ravi Mandla, Jingjing Li, et al.Genome Biology and Evolution|November 7, 2023
Genetic Analysis of Mingrelians Reveals Long-Term Continuity of Populations in Western Georgia (Caucasus)Theodore G Schurr, Ramaz Shengelia, Michel Shamoon-Pour, et al.Nature Communications|January 20, 2026
Preventing premature deaths through polygenic risk scoresMelisa Chuong, Deborah Thompson, Michael E Weale, et al.Nature Communications|April 6, 2022
Identification of host-pathogen-disease relationships using a scalable multiplex serology platform in UK BiobankAlexander J Mentzer, Nicole Brenner, Naomi Allen, et al.Elife|July 13, 2019
The origins and relatedness structure of mixed infections vary with local prevalence of P. falciparum malariaSha Joe Zhu, Jason A Hendry, Jacob Almagro-Garcia, et al.Pageof 16