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Journal Abstract Search

204 related items for PubMed ID: 18271397

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  • 3. Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues.
    Dykens EM, Sutcliffe JS, Levitt P.
    Ment Retard Dev Disabil Res Rev; 2004; 10(4):284-91. PubMed ID: 15666333
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  • 4. [Molecular analysis of the GABRB3 gene in autistic patients: an exploratory study].
    Solís-Añez E, Delgado-Luengo W, Borjas-Fuentes L, Zabala W, Arráiz N, Pineda L, Portillo MG, González-Ferrer S, Chacín JA, Peña J, Montiel C, Morales A, Rojas de Atencio A, Cañizales J, González R, Miranda LE, Abreu N, Delgado J.
    Invest Clin; 2007 Jun; 48(2):225-42. PubMed ID: 17598645
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  • 5. An analysis paradigm for investigating multi-locus effects in complex disease: examination of three GABA receptor subunit genes on 15q11-q13 as risk factors for autistic disorder.
    Ashley-Koch AE, Mei H, Jaworski J, Ma DQ, Ritchie MD, Menold MM, Delong GR, Abramson RK, Wright HH, Hussman JP, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.
    Ann Hum Genet; 2006 May; 70(Pt 3):281-92. PubMed ID: 16674551
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  • 6. Association analysis of chromosome 15 gabaa receptor subunit genes in autistic disorder.
    Menold MM, Shao Y, Wolpert CM, Donnelly SL, Raiford KL, Martin ER, Ravan SA, Abramson RK, Wright HH, Delong GR, Cuccaro ML, Pericak-Vance MA, Gilbert JR.
    J Neurogenet; 2001 May; 15(3-4):245-59. PubMed ID: 12092907
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  • 7. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
    Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, Folstein SE, Haines JL, Sutcliffe JS.
    Genomics; 2001 Sep; 77(1-2):105-13. PubMed ID: 11543639
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  • 8. Autism: an overview of genetic aetiology.
    Bayou N, M'rad R, Ahlem B, Béchir Helayem M, Chaabouni H.
    Tunis Med; 2008 Jun; 86(6):573-8. PubMed ID: 19216451
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  • 10. Shared susceptibility region on chromosome 15 between autism and catatonia.
    Chagnon YC.
    Int Rev Neurobiol; 2006 Jun; 72():165-78. PubMed ID: 16697297
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  • 11. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.
    Sutcliffe JS, Nurmi EL, Lombroso PJ.
    J Am Acad Child Adolesc Psychiatry; 2003 Feb; 42(2):253-6. PubMed ID: 12544187
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  • 13. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T, Vermeesch JR, Holvoet M, Fryns JP, Devriendt K.
    Genet Couns; 2004 Feb; 15(3):293-301. PubMed ID: 15517821
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  • 14. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
    Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS.
    Mol Psychiatry; 2003 Jun; 8(6):624-34, 570. PubMed ID: 12851639
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  • 17. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13.
    Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS.
    J Am Acad Child Adolesc Psychiatry; 2003 Jul; 42(7):856-63. PubMed ID: 12819446
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  • 18. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
    Samaco RC, Hogart A, LaSalle JM.
    Hum Mol Genet; 2005 Feb 15; 14(4):483-92. PubMed ID: 15615769
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  • 20. [Genetics of autism: from genome scans to candidate genes].
    Jamain S, Betancur C, Giros B, Leboyer M, Bourgeron T.
    Med Sci (Paris); 2003 Nov 15; 19(11):1081-90. PubMed ID: 14648479
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