Orhan Kerim Inci is an expert in Genetics at Gazi University (Turkey). Orhan Kerim Inci has authored 8 publications, the most recent in 2025. SLR score: 28 (community average: 125). How the SLR is computed.

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Orhan Kerim Inci Gazi University Turkey
28 ScienceLeadR Reputation 28
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Genetics

Subspecialties:

Full career – Last 3 years

Main Topics

Publications and Clinical Studies

Publications – Clinical Studies

Profile data updated on

Organizations

Career arc: 2021 - 2026

Source: PubMed

Gazi University

Publications Synthesis

Sources: PubMed, OpenAlex

Number : 8

Citations

Citations: 15 1st author: 5 Last author: 0 Unique author: 0


Best Journals

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Latest Publications

5 most recent indexed articles

Source: Pubmed

Title Journal Year Citations
Yeast-Produced Human Recombinant Lysosomal β-Hexosaminidase Efficiently Rescues GM2 Ganglioside Accumulation in Tay-Sachs Disease.
PMID 40423067 — hexosaminidases, cells, genes, yeasts, microscopy, electron, scanning transmission, stem cells, neuroglia, enzymes, tay-sachs disease, fibroblasts, therapeutics, g(m2) ganglioside, gangliosides
J Pers Med20251
Combined treatment of Ketogenic diet and propagermanium reduces neuroinflammation in Tay-Sachs disease mouse model.
PMID 40019557 — diet, tay-sachs disease, diet, ketogenic, therapeutics, g(m2) ganglioside
Metab Brain Dis20250
Human Recombinant Lysosomal β-Hexosaminidase A produced in P.pastoris efficiently reduced GM2 ganglioside accumulation in Tay- Sachs Disease
OpenAlex W4400578005 — hexosaminidases, cells, tay-sachs disease, hexosaminidase a, therapeutics, g(m2) ganglioside, gangliosides
Research Square (Research Square)20240
Gangliosides as Therapeutic Targets for Neurodegenerative Diseases.
PMID 38623278 — cells, therapeutics, neurodegenerative diseases, gangliosides
J Lipids20245
Molecular Trojan Horses for treating lysosomal storage diseases.
PMID 37598508 — cells, genes, extracellular vesicles, metabolic diseases, molecular biology, pharmaceutical preparations, lysosomal storage diseases, therapeutics, tissues, endocrine system diseases
Mol Genet Metab20233

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