Author

G. L. Robertson

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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Cell Biology· 3 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 4 Approach:experimental assay· 4 Organism:human· 4 Research Focus:development & morphogenesis· 2 Research Focus:metabolism & bioenergetics· 2 Assay:scRNA-seq· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1

Frequent Co-Authors

V. Gama· 4 shared A. I. Romero-Morales· 2 shared A. Hinton· 1 shared A. Marshall· 1 shared A. R. Patterson· 1 shared A. Rastogi· 1 shared A. Sugiura· 1 shared B. A. Millis· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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4 shared papersCell Biology

V. Gama

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Leptomeningeal Neural Organoid (LMNO) Fusions as Models to Study Meninges-Brain Signaling

H. E. Jones, G. L. Robertson, A. I. Romero-Morales, R. O'Rourke, J. A. Siegenthaler, V. Gama

The paper develops a co-culture model of human iPSC-derived neural organoids fused with mouse leptomeninges to study meninges-brain signaling and assesses its stability and utility.

bioRxiv · Dec 1, 2023Cell Biology

Functional Overlap of Inborn Errors of Immunity and Metabolism Genes Define T Cell Immunometabolic Vulnerabilities

A. R. Patterson, G. A. Needle, A. Sugiura, C. Chi, K. K. Steiner, E. L. Fisher, G. L. Robertson, C. Bodnya, J. G. Markle, V. Gama, J. C. Rathmell

The paper identifies functional overlap between inborn errors of immunity and metabolism genes, revealing immunometabolic vulnerabilities in T cells.

bioRxiv · Jan 24, 2023 · PreprintImmunology

DRP1-mediated mitochondrial fission is essential to maintain cristae morphology and bioenergetics

G. L. Robertson, S. N. Riffle, M. Patel, A. Marshall, H. Beasley, E. Garza-Lopez, J. Shao, Z. Vue, M. S. Stoll, S. de Wet, R. P. Theart, B. Loos, A. Hinton, J. A. Mears, V. Gama

This study investigates how DRP1 mutations affect mitochondrial and peroxisomal dynamics, leading to metabolic dysfunction and structural abnormalities in EMPF1 patient fibroblasts.

bioRxiv · Dec 31, 2021Cell Biology

Human iPSC-derived cerebral organoids model features of Leigh Syndrome and reveal abnormal corticogenesis

A. I. Romero-Morales, G. L. Robertson, A. Rastogi, M. L. Rasmussen, H. Temuri, R. P. Chakrabarty, G. S. McElroy, L. Hsu, P. M. Almonacid, B. A. Millis, N. S. Chandel, J.-P. Cartailler, V. Gama

This study uses iPSC-derived cerebral organoids to model Leigh Syndrome, identifying defects in brain development and mitochondrial morphology.

bioRxiv · Apr 21, 2020 · PreprintCell Biology