Author

Pablo Kuri Morales

Universidad Nacional Autónoma de México

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 Organism:human· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aris BarasiD· 2 shared Gonçalo R. AbecasisiD· 2 shared Jaime Berumen-CamposiD· 2 shared Jason TorresiD· 2 shared Joelle S. MbatchouiD· 2 shared Jonathan MarchiniiD· 2 shared Kyoko WatanabeiD· 2 shared Michael D. KessleriD· 2 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Aris BarasORCID

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2 papers

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

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