Absence of association between a polymorphic GGC repeat in the 5′ untranslated region of the reelin gene and autism (original) (raw)
Lamb JA, Moore J, Bailey A, Monaco AP . Autism: recent molecular genetic advances Hum Mol Genet 2000; 9: 861–868 ArticleCASPubMed Google Scholar
DeSilva U, D'Arcangelo G, Braden VV, Chen J, Miao GG, Curran T et al. The human reelin gene: isolation, sequencing, and mapping on chromosome 7 Genome Res 1997; 7: 157–164 ArticleCASPubMed Google Scholar
International Molecular Genetic Study of Autism Consortium. A full genome screen for autism with evidence for linkage to a region on chromosome 7q Hum Mol Genet 1998; 7: 571–578
Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Rastam M, Sponheim E et al. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study Hum Mol Genet 1999; 8: 805–812 ArticleCASPubMed Google Scholar
Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL et al. Genetic studies of autistic disorder and chromosome 7 Genomics 1999; 61: 227–236 ArticleCASPubMed Google Scholar
Barrett S, Beck JC, Bernier R, Bisson E, Braun TA, Casavant TL et al. An autosomal genomic screen for autism. Collaborative linkage study of autism Am J Med Genet 1999; 88: 609–615 ArticleCASPubMed Google Scholar
Buxbaum JD, Silverman JM, Smith CJ, Kilifarski M, Reichert J, Hollander E et al. Evidence for a susceptibility gene for autism onchromosome 2 and for genetic heterogeneity Am J Hum Genet 2001; 68: 1514–1520 ArticleCASPubMedPubMed Central Google Scholar
International Molecular Genetic Study of Autism Consortium. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p Am J Hum Genet 2001; 69: 570–581
Persico AM, D'Agruma L, Maiorano N, Totaro A, Militerni R, Bravaccio C et al. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder Mol Psychiatry 2001; 6: 150–159 ArticleCASPubMed Google Scholar
Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E et al. Autism as a strongly genetic disorder: evidence from aBritish twin study Psychol Med 1995; 25: 63–77 ArticleCASPubMed Google Scholar
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden J Child Psychol Psychiatry 1989; 30: 405–416 ArticleCASPubMed Google Scholar
Ritvo ER, Jorde LB, Mason-Brothers A, Freeman BJ, Pingree C, Jones MB et al. The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling Am J Psychiatry 1989; 146: 1032–1036 ArticleCASPubMed Google Scholar
Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH et al. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism Am J Hum Genet 1995; 57: 717–726 CASPubMedPubMed Central Google Scholar
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J et al. A genomic screen of autism: evidence for a multilocus etiology Am J Hum Genet 1999; 65: 493–507 ArticleCASPubMedPubMed Central Google Scholar
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D et al. A genomewide screen for autism susceptibility loci Am J Hum Genet 2001; 69: 327–340 ArticleCASPubMedPubMed Central Google Scholar
Teitelbaum P, Teitelbaum O, Nye J, Fryman J, Maurer RG . Movement analysis in infancy may be useful for early diagnosis of autism Proc Natl Acad Sci USA 1998; 95: 13982–13987 ArticleCASPubMedPubMed Central Google Scholar
Courchesne E . Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism Curr Opin Neurobiol 1997; 7: 269–278 ArticleCASPubMed Google Scholar
Bailey A, Luthert P, Dean A, Harding B, Janota I, Montgomery M et al. A clinicopathological study of autism Brain 1998; 121: 889–905 ArticlePubMed Google Scholar
Fatemi SH . Reelin mutations in mouse and man: from reeler mouse to schizophrenia, mood disorders, autism and lissencephaly Mol Psychiatry 2001; 6: 129–133 ArticleCASPubMed Google Scholar
Fatemi SH, Earle JA, McMenomy T . Reduction in Reelin immunoreactivity in hippocampus of subjects with schizophrenia, bipolar disorder and major depression Mol Psychiatry 2000; 5: 654–663 ArticleCASPubMed Google Scholar
Guidotti A, Auta J, Davis JM, Gerevini VD, Dwivedi Y, Grayson DR et al. Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study Arch Gen Psychiatry 2000; 57: 1061–1069 ArticleCASPubMed Google Scholar
Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO et al. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations Nat Genet 2000; 26: 93–96 ArticleCASPubMed Google Scholar
Rice DS, Curran T . Mutant mice with scrambled brains: understanding the signaling pathways that control cell positioning in the CNS Genes Dev 1999; 13: 2758–2773 ArticleCASPubMed Google Scholar
Sham PC, Curtis D . An extended transmission/disequilibrium test (TDT) for multi-allele marker loci Ann Hum Genet 1995; 59: 323–336 ArticleCASPubMed Google Scholar
Ohshima T, Ogawa M, Veeranna, Hirasawa M, Longenecker G, Ishiguro K et al. Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain Proc Natl Acad Sci USA 2001; 98: 2764–2769 ArticleCASPubMedPubMed Central Google Scholar
Sheldon M, Rice DS, D'Arcangelo G, Yoneshima H, Nakajima K, Mikoshiba K et al. Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice Nature 1997; 389: 730–733 ArticleCASPubMed Google Scholar
Hiesberger T, Trommsdorff M, Howell BW, Goffinet A, Mumby MC, Cooper JA et al. Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation Neuron 1999; 24: 481–489 ArticleCASPubMed Google Scholar
Mallamaci A, Mercurio S, Muzio L, Cecchi C, Pardini CL, Gruss P et al. The lack of Emx2 causes impairment of Reelin signaling and defects of neuronal migration in the developing cerebral cortex J Neurosci 2000; 20: 1109–1118 ArticleCASPubMedPubMed Central Google Scholar
Ringstedt T, Linnarsson S, Wagner J, Lendahl U, Kokaia Z, Arenas E et al. BDNF regulates reelin expression and Cajal–Retzius cell development in the cerebral cortex Neuron 1998; 21: 305–315 ArticleCASPubMed Google Scholar
Lord C, Rutter M, Le Couteur A . Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders J Autism Dev Disord 1994; 24: 659–685 ArticleCASPubMed Google Scholar