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List of works by Jeroen Klevering

A Nonsense Mutation in FAM161A Is a Recurrent Founder Allele in Dutch and Belgian Individuals With Autosomal Recessive Retinitis Pigmentosa.

scientific article published on November 2015

A man with progressive diplopia

scientific article published on January 1, 2012

A pilot study on slit lamp-adapted optical coherence tomography imaging of trabeculectomy filtering blebs.

scientific article published on 22 November 2006

ARE INTRAVITREAL INJECTIONS WITH ULTRATHIN 33-G NEEDLES LESS PAINFUL THAN THE COMMONLY USED 30-G NEEDLES?

scientific article published on 20 April 2015

Association analysis of genetic and environmental risk factors in the cuticular drusen subtype of age-related macular degeneration ⬇️

scientific article published on August 18, 2012

Association of Smoking and CFH and ARMS2 Risk Variants With Younger Age at Onset of Neovascular Age-Related Macular Degeneration.

scientific article published on May 2015

Asymmetric Inter-Eye Progression in Stargardt Disease.

scientific article published in December 2016

Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome

scientific article published on 2 April 2004

Basal laminar drusen caused by compound heterozygous variants in the CFH gene

scientific article published on February 2008

Carbonic Anhydrase Inhibitors for the Treatment of Cystic Macular Lesions in Children With X-Linked Juvenile Retinoschisis

scientific article published in October 2016

Central areolar choroidal dystrophy

scientific article published on 25 February 2009

Central areolar choroidal dystrophy (CACD) and age-related macular degeneration (AMD): differentiating characteristics in multimodal imaging

scientific article

Central areolar choroidal dystrophy associated with dominantly inherited drusen

scientific article

Clinical and genetic heterogeneity in multifocal vitelliform dystrophy

scientific article published in August 2007

Cumulative Effect of Risk Alleles in CFH, ARMS2, and VEGFA on the Response to Ranibizumab Treatment in Age-related Macular Degeneration ⬇️

scientific article published on July 26, 2012

Cuticular drusen: stars in the sky.

scientific article published on 09 September 2013

Eccentric Gaze Direction in Patients with Central Field Loss ⬇️

scientific article published on October 1, 2011

Evaluation of Serum Lipid Concentrations and Genetic Variants at High-Density Lipoprotein Metabolism Loci andTIMP3in Age-Related Macular Degeneration ⬇️

scientific article published on July 25, 2011

Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa.

scientific article

Foveal sparing in Stargardt disease.

scientific article published on 16 October 2014

Genetic, behavioral, and sociodemographic risk factors for second eye progression in age-related macular degeneration

scientific article published on 24 August 2012

Heterozygous Deep-Intronic Variants and Deletions inABCA4in Persons with Retinal Dystrophies and One ExonicABCA4Variant

High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population

scientific article published on 06 April 2011

Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt disease

scientific article

Hyperreflective foci on optical coherence tomography associate with treatment outcome for anti-VEGF in patients with diabetic macular edema

scientific article published in PLoS ONE

Identification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosa

scientific article

Impact of motion-associated noise on intrinsic optical signal imaging in humans with optical coherence tomography.

scientific article published on 9 April 2015

Intraocular inflammation following endotamponade with high-density silicone oil.

scientific article published on 17 March 2004

Lipofuscin-associated photo-oxidative stress during fundus autofluorescence imaging

scientific article

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa

scientific article

Multimodal imaging of the disease progression of birdshot chorioretinopathy

scientific article published on 27 May 2016

Multimodal imaging of the macula in hereditary and acquired lack of macular pigment.

scientific article

Mutations in C2ORF71 cause autosomal-recessive retinitis pigmentosa

scientific article published on 15 April 2010

Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement

scientific journal article

Mutations in the EYS gene account for approximately 5% of autosomal recessive retinitis pigmentosa and cause a fairly homogeneous phenotype

scientific article published in October 2010

Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus

scientific article

Near-infrared reflectance imaging of neovascular age-related macular degeneration

scientific article

Next Generation Genetic Testing for Retinitis Pigmentosa

Next-generation genetic testing for retinitis pigmentosa

scientific article

Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosis

scientific article

Outcome of ABCA4 microarray screening in routine clinical practice

scientific article published on 20 December 2009

Peripheral retinal nonperfusion associated with chronic myeloid leukemia

scientific article

Phenotypic spectrum of autosomal recessive cone-rod dystrophies caused by mutations in the ABCA4 (ABCR) gene.

scientific article published in June 2002

Risk Alleles in CFH and ARMS2 Are Independently Associated with Systemic Complement Activation in Age-related Macular Degeneration

scientific article published on 30 November 2011

Risk factors for development and progression of diabetic retinopathy in Dutch patients with type 1 diabetes mellitus

article

Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations

scientific article

The RD5000 database: facilitating clinical, genetic, and therapeutic studies on inherited retinal diseases

scientific article (publication date: November 2014)

The efficacy of microarray screening for autosomal recessive retinitis pigmentosa in routine clinical practice

scientific article published on 28 April 2015

The identification of a RNA splice variant in TULP1 in two siblings with early-onset photoreceptor dystrophy

scientific article published on 04 April 2019

The spectrum of ocular phenotypes caused by mutations in the BEST1 gene

scientific article published on 16 April 2009

The spectrum of phenotypes caused by variants in the CFH gene.

scientific article

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene

scientific article published on 26 January 2008

The spectrum of retinal phenotypes caused by mutations in the ABCA4 gene

scientific article published on 22 December 2004

The transconjunctival approach with lateral canthal extension for three-wall orbital decompression in thyroid orbitopathy

scientific article published on 03 December 2008

Three families displaying the combination of Stargardt's disease with cone-rod dystrophy or retinitis pigmentosa

scientific article published in March 2004

Whole-genome copy-number analysis identifies new leads for chromosomal aberrations involved in the oncogenesis and metastastic behavior of uveal melanomas

scientific article published on June 2015

Zinc supplementation inhibits complement activation in age-related macular degeneration

scientific article

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