Nichols, B.E., Stone, E.M., Brody, J.M., Johnson, A.T., Raphtis, M.E., and Thompson, H.S., A Single Rack of the FM-100 is as Sensitive and Specific as the Entire Test for Monitoring Optic Neuropathies, (abstr.), Invest. Ophthalmol. Vis. Sci. (30-suppl.) 244, 1989.
Nichols, B.E., Stone, E.M., and Thompson, H.S., A Revised Version of the FM-100 for Evaluating Optic Neuropathies, presented at the 21st annual Midwest Student Medical Research Forum, 1990 and the National Student Research Forum, 1990.
Wolken, M.S., Nichols, B.E., Vockrodt, L.J., Montague, P.R., and Stone, E.M., An 83 Hue Color Vision Test Has a More Even Error Distribution than Farnsworth’s 84 Hue Test, (abstr.), Invest. Ophthalmol. Vis. Sci. (32-suppl.) 1283, 1991.
Nichols, B.E., Massicotte, S.J., Slavin, M.L., Folberg, R., and Stone, E.M., Light Microscopy of the Eyes of a Patient With Non-Wallace-Type Leber’s Hereditary Optic Neuropathy, (abstr.), Invest. Ophthalmol. Vis. Sci. (32-suppl.) 857, 1991.
Nichols, B.E., Thompson, H.S., and Stone, E.M., Normative Data and Standardized Testing Conditions for an 83 Hue Color Vision Test, presented at the 11th meeting of the International Research Group on Color Vision Deficiencies, 1991.
Nichols, B.E., Stone, E.M., and Sheffield, V.C., Mitochondrial DNA Polymorphisms Detected with GC-Clamped Gradient Gel Electrophoresis, (abstr.), Am. J. Hum. Genet. (49-suppl.), 2520, 1991.
Coppinger, J.M., Nichols, B.E., Streb, L.M., Mack, R.J., Sheffield, V.C., and Stone, E.M., Identification of Mitochondrial Gene Mutations Associated with Leber’s Hereditary Optic Neuropathy by GC-Clamped Denaturing Gradient Gel Electrophoresis, (abstr.), Invest. Ophthalmol. Vis. Sci. (33-suppl.), 2631, 1992.
Sheffield, V.C., Kimura, A.E., Folk, J.C., Bennett, S.R., Streb, L.M., Nichols, B.E., and Stone, E.M., The Gene for Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy Maps to 11q13, (abstr.), Am. J. Hum. Genet. (51-suppl.), A35, 1992.
Nichols, B.E., Sheffield, V.C, and Stone, E.M., A User-Friendly Macintosh Interface for DOS-Based Linkage Analysis, (abstr.), Am. J. Hum. Genet. (51-suppl.), A369, 1992.
Stone, E.M., Nichols, B.E., McInnes, R.R., Bascom, R.A., Kimura, A.E., Streb, L.M., and Sheffield, V.C., The Gene for Best’s Disease (Vitelliform Macular Dystrophy) Maps to Chromosome 11q13, (abstr.), Am. J. Hum. Genet. (51-suppl.), A35, 1992.
Brown, D.M., Nichols, B.E., Weingeist, T.A., Kimura, A.E., Sheffield, V.C., and Stone, E.M., Type II Procollagen Gene Mutation in Stickler Syndrome, (abstr.), Am. J. Hum Genet. (51-suppl.), A301, 1992.
Nichols, B.E., Kimura, A.E., Streb, L.M., Sheffield, V.C., and Stone, E.M., Mutations in the RDS Gene are Associated with Butterfly-Shaped Pigment Dystrophy of the Fovea, (abstr.), Invest. Ophthalmol. Vis. Sci. (34-suppl.), 2194, 1993.
Stone, E.M., Nichols, B.E., Kimura, A.E., Weleber, R.G., Gorin, M.B., Fishman, G.A., Jacobson, S.G., Gass, J.D.M., Drack, A.V., Vandenburgh, K., and Sheffield, V.C., Mutations in the RDS/Peripherin Gene Cause Widely Different Phenotypes Between and Within Affected Families, (abstr.), Am. J. Hum. Genet. (53-suppl.), 14, 1993.
Nichols, B.E., Bascom, R.A., Litt, M., McInnes, R., Taylor, C.M., Sheffield, V.C., and Stone, E.M., Fine Mapping of the Best’s Disease Locus and Mutations Analysis of the Candidate Gene ROM1, (abstr.), Am. J. Hum. Genet. (53-suppl.), 1050, 1993.
Sheffield, V.C., Nichols, B.E., Alward, W.L.M., Drack, A.V., Johnson, A.T., Streb, L.M., and Stone, E.M., Genetic Mapping of Familial Open Angle Glaucoma to Chromosome 1q21-q31 and Analysis of Candidate Genes, (abstr.), Am. J. Hum. Genet. (53-suppl.), 1075, 1993.
Brown, D.M., Vandenburgh, K., Nichols, B.E., Erhart, A.R., Kimura, A.E., Weingeist, T.A., Sheffield, V.C., and Stone, E.M., Genetic Mutations at the C-Terminal End of the Procollagen II Gene in Stickler Syndrome (Hereditary Arthro-Ophthalmopathy) and Identification and Phenotypic Description of a New Mutation, (abstr.), Am. J. Hum. Genet. (53-suppl.), 1133, 1993.
Sheffield, V.C., Nichols, B.E., Alward, W.L.M., Drack, A.V., Johnson, A.T., Streb, L.M., Stone, E.M., Genetic Mapping of Familial Open Angle Glaucoma to Chromosome 1q21-q31 and Analysis of Candidate Genes, (abstr.), American Journal of Human Genetics, (53-suppl.), 1075, 1993.
Rokhlina, T., McClain, A.M., Mattes, G.E., Sunden, S.L.F., Nichols, B.E., Duyk, G.M., Stone, E.M., Sheffield, V.C., Rapid Genome-wide Linkage Analysis Using a Set of Tri and Tetranucleotide Repeat Markers and Automated Silver Staining, (abstr.), American Journal of Human Genetics, (55-suppl.), 1173, 1994.
Sheffield, V.C., Kwitek-Black, A.E., Carmi, R., Nichols, B.E., Rokhlina, T., Buetow, K.H., Duyk, G.M., Stone, E.M., Evaluation of an Efficient Approach for Identifying Genetic Disease Loci, (abstr.), American Journal of Human Genetics, (55-suppl.), 266, 1994.
Sunden, S.L.F., Nichols, B.E., Alward, W.L.M., Raymond, M., Ludwigsen, S., Stone, E.M., Sheffield, V.C., Exclusion of Candidate Genes from the Chromosome 1q Juvenile Glaucoma Region and Mapping of the Peripheral Cannabis Receptor Gene (CNR2) to Chromsome 1, (abstr.), American Journal of Human Genetics, (55-suppl.), 1190 1994.
Nichols, B.E., Alward, W.L.M., Ritch, R., Streb, L.M., Taylor, C.M., Sunden, S.L.F., Sheffield, V.C., Stone, E.M., Fine Mapping of the Primary Open Angle Glaucoma Locus on Chromosome 1, (abstr.), Invest. Ophthalmol. Vis. Sci., (35-suppl.), 1009, 1994.
Brown, D.M., Vandenburgh, K., Nichols, B.E., Kimura, A.E., Weingeist, T.A., Sheffield, V.C., Stone, E.M., Incidence of Frameshift Mutations in the Procollagen II Gene in Stickler Syndrome and Identification of Four New Mutations, (abstr.), Invest. Ophthalmol. Vis. Sci., (35-suppl.), 2159, 1994.
Stone, E.M., Nichols, B.E., Kimura, A.E., Weingeist, T.A., Drack, A.V., Sheffield, V.C., Genetic Linkage of a Stargardt-Like Dominant Progressive Macular Dystrophy to Chromosome 6, (abstr.), Invest. Ophthalmol. Vis. Sci., (35-suppl.), 2160, 1994.
Sunden, S.L.F., Nichols, B.E., Alward, W.L.M., Nishimura, D.Y., Stone, E.M., Sheffield, V.C., Physical and Genetic Fine Mapping of the Juvenile Open Angle Glaucoma Region (1q21-q31), (abstr.), American Journal of Human Genetics, (57-suppl.), 1174, 1995.
Sheffield, V.C., Sunden, S.L.F., Alward, W.L.M., Rohklina, T.R., Nichols, B.E., Stone, E.M., High-Density Mapping of the Juvenile Open Angle Glaucoma Region, (abstr.), Invest. Ophthalmol. Vis. Sci., (37-suppl.), 2078, 1996.
Sunden, S.L.F., Alward, W.L.M., Nichols, B.E., Rokhlina, T., Nystuen, A., Fingert, J., Stone, E.M., Sheffield, V.C., Narrowing the GLC1A Critical Region Using a Late-Onset Autosomal Dominant Open Angle Glaucoma Family, (abstr.), American Journal of Human Genetics, (59-suppl.), 1369, 1996.
Fingert, J.H., Alward, W.L.M., Sunden, S.L.F., Nishimura, D., Nystuen, A., Nichols, B.E., Mackey, D.A., Ritch, R., Kalenak, J.W., Craven, E.R., Beck, G.E., Streb, L.M., Sheffield, V.C., Stone, E.M., Identification of the Gene Causing 1Q-Linked Juvenile Onset Open Angle Glaucoma (GLC1A) and Evidence for Its Involvement in Adult Primary Open Angle Glaucoma, (abstr.) Invest. Ophthalmol. Vis. Sci., (38-suppl.) 4333, 1997.
Brown, Jr., J., Nichols, B.E., Wiles, C.D., Butler, N., Sheffield, V.C., Stone, E.M., Clinical Characterization and Linkage Analysis of a Four Generation Family with Cone-Rod Dystrophy, (abstr.) Invest. Ophthalmol. Vis. Sci., (38-suppl.) 5339, 1997.
Nichols, B.E., Butler, N.B., Sheffield, V.C., Stone, E.M., Prevalence of mitochondrial nt3243 mutation in non-syndromic pattern dystrophy, (abstr.) Invest. Ophthalmol. Vis. Sci., (-suppl.) B224, 1998.