Author

Ariane H. Ayer

Regeneron (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

Alan R. ShuldineriD· 2 shared Aris BarasiD· 2 shared Deepika SharmaiD· 2 shared Esteban Chen· 2 shared Giovanni CoppolaiD· 2 shared Kavita Praveen· 2 shared Michael N CantoriD· 2 shared Michelle G. LeBlanciD· 2 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Alan R. ShuldinerORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 27, 2022

Rare coding variants in CHRNB2 reduce the likelihood of smoking

Veera Manikandan Rajagopal, Kyoko Watanabe, Joelle S. Mbatchou…·Giovanni Coppola

The paper identifies rare coding variants in CHRNB2 associated with reduced smoking likelihood and links them to downstream smoking-related phenotypes.

3 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicineCommunications BiologyPeer-reviewedJun 3, 2022

Population-scale analysis of common and rare genetic variation associated with hearing loss in adults

Kavita Praveen, Lee Dobbyn, Lauren Gurski…·Joe Burns

This study identifies 53 genetic loci associated with hearing loss, including 15 novel ones, using genome-wide and exome-sequencing data from multiple cohorts.

36 citations

humanGWAS summary statistics

𝕏 PostBluesky