An atypical deletion of the Williams–Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism von Edelmann, Lisa, Prosnitz, Aaron, Pardo, Sherly, Bhatt, Jahnavi, Cohen, Ninette, Lauriat, Tara, Ouchanov, Leonid, González, Patricia J, Manghi, Elina R, Bondy, Pamela, Esquivel, Marcela, Monge, Silvia, Delgado, Marietha F, Splendore, Alessandra, Francke, Uta, Burton, Barbara K, McInnes, L Alison

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RNA metabolism and dysmyelination in schizophrenia von McInnes, L. Alison, Lauriat, Tara L.

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A quantitative regional expression profile of EAAT2 known and novel splice variants reopens the question of aberrant EAAT2 splicing in disease von Lauriat, Tara L., Richler, Esther, McInnes, L. Alison

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Characterization of KIAA0513, a novel signaling molecule that interacts with modulators of neuroplasticity, apoptosis, and the cytoskeleton von Lauriat, Tara L., Dracheva, Stella, Kremerskothen, Joachim, Duning, Kerstin, Haroutunian, Vahram, Buxbaum, Joseph D., Hyde, Thomas M., Kleinman, Joel E., Alison McInnes, L.

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Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23 von Batki, Steven, Tyler, David J, Blankenship, Kathleen, Leon, Pedro, Fournier, Eduardo, Smith, Lauren B, Spesny, Mitzi, Service, Susan K, Freimer, Nelson B, Reus, Victor I, Silva, Sandra, Gallegos, Alvaro, Sandkuijl, Lodewijk A, Escamilla, Michael A, Meza, Luis, Rojas, Eugenia, Baharloo, Siamak, Vinogradov, Sophia, Barondes, Samuel H, Weissenbach, Jean, Mclnnes, L. Alison

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