Author

Brian Tomlinson

Centre for Human GeneticsORCID 0000-0001-6717-5444Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Anubha MahajaniD· 2 shared Ching‐Yu ChengiD· 2 shared Claudia H.T. TamiD· 2 shared Donald W. BowdeniD· 2 shared Jianjun LiuiD· 2 shared John Campbell ChambersiD· 2 shared Maggie C.Y. NgiD· 2 shared Myron D. Gross· 2 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Anubha MahajanORCID

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2 papers

Recent·Most cited

GeneticsNaturePeer-reviewedMay 6, 2020

Identification of type 2 diabetes loci in 433,540 East Asian individuals

Cassandra Nichole Spracklen, Momoko Horikoshi, Young Jin Kim…·Kyong Soo Park

This paper identifies 56 new type 2 diabetes loci in 433,540 East Asian individuals through a meta-analysis of GWAS data.

442 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 31, 2018

Genetic discovery and translational decision support from exome sequencing of 20,791 type 2 diabetes cases and 24,440 controls from five ancestries

Jason A. Flannick, Josep Maria Mercader, Christian Fuchsberger…·Markku Laakso

This study identifies rare genetic variants associated with type 2 diabetes using exome sequencing of 20,791 cases and 24,440 controls, and provides a Bayesian framework to improve variant prioritization.

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky