Author

Zachary B. Rodriguez

University of PennsylvaniaORCID 0000-0002-4591-803XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Organism:human· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Anurag VermaiD· 2 shared Athanasios KousathanasiD· 1 shared Augusto RendoniD· 1 shared Barney HilliD· 1 shared Benjamin M. NealeiD· 1 shared Cecilia M. LindgreniD· 1 shared Christopher C. CarsoniD· 1 shared Christopher R. GignouxiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersBioinformatics

Anurag VermaORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

PMBB Geno-Pheno Toolkit: A suite of scalable, reproducible pipelines for cross-biobank association analyses

Zachary B. Rodriguez, Lindsay A. Guare, Lannawill Caruth, Katie M. Cardone, Christopher C. Carson, Tess Cherlin, Stephanie Mohammed, Hritvik Gupta, Rachit Kumar, Karl Keat, Shefali S. Verma, Anurag Verma

The PMBB Geno-Pheno Toolkit provides modular pipelines for cross-biobank association analyses, supporting GWAS, ExWAS, and PheWAS with containerized workflows.

bioRxiv · Jul 26, 2026 · PreprintBioinformatics

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration

Duncan S. Palmer, Barney Hill, Sam Hodgson, Maarja Jõeloo, Georgios Kalantzis, Athanasios Kousathanas, Satoshi Koyama, Wenhan Lu, Shinichi Namba, Zachary B. Rodriguez, Jonathan Shortt, Kyuto Sonehara, Nicholas Vartanian, Ha My T. Vy, Isaac Wade, , Benjamin M. Neale

The paper establishes a global consortium to discover rare genetic associations by integrating data from multiple biobanks, identifying 514 gene-trait associations, many detectable only through cross-ancestry meta-analysis.

medRxiv · May 24, 2026 · PreprintGenetic & Genomic Medicine