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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Analysis of the RELN gene as a genetic risk factor for autism von Skaar, D A, Shao, Y, Haines, J L, Stenger, J E, Jaworski, J, Martin, E R, DeLong, G R, Moore, J H, McCauley, J L, Sutcliffe, J S, Ashley-Koch, A E, Cuccaro, M L, Folstein, S E, 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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Multifactor Dimensionality Reduction–Phenomics: A Novel Method to Capture Genetic Heterogeneity with Use of Phenotypic Variables von Mei, H., Cuccaro, M.L., Martin, E.R.

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Multiple rare SAPAP3 missense variants in trichotillomania and OCD von Züchner, S, Wendland, J R, Ashley-Koch, A E, Collins, A L, Tran-Viet, K N, Quinn, K, Timpano, K C, Cuccaro, M L, Pericak-Vance, M A, Steffens, D C, Krishnan, K R, Feng, G, Murphy, D L

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Association and gene-gene interaction of SLC6A4 and ITGB3 in autism von Ma, D.Q., Rabionet, R., Konidari, I., Jaworski, J., Cukier, H.N., Wright, H.H., Abramson, R.K., Gilbert, J.R., Cuccaro, M.L., Pericak-Vance, M.A., Martin, E.R.

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Examination of association of genes in the serotonin system to autism von Anderson, B. M., Schnetz-Boutaud, N. C., Bartlett, J., Wotawa, A. M., Wright, H. H., Abramson, R. K., Cuccaro, M. L., Gilbert, J. R., Pericak-Vance, M. A., Haines, J. L.

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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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Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14 von Ma, D Q, Cuccaro, M L, Jaworski, J M, Haynes, C S, Stephan, D A, Parod, J, Abramson, R K, Wright, H H, Gilbert, J R, Haines, J L, Pericak-Vance, M A

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Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease von Kunkle, B.W., Carney, R.M., Kohli, M.A., Naj, A.C., Hamilton-Nelson, K.L., Whitehead, P.L., Wang, L., Lang, R., Cuccaro, M.L., Vance, J.M., Byrd, G.S., Beecham, G.W., Gilbert, J.R., Martin, E.R., Haines, J.L., Pericak-Vance, M.A.

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An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder von Ashley-Koch, A E, Mei, H, Jaworski, J, Ma, D Q, Ritchie, M D, Menold, M M, Delong, G R, Abramson, R K, Wright, H H, Hussman, J P, Cuccaro, M L, Gilbert, J R, Martin, E R, Pericak-Vance, M A

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The Relationship between Restrictive and Repetitive Behaviors in Individuals with Autism and Obsessive Compulsive Symptoms in Parents von Abramson, R. K, Ravan, S. A, Wright, H. H, Wieduwilt, K, Wolpert, C. M, Donnelly, S. A, Pericak-Vance, M. A, Cuccaro, M. L

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SLITRK1 mutations in Trichotillomania von Zuchner, S, Cuccaro, M L, Tran-Viet, K N, Cope, H, Krishnan, R R, Pericak-Vance, M A, Wright, H H, Ashley-Koch, A

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SLITRK1 mutations in trichotillomania von Zuchner, S, Cuccaro, M L, Tran-Viet, K N, Cope, H, Krishnan, R R, Pericak-Vance, M A, Wright, H H, Ashley-Koch, 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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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways von O'Dushlaine, C., Rossin, L., Lee P., H., Duncan, L., Parikshak N., N., Newhouse, S., Ripke, S., Neale B., M., Purcell S., M., Posthuma, D., Nurnberger J., I., Lee S., H., Faraone S., V., Perlis R., H., Mowry B., J., Thapar, A., Goddard M., E., Witte J., S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen O., A., Anjorin, A., Anney, R., Anttila, V., Arking D., E., Asherson, P., Azevedo M., H., Backlund, L., Badner J., A., Bailey A., J., Banaschewski, T., Barchas J., D., Barnes M., R., Barrett T., B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen S., E., Berrettini, W., Betancur, Catalina, Bettecken, T., Biederman, J., Binder E., B., Black D., W., Blackwood D., H., Bloss C., S., Boehnke, M., Boomsma D., I., Breuer, R., Bruggeman, R., Cormican, P., Buccola N., G., Buitelaar J., K., Bunney W., E., Buxbaum J., D., Byerley W., F., Byrne E., M., Caesar, S., Cahn, W., Cantor R., M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Mattheisen, M., Cloninger C., R., Collier D., A., Cook E., H., Coon, H., Cormand, B., Corvin, A., Coryell W., H., Craig D., W., Craig I., W., Crosbie, J., Cuccaro M., L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., de Geus E., J., Degenhardt, F., Djurovic, S., Donohoe G., J., Doyle A., E., Duan, J., Dudbridge, F., Duketis, E., Ebstein R., P., Edenberg H., J., Elia, J., Ennis, S., Etain, B., Fanous, F.

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Variants in several genomic regions associated with asperger disorder von Salyakina, D., Ma, D.Q., Jaworski, J.M., Konidari, I., Whitehead, P.L., Henson, R., Martinez, D., Robinson, J.L., Sacharow, S., Wright, H.H., Abramson, R.K., Gilbert, J.R., Cuccaro, M.L., Pericak-Vance, M.A.

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De novo partial duplication of chromosome 7p in a male with autistic disorder von Wolpert, C.M., Donnelly, S.L., Cuccaro, M.L., Hedges, D.J., Poole, C.P., Wright, H.H., Gilbert, J.R., Pericak-Vance, M.A.

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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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