Isabelle Russell‐Eggitt

Great Ormond Street Hospital for Children NHS Foundation Trust — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

32h-index4.2kcitations72works0.02yr avg
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Research Topics

Retinal Development and Disorders(14), Glaucoma and retinal disorders(10), Ophthalmology and Visual Impairment Studies(8), Ocular Disorders and Treatments(8), Genetic and Kidney Cyst Diseases(7)

Publications71 total

Study of Optimal Perimetric Testing In Children (OPTIC): developing consensus and setting research priorities for perimetry in the management of children with glaucoma
Eye·2021· 8 citedOpen Access
Comparison of Quality and Output of Different Optimal Perimetric Testing Approaches in Children With Glaucoma
JAMA Ophthalmology·2017· 15 citedOpen Access
Study of Optimal Perimetric Testing In Children (OPTIC): development and feasibility of the kinetic perimetry reliability measure (KPRM)
British Journal of Ophthalmology·2016· 5 cited
OPTIC study: Feasibility and reliability of perimetry in children with glaucoma
UCL Discovery (University College London)·2016Open Access
Genetic Analysis of ‘PAX6-Negative’ Individuals with Aniridia or Gillespie Syndrome
PLoS ONE·2016· 83 citedOpen Access
Study of Optimal Perimetric Testing in Children (OPTIC): Feasibility, Reliability and Repeatability of Perimetry in Children
PLoS ONE·2015· 59 citedOpen Access
Study of Optimal Perimetric Testing In Children (OPTIC)
Ophthalmology·2015· 37 citedOpen Access
Study of Optimal Perimetric Testing In Children (OPTIC) - Comparison of outputs and normative data for Goldmann and Octopus kinetic perimetry
UCL Discovery (University College London)·2015
Risks and outcomes associated with primary intraocular lens implantation in children under 2 years of age: the IoLunder2 cohort study
British Journal of Ophthalmology·2015· 109 citedOpen Access
Active surveillance of visual impairment due to adverse drug reactions: findings from a national study in the United Kingdom
Pharmacology Research & Perspectives·2014· 5 citedOpen Access
Risks and outcomes associated with primary intraocular lens implantation in children under 2 years old with congenital and infantile cataract: the UK and Ireland IoLunder2 cohort study
The Lancet·2014· 2 citedOpen Access
Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness
PLoS ONE·2014· 35 citedOpen Access
Visual Impairment Owing to Adverse Drug Reaction: Incidence and Routine Monitoring in the United Kingdom
Ophthalmology·2014· 2 citedOpen Access
How should we assess reliability of visual field assessment in children
Investigative Ophthalmology & Visual Science·2013· 1 cited
Accuracy of routine data on paediatric cataract in the UK compared to active surveillance: lessons from the IOLu2 study
British Journal of Ophthalmology·2013· 9 cited
Retinal characteristics of the congenital disorder of glycosylation PMM2‐CDG
Journal of Inherited Metabolic Disease·2013· 19 cited
Homozygosity for piebaldism with a proven KIT mutation resulting in depigmentation of the skin and hair, deafness, developmental delay and autism spectrum disorder
Clinical Dysmorphology·2013· 24 cited
The blind kidney: disorders affecting kidneys and eyes
Pediatric Nephrology·2013· 8 cited
Albinism
Elsevier eBooks·2013
Retinal On-Pathway Deficit in Congenital Disorder of Glycosylation Due to Phosphomannomutase Deficiency
Archives of Ophthalmology·2012· 13 citedOpen Access
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Frequent Co-authors

Dorothy Thompson(12), Jugnoo S. Rahi(8), David Taylor(8), A Kriss(8), Fatima Shawkat(6), Christine Timms(4), Ken K. Nischal(4), Phillippa Cumberland(4), David S. Taylor(4), Christopher M. Harris(4), Jane C. Sowden(3), Mario Cortina‐Borja(3), Peng T. Khaw(3), Anthony T. Moore(3), Kling Chong(3), Stephanie Grünewald(3), Dipesh E. Patel(3), Bronwen Walters(3), Gayle B. Collin(2), Jan D. Marshall(2)