D. Joshua Cameron

A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.

Amino-retinoid compounds in the human retinal pigment epithelium.

Elovl4 haploinsufficiency does not induce early onset retinal degeneration in mice.

Essential role of Elovl4 in very long chain fatty acid synthesis, skin permeability barrier function, and neonatal survival.

HTRA1 variant confers similar risks to geographic atrophy and neovascular age-related macular degeneration.

Murine ccl2/cx3cr1 deficiency results in retinal lesions mimicking human age-related macular degeneration.

HTRA1 variant increases risk to neovascular age-related macular degeneration in Chinese population.

10q26 is associated with increased risk of age-related macular degeneration in the Utah population.

Association of HTRA1 polymorphism and bilaterality in advanced age-related macular degeneration.

Further mapping of 10q26 supports strong association of HTRA1 polymorphisms with age-related macular degeneration.

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.

Alzheimer's-related peptide amyloid-β plays a conserved role in angiogenesis.

Early retinoic acid deprivation in developing zebrafish results in microphthalmia.

Amyloid-β increases capillary bed density in the adult zebrafish retina.

Introductory editorial.

Amyloid-β and APP Deficiencies Cause Severe Cerebrovascular Defects: Important Work for an Old Villain.