Author

Rene Hoffman

Stanford Medicine

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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Systems Biology· 2

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:database / resource· 1 Approach:experimental assay· 1

Frequent Co-Authors

Guangwen WangiD· 2 shared Michael P. SnyderiD· 2 shared Songjie CheniD· 2 shared Benedikt RauscheriD· 1 shared Bettina HaaseiD· 1 shared Daniel HornburgiD· 1 shared Gerard DrewesiD· 1 shared Han SuniD· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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2 shared papersSystems Biology

Guangwen WangORCID

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2 papers

Recent·Most cited

Patient-derived gene and protein expression signatures of NGLY1 deficiency

Benedikt Rauscher, William F. Mueller, Sandra Clauder‐Münster, Petra Jakob, Mohammad Saiful Islam, Han Sun, Sonja Ghidelli, Markus Böesche, Marcus Bantscheff, Hannah Pflaumer, Paul G. Collier, Bettina Haase, Songjie Chen, Rene Hoffman, Guangwen Wang, , Lars Michael Steinmetz

The paper characterizes gene and protein expression changes in NGLY1 deficiency using patient-derived cells and provides a web resource for the data.

The Journal of Biochemistry · Dec 6, 2021Peer-reviewedSystems Biology

Integration and comparison of multi-omics profiles of NGLY1 deficiency plasma and cellular models to identify clinically relevant molecular phenotypes

Songjie Chen, Guangwen Wang, Xiaotao Shen, Daniel Hornburg, Shannon M. Rego, Rene Hoffman, Stephanie A. Nevins, Xun Cheng, Michael P. Snyder

This study integrates metabolomics and proteomics data from NGLY1 deficiency patient samples and cellular models to identify molecular phenotypes linked to immune activation and metabolic disturbances.

bioRxiv · May 28, 2021 · PreprintSystems Biology