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R. V. van Huet · SciRah

Researcher profile · Semantic Scholar

R. V. van Huet

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R. V. van Huet — researcher profile on SciRah

h-index: 19
Works: 42
Citations: 2,071

Most-cited papers

Non‐syndromic retinitis pigmentosa
S. K. Verbakel, R. V. van Huet, C. Boon, A. den Hollander +5 more
2018Progress in retinal and eye research859 citations Open access
Semantic Scholar
Next-generation genetic testing for retinitis pigmentosa
K. Neveling, R. W. Collin, C. Gilissen, R. V. van Huet +19 more
2012Human Mutation303 citations Open access
Semantic Scholar
Early-onset stargardt disease: phenotypic and genotypic characteristics.
S. Lambertus, R. V. van Huet, N. Bax, L. Hoefsloot +4 more
2015Ophthalmology (Rochester, Minn.)151 citations Open access
Semantic Scholar
Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement.
Alejandro Estrada-Cuzcano, K. Neveling, S. Kohl, E. Banin +19 more
2012American Journal of Human Genetics99 citations Open access
Semantic Scholar
Central areolar choroidal dystrophy (CACD) and age-related macular degeneration (AMD): differentiating characteristics in multimodal imaging.
D. Smailhodzic, M. Fleckenstein, T. Theelen, C. Boon +8 more
2011Investigative Ophthalmology and Visual Science71 citations Open access
Semantic Scholar
Foveal sparing in Stargardt disease.
R. V. van Huet, N. Bax, Sarah C. Westeneng-Van Haaften, M. Muhamad +6 more
2014Investigative Ophthalmology and Visual Science68 citations Open access
Semantic Scholar
Long‐term outcomes of vitrectomy for proliferative diabetic retinopathy
Vivian Schreur, J. Brouwers, R. V. van Huet, S. Smeets +4 more
2020Acta ophthalmologica55 citations Open access
Semantic Scholar
Exome sequencing extends the phenotypic spectrum for ABHD12 mutations: from syndromic to nonsyndromic retinal degeneration.
K. Nishiguchi, A. Ávila-Fernández, R. V. van Huet, M. Cortón +18 more
2014Ophthalmology (Rochester, Minn.)54 citations
Semantic Scholar
Zinc Supplementation Inhibits Complement Activation in Age-Related Macular Degeneration
D. Smailhodzic, F. van Asten, A. Blom, F. Mohlin +13 more
2014PLoS ONE54 citations Open access
Semantic Scholar
IMPG2-associated retinitis pigmentosa displays relatively early macular involvement.
R. V. van Huet, R. W. Collin, A. Siemiątkowska, C. Klaver +10 more
2014Investigative Ophthalmology and Visual Science40 citations Open access
Semantic Scholar
Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum.
S. K. Verbakel, R. V. van Huet, A. den Hollander, M. Geerlings +15 more
2019Investigative Ophthalmology and Visual Science38 citations Open access
Semantic Scholar
The effect of light deprivation in patients with Stargardt disease.
M. Teussink, Michele D. Lee, R. T. Smith, R. V. van Huet +4 more
2015American journal of ophthalmology-glaucoma38 citations Open access
Semantic Scholar
The RD5000 database: facilitating clinical, genetic, and therapeutic studies on inherited retinal diseases.
R. V. van Huet, C. Oomen, A. Plomp, M. V. van Genderen +5 more
2014Investigative Ophthalmology and Visual Science36 citations Open access
Semantic Scholar
The efficacy of microarray screening for autosomal recessive retinitis pigmentosa in routine clinical practice
R. V. van Huet, L. Pierrache, M. Meester-Smoor, C. Klaver +6 more
2015Molecular Vision31 citations
Semantic Scholar
Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.
R. V. van Huet, Alejandro Estrada-Cuzcano, E. Banin, Y. Rotenstreich +6 more
2013Investigative Ophthalmology and Visual Science31 citations Open access
Semantic Scholar
The genetics and disease mechanisms of rhegmatogenous retinal detachment.
B. M. Govers, R. V. van Huet, S. Roosing, S. Keijser +3 more
2023Progress in retinal and eye research30 citations Open access
Semantic Scholar
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosis
A. Siemiątkowska, L. I. van den Born, M. V. van Genderen, Mette Bertelsen +11 more
2014Molecular Vision28 citations
Semantic Scholar
Nonsyndromic Hearing Loss Caused by USH1G Mutations: Widening the USH1G Disease Spectrum
Anne Marthe Maria Oonk, R. V. van Huet, Joop M. Leijendeckers, Jaap Oostrik +8 more
2015Ear and Hearing20 citations
Semantic Scholar
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra‐ocular features
R. V. van Huet, A. Siemiątkowska, R. Özgül, D. Yücel +10 more
2015Acta ophthalmologica19 citations Open access
Semantic Scholar
Dominant cystoid macular dystrophy.
N. Saksens, R. V. van Huet, J. J. V. van Lith-Verhoeven, A. den Hollander +2 more
2015Ophthalmology (Rochester, Minn.)12 citations
Semantic Scholar
Risk factors and management of primary giant retinal tears
Birgit M. Govers, R. V. van Huet, M. el Kandoussi, A. den Hollander +2 more
2023Acta ophthalmologica9 citations Open access
Semantic Scholar
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis
E. L. de Groot, Jeannette Ossewaarde-van Norel, J. D. de Boer, S. Hiddingh +14 more
2023JAMA ophthalmology8 citations Open access
Semantic Scholar
Idiopathic multifocal choroiditis and punctate inner choroidopathy: an evaluation in pregnancy
E. L. de Groot, R. V. van Huet, K. Bloemenkamp, J. D. de Boer +1 more
2021Acta ophthalmologica8 citations Open access
Semantic Scholar
Next Generation Genetic Testing for Retinitis Pigmentosa
K. Neveling, R. W. Collin, C. Gilissen, R. V. van Huet +19 more
20136 citations Open access
Semantic Scholar
Novel compound heterozygous NMNAT 1 variants associated with Leber congenital amaurosis
A. Siemiątkowska, L. I. van den Born, M. V. van Genderen, Mette Bertelsen +14 more
20174 citations
Semantic Scholar
Retina Clinical Characteristics of Rod and Cone Photoreceptor Dystrophies in Patients With Mutations in the C 8 orf 37 Gene
R. V. van Huet, Alejandro Estrada-Cuzcano, E. Banin, Y. Rotenstreich +6 more
20134 citations
Semantic Scholar
Cross-Phenotype Plasma Proteomics Reveals Molecular Heterogeneity in Neovascular AMD
R. Rijken, E. M. Pameijer, A. D. de Ligt, M. Stehouwer +20 more
2026medRxiv0 citations Open access
Semantic Scholar
Peer Review #1 of "Ultrastructural alterations in the retinal pigment epithelium and photoreceptors of a Stargardt patient and three Stargardt mouse models: indication for the central role of RPE melanin in oxidative stress (v0.1)"
Tatjana Taubitz, A. Tschulakow, M. Tikhonovich, B. Illing +425 more
20180 citations Open access
Semantic Scholar
Retina Foveal Sparing in Stargardt Disease
R. V. van Huet, N. Bax, Sarah C. Westeneng-Van Haaften, M. Muhamad +6 more
20170 citations
Semantic Scholar
Insensitive short-term clinical trial endpoint in Stargardt disease: progression of best-corrected visual acuity
S. K. Verbakel, S. Lambertus, N. Bax, Dyon Valkenburg +3 more
20170 citations
Semantic Scholar
The clinical spectrum of IMPG2-associated retinal dystrophies
A. Thiadens, A. D. de Boer, J. Kievit, V. Verhoeven +3 more
20170 citations
Semantic Scholar
Macular Changes in Generalized Retinal Dystrophies and in Cone Dystrophies
C. Hoyng, R. V. van Huet
20160 citations
Semantic Scholar
Inherited retinal dystrophies. Studies on the clinical and genetic characteristics
R. V. van Huet
20150 citations
Semantic Scholar
Reply: To PMID 25267528.
N. Saksens, R. V. van Huet, J. J. V. van Lith-Verhoeven, A. den Hollander +2 more
2015Ophthalmology (Rochester, Minn.)0 citations Open access
Semantic Scholar
The Effect of Light Deprivation in Human STGD1 Patients
M. Teussink, Michele D. Lee, Theodore R. Smith, R. V. van Huet +4 more
20140 citations
Semantic Scholar
The natural progression of early-onset Stargardt disease
S. Lambertus, R. V. van Huet, N. Bax, Ellen van den Wittenboer +4 more
20140 citations
Semantic Scholar
Analysis of ABCA4- related retinal dystrophies without fundus abnormalities.
N. Bax, S. Lambertus, R. V. van Huet, F. Cremers +1 more
20140 citations
Semantic Scholar
Functional Optical Coherence Tomography with a Commercial Device - A Pilot Study
M. Teussink, M. V. van Grinsven, R. V. van Huet, B. Cense +3 more
20130 citations
Semantic Scholar
Clinical evaluation of foveal sparing in patients with Stargardt disease
R. V. van Huet, Sarah Westeneng van Haaften, M. Muhamad, F. Cremers +3 more
20130 citations
Semantic Scholar
Clinical Features In Patients With Cone-Rod Dystrophy Or Retinitis Pigmentosa Due To Mutations In C8orf37
R. V. van Huet, A. E. Cuzcano, E. Banin, Y. Rotenstreich +6 more
20120 citations
Semantic Scholar
Mutations In IMPG2 Are Causative For Autosomal Recessive Retinitis Pigmentosa Combined With Bull’s Eye Maculopathy
R. V. van Huet, L. I. van den Born, K. Neveling, A. Siemiątkowska +4 more
20110 citations
Semantic Scholar
Rondom de metro: Een onderzoek naar de fysieke inrichtingspotentie van metrostationsomgevingen in de autogeorienteerde regio Rotterdam
R. V. van Huet
20110 citations
Semantic Scholar

Frequent co-authors

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C. Hoyng×31
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C. Hoyng — researcher profile on SciRah
B. Klevering×27
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B. Klevering — researcher profile on SciRah
A. den Hollander×20
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A. den Hollander — researcher profile on SciRah
F. Cremers×16
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×13

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R. W. Collin — researcher profile on SciRah

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C. Boon — researcher profile on SciRah

L. I. van den Born×10

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L. I. van den Born — researcher profile on SciRah

L. Hoefsloot×9

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L. Hoefsloot — researcher profile on SciRah

A. Siemiątkowska×7

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A. Siemiątkowska — researcher profile on SciRah

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N. Bax — researcher profile on SciRah

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E. Banin — researcher profile on SciRah

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T. Theelen — researcher profile on SciRah