A Systematic Single Nucleotide Polymorphism Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association With a Novel Susceptibility Gene ACN9 von Dick, Danielle M, Aliev, Fazil, Wang, Jen C, Saccone, Scott, Hinrichs, Anthony, Bertelsen, Sarah, Budde, John, Saccone, Nancy, Foroud, Tatiana, Nurnberger, John, Xuei, Xiaoling, Conneally, P.M, Schuckit, Marc, Almasy, Laura, Crowe, Raymond, Kuperman, Samuel, Kramer, John, Tischfield, Jay A, Hesselbrock, Victor, Edenberg, Howard J, Porjesz, Bernice, Rice, John P, Bierut, Laura, Goate, Alison

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Heterozygosity for a mutation in the Parkin gene leads to later onset Parkinson disease von FOROUD, T, UNIACKE, S. K, LIU, L, PANKRATZ, N, RUDOLPH, A, HALTER, C, SHULTS, C, MARDER, K, CONNEALLY, P. M, NICHOLS, W. C

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Identification of Novel Genes in Late-Onset Alzheimer's Disease von Pericak-Vance, M.A., Grubber, J., Bailey, L.R., Hedges, D., West, S., Santoro, L., Kemmerer, B., Hall, J.L., Saunders, A.M., Roses, A.D., Small, G.W., Scott, W.K., Conneally, P.M., Vance, J.M., Haines, J.L.

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Fine Mapping of the Chromosome 12 Late-Onset Alzheimer Disease Locus: Potential Genetic and Phenotypic Heterogeneity von Scott, W.K., Grubber, J.M., Conneally, P.M., Small, G.W., Hulette, C.M., Rosenberg, C.K., Saunders, A.M., Roses, A.D., Haines, J.L., Pericak-Vance, M.A.

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Anxiety proneness linked to epistatic loci in genome scan of human personality traits von Cloninger, C.R., Van Eerdewegh, P., Goate, A., Edenberg, H.J., Blangero, J., Hesselbrock, V., Reich, T., Nurnberger Jr, J., Schuckit, M., Porjesz, B., Crowe, R., Rice, J.P., Foroud, T., Przybeck, T.R., Almasy, L., Bucholz, K., Wu, W., Shears, S., Carr, K., Crose, C., Willig, C., Zhao, J., Tischfield, J.A., Li, T.-K., Conneally, P.M., Begleiter, H.

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Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus von Takacs, I, Koller, D.L, Peacock, M, Christian, J.C, Evans, W.E, Hui, S.L, Conneally, P.M, Johnston, C.C, Foroud, T, Econs, M.J

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A Systematic SNP Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association with a Novel Susceptibility Gene ACN9 von Dick, Danielle M., Aliev, Fazil, Wang, Jen C., Saccone, Scott, Hinrichs, Anthony, Bertelsen, Sarah, Budde, John, Saccone, Nancy, Foroud, Tatiana, Nurnberger, John, Xuei, Xiaoling, Conneally, P.M., Schuckit, Marc, Almasy, Laura, Crowe, Raymond, Kuperman, Samuel, Kramer, John, Tischfield, Jay A., Hesselbrock, Victor, Edenberg, Howard J., Porjesz, Bernice, Rice, John P., Bierut, Laura, Goate, Alison

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Quantitative trait loci analysis of human event-related brain potentials: P3 voltage von Begleiter, H, Porjesz, B, Reich, T, Edenberg, H.J, Goate, A, Blangero, J, Almasy, L, Foroud, T, Van Eerdewegh, P, Polich, J, Rohrbaugh, J, Kuperman, S, Bauer, L.O, O'Connor, S.J, Chorlian, D.B, Li, T.K, Conneally, P.M, Hesselbrock, V, Rice, J.P, Schuckit, M.A, Cloninger, R, Nurnberger, J, Crowe, R, Bloom, F.E

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Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K) von Grubber, Janet M., Saunders, Ann M., Crane-Gatherum, Alison R., Scott, William K., Martin, Eden R., Haynes, Carol S., Conneally, P.M., Small, Gary W., Roses, Allen D., Haines, Jonathan L., Pericak-Vance, Margaret A.

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No Genetic Effect of α1-Antichymotrypsin in Alzheimer Disease von Haines, J.L., Pritchard, M.L., Saunders, A.M., Schildkraut, J.M., Growdon, J.H., Gaskell, P.C., Farrer, L.A., Auerbach, S.A., Gusella, J.F., Locke, P.A., Rosi, B.L., Yamaoka, L., Small, G.W., Conneally, P.M., Roses, A.D., Pericak-Vance, M.A.

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Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease von Pericak-Vance, M.A, Bass, M.L, Yamaoka, L.H, Gaskell, P.C, Scott, W.K, Terwedow, H.A, Menold, M.M, Conneally, P.M, Small, G.W, Saunders, A.M, Roses, A.D, Haines, J.L

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Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant von Trofatter, James A., Dlouhy, Stephen R., DeMyer, William, Conneally, P. Michael, Hodes, M. E.

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Description of the genetic analysis workshop 11 collaborative study on the genetics of alcoholism von Begleiter, H., Reich, T., Nurnberger Jr, J., Li, T.K., Conneally, P.M., Edenberg, H., Crowe, R., Kuperman, S., Schuckit, M., Bloom, F., Hesselbrock, V., Porjesz, B., Cloninger, C.R., Rice, J., Goate, A.

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The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD von FARRER, L. A, CUPPLES, L. A, WIATER, P, CONNEALLY, P. M, GUSELLA, J. F, MYERS, R. H

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No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians von Pritchard, M.L., Saunders, A.M., Gaskell, P.C., Small, G.W., Conneally, P.M., Rosi, B., Yamaoka, L.H., Roses, A.D., Haines, J.L., Pericak-Vance, M.A.

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Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15 von Young, K., Foroud, T., Williams, P., Jackson, C.E., Beckmann, J.S., Cohen, D., Conneally, P.M., Tischfield, J., Hodes, M.E.

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Association of 3'-UTR polymorphisms of the oxidised LDL receptor 1 von Lambert, J-C, Luedecking-Zimmer, E, Merrot, S, Hayes, A, Thaker, U, Desai, P, Houzet, A, Hermant, X, Cottel, D, Pritchard, A, Iwatsubo, T, Pasquier, F, Frigard, B, Conneally, P.M, Cha, DeKosky, S.T, Lendon, C, Mann, D, Kamboh, M.I, Amouyel, P

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Genetic heterogeneity of autosomal recessive limbgirdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus von Allamand, V., Broux, O., Bourg, N., Richard, I., Tischfield, J.A., Hodes, M.E., Conneally, P.M., Fardeau, M., Jackson, C.E., Beckmann, J.S.

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No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease von Scott, W.K., Yamaoka, L.H., Locke, P.A., Rosi, B.L., Gaskell, P.C., Saunders, A.M., Conneally, P.M., Small, G.W., Farrer, L.A., Growdon, J.H., Roses, A.D., Pericak-Vance, M.A., Haines, J.L.

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Genetics of Alcoholism von Edenberg, Howard J., Foroud, Tatiana, Goate, Alison, Rice, John, Reich, Theodore, Cloninger, C. Robert, Nurnberger, John I., T.-K. Li, Conneally, P. M., Tischfield, Jay A., Crowe, Raymond, Hesselbrock, Victor, Schuckit, Marc, Porjesz, Bernice, Begleiter, Henri

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