Author

Russell Bowler

National Jewish Health

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· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Allison E. Ashley‐KochiD· 3 shared Álvaro AlonsoiD· 3 shared Donald W. BowdeniD· 3 shared Donna K. ArnettiD· 3 shared François AguetiD· 3 shared John BarnardiD· 3 shared John BlangeroiD· 3 shared Kristin ArdlieiD· 3 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Allison E. Ashley‐KochORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Local ancestry-aware genome-wide meta-analysis uncovers novel genetic loci for sickle cell disease nephropathy

Melanie E. Garrett, Seyed Mehdi Nouraie, Roberto F. Machado, Victor R. Gordeuk, Mark T. Gladwin, Marilyn J. Telen, Allison E. Ashley‐Koch, Gonçalo Abecasis, François Aguet, Christine Albert, Laura Almasy, Álvaro Alonso, Seth Ament, Peter Anderson, Pramod Anugu, , Mao Fu

This paper performs a local ancestry-aware GWAS on SCD cohorts to identify novel genetic loci associated with eGFR, uncovering regions linked to inflammation, ECM integrity, and other pathways relevant to SCD nephropathy.

Blood Advances · Aug 19, 2026Peer-reviewedGenetic & 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

Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity

Ali Reza Keramati, Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady J. Gaynor, Kathleen A. Ryan, Jennifer A. Brody, Xue Yun Zhong, Qiang Wei, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura A. Almasy, , Paul S. de Vries

The paper uses whole genome sequencing to identify genetic loci associated with platelet aggregation, including novel variants in RGS18, SVEP1, and PEAR1.

Nature Communications · Jun 15, 2021Peer-reviewedGenomics