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Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

• Authors : Nguyen, L S; Jolly, L; Shoubridge, C

Subjects: MESSENGER RNA; LYMPHOBLASTOID cell lines; INTELLECT

• Source: Molecular Psychiatry. Nov2012, Vol. 17 Issue 11, p1103-1115. 13p. 2 Charts, 3 Graphs.

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Common functional polymorphisms of DISC1 and cortical maturation in typically developing children and adolescents.

• Authors : Raznahan, A.; Lee, Y.; Long, R.

Subjects: GENETIC polymorphisms; SCHIZOPHRENIA; PREFRONTAL cortex

• Source: Molecular Psychiatry. Sep2011, Vol. 16 Issue 9, p917-926. 10p. 1 Color Photograph, 2 Charts, 2 Graphs.

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A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.

• Authors : Arcos-Burgos, M.; Jain, M.; Acosta, M. T.

Subjects: ATTENTION-deficit hyperactivity disorder; PHENOTYPES; INTERGENERATIONAL households

• Source: Molecular Psychiatry. Nov2010, Vol. 15 Issue 11, p1053-1066. 14p. 1 Color Photograph, 2 Charts, 4 Graphs.

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Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.

• Authors : Addington, A. M.; Gornick, M. C.; Shaw, P.

Subjects: SCHIZOPHRENIA; JUVENILE diseases; DEVELOPMENTAL disabilities

• Source: Molecular Psychiatry. Feb2007, Vol. 12 Issue 2, p195-205. 11p. 4 Charts, 2 Graphs.

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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

• Authors : Addington, A. M.; Gauthier, J.; Piton, A.

Subjects: LETTERS to the editor; GENETICS of schizophrenia

• Source: Molecular Psychiatry. Mar2011, Vol. 16 Issue 3, p238-239. 2p. 1 Graph.

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Sex chromosome anomalies in childhood onset schizophrenia: an update.

• Authors : Eckstrand, K; Addington, A M; Stromberg, T

Subjects: SCHIZOPHRENIA in children; SEX chromosome abnormalities; SCHIZOPHRENIA

• Source: Molecular Psychiatry. Oct2008, Vol. 13 Issue 10, p910-911. 2p. 1 Chart.

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A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

• Authors : Addington, A M; Gauthier, J; Piton, A

Subjects: SCHIZOPHRENIA

• Source: Molecular Psychiatry. Apr2012, Vol. 17 Issue 4, p468-468. 1p. 1 Graph.

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Castellanos replies

• Authors : Castellanos F; National Institute of Mental Health, Bethesda, MD, USA.; Lau E

• Source: Molecular psychiatry [Mol Psychiatry] 1999 Sep; Vol. 4 (5), pp. 414.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Internet

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Lack of an association between a dopamine-4 receptor polymorphism and attention-deficit/hyperactivity disorder: genetic and brain morphometric analyses.

• Authors : Castellanos FX; Child Psychiatry Branch, National Institute of Mental Health, Bethesda, MD 20892-1600, USA. ; Lau E

Subjects: Child Behavior* ; Polymorphism, Genetic*; Attention Deficit Disorder with Hyperactivity/Attention Deficit Disorder with Hyperactivity/Attention Deficit Disorder with Hyperactivity/*genetics

• Source: Molecular psychiatry [Mol Psychiatry] 1998 Sep; Vol. 3 (5), pp. 431-4.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

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Large CAG/CTG repeats are associated with childhood-onset schizophrenia.

• Authors : Burgess CE; Neurogenetics Unit, Karolinska Hospital, Stockholm, Sweden.; Lindblad K

Subjects: Trinucleotide Repeats*; Schizophrenia/Schizophrenia/Schizophrenia/*genetics; Adolescent

• Source: Molecular psychiatry [Mol Psychiatry] 1998 Jul; Vol. 3 (4), pp. 321-7.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print Cited Medium: Print

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