Rando Allikmets

Columbia University Irving Medical Center — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

72h-index30.0kcitations365works8.22yr avg
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Research Topics

Retinal Development and Disorders(217), Retinal Diseases and Treatments(187), Glaucoma and retinal disorders(59), Retinal Imaging and Analysis(41), Photoreceptor and optogenetics research(29)

Publications357 total

Characterization of the Subclinical Perilesional Zone in the Macula of Early-Stage ABCA4 Disease
Translational Vision Science & Technology·2025Open Access
Characterization of the Subclinical Perilesional Zone in the Macula of Early-Stage ABCA4 Disease
2024· 1 citedOpen Access
Serine and glycine physiology reversibly modulate retinal and peripheral nerve function
Cell Metabolism·2024· 12 cited
Cross-Sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter Study
American Journal of Ophthalmology·2024· 1 citedOpen Access
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Biomolecules·2024· 7 citedOpen Access
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability
Human Genetics and Genomics Advances·2023· 12 citedOpen Access
Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence
Translational Vision Science & Technology·2023· 6 citedOpen Access
iPSC–derived retinal pigmented epithelial cells from patients with macular telangiectasia show decreased mitochondrial function
Journal of Clinical Investigation·2023· 12 citedOpen Access
Re: Agrón et al.: Reticular pseudodrusen status, ARMS2/HTRA1 genotype, and geographic atrophy enlargement: Age-Related Eye Disease Study 2 Report 32. (Ophthalmology. 2022;129:1107–1119)
Ophthalmology·2023Open Access
Insights Into <i>PROM1</i>-Macular Disease Using Multimodal Imaging
Investigative Ophthalmology & Visual Science·2023· 6 citedOpen Access
Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture
Stem Cell Research·2022· 4 citedOpen Access
A pathogenic in-frame deletion-insertion variant in BEST1 phenocopies Stargardt disease
JCI Insight·2022· 4 citedOpen Access
Systems genomics in age-related macular degeneration
Experimental Eye Research·2022· 39 citedOpen Access
The human ATP‐binding cassette (ABC) transporter superfamily
Human Mutation·2022· 146 citedOpen Access
Longitudinal Analysis of a Resolving Foveomacular Vitelliform Lesion in ABCA4 Disease
Ophthalmology Retina·2022· 2 citedOpen Access
Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series
Orphanet Journal of Rare Diseases·2022· 7 citedOpen Access
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease
PLoS Genetics·2022· 15 citedOpen Access
Comparisons Among Optical Coherence Tomography and Fundus Autofluorescence Modalities as Measurements of Atrophy in <i>ABCA4</i>-Associated Disease
Translational Vision Science & Technology·2022· 6 citedOpen Access
The Human ATP-Binding Cassette (ABC) Transporter Superfamily
2021· 14 citedOpen Access
A genotype-phenotype correlation matrix for ABCA4 disease based on long-term prognostic outcomes
JCI Insight·2021· 51 citedOpen Access
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Frequent Co-authors

Michael Dean(21), Jana Zernant(14), Amy Hutchinson(8), Frans P.M. Cremers(7), Stephen H. Tsang(6), Gaetano R. Barile(5), R. Theodore Smith(5), Joanna E. Merriam(5), Nanda Singh(5), James R. Lupski(5), Paul S. Bernstein(5), Winston Lee(5), Janet R. Sparrow(5), Noah F. Shroyer(4), Bernard Gerrard(4), Richard A. Lewis(4), Mark Leppert(4), Johanna M. Seddon(4), Carel B. Hoyng(4), Gerald A. Fishman(4)