Author

Robert L. Hanson

National Institute of Diabetes and Digestive and Kidney DiseasesORCID 0000-0002-4252-7068Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Leslie J. BaieriD· 2 shared Aaron J. DeutschiD· 1 shared Aaron LeongiD· 1 shared Alan R. ShuldineriD· 1 shared Alicia Huerta‐ChagoyaiD· 1 shared Alicia R. MartiniD· 1 shared Alisa Knodle ManningiD· 1 shared Andrés Moreno‐EstradaiD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Leslie J. BaierORCID

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2 papers

Recent·Most cited

The power of TOPMed imputation for the discovery of Latino enriched rare variants associated with type 2 diabetes

Alicia Huerta‐Chagoya, Philip H. Schroeder, Ravi Mandla, Aaron J. Deutsch, Wanying Zhu, Lauren E. Petty, Xiaoyan Yi, Joanne B. Cole, Miriam S. Udler, Peter Dornbos, Bianca Porneala, DANIEL A. DICORPO, Ching‐Ti Liu, Josephine H. Li, Łukasz Szczerbiński, , Josep Maria Mercader

The paper demonstrates that TOPMed imputation improves the identification of rare variants associated with type 2 diabetes in Latino populations, leading to novel associations and better polygenic scores.

Diabetologia · May 6, 2023Peer-reviewedGenetic & Genomic Medicine

Characterization of exome variants and their metabolic impact in 6,716 American Indians from Southwest US

Hye In Kim, Bin Ye, Nehal Gosalia, Çiğdem Köroğlu, Robert L. Hanson, Wen‐Chi Hsueh, William C. Knowler, Leslie J. Baier, Clifton Bogardus, Alan R. Shuldiner, Cristopher V. Van Hout

This study uses whole exome sequencing in 6,716 American Indians to identify metabolic trait-associated variants, finding unique pLOF and nonsynonymous variants linked to BMI, diabetes, and lipid levels.

The American Journal of Human Genetics · Jul 7, 2020Peer-reviewedGenetics