Author

Brian Miller

Oregon National Primate Research CenterPrimary ORCID profile (0000-0001-7615-3044 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Brian MilleriD1 paper · Australian Antarctic Division

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 3 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Donald F. ConradiD· 2 shared Katinka A. Vigh‐ConradiD· 2 shared Liina NagirnajaiD· 2 shared Adrian M. E. PilatziD· 1 shared Alberto BarrosiD· 1 shared Alem Abebe· 1 shared Alexandra M. StendahliD· 1 shared Alexandra Manuel LopesiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenomics

Donald F. ConradORCID

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Author profile →

3 papers

Recent·Most cited

Autolab HBH: A Rapid Hyperbaric Heating Device for Streamlined, PCR-Ready Sample Preparation Across Diverse Biological Matrices and Organisms

Alem Abebe, Brian Miller, Thea Heeren, Sarkis Babikian, Kirk Allen, Jozef Hambálek, David Wright, Régis Peytavi

The paper introduces a rapid hyperbaric heating device for nucleic acid extraction, demonstrating its effectiveness across diverse biological samples and organisms.

bioRxiv · Jan 22, 2026 · PreprintMolecular Biology

The origins and functional effects of postzygotic mutations throughout the human lifespan

Nicole B. Rockweiler, Avinash Ramu, Liina Nagirnaja, Winghing Wong, Michiel J. Noordam, Casey W. Drubin, Ni Huang, Brian Miller, Ellen Z. Todres, Katinka A. Vigh‐Conrad, Antonino Zito, Kerrin S. Small, Kristin Ardlie, Barak A. Cohen, Donald F. Conrad

This study maps postzygotic mutations across tissues and lifespan, showing their functional variation and selection pressures, suggesting multiple dynamic genomes per individual.

Science · Apr 13, 2023Peer-reviewedGenomics

Diverse Monogenic Subforms of Human Spermatogenic Failure

Liina Nagirnaja, Alexandra Manuel Lopes, Wu‐Lin Charng, Brian Miller, Rytis Stakaitis, Ieva Golubickaitė, Alexandra M. Stendahl, Tianpengcheng Luan, Corinna Friedrich, Eisa Mahyari, Eloise Fadial, Laura Kasak, Katinka A. Vigh‐Conrad, Manon S. Oud, Miguel Joao Xavier, , Donald F. Conrad

This study identifies genetic subforms of non-obstructive azoospermia using exome sequencing and single-cell RNA sequencing, revealing molecular groups of genes involved in spermatogenesis.

Nature Communications · Dec 26, 2022Peer-reviewedGenetic & Genomic Medicine