Author

Brendan Jamison

Endeavor HealthORCID 0000-0002-0208-9307Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:gene regulatory network inference· 2 Assay:ATAC-seq· 1 Research Focus:benchmarking· 1 Organism:mouse· 1

Frequent Co-Authors

Alan R. SandersiD· 2 shared Alena KozlovaiD· 2 shared Hanwen ZhangiD· 2 shared Jubao DuaniD· 2 shared Siwei ZhangiD· 2 shared Zhiping P. PangiD· 2 shared Ada McCarrolliD· 1 shared Alex KotlariD· 1 shared

Activity by Year

2022-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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2 shared papersNeuroscience

Alan R. SandersORCID

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3 papers

Recent·Most cited

Single-cell multiomics of neuron activation reveals context-specific genetics of brain disorders

Lifan Liang, Siwei Zhang, Zicheng Wang, Hanwen Zhang, C Li, Christina Thapa, E. Oh, David Sirkin, Xiaotong Sun, Alexandra Barishman, Ada McCarroll, Alexandra C. Duhe, Sheng Qian, Xiaoyuan Zhong, Brendan Jamison, , Jubao Duan

The paper identifies context-specific genetic effects in neuronal activation using single-cell multiomics, revealing NPD risk variants and genes active during stimulation.

Science · Jun 25, 2026Peer-reviewedNeuroscience

Beyond the mean: genetic control of gene expression fidelity and dispersion

Brendan Jamison, Alexander Chen, Kenneth Barr, Erik McIntire, Xin He, Yoav Gilad

This paper shows that gene expression dispersion, not just mean expression, is a genetically controlled regulatory feature reflecting fidelity across species and cell types.

bioRxiv · Apr 7, 2026 · PreprintGenomics

Loss-of-function of OTUD7A in the schizophrenia-associated 15q13.3 deletion impairs synapse development and function in human neurons

Alena Kozlova, Siwei Zhang, Alex Kotlar, Brendan Jamison, Hanwen Zhang, Serena Qinyun Z. Shi, Marc P. Forrest, John McDaid, David J. Cutler, Michael P. Epstein, Michael E. Zwick, Zhiping P. Pang, Alan R. Sanders, Stephen T. Warren, Pablo V. Gejman, , Jubao Duan

The paper identifies OTUD7A loss-of-function mutations in schizophrenia-associated 15q13.3 deletions and shows they impair synapse development and function in human neurons.

The American Journal of Human Genetics · Aug 1, 2022Peer-reviewedNeuroscience