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Academic Journal

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Authors : Merikangas, A K; Segurado, R; Heron, E A

Subjects: DNA copy number variations; AUTISM spectrum disorders; HYPERLEXIA

Source: Molecular Psychiatry. Nov2015, Vol. 20 Issue 11, p1366-1372. 7p.

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Academic Journal

2,3,7,8-Tetrachlorodibenzo-p-dioxin in breast milk increases autistic traits of 3-year-old children in Vietnam.

Authors : Nishijo, M; Pham, T T; Nguyen, A T N

Subjects: AUTISM; DEVELOPMENTAL disabilities; AUTISM spectrum disorders

Source: Molecular Psychiatry. Nov2014, Vol. 19 Issue 11, p1220-1226. 7p.

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Academic Journal

Common genetic variants on 1p13.2 associate with risk of autism.

Authors : Xia, K; Guo, H; Hu, Z

Subjects: AUTISM; AUTISM spectrum disorders; DEVELOPMENTAL disabilities

Source: Molecular Psychiatry. Nov2014, Vol. 19 Issue 11, p1212-1219. 8p.

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Academic Journal

Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.

Authors : Frazier, T W; Embacher, R; Tilot, A K

Subjects: PHENOTYPES; GERM cells; GENETIC mutation

Source: Molecular Psychiatry. Sep2015, Vol. 20 Issue 9, p1132-1138. 7p.

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Academic Journal

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

Authors : Moreno-De-Luca, D; Sanders, S J; Willsey, A J

Subjects: DNA copy number variations; AUTISM; COHORT analysis

Source: Molecular Psychiatry. Oct2013, Vol. 18 Issue 10, p1090-1095. 6p.

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Academic Journal

Schizophrenia genetics: emerging themes for a complex disorder.

Authors : Kavanagh, D H; Tansey, K E; O'Donovan, M C

Subjects: BIPOLAR disorder; SCHIZOAFFECTIVE disorders; AUTISM

Source: Molecular Psychiatry. Jan2015, Vol. 20 Issue 1, p72-76. 5p.

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Academic Journal

Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.

Authors : Mohn, J L; Alexander, J; Pirone, A

Subjects: AUTISM; INTELLECTUAL disabilities; ADENOMATOUS polyposis coli

Source: Molecular Psychiatry. Oct2014, Vol. 19 Issue 10, p1133-1142. 10p.

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Academic Journal

A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.

Authors : Gershon, E S; Grennan, K; Busnello, J

Subjects: BIPOLAR disorder; GENETIC mutation; CALCIUM channels

Source: Molecular Psychiatry. Aug2014, Vol. 19 Issue 8, p890-894. 5p.

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Academic Journal

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.

Authors : Toma, C; Torrico, B; Hervás, A

Subjects: DEVELOPMENTAL disabilities; AUTISM; PROTEIN-protein interactions

Source: Molecular Psychiatry. Jul2014, Vol. 19 Issue 7, p784-790. 7p.

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Academic Journal

Prenatal stress and inhibitory neuron systems: implications for neuropsychiatric disorders.

Authors : Fine, R; Zhang, J; Stevens, H E

Subjects: NEUROBEHAVIORAL disorders; NEURAL physiology; PATHOLOGICAL physiology

Source: Molecular Psychiatry. Jun2014, Vol. 19 Issue 6, p641-651. 11p.

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Academic Journal

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.

Authors : McCarthy, S E; Gillis, J; Kramer, M

Subjects: GENETICS of schizophrenia; CHROMATIN-remodeling complexes; AUTISM

Source: Molecular Psychiatry. Jun2014, Vol. 19 Issue 6, p652-658. 7p.

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Academic Journal

Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disorders.

Authors : Lotan, A; Lifschytz, T; Slonimsky, A

Subjects: NEURAL development; ABL1 gene; SCHIZOPHRENIA

Source: Molecular Psychiatry. Feb2014, Vol. 19 Issue 2, p243-252. 10p.

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Academic Journal

Elevated maternal C-reactive protein and autism in a national birth cohort.

Authors : Brown, A S; Sourander, A; Hinkka-Yli-Salomäki, S

Subjects: AUTISM; NEUROBEHAVIORAL disorders; IMMUNOLOGY of inflammation

Source: Molecular Psychiatry. Feb2014, Vol. 19 Issue 2, p259-264. 6p.

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Academic Journal

β2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort.

Authors : Cheslack-Postava, K.; Fallin, M. D.; Avramopoulos, D.

Subjects: ADRENERGIC receptors; DIAGNOSIS of autism; GENETIC polymorphisms

Source: Molecular Psychiatry. Mar2007, Vol. 12 Issue 3, p283-291. 9p.

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Academic Journal

A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins.

Authors : Corbett, B. A.; Kantor, A. B.; Schulman, H.

Subjects: PROTEIN analysis; AUTISM; BLOOD proteins

Source: Molecular Psychiatry. Mar2007, Vol. 12 Issue 3, p292-306. 15p.

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Academic Journal

Evidence for multiple loci from a genome scan of autism kindreds.

Authors : Schellenberg, G. D.; Dawson, G.; Sung, Y. J.

Subjects: GENETICS of autism; HUMAN genome; IMMUNOGENETICS

Source: Molecular Psychiatry. Nov2006, Vol. 11 Issue 11, p1049-1060. 12p. 2 Charts, 7 Graphs.

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Academic Journal

Autism and the serotonin transporter: the long and short of it.

Authors : Devlin, B.; Cook Jr., E. H.; Coon, H.

Subjects: AUTISM; AUTISM in children; DIAGNOSIS of autism

Source: Molecular Psychiatry. Dec2005, Vol. 10 Issue 12, p1110-1116. 7p. 4 Charts.

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Academic Journal

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

Authors : Molloy, C. A.; Keddache, M.; Martin, L. J.

Subjects: AUTISM in children; AUTISM; DEVELOPMENTAL disabilities

Source: Molecular Psychiatry. Aug2005, Vol. 10 Issue 8, p741-746. 6p.

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Academic Journal

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.

Authors : Auranen, M.; Varilo, T.; Alen, R.

Subjects: GENETICS; AUTISM in children; ASPERGER'S syndrome

Source: Molecular Psychiatry. 2003, Vol. 8 Issue 10, p879. 6p.

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Academic Journal

Disorder-specific functional abnormalities during sustained attention in youth with Attention Deficit Hyperactivity Disorder (ADHD) and with Autism.

Authors : Christakou, A; Murphy, C M; Chantiluke, K

Subjects: ATTENTION-deficit hyperactivity disorder; BEHAVIOR disorders in children; DEVELOPMENTAL disabilities

Source: Molecular Psychiatry. Feb2013, Vol. 18 Issue 2, p236-244. 9p. 1 Diagram, 2 Charts, 2 Graphs.

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Academic Journal

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders.

Authors : Lu, A T-H; Yoon, J; Geschwind, D H

Subjects: DEVELOPMENTAL disabilities; AUTISM; CYTOKINES

Source: Molecular Psychiatry. Feb2013, Vol. 18 Issue 2, p226-235. 10p. 1 Diagram, 2 Charts, 3 Graphs.

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Academic Journal

Modeling the functional genomics of autism using human neurons.

Authors : Konopka, G; Wexler, E; Rosen, E

Subjects: FUNCTIONAL genomics; AUTISM; NEURONS

Source: Molecular Psychiatry. Feb2012, Vol. 17 Issue 2, p202-214. 13p. 1 Diagram, 2 Charts, 2 Graphs.

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Academic Journal

The psychiatric disease risk factors DISC1 and TNIK interact to regulate synapse composition and function.

Authors : Wang, Q.; Charych, E. I.; Pulito, V. L.

Subjects: GENETICS of schizophrenia; DISEASE risk factors; PROTEIN-protein interactions

Source: Molecular Psychiatry. Oct2011, Vol. 16 Issue 10, p1006-1023. 18p. 1 Color Photograph, 1 Black and White Photograph, 6 Graphs.

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Academic Journal

A twin study of autism symptoms in Sweden.

Authors : Ronald, A.; Larsson, H.; Anckarsäter, H.

Subjects: PEDIATRIC diagnosis; DIAGNOSIS of autism; FACTOR analysis

Source: Molecular Psychiatry. Oct2011, Vol. 16 Issue 10, p1039-1047. 9p. 5 Charts, 1 Graph.

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Academic Journal

The role of neurotrophic factors in autism.

Authors : Nickl-Jockschat, T.; Michel, T. M.

Subjects: AUTISM spectrum disorders; NEUROPLASTICITY; NEUROTROPHINS

Source: Molecular Psychiatry. May2011, Vol. 16 Issue 5, p478-490. 13p.

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Search Results

Your Filters

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

2,3,7,8-Tetrachlorodibenzo-p-dioxin in breast milk increases autistic traits of 3-year-old children in Vietnam.

Common genetic variants on 1p13.2 associate with risk of autism.

Molecular and phenotypic abnormalities in individuals with germline heterozygous PTEN mutations and autism.

Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts.

Schizophrenia genetics: emerging themes for a complex disorder.

Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.

A rare mutation of CACNA1C in a patient with bipolar disorder, and decreased gene expression associated with a bipolar-associated common SNP of CACNA1C in brain.

Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.

Prenatal stress and inhibitory neuron systems: implications for neuropsychiatric disorders.

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.

Neural mechanisms underlying stress resilience in Ahi1 knockout mice: relevance to neuropsychiatric disorders.

Elevated maternal C-reactive protein and autism in a national birth cohort.

β2-Adrenergic receptor gene variants and risk for autism in the AGRE cohort.

A proteomic study of serum from children with autism showing differential expression of apolipoproteins and complement proteins.

Evidence for multiple loci from a genome scan of autism kindreds.

Autism and the serotonin transporter: the long and short of it.

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.

Disorder-specific functional abnormalities during sustained attention in youth with Attention Deficit Hyperactivity Disorder (ADHD) and with Autism.

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders.

Modeling the functional genomics of autism using human neurons.

The psychiatric disease risk factors DISC1 and TNIK interact to regulate synapse composition and function.

A twin study of autism symptoms in Sweden.

The role of neurotrophic factors in autism.

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