Peachey, Neal S.

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., Burdon, K. P., Hebbring, S. J., Wen, C., Gorski, M., et al. (2016) · Nature Genetics

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 1,544

Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration

Chen, W., Stambolian, D., Edwards, A. O., Branham, K. E., Othman, M., Jakobsdottir, J., Tosakulwong, N., Pericak-Vance, M. A., Campochiaro, P. A., Klein, M. L., et al. (2010) · Proceedings of the National Academy of Sciences

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 506

Neuronal Pentraxins Mediate Synaptic Refinement in the Developing Visual System

Bjartmar, L., Huberman, A. D., Ullian, E. M., Renteria, R. C., Liu, X., Xu, W., Prezioso, J., Susman, M. W., Stellwagen, D., Stokes, C. C., et al. (2006) · Journal of Neuroscience

Neuroscience and Neuropharmacology ResearchBiomarkers in Disease Mechanisms

Cited by 179

Modulating GLUT1 expression in retinal pigment epithelium decreases glucose levels in the retina: impact on photoreceptors and Muller glial cells

Swarup, A., Samuels, I. S., Bell, B. A., Han, J. Y. S., Du, J., Massenzio, E., Abel, E. D., Boesze-Battaglia, K., Peachey, N. S., & Philp, N. J. (2019) · American Journal of Physiology-Cell Physiology

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 122

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Strunz, T., Lauwen, S., Kiel, C., International AMD Genomics Consortium (IAMDGC), Fritsche, L. G., Igl, W., Bailey, J. N. C., Grassmann, F., Sengupta, S., Bragg-Gresham, J. L., et al. (2020) · Scientific Reports

Genetic Associations and EpidemiologyRetinal Diseases and Treatments

Cited by 60

Mouse models of human ocular disease for translational research

Krebs, M. P., Collin, G. B., Hicks, W. L., Yu, M., Charette, J. R., Shi, L. Y., Wang, J., Naggert, J. K., Peachey, N. S., & Nishina, P. M. (2017) · PLOS ONE

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 51

Microtubule-associated protein 1 light chain 3B, (LC3B) is necessary to maintain lipid-mediated homeostasis in the retinal pigment epithelium

Dhingra, A., Bell, B. A., Peachey, N. S., Daniele, L. L., Reyes-Reveles, J., Sharp, R. C., Jun, B., Bazan, N. G., Sparrow, J. R., Kim, H. J., et al. (2018) · Frontiers in Cellular Neuroscience

Autophagy in Disease and TherapyRetinal Diseases and Treatments

Cited by 41

A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation

Gorman, B. R., Francis, M., Nealon, C. L., Halladay, C. W., Duro, N., Markianos, K., Genovese, G., Hysi, P. G., Choquet, H., Afshari, N. A., et al. (2024) · Communications Biology

Corneal surgery and disordersGenetic Associations and Epidemiology

Cited by 23

Membrane frizzled-related protein is necessary for the normal development and maintenance of photoreceptor outer segments

WON, J., SMITH, R. S., PEACHEY, N. S., WU, J., HICKS, W. L., NAGGERT, J. K., & NISHINA, P. M. (2008) · Visual Neuroscience

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 13