Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism von Ma, D.Q., Whitehead, P.L., Menold, M.M., Martin, E.R., Ashley-Koch, A.E., Mei, H., Ritchie, M.D., DeLong, G.R., Abramson, R.K., Wright, H.H., Cuccaro, M.L., Hussman, J.P., Gilbert, J.R., Pericak-Vance, M.A.

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Fine Mapping of Autistic Disorder to Chromosome 15q11-q13 by Use of Phenotypic Subtypes von Shao, Yujun, Cuccaro, M.L., Hauser, E.R., Raiford, K.L., Menold, M.M., Wolpert, C.M., Ravan, S.A., Elston, L., Decena, K., Donnelly, S.L., Abramson, R.K., Wright, H.H., DeLong, G.R., Gilbert, J.R., Pericak-Vance, M.A.

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Genetic Studies of Autistic Disorder and Chromosome 7 von Ashley-Koch, A., Wolpert, C.M., Menold, M.M., Zaeem, L., Basu, S., Donnelly, S.L., Ravan, S.A., Powell, C.M., Qumsiyeh, M.B., Aylsworth, A.S., Vance, J.M., Gilbert, J.R., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

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Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder von Martin, E.R., Menold, M.M., Wolpert, C.M., Bass, M.P., Donnelly, S.L., Ravan, S.A., Zimmerman, A., Gilbert, J.R., Vance, J.M., Maddox, L.O., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

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Ordered-subset analysis of savant skills in autism for 15q11-q13 von Ma, D.Q., Jaworski, J., Menold, M.M., Donnelly, S., Abramson, R.K., Wright, H.H., Delong, G.R., Gilbert, J.R., Pericak-Vance, M.A., Cuccaro, Michael L.

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No association between the APOE gene and autism von Raiford, K.L., Shao, Y., Allen, I.C., Martin, E.R., Menold, M.M., Wright, H.H., Abramson, R.K., Worley, G., DeLong, G.R., Vance, J.M., Cuccaro, M.L., Gilbert, J.R., 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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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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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia von Scott, W K, Gaskell, P C, Lennon, F, Wolpert, C M, Menold, M M, Aylsworth, A S, Warner, C, Farrell, C D, Boustany, R M, Albright, S G, Boyd, E, Kingston, H M, Cumming, W J, Vance, J M, Pericak-Vance, M A

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Increased concentration of spectrin is observed in avian dystrophic muscle von Repasky, E.A, Pollina, C.M, Menold, M.M, Hudecki, M.S

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Analysis of linkage disequilibrium in ?-aminobutyric acid receptor subunit genes in autistic disorder von Martin, E.R., Menold, M.M., Wolpert, C.M., Bass, M.P., Donnelly, S.L., Ravan, S.A., Zimmerman, A., Gilbert, J.R., Vance, J.M., Maddox, L.O., Wright, H.H., Abramson, R.K., DeLong, G.R., Cuccaro, M.L., Pericak-Vance, M.A.

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