List of works - Robert Henderson

A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity

scientific article

A novel technique for high-density silicone oil removal

scientific article published on 01 September 2012

Accuracy of scleral transillumination techniques to identify infant ciliary body for sclerostomy and intravitreal injections

scientific article published on 10 December 2018

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy

scientific article published in December 2007

Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa

scientific article published on 5 January 2017

Early Onset Retinal Dystrophy Due to Mutations inLRAT: Molecular Analysis and Detailed Phenotypic Study

article

Effect of gene therapy on visual function in Leber's congenital amaurosis

scientific article

Group A streptococcal endophthalmitis complicating a sore throat in a 2-year-old child

scientific article

Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter Study.

scientific article

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

scientific article

Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndrome

scientific article published on 02 July 2020

Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females

scientific article published on 2 October 2017

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

scientific article

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

scientific article published on 17 October 2010

RDH12 retinopathy: novel mutations and phenotypic description.

scientific article published on 19 October 2011

Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

scientific article

The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders

scientific article published on 14 January 2019

Wound-related complications and clinical outcomes following open globe injury repair

scientific article published on 19 June 2015

List of works by Robert Henderson

A homozygous mutation in the TUB gene associated with retinal dystrophy and obesity

A novel technique for high-density silicone oil removal

Accuracy of scleral transillumination techniques to identify infant ciliary body for sclerostomy and intravitreal injections

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy

Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa

Early Onset Retinal Dystrophy Due to Mutations inLRAT: Molecular Analysis and Detailed Phenotypic Study

Effect of gene therapy on visual function in Leber's congenital amaurosis

Group A streptococcal endophthalmitis complicating a sore throat in a 2-year-old child

Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter Study.

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy.

Misaligned foveal morphology and sector retinal dysfunction in AKT1-mosaic Proteus syndrome

Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females

Novel mutations in MERTK associated with childhood onset rod-cone dystrophy

Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.

RDH12 retinopathy: novel mutations and phenotypic description.

Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations.

The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders

Wound-related complications and clinical outcomes following open globe injury repair