Author

Esteban Chen

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 Ariane H. Ayer· 2 shared Aris BarasiD· 2 shared Deepika SharmaiD· 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

Rare coding variants in CHRNB2 reduce the likelihood of smoking

Veera Manikandan Rajagopal, Kyoko Watanabe, Joelle S. Mbatchou, Ariane H. Ayer, Peter Quon, Deepika Sharma, Michael D. Kessler, Kavita Praveen, Sahar Gelfman, Neelroop Parikshak, Jacqueline M. Otto, Suying Bao, Shek Man Chim, Elias Pavlopoulos, Andreja Avberšek, , Giovanni Coppola

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

medRxiv · Oct 27, 2022 · PreprintGenetic & Genomic Medicine

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

Kavita Praveen, Lee Dobbyn, Lauren Gurski, Ariane H. Ayer, Jeffrey C. Staples, Shawn Mishra, Yu Bai, Alexandra M. Kaufman, Arden Moscati, Christian Benner, Esteban Chen, Siying Chen, Alexander Popov, Janell Smith, Lance J. Adams, , 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.

Communications Biology · Jun 3, 2022Peer-reviewedGenetic & Genomic Medicine