Robert E MacLaren
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Explore the profile of Robert E MacLaren including associated specialties, affiliations and a list of published articles.
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332
Citations
6241
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Recent Articles
31.
Fry L, MacLaren R
Genes (Basel)
. 2023 Dec;
14(12).
PMID: 38136982
The recent publication of Di Giosaffatte et al. [...].
32.
Kiraly P, Cottriall C, Taylor L, Jolly J, Cehajic-Kapetanovic J, Yusuf I, et al.
Biomolecules
. 2023 Oct;
13(10).
PMID: 37892166
Our study evaluated the morphological and functional outcomes, and the side effects, of voretigene neparvovec (VN) gene therapy for RPE65-mediated inherited retinal dystrophies (IRDs) in 12 eyes (six patients) at...
33.
MacLaren R, Fischer M, Gow J, Lam B, Sankila E, Girach A, et al.
Nat Med
. 2023 Oct;
29(10):2464-2472.
PMID: 37814062
Choroideremia is a rare, X-linked retinal degeneration resulting in progressive vision loss. A randomized, masked, phase 3 clinical trial evaluated the safety and efficacy over 12 months of follow-up in...
34.
Birtel J, Caswell R, de Silva S, Herrmann P, Rehman S, Lotery A, et al.
Am J Ophthalmol
. 2023 Oct;
258:32-42.
PMID: 37806544
Purpose: To investigate the phenotype, variability, and penetrance of IMPG2-related maculopathy. Design: Retrospective observational case series. Methods: Clinical evaluation, multimodal retinal imaging, genetic testing, and molecular modeling. Results: A total...
35.
Poli F, Yusuf I, Jolly J, Taylor L, Adeyoju D, Josan A, et al.
Transl Vis Sci Technol
. 2023 Sep;
12(9):24.
PMID: 37773503
Purpose: In patients with choroideremia, it is not known how smooth and mottled patterns on short-wavelength fundus autofluorescence (AF) imaging relate to retinal function. Methods: A retrospective case-note review was...
36.
Abdalla Elsayed M, Taylor L, Josan A, Fischer M, MacLaren R
Int J Mol Sci
. 2023 Sep;
24(18).
PMID: 37762657
Choroideremia is an X-linked retinal degeneration resulting from the progressive, centripetal loss of photoreceptors and choriocapillaris, secondary to the degeneration of the retinal pigment epithelium. Affected individuals present in late...
37.
Liu W, Taylor L, MacLaren R, Jolly J
Clin Ophthalmol
. 2023 Sep;
17:2729-2735.
PMID: 37743890
Purpose: Clinical research brings the potential of improved diagnostics, sight-saving treatments, and more accessible services to those suffering with severe sight impairment (SSI). This report investigates whether registered ophthalmology clinical...
38.
Farag S, Yusuf I, Kaukonen M, Taylor L, Charbel Issa P, MacLaren R
Ophthalmic Genet
. 2023 Sep;
45(2):201-206.
PMID: 37728066
Purpose: Retinitis pigmentosa (RP) associated with biallelic variants in CDHR1 has rarely been reported, and detailed phenotyping data are not available. RP implies relative preservation of foveal cones, when compared...
39.
Borchert G, Shamsnajafabadi H, Hu M, de Silva S, Downes S, MacLaren R, et al.
Cells
. 2023 Aug;
12(16).
PMID: 37626902
Age-related macular degeneration (AMD) is the leading cause of vision loss and visual impairment in people over 50 years of age. In the current therapeutic landscape, intravitreal anti-vascular endothelial growth...
40.
Shamsnajafabadi H, MacLaren R, Cehajic-Kapetanovic J
Cells
. 2023 Aug;
12(15).
PMID: 37566092
Leber hereditary optic neuropathy (LHON) is the most common primary mitochondrial genetic disease that causes blindness in young adults. Over 50 inherited mitochondrial DNA (mtDNA) variations are associated with LHON;...