Tamas Kozicz

19PUBLICATIONS
52CO-AUTHORS
Medical devicesMedical molecular engineering of nucleic acids and proteinsGlycoconjugatesNeurogeneticsMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (19)

|Jun 21, 2026
Mitochondrial DNA heteroplasmy drives cortical neuronal disturbances in human organoids harbouring the common m.3243A>G mutation.

|Jun 12, 2026
DHDDS-related juvenile parkinsonism is caused by impaired lipid metabolism, glycosylation, and mitochondrial dysfunction, which can be rescued by NAD⁺ treatment.

|Feb 24, 2026
Extensive Hypoglycosylation of Serum N-Glycoproteins in SRD5A3 Deficiency.

Anu Jain, Rohit Budhraja, Kishore Garapati

|Jan 28, 2026
Network Hypoactivity in ALG13-CDG: Disrupted Developmental Pathways and E/I Imbalance as Early Drivers of Neurological Features in CDG.

Rameen Shah, Rohit Budhraja, Silvia Radenkovic

|Jul 09, 2025
PGM1 deficiency disrupts sarcomere and mitochondrial function in a stem-cell cardiomyocyte model.

Silvia Radenkovic, Graeme Preston, Rohit Budhraja

|May 06, 2025
Mitochondria as the key to understanding neuroinflammation.

Tamas Kozicz, Eva Morava

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Frequent Collaborators

7 joint publications

Eva Morava

4 joint publications

Akhilesh Pandey

3 joint publications

I J J Muffels

3 joint publications

Beata Bystrowska