Author

Graeme J. Preston

Mayo ClinicORCID 0000-0001-6810-9326Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Organism:human· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Assay:proteomics· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:metabolomics· 1

Frequent Co-Authors

Ibrahim ShammasiD· 3 shared Tamás KozicziD· 3 shared Akhilesh PandeyiD· 2 shared Éva MoravaiD· 2 shared Nathan P. StaffiD· 2 shared Rameen ShahiD· 2 shared Rohit BudhrajaiD· 2 shared Silvia RadenkoviciD· 2 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersNeuroscience

Ibrahim ShammasORCID

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3 papers

Recent·Most cited

NeurosciencebioRxivPreprintFeb 20, 2026

Multilevel impairment of mitochondrial respiration with sex-specific signatures in inclusion body myositis

Ibrahim Shammas, Hazem Iaali, Jens O. Watzlawik…·Elie Naddaf

This study profiles mitochondrial respiration in IBM muscle tissue, identifying sex-specific impairments in respiration and OXPHOS complexes, along with correlations with disease severity.

DOI 10.64898/2026.02.18.706692

humanbulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintJul 9, 2025

ALG13 loss-of-function alters glycosylation, impairs neuronal maturation, and drives network hypoactivity in a cortical organoid model of CDG

Rameen Shah, Rohit Budhraja, Silvia Radenkovic…·Tamás Kozicz

This study uses cortical organoids to show that ALG13 loss-of-function causes glycosylation defects, neuronal maturation issues, and network hypoactivity in CDG.

DOI 10.1101/2025.07.09.663964

humanscRNA-seq

𝕏 PostBluesky

BiochemistrybioRxivPreprintJul 1, 2025

PGM1 deficiency disrupts sarcomere and mitochondrial function in a stem-cell cardiomyocyte model

Silvia Radenkovic, Graeme J. Preston, Rohit Budhraja…·Tamás Kozicz

This paper investigates the role of PGM1 in cardiomyocytes using patient-derived stem cells, finding disruptions in sarcomere and mitochondrial function, and suggesting potential therapeutic targets.

2 citations

humanproteomics

𝕏 PostBluesky