A functional alternative splicing mutation in human tryptophan hydroxylase-2 von Zhang, X, Nicholls, P J, Laje, G, Sotnikova, T D, Gainetdinov, R R, Albert, P R, Rajkowska, G, Stockmeier, C A, Speer, M C, Steffens, D C, Austin, M C, McMahon, F J, Krishnan, K R R, Garcia-Blanco, M A, Caron, M G

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Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE) von Krupp, Deidre R., Xu, Pu-Ting, Thomas, Sophie, Dellinger, Andrew, Etchevers, Heather C., Vekemans, Michel, Gilbert, John R., Speer, Marcy C., Ashley-Koch, Allison E., Gregory, Simon G.

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Natural Food Folate and Late-Life Depression von Payne, M.E, Jamerson, B.D, Potocky, C.F, Ashley-Koch, A.E, Speer, M.C, Steffens, D.C

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Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when... von Rampersaud, E., Morris, R.W., Weinberg, C.R., Speer, M.C., Martin, E.R.

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The genes encoding for D4Z4 binding proteins HMGB2, YY1, NCL, and MYOD1 are excluded as candidate genes for FSHD1B von Bastress, K.L., Stajich, J.M., Speer, M.C., Gilbert, J.R.

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Dinucleotide repeat polymorphism at the DXS1683 locus von Econs, M.J., Francis, F., Rowe, P.S.N., Speer, M.C., O'Riordan, J.L.H., Lehrach, H., Becker, P.A.

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A Microsatellite Genetic Linkage Map of Human Chromosome 18 von Straub, Richard E., Speer, Marcy C., Luo, Ying, Rojas, Katherine, Overhauser, Joan, Ott, Jurg, Gilliam, T.Conrad

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No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives von Rampersaud, E., Brusato, C., Melvin, E.C., Speer, M.C., Metcalf, K.

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Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17 von Vance, J.M., Nicholson, G.A., Yamaoka, L.H., Stajich, J., Stewart, C.S., Speer, M.C., Hung, W.-Y., Roses, A.D., Barker, D., Pericak-Vance, M.A.

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Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD) von GILBERT, J. R, STAJICH, J. M, ROZEAR, M, SAMSON, F, FARDEAU, M, ROSES, A. D, PERICAK-VANCE, M. A, WALL, S, CARTER, S. C, QIU, H, VANCE, J. M, STEWART, C. S, SPEER, M. C, PUFKY, J, YAMAOKA, L. H

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Cloning and characterization of an inversion breakpoint at 6q23.3 suggests a role for Map7 in sacral dysgenesis von Sood, R., Bader, P.I., Speer, M.C., Edwards, Y.H., Eddings, E.M., Blair, R.T., Hu, P., Faruque, M.U., Robbins, C.M., Zhang, H., Leuders, J., Morrison, K., Thompson, D., Schwartzberg, P.L., Meltzer, P.S., Trent, J.M.

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Refined Assignment of the Infantile Neuronal Ceroid Lipofuscinosis (INCL, CLN1) Locus at 1p32: Incorporation of Linkage Disequilibrium in Multipoint Analysis von Hellsten, Elina, Vesa, Jouni, Speer, Marcy C., Mäkelä, Tomi P., Järvelä, Irma, Alitalo, Kari, Ott, Jürg, Peltonen, Leena

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The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians von Speer, M.C., Worley, G., Mackey, J.F., Melvin, E., Oakes, W.J., George, T.M.

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Genetic linkage studies in Alzheimer's disease families von Pericak-Vance, M.A., Yamaoka, L.H., Haynes, C.S., Speer, M.C., Haines, J.L., Gaskell, P.C., Hung, W.-Y., Clark, C.M., Heyman, A.L., Trofatter, J.A., Eisenmenger, J.P., Gilbert, J.R., Lee, J.E., Alberts, M.J., Dawson, D.V., Bartlett, R.J., Earl, N.L., Siddique, T., Vance, J.M., Conneall, P.M., Roses, A.D.

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A Microsatellite Genetic Linkage Map of Human Chromosome 13 von Petrukhin, Konstantin E., Speer, Marcy C., Cayanis, Eftihia, Bonaldo, Maria de Fátima, Tantravahi, Umadevi, Soares, Marcelo Bento, Fischer, Stuart G., Warburton, Dorothy, Gilliam, T.Conrad, Ott, Jurg

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Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity von Pericak-Vance, M A, Speer, M C, Lennon, F, West, S G, Menold, M M, Stajich, J M, Wolpert, C M, Slotterbeck, B D, Saito, M, Tim, R W, Rozear, M P, Middleton, L T, Tsuji, S, Vance, J M

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Genetic and Physical Mapping of the Treacher Collins Syndrome Locus with Respect to Loci in the Chromosome 5q3 Region von Jabs, Ethylin Wang, Li, Xiang, Lovett, Michael, Yamaoka, Larry H., Taylor, Eugene, Speer, Marcy C., Coss, Cathleen, Cadle, Ronald, Hall, Bryan, Brown, Karen, Kidd, Kenneth K., Dolganov, Gregory, Polymeropoulos, Mihael H., Meyers, Deborah A.

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Complete genomic screen for disease susceptibility loci in nuclear families von Anderson, J.L., Hauser, E.R., Martin, E.R., Scott, W.K., Ashley-Koch, A., Kim, K.J., Monks, S.A., Haynes, C.S., Speer, M.C., Pericak-Vance, M.A.

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The human glycine receptor: A new probe that is linked to the X-linked hypophosphatemic rickets gene von Econs, M.J., Pericak-Vance, M.A., Betz, H., Bartlett, R.J., Speer, M.C., Drezner, M.K.

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Confirmation of locus heterogeneity in the pure form of familial spastic paraplegia von Speer, Marcy C., Kingston, Helen M., Boustany, Rose-Mary N., Gaskell, Peter C., Robinson, L. Christi, Lennon, Felicia, Wolpert, Chantelle M., Yamaoka, Larry H., Kahler, Stephen G., Hogan, Edward L., Cumming, W. J. K., Pericak-Vance, Margaret A.

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