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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

240 related items for PubMed ID: 23537858

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  • 4. Longitudinal follow-up of autism spectrum features and sensory behaviors in Angelman syndrome by deletion class.
    Peters SU, Horowitz L, Barbieri-Welge R, Taylor JL, Hundley RJ.
    J Child Psychol Psychiatry; 2012 Feb; 53(2):152-9. PubMed ID: 21831244
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  • 6. Interaction of neurodevelopmental pathways and synaptic plasticity in mental retardation, autism spectrum disorder and schizophrenia: implications for psychiatry.
    Waltereit R, Banaschewski T, Meyer-Lindenberg A, Poustka L.
    World J Biol Psychiatry; 2014 Sep; 15(7):507-16. PubMed ID: 24079538
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  • 7. Microdeletion syndromes.
    Carvill GL, Mefford HC.
    Curr Opin Genet Dev; 2013 Jun; 23(3):232-9. PubMed ID: 23664828
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  • 8. Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
    Sicca F, Imbrici P, D'Adamo MC, Moro F, Bonatti F, Brovedani P, Grottesi A, Guerrini R, Masi G, Santorelli FM, Pessia M.
    Neurobiol Dis; 2011 Jul; 43(1):239-47. PubMed ID: 21458570
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  • 9. Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.
    Chung BH, Drmic I, Marshall CR, Grafodatskaya D, Carter M, Fernandez BA, Weksberg R, Roberts W, Scherer SW.
    Eur J Med Genet; 2011 Jul; 54(5):e516-20. PubMed ID: 21689796
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  • 10. The genetic landscapes of autism spectrum disorders.
    Huguet G, Ey E, Bourgeron T.
    Annu Rev Genomics Hum Genet; 2013 Jul; 14():191-213. PubMed ID: 23875794
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  • 11. Epigenetic impacts on neurodevelopment: pathophysiological mechanisms and genetic modes of action.
    Zahir FR, Brown CJ.
    Pediatr Res; 2011 May; 69(5 Pt 2):92R-100R. PubMed ID: 21293311
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  • 15. [Genetic, environmental, and epigenetic contribution to the susceptibility to autism spectrum disorders].
    Díaz-Anzaldúa A, Díaz-Martínez A.
    Rev Neurol; 2013 Dec 16; 57(12):556-68. PubMed ID: 24288105
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  • 17. Genomic and genetic aspects of autism spectrum disorder.
    Liu X, Takumi T.
    Biochem Biophys Res Commun; 2014 Sep 19; 452(2):244-53. PubMed ID: 25173933
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  • 18. Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
    Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U, Endris V, Roberts W, Szatmari P, Pinto D, Bonin M, Riess A, Engels H, Sprengel R, Scherer SW, Rappold GA.
    Nat Genet; 2010 Jun 19; 42(6):489-91. PubMed ID: 20473310
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  • 19. From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease.
    Ku CS, Tan EK, Cooper DN.
    J Med Genet; 2013 Apr 19; 50(4):203-11. PubMed ID: 23396985
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  • 20. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.
    J Med Genet; 2010 Mar 19; 47(3):195-203. PubMed ID: 19755429
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