Author

Katherine Taylor

Broad Institute

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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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Alisa Knodle ManningiD· 2 shared Josep Maria MercaderiD· 2 shared Sarah FineriD· 2 shared Aaron LeongiD· 1 shared Adebowale AdeyemoiD· 1 shared Adem Y. DawediD· 1 shared Alain Gerald BertoniiD· 1 shared Alexandra M. BleeiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alisa Knodle ManningORCID

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2 papers

Recent·Most cited

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries.

Alicia Huerta‐Chagoya, Joohyun Kim, Ravi Mandla, Yingchang Lu, Suzuki Ken, Lauren E. Petty, Hong Kiat Ng, Jaewon Choi, Simon Lee, Madhusmita Rout, Kuang Lin, Katherine Taylor, Carlos Alberto Aguilar-Salinas, Lourdes García‐García, Clicerio González‐Villalpando, , Xiuqing Guo

This paper develops and validates multi-ancestry polygenic risk scores for type 2 diabetes prediction and complications across diverse populations.

The Lancet Diabetes & Endocrinology · Apr 27, 2026Peer-reviewedGenetic & Genomic Medicine

An ancestry-enriched HNF4A variant and GP2 reveal distinct mechanisms of type 2 diabetes in exome-wide study of 13,674 cases and 41,024 controls

Sam Hodgson, Vi Bui, Siqi Hu, Cyrielle Maroteau, Margherita Bigossi, Alicia Huerta-Chagoya, Trang Nguyen, Adem Y. Dawed, Ryan Koesterer, Maheak Vora, Daniel Stow, Alice Williamson, Alexandra M. Blee, Julia Carrasco-Zanini Sanchez, Viswanathan Baskar, , Moneeza Kalhan Siddiqui

The paper identifies ancestry-specific T2D risk variants in South Asian populations through exome-wide association study and functional validation.

medRxiv · Sep 24, 2025 · PreprintGenetic & Genomic Medicine