These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


170 related items for PubMed ID: 12819446

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P, Pingree C, McMahon W, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Pitts T, Yang J, Hinds D, Myers RM, Risch N.
    Am J Med Genet; 1999 Oct 15; 88(5):551-6. PubMed ID: 10490715
    [Abstract] [Full Text] [Related]

  • 3. Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues.
    Dykens EM, Sutcliffe JS, Levitt P.
    Ment Retard Dev Disabil Res Rev; 2004 Oct 15; 10(4):284-91. PubMed ID: 15666333
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 8(6):624-34, 570. PubMed ID: 12851639
    [Abstract] [Full Text] [Related]

  • 5. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA.
    Mol Psychiatry; 2007 Apr 15; 12(4):376-84. PubMed ID: 17179998
    [Abstract] [Full Text] [Related]

  • 6. Ordered-subset analysis of savant skills in autism for 15q11-q13.
    Ma DQ, Jaworski J, Menold MM, Donnelly S, Abramson RK, Wright HH, Delong GR, Gilbert JR, Pericak-Vance MA, Cuccaro ML.
    Am J Med Genet B Neuropsychiatr Genet; 2005 May 05; 135B(1):38-41. PubMed ID: 15756693
    [Abstract] [Full Text] [Related]

  • 7. No association between the ryanodine receptor 3 gene and autism in a Japanese population.
    Tochigi M, Kato C, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, Sasaki T.
    Psychiatry Clin Neurosci; 2008 Jun 05; 62(3):341-4. PubMed ID: 18588595
    [Abstract] [Full Text] [Related]

  • 8. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

  • 9. Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19.
    Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG.
    Mol Psychiatry; 2004 Feb 15; 9(2):144-50. PubMed ID: 14699429
    [Abstract] [Full Text] [Related]

  • 10. Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
    Ylisaukko-oja T, Alarcón M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Järvelä I, Geschwind DH, Peltonen L.
    Ann Neurol; 2006 Jan 15; 59(1):145-55. PubMed ID: 16288458
    [Abstract] [Full Text] [Related]

  • 11. An autosomal genomic screen for autism.
    Collaborative Linkage Study of Autism.
    Am J Med Genet; 2001 Dec 08; 105(8):609-15. PubMed ID: 11811142
    [Abstract] [Full Text] [Related]

  • 12. A principal components analysis of the Autism Diagnostic Interview-Revised.
    Tadevosyan-Leyfer O, Dowd M, Mankoski R, Winklosky B, Putnam S, McGrath L, Tager-Flusberg H, Folstein SE.
    J Am Acad Child Adolesc Psychiatry; 2003 Jul 08; 42(7):864-72. PubMed ID: 12819447
    [Abstract] [Full Text] [Related]

  • 13. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
    Maddox LO, Menold MM, Bass MP, Rogala AR, Pericak-Vance MA, Vance JM, Gilbert JR.
    Genomics; 1999 Dec 15; 62(3):325-31. PubMed ID: 10644429
    [Abstract] [Full Text] [Related]

  • 14. Genetics of autism.
    Cook EH.
    Child Adolesc Psychiatr Clin N Am; 2001 Apr 15; 10(2):333-50. PubMed ID: 11351802
    [Abstract] [Full Text] [Related]

  • 15. Association between a GABRB3 polymorphism and autism.
    Buxbaum JD, Silverman JM, Smith CJ, Greenberg DA, Kilifarski M, Reichert J, Cook EH, Fang Y, Song CY, Vitale R.
    Mol Psychiatry; 2002 Apr 15; 7(3):311-6. PubMed ID: 11920158
    [Abstract] [Full Text] [Related]

  • 16. A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families.
    Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.
    Autism Res; 2010 Apr 15; 3(2):47-52. PubMed ID: 20437600
    [Abstract] [Full Text] [Related]

  • 17. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.
    Clin Genet; 2006 Feb 15; 69(2):124-34. PubMed ID: 16433693
    [Abstract] [Full Text] [Related]

  • 18. Evidence for multiple loci from a genome scan of autism kindreds.
    Schellenberg GD, Dawson G, Sung YJ, Estes A, Munson J, Rosenthal E, Rothstein J, Flodman P, Smith M, Coon H, Leong L, Yu CE, Stodgell C, Rodier PM, Spence MA, Minshew N, McMahon WM, Wijsman EM.
    Mol Psychiatry; 2006 Nov 15; 11(11):1049-60, 979. PubMed ID: 16880825
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 70(Pt 3):281-92. PubMed ID: 16674551
    [Abstract] [Full Text] [Related]

  • 20. [Autism, chromosome 15 and the GAbaergic dysfunction hypothesis].
    Solís-Añez E, Delgado-Luengo W, Hernández ML.
    Invest Clin; 2007 Dec 15; 48(4):529-41. PubMed ID: 18271397
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.