Warren Laboratory

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Publications - 1995   Kirchgessner, CU, Warren, ST and Willard, HL: X inactivation of the FMR1 fragile X mental retardation gene. Journal of Medical Genetics 32:925-929 (1995). Small, K and Warren, ST: Analysis of FMRP, the protein deficient in fragile X syndrome. Mental Retardation and Developmental Disabilities Research Reviews 1:245-250 (1995). Eichler, EE, Kunst, CB, Lugenbeel, KA, Ryder, OA, Davison, D, Warren, ST and Nelson, DL: Evolution of the cryptic FMR1 CGG repeat. Nature Genetics 11:301-307 (1995). Ashley, CT and Warren, ST: Trinucleotide repeat expansion and human disease. Annual Review of Genetics 29:703-728 (1995).   Andersson, B, Lu, F, Muzny, DM, Warren, ST and Gibbs, RA: Complete sequence of a 38.5-kb human cosmid insert containing the polymorphic marker DXS455 from Xq28. DNA Sequence 5:219-223 (1995). Bione, S, Small, K, Aksmanovic, VMA, Ciccodicola, A, Merlini, L, Morandi, L, Kress, W, Yates, JRW, Warren, ST and Toniolo, D: Identification of new mutations in the Emery Dreifuss dystrophy gene and evidence for genetic heterogeneity of the disease. Human Molecular Genetics 4:1859-1864 (1995). Litt, M, Kramer, P, Kort, E, Fain, P, Cox, S, Root, D, White, R, Weissenbach, J, Donis-Keller, H, Gatti, R, Weber, J, Nakamura, Y, Julier, C, Hayashi, K, Spurr, N, Dean, M, Mandel, J, Kidd, K, Kruse, T, Retief, A, Bale, A, Meo, T, Vergnaud, G, Warren, ST and Willard, HF: The CEPH consortium linkage map of human chromosome 11. Genomics 27:101-112 (1995). Feng, Y, Zhang, F, Lokey, LK, Chastain, JL, Lakkis, L, Eberhart, D and Warren, ST: Translational suppression by trinucleotide repeat expansion at FMR1. Science 268:731-734 (1995).  Warren, ST and Ashley, CT: Triplet repeat expansion mutations: The example of fragile X syndrome. Annual Review of Neuroscience 18:77-99 (1995). Gregor, P, Nash, SR, Caron, MG, Seldin, MF and Warren, ST: Assignment of the creatine transporter gene to human chromosome Xq28 telomeric to G6PD. Genomics 25:332-333 (1995).   Zerylnick, C, Torroni, A, Sherman, SL and Warren, ST: Normal variation at the myotonic dystrophy locus in global human populations. American Journal of Human Genetics 56:123-130 (1995).   Feng, Y, Lakkis, L, Devys D and Warren, ST: Quantitative comparison of FMR1 gene expression in normal and premutation alleles. American Journal of Human Genetics 56:106-113 (1995).

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