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Article

Comparison of standard versus wide-field composite images of the corneal subbasal layer by In vivo confocal microscopy.
Kheirkhah, A., Muller, R., Mikolajczak, J., Ren, A., Kadas, E.M., Zimmermann, H., Pruess, H., Paul, F., Brandt, A.U. and Hamrah, P.
Investigative Ophthalmology & Visual Science 56 (10): 5801-5807. 1 September 2015

Sleeping Beauty transposon-mediated transfection of retinal and iris pigment epithelial cells.
Johnen, S., Izsvak, Z., Stocker, M., Harmening, N., Salz, A.K., Walter, P. and Thumann, G.
Investigative Ophthalmology & Visual Science 53 (8): 4787-4796. 18 July 2012

Mutations in RD3 are associated with an extremely rare and severe form of early onset retinal dystrophy.
Preising, M.N., Hausotter-Will, N., Solbach, M.C., Friedburg, C., Rueschendorf, F. and Lorenz, B.
Investigative Ophthalmology & Visual Science 53 (7): 3463-3472. 8 June 2012

A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Puk, O., Esposito, I., Soeker, T., Loester, J., Budde, B., Nuernberg, P., Michel-Soewarto, D., Fuchs, H., Wolf, E., Hrabe de Angelis, M. and Graw, J.
Investigative Ophthalmology & Visual Science 50 (9): 4311-4318. September 2009

Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Puk, O., Loester, J., Dalke, C., Soewarto, D., Fuchs, H., Budde, B., Nuernberg, P., Wolf, E., de Angelis, M.H. and Graw, J.
Investigative Ophthalmology & Visual Science 49 (4): 1525-1532. April 2008

Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
Wycisk, K.A., Budde, B., Feil, S., Skosyrski, S., Buzzi, F., Neidhardt, J., Glaus, E., Nuernberg, P., Ruether, K. and Berger, W.
Investigative Ophthalmology & Visual Science 47 : 3523-3530. August 2006

Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Graw, J., Loester, J., Puk, O., Muenster, D., Haubst, N., Soewarto, D., Fuchs, H., Meyer, B., Nuernberg, P., Pretsch, W., Selby, P., Favor, J., Wolf, E. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 46 (12): 4671-4683. 1 December 2005

OPA1, the disease gene for autosomal dominant optic atrophy, is specifically expressed in ganglion cells and intrinsic neurons of the retina.
Pesch, U.E.A., Fries, J.E., Bette, S., Kalbacher, H., Wissinger, B., Alexander, C. and Kohler, K.
Investigative Ophthalmology & Visual Science 45 (11): 4217-4225. 1 January 2004

A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.
Thiselton, D.L., Alexander, C., Taanman, J.W., Brooks, S., Rosenberg, T., Eiberg, H., Andreasson, S., Van Regemorter, N., Munier, F.L., Moore, A.T., Bhattacharya, S.S. and Votruba, M.
Investigative Ophthalmology & Visual Science 43 : 1715-1724. 1 June 2002

Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Graw, J., Loester, J., Soewarto, D., Fuchs, H., Meyer, B., Reis, A., Wolf, E., Balling, R. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 42 : 2909-2915. 1 January 2001

Aey2, a new mutation in thebetaB2-crystallin-encoding gene of the mouse.
Graw, J., Loester, J., Soewarto, D., Fuchs, H., Reis, A., Wolf, E., Balling, R. and de Angelis, M.H.
Investigative Ophthalmology & Visual Science 42 : 1574-1580. 1 January 2001

Letter

Retinal segmentation to demonstrate hyperplasia in ataxia of charlevoix-saguenay: critique on study methodology and results.
Albrecht, P., Balk, L., Oberwahrenbrock, T., Petzold, A. and Paul, F.
Investigative Ophthalmology & Visual Science 55 (8): 4728. 4 August 2014