Marko Hawlina

University of Ljubljana — SI

Biochemistry, Genetics and Molecular Biology · Life Sciences

30h-index3.5kcitations206works2.32yr avg
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Research Topics

Retinal Development and Disorders(79), Retinal Diseases and Treatments(58), Connexins and lens biology(33), Intraocular Surgery and Lenses(28), Glaucoma and retinal disorders(22)

Publications206 total

Gap Junctional Versus Paracrine Signaling in the Human Lens Epithelium: Analysis Based on Multicellular Ca²⁺ Imaging and Computational Modeling
Investigative Ophthalmology & Visual Science·2025Open Access
Extracellular Vesicle-Derived Bioactive Molecules for Corneal and Ocular Surface Regeneration
Journal of Clinical Medicine·2025Open Access
Stem Cells for Therapy of Eye Diseases: Current Status
Biochemistry·2024Open Access
Molecular and Cellular Mechanisms of the Therapeutic Effect of Mesenchymal Stem Cells and Extracellular Vesicles in Corneal Regeneration
International Journal of Molecular Sciences·2024· 11 citedOpen Access
Leber hereditary optic neuropathy in Slovenia: quality of life and costs from patient perspective
Orphanet Journal of Rare Diseases·2024· 1 citedOpen Access
Human Primary Lens Epithelial Cultures on Basal Laminas Studied by Synchrotron-Based FTIR Microspectroscopy for Understanding Posterior Capsular Opacification
International Journal of Molecular Sciences·2024Open Access
Peripapillary retinal nerve fibre layer thinning in patients with X-linked retinoschisis
BMJ Open Ophthalmology·2024Open Access
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Documenta Ophthalmologica·2024· 4 citedOpen Access
Morphological and functional parameters in X-linked retinoschisis patients–A multicentre retrospective cohort study
Frontiers in Medicine·2024· 6 citedOpen Access
Leber hereditary optic neuropathy genotype, phenotype and biochemical characteristics
Medicinski podmladak·2024Open Access
Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia
Journal of Clinical Medicine·2023· 4 citedOpen Access
Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia
Preprints.org·2023· 2 citedOpen Access
<i>ABCA4</i> Variant c.5714+5G&amp;gt;A in <i>Trans</i> With Null Alleles Results in Primary RPE Damage
Investigative Ophthalmology & Visual Science·2023· 3 citedOpen Access
Natural History of Stargardt Disease: The Longest Follow-Up Cohort Study
Genes·2023· 5 citedOpen Access
Analysis of the slope between P50 and N95 waves of the large field pattern electroretinogram as an additional indicator of ganglion cell dysfunction
Documenta Ophthalmologica·2023· 6 cited
Inflammation and Oxidative Stress Gene Variability in Retinal Detachment Patients with and without Proliferative Vitreoretinopathy
Genes·2023· 8 citedOpen Access
Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis
Stresses·2023· 3 citedOpen Access
Leber Hereditary Optic Neuropathy in a Family of Carriers of MT-ND5 m.13042G&gt;T (A236S) Novel Variant
Journal of Neuro-Ophthalmology·2023· 1 cited
Natural Disease Course in Usher Syndrome Patients Harboring USH2A Variant p.Cys870* in Exon 13, Amenable to Exon Skipping Therapy
Genes·2023· 3 citedOpen Access
Characterization of Different Types of Epiretinal Proliferations by Synchrotron Radiation-Based Fourier Transform Infrared Micro-Spectroscopy
International Journal of Molecular Sciences·2023· 3 citedOpen Access
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Frequent Co-authors

Damjan Glavač(13), Martina Jarc-Vidmar(9), Ana Fakin(9), Mojca Globočnik Petrovič(9), Sofija Andjelić(7), Aleksandra Kraut(6), Borut Peterlin(6), Daniel Petrovič(6), Xhevat Lumi(5), Goran Petrovski(5), Maja Šuštar(5), Graham E. Holder(4), Metka Ravnik‐Glavač(4), Crystel Bonnet(4), Christine Petit(4), Peter Korošec(4), Špela Štunf(4), Eva Lenassi(4), Anastazija Hvala(4), Jelka Brecelj(4)