Florin Grigorian
Sourced from institutional research profiles (UAMS TRI or ARA).
Assistant Professor
Ophthalmology, College of Medicine
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Florin Grigorian's research focuses on ophthalmology, with a particular emphasis on pediatric eye conditions. His work includes investigations into the diagnosis and management of retinal diseases, such as retinopathy of prematurity and familial exudative vitreoretinopathy. Grigorian has studied the effectiveness of various diagnostic tools, including the Icare tonometer and artificial intelligence-based vascular severity scores, in pediatric populations. His publications also address topics ranging from infectious keratitis to leukemic optic nerve infiltration and the role of dietary factors in age-related macular degeneration.
Grigorian's scholarship metrics include an h-index of 9, with 24 total publications and 197 total citations. He has contributed to research on the genotype-phenotype correlations in metabolic and genetic disorders affecting vision and has explored novel diagnostic methods like oral fluorescein angiography for conditions such as papilledema in children. His recent work also includes the application of machine learning in medical imaging for improved disease diagnosis.
Metrics
- h-index: 9
- Publications: 24
- Citations: 197
Positions
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Assistant Professor 2018–presentUniversity of Arkansas for Medical Sciences Ophthalmology, College of Medicine Institutional directory
Selected Publications
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Association between retinal findings and risk of mortality in pediatric abusive head trauma (2026)
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Oral fluorescein angiography in pediatric ophthalmology (2025)
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Use of an Artificial Intelligence-Generated Vascular Severity Score Improved Plus Disease Diagnosis in Retinopathy of Prematurity (2024)
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Re: Sawyer et al.: Diagnostic role of oral fluorescein angiography in pediatric ambulatory clinics (Ophthalmol Retina. 2024;8:204-206) (2024)
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Paediatric Cogan Syndrome masquerading as IgA vasculitis (2023)
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Oral Fluorescein Angiography for the Diagnosis of Papilledema Versus Pseudopapilledema in Children (2022)
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Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy (2020)
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Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum. (2020)
Collaboration Network
Top Collaborators
- Oral Fluorescein Angiography for the Diagnosis of Papilledema Versus Pseudopapilledema in Children
- Oral fluorescein angiography in pediatric ophthalmology
- Re: Sawyer et al.: Diagnostic role of oral fluorescein angiography in pediatric ambulatory clinics (Ophthalmol Retina. 2024;8:204-206)
- Oral Fluorescein Angiography for the Diagnosis of Papilledema Versus Pseudopapilledema in Children
- Oral fluorescein angiography in pediatric ophthalmology
- Re: Sawyer et al.: Diagnostic role of oral fluorescein angiography in pediatric ambulatory clinics (Ophthalmol Retina. 2024;8:204-206)
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Oral Fluorescein Angiography for the Diagnosis of Papilledema Versus Pseudopapilledema in Children
- Association between retinal findings and risk of mortality in pediatric abusive head trauma
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
- Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy
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