Gal, Andreas

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa

Gal, A., Li, Y., Thompson, D. A., Weir, J., Orth, U., Jacobson, S. G., Apfelstedt-Sylla, E., & Vollrath, D. (2000) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 679

Mutations in RPE65 cause autosomal recessive childhood–onset severe retinal dystrophy

Gu, S.-M., Thompson, D. A., Srikumari, C. R. S., Lorenz, B., Finckh, U., Nicoletti, A., Murthy, K. R., Rathmann, M., Kumaramanickavel, G., Denton, M. J., et al. (1997) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 663

Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

Kurth, I., Pamminger, T., Hennings, J. C., Soehendra, D., Huebner, A. K., Rotthier, A., Baets, J., Senderek, J., Topaloglu, H., Farrell, S. A., et al. (2009) · Nature Genetics

Hereditary Neurological DisordersPain Mechanisms and Treatments

Cited by 260

Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy

Janecke, A. R., Thompson, D. A., Utermann, G., Becker, C., Hübner, C. A., Schmid, E., McHenry, C. L., Nair, A. R., Rüschendorf, F., Heckenlively, J., et al. (2004) · Nature Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 246

Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy

Thompson, D. A., Li, Y., McHenry, C. L., Carlson, T. J., Ding, X., Sieving, P. A., Apfelstedt-Sylla, E., & Gal, A. (2001) · Nature Genetics

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 185

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Kornak, U., Mademan, I., Schinke, M., Voigt, M., Krawitz, P., Hecht, J., Barvencik, F., Schinke, T., Gießelmann, S., Beil, F. T., et al. (2014) · Brain

Hereditary Neurological DisordersCellular transport and secretion

Cited by 109

Missense rhodopsin mutation in a family with recessive RP

Kumaramanickavel, G., Maw, M., Denton, M. J., John, S., Srikumari, C. R. S., Orth, U., Oehlmann, R., & Gal, A. (1994) · Nature Genetics

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

Cited by 94

Missense mutations are frequent in the gene for X-chromosomal adrenoleukodystrophy (ALD)

Fuchs, S., Sarde, C. O., Wedemann, H., Schwinger, E., Mandel, J. L., & Gal, A. (1994) · Human Molecular Genetics

Metabolism and Genetic DisordersLysosomal Storage Disorders Research

Cited by 57

Rdh12 activity and effects on retinoid processing in the murine retina

Chrispell, J. D., Feathers, K. L., Kane, M. A., Kim, C. Y., Brooks, M., Khanna, R., Kurth, I., Hübner, C. A., Gal, A., Mears, A. J., et al. (2009) · Journal of Biological Chemistry

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 56

A New Gene Family (FAM9) of Low-Copy Repeats in Xp22.3 Expressed Exclusively in Testis: Implications for Recombinations in This Region

Martinez-Garay, I., Jablonka, S., Sutajova, M., Steuernagel, P., Gal, A., & Kutsche, K. (2002) · Genomics

Genomic variations and chromosomal abnormalitiesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 54

Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease

Günther, C., Hadeln, K. V., Müller-Thomsen, T., Alberici, A., Binetti, G., Hock, C., Nitsch, R. M., Stoppe, G., Reiss, J., Gal, A., et al. (2004) · Neuroscience Letters

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 53

Genetic defects in vitamin A metabolism of the retinal pigment epithelium

Thompson, D. A., & Gal, A. (2003) · Developments in Ophthalmology

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 47