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Cogan Eye Pathology Laboratory
Ophthalmology - Eye pathology
Yale University School of Medicine, 1976
Pathology
Genetics of hereditary eye disease
Please see the biosketch (click).Also see below.
Ben-Arie-Weintrob Y, Berson EL, Dryja TP. Histopathologic-genotypic correlations in retinitis pigmentosa and allied
diseases. Ophthal Genet 2005;26:91-100.
Dryja TP, McGee TL, Berson EL, et al. Night blindness and abnormal cone ERG ON responses in patients with mutations in
the GRM6 gene encoding the mGluR6 receptor. Proc Natl Acad Sci USA 2005;102:4884-9.
Wada Y, Sandberg MA, McGee TL, et al. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and
clinical features associated with the most common mutation, Asp226Asn. Invest Ophthalmol Vis Sci 2005;46:1735-41.
Nishiguchi KM, Sandberg MA, Kooijman AC, et al. Defects in RGS9 or its anchor protein R9AP in patients with slow
photoreceptor deactivation. Nature 2004;427:75-8.
A complete list of research publications can be seen at www.pubmed.gov. Type the physician's name at the top, where it says 'for' and the physician's research publications will appear.