Search Results - "Rapoport, J.L"

Statistical approach to segmentation of single-channel cerebral MR images by Rajapakse, J.C., Giedd, J.N., Rapoport, J.L.

“…A statistical model is presented that represents the distributions of major tissue classes in single-channel magnetic resonance (MR) cerebral images. Using the…”
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Clinical utility of neuronal cells directly converted from fibroblasts of patients for neuropsychiatric disorders: studies of lysosomal storage diseases and channelopathy by Kano, S, Yuan, M, Cardarelli, R A, Maegawa, G, Higurashi, N, Gaval-Cruz, M, Wilson, A M, Tristan, C, Kondo, M A, Chen, Y, Koga, M, Obie, C, Ishizuka, K, Seshadri, S, Srivastava, R, Kato, T A, Horiuchi, Y, Sedlak, T W, Lee, Y, Rapoport, J L, Hirose, S, Okano, H, Valle, D, O'Donnell, P, Sawa, A, Kai, M

“…Methodologies for generating functional neuronal cells directly from human fibroblasts [induced neuronal (iN) cells] have been recently developed, but the…”
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Sydenham's chorea: Magnetic resonance imaging of the basal ganglia by Giedd, J.N, Rapoport, J.L, Kruesi, M.J.P, Parker, C, Schapiro, M.B, Allen, A.J, Leonard, H.L, Kaysen, D, Dickstein, D.P, Marsh, W.L, Kozuch, P.L, Hamburger, S.D, Swedo, S.E

“…Analysis of cerebral magnetic resonance images of 24 subjects with Sydenham's chorea and 48 age-, height-, weight-, gender-, and handedness-matched controls…”
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Neurodevelopmental model of schizophrenia: update 2012 by Rapoport, J L, Giedd, J N, Gogtay, N

“…The neurodevelopmental model of schizophrenia, which posits that the illness is the end state of abnormal neurodevelopmental processes that started years…”
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Attention-deficit/hyperactivity disorder is characterized by a delay in cortical maturation by Shaw, P, Eckstrand, K, Sharp, W, Blumenthal, J, Lerch, J.P, Greenstein, D, Clasen, L, Evans, A, Giedd, J, Rapoport, J.L

“…There is controversy over the nature of the disturbance in brain development that underpins attention-deficit/hyperactivity disorder (ADHD). In particular, it…”
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Common polygenic variation and risk for childhood-onset schizophrenia by Ahn, K, An, S S, Shugart, Y Y, Rapoport, J L

“…Childhood-onset schizophrenia (COS) is a rare and severe form of the disorder, with more striking abnormalities with respect to prepsychotic developmental…”
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Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia by Piton, A, Gauthier, J, Hamdan, F F, Lafrenière, R G, Yang, Y, Henrion, E, Laurent, S, Noreau, A, Thibodeau, P, Karemera, L, Spiegelman, D, Kuku, F, Duguay, J, Destroismaisons, L, Jolivet, P, Côté, M, Lachapelle, K, Diallo, O, Raymond, A, Marineau, C, Champagne, N, Xiong, L, Gaspar, C, Rivière, J-B, Tarabeux, J, Cossette, P, Krebs, M-O, Rapoport, J L, Addington, A, DeLisi, L E, Mottron, L, Joober, R, Fombonne, E, Drapeau, P, Rouleau, G A

“…Autism spectrum disorder (ASD) and schizophrenia (SCZ) are two common neurodevelopmental syndromes that result from the combined effects of environmental and…”
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High rate of disease-related copy number variations in childhood onset schizophrenia by Ahn, K, Gotay, N, Andersen, T M, Anvari, A A, Gochman, P, Lee, Y, Sanders, S, Guha, S, Darvasi, A, Glessner, J T, Hakonarson, H, Lencz, T, State, M W, Shugart, Y Y, Rapoport, J L

“…Copy number variants (CNVs) are risk factors in neurodevelopmental disorders, including autism, epilepsy, intellectual disability (ID) and schizophrenia…”
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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders by Addington, A M, Gauthier, J, Piton, A, Hamdan, F F, Raymond, A, Gogtay, N, Miller, R, Tossell, J, Bakalar, J, Germain, G, Gochman, P, Long, R, Rapoport, J L, Rouleau, G A

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Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability by Nguyen, L S, Jolly, L, Shoubridge, C, Chan, W K, Huang, L, Laumonnier, F, Raynaud, M, Hackett, A, Field, M, Rodriguez, J, Srivastava, A K, Lee, Y, Long, R, Addington, A M, Rapoport, J L, Suren, S, Hahn, C N, Gamble, J, Wilkinson, M F, Corbett, M A, Gecz, J

“…The nonsense-mediated mRNA decay (NMD) pathway was originally discovered by virtue of its ability to rapidly degrade aberrant mRNAs with premature termination…”
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A Unified Statistical Approach to Deformation-Based Morphometry by Chung, M.K., Worsley, K.J., Paus, T., Cherif, C., Collins, D.L., Giedd, J.N., Rapoport, J.L., Evans, A.C.

“…We present a unified statistical framework for analyzing temporally varying brain morphology using the 3D displacement vector field from a nonlinear…”
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S.18.05 Drug discovery and mood and anxiety disorders of childhood by Rapoport, J.L.

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Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents by Raznahan, A, Lee, Y, Long, R, Greenstein, D, Clasen, L, Addington, A, Rapoport, J L, Giedd, J N

“…Disrupted-in-schizophrenia-1 (DISC1), contains two common non-synonymous single-nucleotide polymorphisms (SNPs)—Leu607Phe and Ser704Cys—that modulate (i)…”
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Association of the dopamine receptor D4 (DRD4) gene 7-repeat allele with children with attention-deficit/hyperactivity disorder (ADHD): An update by Gornick, M.C., Addington, Anjene, Shaw, P., Bobb, A.J., Sharp, W., Greenstein, D., Arepalli, S., Castellanos, F.X., Rapoport, J.L.

“…Polymorphisms of the dopamine receptor D4 gene DRD4, 11p15.5, have previously been associated with attention‐deficit/hyperactivity disorder (ADHD) [Bobb et…”
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Effects of caffeine on development and behavior in infancy and childhood: a review of the published literature by Castellanos, F.X, Rapoport, J.L

“…The Medline literature on the behavioral effects of caffeine in infants and children are reviewed. There has been little recent work in this area. Generally,…”
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Childhood onset schizophrenia: New research by Rapoport, J.L.

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Sex chromosome anomalies in childhood onset schizophrenia: an update by Eckstrand, K, Addington, A M, Stromberg, T, Merriman, B, Miller, R, Gochman, P, Long, R, Dutra, A, Chen, Z, Meltzer, P, Nelson, S F, Rapoport, J L

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Predictors of two-year follow-up in children and adolescents with schizophrenia by Sporn, A.L., Greenstein, D., Gogtay, N., Lenane, M., Gochman, P., Mattai, A., Tossell, J., Rapoport, J.L.

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Progressive cortical gray matter loss in adolescence is specific to schizophrenia by Gogtay, N., Sporn, A., Nicolson, R., Classen, L., Greenstein, D., Giedd, J.N., Gochman, P., Lenane, M., Evans, A., Rapoport, J.L.

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Assessment of voxel-based heritability of white and gray matter density using the intraclass correlation coefficient by Bellera, C., Paus, T., Worsley, K.J., Giedd, J.N., Rapoport, J.L., Zijdenbos, A., Pausova, Z., Evans, A.C.

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