Author

Maoxuan Lin

University of MichiganORCID 0000-0001-5191-1857Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 4 Approach:statistical model· 4 Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 2 Assay:whole-exome sequencing· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Research Focus:fine-mapping· 1

Frequent Co-Authors

Cristen J. WilleriD· 3 shared Gonçalo R. AbecasisiD· 3 shared Jonas Bille NielseniD· 3 shared Kristian HveemiD· 3 shared Lars G. FritscheiD· 3 shared Wei ZhouiD· 3 shared Brooke N. WolfordiD· 2 shared Chad M. BrummettiD· 2 shared

Activity by Year

2018-2021 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Cristen J. WillerORCID

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4 papers

Recent·Most cited

GenomicsVirusesPeer-reviewedAug 23, 2021

APOBEC Mutagenesis is Concordant Between Tumor and Viral Genomes in HPV Positive Head and Neck Squamous Cell Carcinoma

Daniel L. Faden, Krystle A. Lang Kuhs, Maoxuan Lin…·Lisa J. Mirabello

This study shows that APOBEC mutagenesis occurs in both tumor and viral genomes in HPV+ OPSCC, suggesting a direct link between viral restriction and host mutations.

35 citationstop 4%

humanwhole-exome sequencing

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GenomicsNature GeneticsPeer-reviewedAug 8, 2018

Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

Wei Zhou, Jonas Bille Nielsen, Lars G. Fritsche…·Seunggeun Lee

This paper introduces SAIGE, a method that improves the accuracy of genetic association tests in unbalanced case-control studies by using saddlepoint approximation, and demonstrates its effectiveness on UK Biobank data.

1,406 citationstop 1%

humanwhole-exome sequencing

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GeneticsNature GeneticsPeer-reviewedJul 26, 2018

Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

Jonas Bille Nielsen, Rósa B. Þórólfsdóttir, Lars G. Fritsche…·Cristen J. Willer

This study identifies 111 genetic loci and 163 risk variants associated with atrial fibrillation using a GWAS of over 1 million individuals.

876 citationstop 1%

humanGWAS summary statistics

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GeneticsNature CommunicationsPeer-reviewedMar 1, 2018

Genome-wide analysis yields new loci associating with aortic valve stenosis

Anna Helgadóttir, Guðmar Þorleifsson, Sólveig Grétarsdóttir…·Kāri Stefánsson

This study identifies two new genetic loci associated with aortic valve stenosis through a large genome-wide association study.

125 citationstop 1%

humanGWAS summary statistics

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