Child abuse and neglect, monoamine oxidase A, and mental health outcomes: a prospective examination von Nikulina, V, Widom, C.S, Brzustowicz, L.M

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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene von Tanzi, R.E, Petrukhin, K, Chernov, I, Pellequer, J.L, Wasco, W, Ross, B, Romano, D.M, Parano, E, Pavone, L, Brzustowicz, L.M, Devoto, M, Peppercorn, J, Bush, A.I, Sternlieb, I, Pirastu, M, Gusella, J.F, Evgrafov, O, Penchaszadeh, G.K, Honig, B, Edelman, I.S, Soares, M.B, Scheinberg, I.H, Gilliam, T.C

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Recent advances in the genetics of schizophrenia von Waterworth, D.M, Bassett, A.S, Brzustowicz, L.M

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Mapping of a New SGBS Locus to Chromosome Xp22 in a Family with a Severe Form of Simpson-Golabi-Behmel Syndrome von Brzustowicz, L.M., Farrell, S., Khan, M.B., Weksberg, R.

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Use of a Quantitative Trait to Map a Locus Associated with Severity of Positive Symptoms in Familial Schizophrenia to Chromosome 6p von Brzustowicz, L.M., Honer, W.G., Chow, E.W.C., Hogan, J., Hodgkinson, K., Bassett, A.S.

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Recent advances in the genetics of schizophrenia von Waterworth, D.M., Bassett, A.S., Brzustowicz, L.M.

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A Posterior Probability of Linkage-Based Re-Analysis of Schizophrenia Data Yields Evidence of Linkage to Chromosomes 1 and 17 von Logue, M.W., Brzustowicz, L.M., Bassett, A.S., Chow, E.W.C., Vieland, V.J.

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Molecular and statistical approaches to the detection and correction of errors in genotype databases von BRZUSTOWICZ, L. M, MERETTE, C, XIE, X, TOWNSEND, L, GILLIAM, T. C, OTT, J

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Mapping of Human Microtubule-Associated Protein 1B in Proximity to the Spinal Muscular Atrophy Locus at 5q13 von LIEN, L. L, BOYCE, F. M, KLEYN, P, BRZUSTOWICZ, L. M, MENNINGER, J, WARD, D. C, CONRAD GILLIAM, T, KUNKEL, L. M

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Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B von Soares, Vera M., Brzustowicz, Linda M., Kleyn, Patrick W., Knowles, James A., Palmer, David A., Asokan, Susha, Penchaszadeh, Graciela K., Munsat, Theodore L., Gilliam, T.Conrad

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Supplementary Material for: The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels von Vieland, V.J., Walters, K.A., Azaro, M., Brzustowicz, L.M., Lehner, T.

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A susceptibility locus for schizophrenia on chromosome 6 using positive symptom scores as quantitative traits von Bassett, A.S., Honer, W.G., Chow, E., McAlduff, J., Hodgkinson, K.A., Kirkham, S.J., Brzustowicz, L.M.

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Supplementary Material for: Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language-Impaired Famili... von Simmons, T.R., Flax, J.F., Azaro, M.A., Hayter, J.E., Justice, L.M., Petrill, S.A., Bassett, A.S., Tallal, P., Brzustowicz, L.M., Bartlett, C.W.

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Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6 von Brzustowicz, L.M., Kleyn, P.W., Boyce, F.M., Lien, L.L., Monaco, A.P., Penchaszadeh, G.K., Das, K., Wang, C.H., Munsat, T.L., Ott, J., Kunkel, L.M., Gilliam, T.C.

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Linkage analysis of spinal muscular atrophy von Daniels, R.J., Thomas, N.H., MacKinnon, R.N., Lehner, T., Ott, J., Flint, T.J., Dubowitz, V., Ignatius, J., Donner, M., Zerres, K., Rietschel, M., Cookson, W.O.C., Brzustowicz, L.M., Gilliam, T.C., Davies, K.E.

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An Investigation of Genetic Heterogeneity and Linkage Disequilibrium in 161 Families with Spinal Muscular Atrophy von Mérette, C., Brzustowicz, L.M., Daniels, R.J., Davies, K.E., Gilliam, T.C., Melki, J., Munnich, A., Pericak-Vance, M.A., Siddique, T., Voosen, B., Wirth, B., Ott, J.

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Paternal isodisomy for chromosome 5 in a child with spinal muscular atropy von Brzustowicz, L.M., Penchaszadeh, G.K., Gilliam, T.C., Allitto, B.A., Theve, R., Michaud, L., Sugarman, E., Handelin, B.L., Chatkupt, S., Koenigsberger, M.R.

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Assessment of Nonallelic Genetic Heterogeneity of Chronic (Type II and III) Spinal Muscular Atrophy von Brzustowicz, L.M., Mérette, C., Kleyn, P.W., Lehner, T., Castilla, L.H., Penchaszadeh, G.K., Das, K., Munsat, T.L., Ott, J., Gilliam, T.C.

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Construction of a yeast artifical chromosome contig spanning the spinal muscular atrophy disease gene region von Kleyn, P.W., Wang, C.H., Vitale, E., Pan, J., Ross, B.M., Grunn, A., Palmer, D.A., Warburton, D., Brzustowicz, L.M., Gilliam, T.G., Lien, L.L., Kunkel, L.M.

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