The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase von Mukherjee, N, Kidd, K K, Pakstis, A J, Speed, W C, Li, H, Tarnok, Z, Barta, C, Kajuna, S L B, Kidd, J R

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Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins von Tishkoff, S. A., Dietzsch, E., Speed, W., Pakstis, A. J., Kidd, J. R., Cheung, K., Bonné-Tamir, B., Santachiara-Benerecetti, A. S., Moral, P., Krings, M., Pääbo, S., Watson, E., Risch, N., Jenkins, T., Kidd, K. K.

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Population studies of polymorphisms of the serotonin transporter protein gene von Gelernter, J., Cubells, J.F., Kidd, J.R., Pakstis, A.J., Kidd, K.K.

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The Accuracy of Statistical Methods for Estimation of Haplotype Frequencies: An Example from the CD4 Locus von Tishkoff, S.A., Pakstis, A.J., Ruano, G., Kidd, K.K.

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COMT haplotypes suggest P2 promoter region relevance for schizophrenia von Palmatier, M A, Pakstis, A J, Speed, W, Paschou, P, Goldman, D, Odunsi, A, Okonofua, F, Kajuna, S, Karoma, N, Kungulilo, S, Grigorenko, E, Zhukova, O V, Bonne-Tamir, B, Lu, R-B, Parnas, J, Kidd, J R, DeMille, M M C, Kidd, K K

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Genome-wide association study of Tourette's syndrome von Scharf, J M, Yu, D, Mathews, C A, Neale, B M, Stewart, S E, Fagerness, J A, Evans, P, Gamazon, E, Edlund, C K, Service, S K, Tikhomirov, A, Osiecki, L, Illmann, C, Pluzhnikov, A, Konkashbaev, A, Davis, L K, Han, B, Crane, J, Moorjani, P, Crenshaw, A T, Parkin, M A, Reus, V I, Lowe, T L, Rangel-Lugo, M, Chouinard, S, Dion, Y, Girard, S, Cath, D C, Smit, J H, King, R A, Fernandez, T V, Leckman, J F, Kidd, K K, Kidd, J R, Pakstis, A J, State, M W, Herrera, L D, Romero, R, Fournier, E, Sandor, P, Barr, C L, Phan, N, Gross-Tsur, V, Benarroch, F, Pollak, Y, Budman, C L, Bruun, R D, Erenberg, G, Naarden, A L, Lee, P C, Weiss, N, Kremeyer, B, Berrío, G B, Campbell, D D, Cardona Silgado, J C, Ochoa, W C, Mesa Restrepo, S C, Muller, H, Valencia Duarte, A V, Lyon, G J, Leppert, M, Morgan, J, Weiss, R, Grados, M A, Anderson, K, Davarya, S, Singer, H, Walkup, J, Jankovic, J, Tischfield, J A, Heiman, G A, Gilbert, D L, Hoekstra, P J, Robertson, M M, Kurlan, R, Liu, C, Gibbs, J R, Singleton, A, Hardy, J, Strengman, E, Ophoff, R A, Wagner, M, Moessner, R, Mirel, D B, Posthuma, D, Sabatti, C, Eskin, E, Conti, D V, Knowles, J A, Ruiz-Linares, A, Rouleau, G A, Purcell, S, Heutink, P, Oostra, B A, McMahon, W M, Freimer, N B, Cox, N J, Pauls, D L

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Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region von Paschou, P., Feng, Y., Pakstis, A.J., Speed, W.C., DeMille, M.M., Kidd, J.R., Jaghori, B., Kurlan, R., Pauls, D.L., Sandor, P., Barr, C.L., Kidd, K.K.

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A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations von Tishkoff, S.A., Goldman, A., Calafell, F., Speed, W.C., Deinard, A.S., Bonne-Tamir, B., Kidd, J.R., Pakstis, A.J., Jenkins, T., Kidd, K.K.

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Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene von Lee, M-Y, Mukherjee, N, Pakstis, A J, Khaliq, S, Mohyuddin, A, Mehdi, S Q, Speed, W C, Kidd, J R, Kidd, K K

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Linkage Disequilibrium at the ADH2 and ADH3 Loci and Risk of Alcoholism von Osier, Michael, Pakstis, Andrew J., Kidd, Judith R., Lee, Jia-Fu, Yin, Shih-Jiun, Ko, Huei-Chen, Edenberg, Howard J., Lu, Ru-Band, Kidd, Kenneth K.

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The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus von CHANG, F.-M, KIDD, J. R, LIVAK, K. J, PAKSTIS, A. J, KIDD, K. K

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Short Tandem-Repeat Polymorphism/ Alu Haplotype Variation at the PLAT Locus: Implications for Modern Human Origins von Tishkoff, S.A., Pakstis, A.J., Stoneking, M., Kidd, J.R., Destro-Bisol, G., Sanjantila, A., Lu, R.-b., Deinard, A.S., Sirugo, G., Jenkins, T., Kidd, K.K., Clark, A.G.

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Understanding Human DNA Sequence Variation von Kidd, K. K., Pakstis, A. J., Speed, W. C., Kidd, J. R.

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An international two-stage genome-wide search for schizophrenia susceptibility genes von Wiese, C, Hwu, H.-G, Helgason, T, Bui, M.-T, Gottesman, I.I, Macciardi, F, Kidd, K.K, Byerley, W, Yu, M.-H, Pakstis, A.J, Wetterberg, L, Aschauer, H.N, Kennedy, J.L, Kristbjarnarson, H, Sjögren, B, Yang, L, Arolt, V, Blackwood, D, Jang, K, Havsteen, B, Zoega, T, Weissenbach, J, Livesley, W.J, Schwinger, E, Ivarsson, O, Moises, H.W, Liu, X, Commenges, D

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Possible epistatic role of ADH7 in the protection against alcoholism von Osier, M.V., Lu, R.-B., Pakstis, A.J., Kidd, J.R., Huang, S.-Y., Kidd, Kenneth K.

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HAPLOT: a graphical comparison of haplotype blocks, tagSNP sets and SNP variation for multiple populations von Gu, Sheng, Pakstis, Andrew J., Kidd, Kenneth K.

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ALFRED: the ALelle FREquency Database. Update von Rajeevan, H., Osier, M. V., Cheung, K.-H., Deng, H., Druskin, L., Heinzen, R., Kidd, J. R., Stein, S., Pakstis, A. J., Tosches, N. P., Yeh, C.-C., Miller, P. L., Kidd, K. K.

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Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test von GRICE, D. E, LECKMAN, J. F, PAULS, D. L, KURLAN, R, KIDD, K. K, PAKSTIS, A. J, CHANG, F. M, BUXBAUM, J. D, COHEN, D. J, GELERNTER, J

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A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus von KIDD, K. K, MORAR, B, YONG SUK NAM, GRANDY, D. K, JENKINS, T, KIDD, J. R, CASTIGLIONE, C. M, HONGYU ZHAO, PAKSTIS, A. J, SPEED, W. C, BONNE-TAMIR, B, LU, R.-B, GOLDMAN, D, CHAEYOUNG LEE

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Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17 von GELERNTER, J, PAKSTIS, A. J, KIDD, K. K

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