Author

David Blair

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

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Adam E. LockeiD· 1 shared Adrián I. CamposiD· 1 shared Alexander W. CharneyiD· 1 shared Andrey ZiyatdinoviD· 1 shared Aris BarasiD· 1 shared BELIEVE Study Group· 1 shared Chuanyi ZhangiD· 1 shared Gonçalo R. AbecasisiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Adam E. LockeORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Rare protein-coding variation and the genetic architecture of height in >1.4 million individuals

Jack A. Kosmicki, Liron Ganel, Kyoko Watanabe, Tyler Joseph, Sheila M. Gaynor, Michael D. Kessler, Joshua Backman, Joelle S. Mbatchou, Andrey Ziyatdinov, David Blair, Jonas Bovijn, Niek Verweij, Kathie Sun, Chuanyi Zhang, Suganthi Balasubramanian, , Adam E. Locke

This study identifies 207 height-associated genes using rare protein-altering variants from over 1.4 million individuals, showing large effect sizes and overlap with Mendelian height syndromes.

medRxiv · Jun 24, 2026 · PreprintGenetic & Genomic Medicine