Age-related maculopathy: its genetic basis

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation.

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Exploring the choroidal vascular labyrinth and its molecular and structural roles in health and disease.

Progress in retinal and eye research·2021

Serum fatty acid chain length associates with prevalent symptomatic end-stage osteoarthritis, independent of BMI.

Scientific reports·2020

A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.

Behavior genetics·2019

Stem Cell Derived Retinal Pigment Epithelium: The Role of Pigmentation as Maturation Marker and Gene Expression Profile Comparison with Human Endogenous Retinal Pigment Epithelium.

Stem cell reviews and reports·2017

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts.

Translational psychiatry·2017

Patterns of appointment cancellations and no-shows across and within ophthalmology subspecialties.

Eye (London, England)·2026

Barriers to accessible ophthalmic imaging device uptake: an exploratory study of ophthalmology care provider perspectives.

Eye (London, England)·2026

Bridging the gap: A new perspective on lid wiper epitheliopathy and meibomian gland inversion.

Eye (London, England)·2026

Long-term outcomes of the Paul glaucoma implant in a paediatric population: A retrospective cohort study.

Eye (London, England)·2026

Long-term clinical outcomes of dome-shaped macula: a contralateral eye comparison.

Eye (London, England)·2026

Revisiting the sclera as a target for glaucoma therapy.

Eye (London, England)·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

Age-related maculopathy: its genetic basis

Related Concept Videos

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation.

Exploring the choroidal vascular labyrinth and its molecular and structural roles in health and disease.

Serum fatty acid chain length associates with prevalent symptomatic end-stage osteoarthritis, independent of BMI.

A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms.

Stem Cell Derived Retinal Pigment Epithelium: The Role of Pigmentation as Maturation Marker and Gene Expression Profile Comparison with Human Endogenous Retinal Pigment Epithelium.

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts.

Patterns of appointment cancellations and no-shows across and within ophthalmology subspecialties.

Barriers to accessible ophthalmic imaging device uptake: an exploratory study of ophthalmology care provider perspectives.

Bridging the gap: A new perspective on lid wiper epitheliopathy and meibomian gland inversion.

Long-term outcomes of the Paul glaucoma implant in a paediatric population: A retrospective cohort study.

Long-term clinical outcomes of dome-shaped macula: a contralateral eye comparison.

Revisiting the sclera as a target for glaucoma therapy.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

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The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

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Age-related maculopathy: its genetic basis

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