Genomic screen and follow-up analysis for autistic disorder von Shao, Yujun, Wolpert, Chantelle M., Raiford, Kimberly L., Menold, Marisa M., Donnelly, Shannon L., Ravan, Sarah A., Bass, Meredyth P., McClain, Cate, von Wendt, Lennart, Vance, Jeffery M., Abramson, Ruth H., Wright, Harry H., Ashley-Koch, Allison, Gilbert, John R., DeLong, Robert G., Cuccaro, Michael L., Pericak-Vance, Margaret A.

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Ordered subset analysis in genetic linkage mapping of complex traits von Hauser, Elizabeth R., Watanabe, Richard M., Duren, William L., Bass, Meredyth P., Langefeld, Carl D., Boehnke, Michael

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Correcting for a Potential Bias in the Pedigree Disequilibrium Test von Martin, Eden R., Bass, Meredyth P., Kaplan, Norman L.

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Accounting for Linkage in Family-Based Tests of Association with Missing Parental Genotypes von Martin, Eden R., Bass, Meredyth P., Hauser, Elizabeth R., Kaplan, Norman L.

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Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing von Boyles, Abee L., Scott, William K., Martin, Eden R., Schmidt, Silke, Li, Yi-Ju, Ashley-Koch, Allison, Bass, Meredyth P., Schmidt, Michael, Pericak-Vance, Margaret A., Speer, Marcy C., Hauser, Elizabeth R.

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Behavioral Comparisons in Autistic Individuals from Multiplex and Singleton Families von Cuccaro, Michael L, Shao, Yujun, Bass, Meredyth P, Abramson, Ruth K, Ravan, Sarah A, Wright, Harry H, Wolpert, Chantelle M, Donnelly, Shannon L, Pericak-Vance, Margaret A

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Autistic Disorder and Chromosome 15q11–q13: Construction and Analysis of a BAC/PAC Contig von Maddox, Lewis O., Menold, Marisa M., Bass, Meredyth P., Rogala, Allison R., Pericak-Vance, Margaret A., Vance, Jeffery M., Gilbert, John R.

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No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease von Scott, W K, Yamaoka, L H, Bass, M P, Gaskell, P C, Conneally, P M, Small, G W, Farrer, L A, Auerbach, S A, Saunders, A M, Roses, A D, Haines, J L, Pericak-Vance, M A

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No association of α1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients von Bass, Meredyth P, Yamaoka, Larry H, Scott, William K, Craig Gaskell, P, Welsh-Bohmer, Kathleen A, Roses, Allen D, Saunders, Ann M, Haines, Jonathan L, Pericak-Vance, Margaret A

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Three probands with autistic disorder and isodicentric chromosome 15 von Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Qumsiyeh, Mazin B., Donnelly, Shannon L., Ravan, Sarah A., Vance, Jeffery M., Gilbert, John R., Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L., Pericak-Vance, Margaret A.

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Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome von Donnelly, Shannon L., Wolpert, Chantelle M., Menold, Marisa M., Bass, Meredyth P., Gilbert, John R., Cuccaro, Michael L., Delong, G. Robert, Pericak-Vance, Margaret A.

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Genetic studies in autistic disorder and chromosome 15 von BASS, M. P, MENOLD, M. M, GILBERT, J. R, CUCCARO, M. L, DELONG, G. R, PERICAK-VANCE, M. A, WOLPERT, C. M, DONNELLY, S. L, RAVAN, S. A, HAUSER, E. R, MADDOX, L. O, VANCE, J. M, ABRAMSON, R. K, WRIGHT, H. H

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