Ian C. Lloyd

Oxford Rd
Manchester, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 22 publications

Genomic Approaches to Diagnosis in Congenital and Developmental Cataract: Comparison of Panel Versus Whole Genome Sequencing, Diagnostic Yield, Variant Spectrum, Genotype-Phenotype Correlations, and Implications for Counseling.

Genomic Approaches to Diagnosis in Congenital and Developmental Cataract: Comparison of Panel Versus Whole Genome Sequencing, Diagnostic Yield, Variant Spectrum, Genotype-Phenotype Correlations, and Implications for Counseling.

Journal: American journal of ophthalmology

Published: December 31, 2025

A novel PAX2 heterozygous mutation in a male with anterior segment dysgenesis, colobomatous optic nerves and atypical retinal findings: a case report.

A novel PAX2 heterozygous mutation in a male with anterior segment dysgenesis, colobomatous optic nerves and atypical retinal findings: a case report.

Journal: Ophthalmic genetics

Published: June 29, 2025

The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular Disease.

The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular Disease.

Journal: Clinical genetics

Published: June 26, 2025

Update on pediatric cataract surgery.

Update on pediatric cataract surgery.

Journal: Asia-Pacific journal of ophthalmology (Philadelphia, Pa.)

Published: May 23, 2025

Abusive head trauma and the eye in infants and children - clinical guideline update by the royal college of ophthalmologists and the royal college of paediatrics and child health: executive summary.

Abusive head trauma and the eye in infants and children - clinical guideline update by the royal college of ophthalmologists and the royal college of paediatrics and child health: executive summary.

Journal: Eye (London, England)

Published: January 16, 2024

Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation.

Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation.

Journal: Clinical dysmorphology

Published: October 15, 2021

Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia.

Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia.

Journal: Orphanet journal of rare diseases

Published: June 10, 2021

EPHA2 Segregates with Microphthalmia and Congenital Cataracts in Two Unrelated Families.

EPHA2 Segregates with Microphthalmia and Congenital Cataracts in Two Unrelated Families.

Journal: International journal of molecular sciences

Published: January 06, 2021

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

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

Journal: Genes

Published: November 27, 2020

Study of Optimal Perimetric Testing In Children (OPTIC): developing consensus and setting research priorities for perimetry in the management of children with glaucoma.

Study of Optimal Perimetric Testing In Children (OPTIC): developing consensus and setting research priorities for perimetry in the management of children with glaucoma.

Journal: Eye (London, England)

Published: November 02, 2020

Re: Lambert et al.: Intraocular lens implantation during early childhood: a report by the American Academy of Ophthalmology (Ophthalmology. 2019;126:1454-1461).

Re: Lambert et al.: Intraocular lens implantation during early childhood: a report by the American Academy of Ophthalmology (Ophthalmology. 2019;126:1454-1461).

Journal: Ophthalmology

Published: September 11, 2019

Traboulsi syndrome due to ASPH mutation: an under-recognised cause of ectopia lentis.

Traboulsi syndrome due to ASPH mutation: an under-recognised cause of ectopia lentis.

Journal: Clinical dysmorphology

Published: July 06, 2019

Showing 1-12 of 22

Last Updated: 09/26/2026