Author

Briana Cameron

23andMe (United States)

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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Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Organism:human· 2 Approach:statistical model· 2

Frequent Co-Authors

Adam AutoniD· 2 shared Devika Dhamija· 2 shared Suyash ShringarpureiD· 2 shared Yunxuan JiangiD· 2 shared A. A. Jubb· 1 shared Aaron A. Petrakovitz· 1 shared Aaron Kleinman· 1 shared Adrián I. CamposiD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adam AutonORCID

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2 papers

Recent·Most cited

Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring

Adrián I. Campos, Nathan Ingold, Yunru Huang, Brittany L. Mitchell, Pik Fang Kho, Xikun Han, Luis M. García‐Marín, Jue‐Sheng Ong, Michelle Agee, Stella Aslibekyan, Adam Auton, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, , Miguel E. Rentería

This study identifies 49 genetic loci associated with sleep apnoea risk using multi-trait GWAS, with 29 replicated in a large cohort, and finds genetic correlations with several complex traits.

SLEEP · Dec 16, 2022Peer-reviewedGenetic & Genomic Medicine

Large-scale trans-ethnic replication and discovery of genetic associations for rare diseases with self-reported medical data

Suyash Shringarpure, Wei Ting Wang, Yunxuan Jiang, Alison Acevedo, Devika Dhamija, Briana Cameron, A. A. Jubb, Peng Yue, Lea Sarov‐Blat, Robert C. Gentleman, Adam Auton

This paper uses self-reported medical data to perform GWAS on 33 rare diseases, rediscovering known associations and finding novel ones, validated across multiple populations.

medRxiv · Jun 9, 2021 · PreprintGenetic & Genomic Medicine