Author

Kurt K. Lohman

Wake Forest University Health Sciences

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 2 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alisa Knodle ManningiD· 2 shared Amy R. BentleyiD· 2 shared André Gerardus UitterlindeniD· 2 shared Andréa R. V. R. HorimotoiD· 2 shared Andres MetspaluiD· 2 shared Annemarie Ida LuikiD· 2 shared Annette PetersiD· 2 shared Brian E. CadeiD· 2 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Alisa Knodle ManningORCID

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3 papers

Recent·Most cited

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

Heming Wang, Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee, Yun Ju Sung, Amy R. Bentley, Alisa Knodle Manning, Hugues Aschard, Tuomas O. Kilpeläinen, Marjan Ilkov, Michael R. Brown, Andréa R. V. R. Horimoto, Melissa A. Richard, , Wei Zheng

The paper identifies novel genetic loci associated with blood pressure that interact with sleep duration across multiple ancestries.

Molecular Psychiatry · Apr 15, 2021Peer-reviewedGenomics

Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

Raymond Noordam, Maxime M. Bos, Heming Wang, Thomas W. Winkler, Amy R. Bentley, Tuomas O. Kilpeläinen, Paul S. de Vries, Yun Ju Sung, Karen Schwander, Brian E. Cade, Alisa Knodle Manning, Hugues Aschard, Michael R Brown, Han Chen, Nora Franceschini, , André Gerardus Uitterlinden

The paper identifies 49 novel blood lipid loci associated with gene-sleep interactions in 126,926 individuals across 5 ancestry groups, with gene-short-sleep interactions explaining 4.25% of triglyceride variance.

bioRxiv · Feb 25, 2019 · PreprintGenomics

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

Anubha Mahajan, Jennifer Wessel, Sara M. Willems, Wei Zhao, Neil R. Robertson, Audrey Y. Chu, Wei Gan, Hidetoshi Kitajima, Daniel Taliun, Nigel William Rayner, Xiuqing Guo, Yingchang Lu, Man Li, Richard A. Jensen, Yao Hu, , Jun Liu

This study identifies 16 causal coding variants in type 2 diabetes using fine-mapping and shows that one third of signals are false leads.

Nature Genetics · Apr 1, 2018Peer-reviewedGenetics