A. Churchill

J. Rankin, P. Rizzu, M. S. van der Knaap, 2010, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation

E. Héon, M. Hosseini, A. Churchill, 2010, Acta ophthalmologica.

Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.

J. Clayton-Smith, D. Taylor, R. Winter, 2000, Investigative ophthalmology & visual science.

Clinical manifestations of protein C deficiency: a spectrum within one family

A. Churchill, A. Minford, M. Gallagher, 2001, The British journal of ophthalmology.

Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.

Jonathan E. Moore, D. Frazer, C. Willoughby, 2013, Investigative ophthalmology & visual science.

Polymicrogyria and absence of pineal gland due to PAX6 mutation

S. Shorvon, J. Stevens, S. Sisodiya, 2003, Annals of neurology.

Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.

P. Carlsson, S. Enerbäck, A. Churchill, 2002, Investigative ophthalmology & visual science.

PAX 6 is normal in most cases of Peters' anomaly

A. Markham, A. Booth, A. Churchill, 1998, Eye.

Factors affecting visual outcome in children following uniocular traumatic cataract

A. Churchill, B. Noble, D. Etchells, 1995, Eye.

Prenatal diagnosis of aniridia.

A. Markham, I. Hanson, A. Churchill, 2000, Ophthalmology.

Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.

Jonathan E. Moore, D. Frazer, C. Willoughby, 2013, Investigative ophthalmology & visual science.

Tumor necrosis factor polymorphisms associated with tumor necrosis factor production influence the risk of idiopathic intermediate uveitis

J. Forrester, A. Dick, J. Bidwell, 2013, Molecular vision.

Clinical and experimental advances in congenital and paediatric cataracts

J. Graw, A. Churchill, 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.

Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease

D. Mackey, J. Craig, C. Inglehearn, 2002, Journal of medical genetics.

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy.

D. Mackey, R. Newbury-Ecob, A. Markham, 2001, Human molecular genetics.

Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.

R. Axton, J. Love, F. Meire, 1999, Human molecular genetics.

A new set of primers for mutation analysis of the human PAX6 gene

R. Axton, J. Love, I. Hanson, 1998, Human mutation.

Punctate inner choroidopathy and multifocal choroiditis with panuveitis share haplotypic associations with IL10 and TNF loci.

J. Forrester, A. Dick, J. Bidwell, 2011, Investigative ophthalmology & visual science.

A Combined in silico, in vitro and Clinical Approach to Characterize Novel Pathogenic Missense Variants in PRPF31 in Retinitis Pigmentosa

G. Wheway, A. Churchill, S. Hunt, 2019, Front. Genet..

A combined in silico, in vitro and clinical approach to characterise novel pathogenic missense variants in PRPF31 in retinitis pigmentosa

G. Wheway, A. Churchill, S. Hunt, 2018, bioRxiv.

Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8.

G. Holder, S. Bhattacharya, A. Webster, 2011, Investigative ophthalmology & visual science.

Cytokine polymorphism in noninfectious uveitis.

J. Forrester, A. Dick, J. Bidwell, 2010, Investigative ophthalmology & visual science.

Regulation of alternative VEGF-A mRNA splicing is a therapeutic target for analgesia

H. Kennedy, S. Harper, D. Bates, 2014, Neurobiology of Disease.

Progressive neurodegenerative disorder in a patient with nonketotic hyperglycinemia

A. Churchill, Bzoch Kr, L. Swisher, 1981 .

Recombinant human VEGF165b inhibits experimental choroidal neovascularization.

S. Harper, D. Bates, S. Kase, 2010, Investigative ophthalmology & visual science.

VEGF-A165b is cytoprotective and antiangiogenic in the retina.

S. Harper, D. Bates, M. Gammons, 2010, Investigative ophthalmology & visual science.

The genetics of primary open angle glaucoma

A. Booth, A. Churchill, R. Anwar, 1997, The British journal of ophthalmology.

Should myopes have routine axial length measurements before retrobulbar or peribulbar injections?

A. Churchill, T. E. James, 1996, The British journal of ophthalmology.

VEGF-A165b is an endogenous neuroprotective splice isoform of vascular endothelial growth factor A in vivo and in vitro.

P. Kehoe, S. Harper, D. Bates, 2013, The American journal of pathology.

What factors influence cataract waiting list time?

O. Backhouse, A. Churchill, O. Stewart, 2000, The British journal of ophthalmology.

New macular findings in individuals with biallelic KLHL7 gene mutation

R. Newbury-Ecob, L. Heng, S. Smithson, 2019, BMJ Open Ophthalmology.

Polymorphisms in OPA1 are associated with normal tension glaucoma.

C. Inglehearn, C. Toomes, P. Spry, 2003, Molecular vision.

Polymorphisms in OPA 1 are associated with normal tension glaucoma

C. Inglehearn, C. Toomes, P. Spry, 2003 .

Diabetic retinopathy is associated with a switch in splicing from anti- to pro-angiogenic isoforms of vascular endothelial growth factor

S. Harper, D. Bates, A. Churchill, 2005, Diabetologia.

Analysis of SERPING1 and its association with age‐related macular degeneration

A. Churchill, James G Carter, 2009, Acta ophthalmologica.

An alternative and more cost effective method of delivery of radiotherapy in age related macular degeneration

D. Ash, A. Churchill, W. Franks, 1998, The British journal of ophthalmology.

Quantitative MR image analysis in subjects with defects in the PAX6 gene

Samantha L. Free, Veronica van Heyningen, Sanjay M. Sisodiya, 2003, NeuroImage.

Clinical Reasoning: Complex ataxia

A. Churchill, K. Vijayakumar, T. Abkur, 2020, Neurology.

A potential therapeutic target in age-related macular degeneration

A. Churchill, James G Carter, 2007 .

β‐Defensin 1 haplotype associated with postoperative endophthalmitis

A. Churchill, James G Carter, R. Haynes, 2010, Acta ophthalmologica.

A case of bilateral endophthalmitis and carriage of &bgr;-defensin 1 –44CC genotype

A. Churchill, James G Carter, R. Haynes, 2007, British Journal of Ophthalmology.

The carboxyl terminus of VEGF-A is a potential target for anti-angiogenic therapy

G. Damodaran, S. Harper, D. Bates, 2014, Angiogenesis.

Paediatric outpatient clinics: A unique case for expanded clinic provision?

A. Churchill, R. Harrison, 2017 .

Public opinion on weekend and evening outpatient clinics

S. Anand, A. Churchill, C. Gibbon, 2003, British Journal of Ophthalmology.

Cytokine polymorphism in noninfectious uveitis.

J. Forrester, A. Dick, J. Bidwell, 2010, Investigative Ophthalmology and Visual Science.

β‐Defensin 1 haplotype associated with postoperative endophthalmitis

A. Churchill, James G Carter, R. Haynes, 2010, Acta ophthalmologica.

Allergic eye disease in children: identifying the signs and symptoms

A. Churchill, D. Tole, P. Choleva, 2014 .