I. C. Lloyd

I. C. Lloyd, Deborah M. Costakos, E. Héon, 2019, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Combined trabeculotomy–trabeculectomy augmented with 5‐fluorouracil in paediatric glaucoma

I. C. Lloyd, L. Au, S. Biswas, 2011, Clinical & experimental ophthalmology.

Optic atrophy in association with cobalamin C (cblC) disease

I. C. Lloyd, S. Beatty, N. Patton, 2000, Ophthalmic genetics.

Does the timing of treatment affect the ocular phenotype in patients with Mucopolysaccharidosis I homozygous for the L490P mutation?

I. C. Lloyd, S. Biswas, J. Ashworth, 2013, Eye.

The Use of Autozygosity Mapping and Next-Generation Sequencing in Understanding Anterior Segment Defects Caused by an Abnormal Development of the Lens

I. C. Lloyd, G. Black, R. Gillespie, 2014, Human Heredity.

Investigation of microbial keratitis: an audit from 1988-1992.

I. C. Lloyd, P. Simcock, J. Butcher, 2009, Acta ophthalmologica Scandinavica.

Primary IOL implantation in children: a risk analysis of foldable acrylic v PMMA lenses

I. C. Lloyd, S. Biswas, N. Rowe, 2004, British Journal of Ophthalmology.

Accuracy of intraocular lens power calculation in paediatric cataract surgery

I. C. Lloyd, C. Tromans, S. Biswas, 2001, The British journal of ophthalmology.

Cataract management in children: a review of the literature and current practice across five large UK centres

I. C. Lloyd, M. Parulekar, A. L. Solebo, 2020, Eye.

Neonatal cataract: Aetiology, pathogenesis and management

I. C. Lloyd, D. Taylor, A. Kriss, 1992, Eye.

Aspects of albinism.

I. C. Lloyd, A. Kriss, C. Harris, 1992, Ophthalmic paediatrics and genetics.

Oculocutaneous albinism

I. C. Lloyd, S. Biswas, 1999, Archives of disease in childhood.

Anterior segment dysgenesis in mosaic Turner syndrome

I. C. Lloyd, J. Clayton-Smith, D. Donnai, 1997, The British journal of ophthalmology.

Dominantly inherited unilateral retinal dysplasia.

I. C. Lloyd, R. Bonshek, A. Tullo, 1993, The British journal of ophthalmology.

Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation

I. C. Lloyd, D. Smedley, M. McEntagart, 2021, Clinical dysmorphology.

Educational paper

I. C. Lloyd, S. Biswas, J. Ashworth, 2012, European Journal of Pediatrics.

Mutations in SIPA1L3 cause eye defects through disruption of cell polarity and cytoskeleton organization.

Silke Rinkwitz, I. C. Lloyd, Marija Mihelec, 2015, Human molecular genetics.

Congenital and infantile cataract: aetiology and management.

I. C. Lloyd, S. Biswas, J. Ashworth, 2012, European journal of pediatrics.

Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation

I. C. Lloyd, P. Scambler, P. Tam, 2007, Human mutation.

Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric Cataract.

I. C. Lloyd, J. Clayton-Smith, S. Williams, 2016, Ophthalmology.

Molecular findings from 537 individuals with inherited retinal disease

I. C. Lloyd, J. Lamb, S. Daiger, 2016, Journal of Medical Genetics.

The ophthalmic findings in Cohen syndrome

I. C. Lloyd, K E Chandler, J. Clayton-Smith, 2002, The British journal of ophthalmology.

MRI and CT in pediatric ophthalmology: a guide to their use.

I. C. Lloyd, D. Taylor, B. Kendall, 1991, Seminars in ophthalmology.

Endocrine status in patients with optic nerve hypoplasia: relationship to midline central nervous system abnormalities and appearance of the hypothalamic-pituitary axis on magnetic resonance imaging.

I. C. Lloyd, P. Clayton, L. Patel, 2003, The Journal of clinical endocrinology and metabolism.

Geographical distribution of optic nerve hypoplasia and septo-optic dysplasia in Northwest England.

I. C. Lloyd, P. Clayton, R. McNally, 2006, The Journal of pediatrics.

Optic nerve size evaluated by magnetic resonance imaging in children with optic nerve hypoplasia, multiple pituitary hormone deficiency, isolated growth hormone deficiency, and idiopathic short stature.

I. C. Lloyd, P. Clayton, L. Patel, 2004, The Journal of pediatrics.

Flecked retina associated with ring 17 chromosome

I. C. Lloyd, J. Doré, R. Kumari, 2009, Eye.

Ectopia lentis et pupillae: the genetic aspects and differential diagnosis.

I. C. Lloyd, D. Donnai, A. Colley, 1991, Journal of medical genetics.

Nystagmus in the child with congenital cataract

I. C. Lloyd, J. Self, 2017 .

Refractive outcomes after primary intraocular lens implantation in infants

I. C. Lloyd, A. Maino, S. Biswas, 2006, British Journal of Ophthalmology.

Bardet-Biedl Syndrome: An Atypical Phenotype in Brothers with a Proven BBS1 Mutation

I. C. Lloyd, J. Clayton-Smith, P. Beales, 2008, Ophthalmic genetics.

Clinical and molecular genetic findings in autosomal dominant OPA3-related optic neuropathy

Jennifer R. Davies, I. C. Lloyd, M. Votruba, 2014, neurogenetics.

Clinical Spectrum and Genetic Diagnosis of 54 Consecutive Patients Aged 0–25 with Bilateral Cataracts

I. C. Lloyd, S. Malka, M. Moosajee, 2021, Genes.

Nidek MP-1 microperimetry and Fourier domain optical coherence tomography (FD-OCT) in X linked retinoschisis

I. C. Lloyd, P. Stanga, S. Biswas, 2010, British Journal of Ophthalmology.

Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome

I. C. Lloyd, S. Bhaskar, G. Hall, 2015, The Lancet.

Modulation of amblyopia therapy following early surgery for unilateral congenital cataracts.

I. C. Lloyd, D. Taylor, A. Kriss, 1995, The British journal of ophthalmology.

Intraocular Lens Implantation in the Capsular Bag and Posterior Capsulotomy Techniques

I. C. Lloyd, J. Ashworth, I. Lloyd, 2017 .