The Genetic Architecture of Selection at the Human Dopamine Receptor D4 ( DRD4) Gene Locus von Wang, E., Ding, Y.-C., Flodman, P., Kidd, J.R., Kidd, K.K., Grady, D.L., Ryder, O.A., Spence, M.A., Swanson, J.M., Moyzis, R.K.

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Evidence for multiple loci from a genome scan of autism kindreds von Schellenberg, G D, Dawson, G, Sung, Y J, Estes, A, Munson, J, Rosenthal, E, Rothstein, J, Flodman, P, Smith, M, Coon, H, Leong, L, Yu, C-E, Stodgell, C, Rodier, P M, Spence, M A, Minshew, N, McMahon, W M, Wijsman, E M

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High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder von Grady, D L, Chi, H-C, Ding, Y-C, Smith, M, Wang, E, Schuck, S, Flodman, P, Spence, M A, Swanson, J M, Moyzis, R K

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A new βA1-crystallin splice junction mutation in autosomal dominant cataract von BATEMAN, J. Bronwyn, GEYER, David D, FLODMAN, Pamela, JOHANNES, Meriam, SIKELA, James, WALTER, Nicole, MOREIRA, Ana Teresa, CLANCY, Kevin, SPENCE, M. Anne

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Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease von Kandt, R. S., Haines, J. L., Smith, M., Northrup, H., Gardner, R. J. M., Short, M. P., Dumars, K., Roach, E. S., Steingold, S., Wall, S., Blanton, S. H., Flodman, P., Kwiatkowski, D. J., Jewell, A., Weber, J. L., Roses, A. D., Pericak-Vance, M. A.

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Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific von Grady, D.L., Harxhi, A., Smith, M., Flodman, P., Spence, M.A., Swanson, J.M., Moyzis, R.K.

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Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus von Ding, Yuan-Chun, Chi, Han-Chang, Grady, Deborah L., Morishima, Atsuyuki, Kidd, Judith R., Kidd, Kenneth K., Flodman, Pamela, Spence, M. Anne, Schuck, Sabrina, Swanson, James M., Zhang, Ya-Ping, Moyzis, Robert K.

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Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives von Neuhausen, Susan L, Steele, Linda, Ryan, Sarah, Mousavi, Maryam, Pinto, Marie, Osann, Kathryn E, Flodman, Pamela, Zone, John J

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A genetic linkage map of the rat derived from recombinant inbred strains von Pravenec, M, Gauguier, D, Schott, J J, Buard, J, Kren, V, Bílá, V, Szpirer, C, Szpirer, J, Wang, J M, Huang, H, St Lezin, E, Spence, M A, Flodman, P, Printz, M, Lathrop, G M, Vergnaud, G, Kurtz, T W

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Evidence for genetic linkage of autism to chromosomes 7 and 4 von Schellenberg, G D, Dawson, G, Sung, Y J, Estes, A, Munson, J, Rosenthal, E, Rothstein, J, Flodman, P, Smith, M, Coon, H, Leong, L, Yu, C-E, Stodgell, C, Rodier, P M, Spence, M A, Minshew, N, McMahon, W M, Wijsman, E M

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Molecular genetic delineation of a deletion of chromosome 13q12→q13 in a patient with autism and auditory processing deficits von Smith, M., Woodroffe, A., Smith, R., Holguin, S., Martinez, J., Filipek, P.A., Modahl, C., Moore, B., Bocian, M.E., Mays, L., Laulhere, T., Flodman, P., Spence, M.A.

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Language and other regression: Assessment and timing von GOLDBERG, Wendy A, OSANN, Kathy, FILIPEK, Pauline A, LAULHERE, Tracy, JARVIS, Kelly, MODAHL, Charlotte, FLODMAN, Pamela, SPENCE, M. Anne

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Bipolar disorder: Evidence for a major locus von Spence, M. Anne, Flodman, Pamela L., Sadovnick, A. Dessa, Bailey-Wilson, Joan E., Ameli, Hossein, Remick, Ronald A.

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A Genome Survey Indicates a Possible Susceptibility Locus for Bipolar Disorder on Chromosome 22 von Kelsoe, John R., Spence, M. Anne, Loetscher, Erika, Foguet, Montserrat, Sadovnick, A. Dessa, Remick, Ronald A., Flodman, Pamela, Khristich, Jason, Mroczkowski-Parker, Zofi, Brown, John L., Masser, Diane, Ungerleider, Sharon, Rapaport, Mark H., Wishart, William L., Luebbert, Hermann

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Molecular genetic delineation of 2q37.3 deletion in autism and osteodystrophy: report of a case and of new markers for deletion screening by PCR von Smith, M., Escamilla, J.R., Filipek, P., Bocian, M.E., Modahl, C., Flodman, P., Spence, M.A.

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Dopamine genes and ADHD von Swanson, J.M, Flodman, Pamela, Kennedy, James, Spence, M.Anne, Moyzis, Robert, Schuck, Sabrina, Murias, Michael, Moriarity, Joan, Barr, Cathy, Smith, Moyra, Posner, Michael

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Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract von Geyer, David D., Spence, M. Anne, Johannes, Meriam, Flodman, Pamela, Clancy, Kevin P., Berry, Rebecca, Sparkes, Robert S., Jonsen, Matthew D., Isenberg, Sherwin J., Bateman, J. Bronwyn

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Attention Deficit/Hyperactivity Disorder Children with a 7-Repeat Allele of the Dopamine Receptor D4 Gene Have Extreme Behavior but Normal Performance on Critical Neuropsychologica... von Swanson, James, Oosterlaan, Jaap, Murias, Michael, Schuck, Sabrina, Flodman, Pamela, Spence, M. Anne, Wasdell, Michael, Ding, Yuanchun, Chi, Han-Chang, Smith, Moyra, Mann, Miranda, Carlson, Caryn, Kennedy, James L., Sergeant, Joseph A., Leung, Patrick, Zhang, Ya-Ping, Sadeh, Avi, Chen, Chuansheng, Whalen, Carol K., Babb, Kimberley A., Moyzis, Robert, Posner, Michael I.

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Preliminary Implementation of New Data Mining Techniques for the Analysis of Simulation Data from Genetic Analysis Workshop 12: Problem 2 von Flodman, Pamela, Macula, Anthony J., Spence, M. Anne, Torney, David C.

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Dopamine receptor D4 (DRD4) gene in Han Chinese children with attention-deficit/hyperactivity disorder (ADHD): Increased prevalence of the 2-repeat allele von Leung, Patrick W.L., Lee, C.C., Hung, S.F., Ho, T.P., Tang, C.P., Kwong, S.L., Leung, S.Y., Yuen, S.T., Lieh-Mak, F., Oosterlaan, Jaap, Grady, Deborah, Harxhi, Ante, Ding, Y.C., Chi, H.C., Flodman, Pamela, Schuck, Sabrina, Spence, M. Anne, Moyzis, Robert, Swanson, James

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