Author

Take Naseri

Brown University

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 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:whole-genome sequencing· 2 Assay:GWAS summary statistics· 1 Assay:scATAC-seq· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alex P. ReineriD· 2 shared Braxton D. MitchelliD· 2 shared Bruce M. PsatyiD· 2 shared Charles L KooperbergiD· 2 shared Christine M. AlbertiD· 2 shared Donald W. BowdeniD· 2 shared Donna K. ArnettiD· 2 shared Eric BoerwinkleiD· 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 papersGenetics

Alex P. ReinerORCID

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Author profile →

3 papers

Recent·Most cited

Meta-analysis of over 8,000 individuals from Hawai'i and Samoa for genetic associations to cardiometabolic phenotypes

Bryan L. Dinh, Xinran Wang, Xin Sheng, P. C. Wan, Amit K. Srivastava, Take Naseri, Satupa’itea Viali, Lynne Ross Wilkens, Loı̈c Le Marchand, Christopher A. Haiman, Daniel E. Weeks, Charleston W. K. Chiang, Jenna C. Carlson

This study conducts a GWAS of Native Hawaiians and Polynesian-ancestry populations to identify population-enriched genetic associations for cardiometabolic traits, confirming some variants and highlighting the need for larger cohorts.

medRxiv · May 12, 2026 · PreprintGenetic & Genomic Medicine

cellSTAAR: Incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of non-coding regions

Eric Van Buren, Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou, Nicholette D. Palmer, Donna K. Arnett, John Blangero, Eric Boerwinkle, Brian E. Cade, Jenna C. Carlson, April P. Carson, Yii-Der Ida Chen, Joanne E. Curran, , Russell Bowler

cellSTAAR integrates single-cell ATAC-seq with whole-genome sequencing to enhance power and interpretation of rare variant association tests in non-coding regions.

Nature Methods · Dec 31, 2025Peer-reviewedGenetics

Genomic and phenomic landscape of clonal hematopoiesis in over a million ancestrally diverse participants

Md Mesbah Uddin, Zhi Yu, Joshua S. Weinstock, Abhishek Niroula, Caitlyn Vlasschaert, Satoshi Koyama, Tetsushi Nakao, Sarah Urbut, Seyedeh Maryam Zekavat, Kaavya Paruchuri, Buu Minh Thanh Truong, Alexander James Silver, Taralynn Mack, Megan Y. Wong, Sara Haidermota, , Pradeep Natarajan

This study analyzes clonal hematopoiesis in over a million diverse individuals, identifying 72 genome-wide significant loci and linking CHIP to various phenotypes.

medRxiv · Jul 29, 2022 · PreprintGenetic & Genomic Medicine