Genetic advances in autism: heterogeneity and convergence on shared pathways.
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[1] Daniel P. Kennedy,et al. Mapping Early Brain Development in Autism , 2007, Neuron.
[2] Thomas Bourgeron,et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements , 2007, Nature Genetics.
[3] D. Conrad,et al. Recurrent 16p11.2 microdeletions in autism. , 2007, Human molecular genetics.
[4] I. Gottesman,et al. The endophenotype concept in psychiatry: etymology and strategic intentions. , 2003, The American journal of psychiatry.
[5] D. Geschwind,et al. Replication of autism linkage: fine-mapping peak at 17q21. , 2005, American journal of human genetics.
[6] A. Zimmerman,et al. Neuroglial activation and neuroinflammation in the brain of patients with autism , 2005, Annals of neurology.
[7] A. Couteur,et al. Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders , 1994, Journal of autism and developmental disorders.
[8] C. Walsh,et al. Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome , 2004, Nature Genetics.
[9] C. Francks,et al. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium. , 1998, Human molecular genetics.
[10] D. Stephan,et al. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. , 2006, The New England journal of medicine.
[11] T. Gilliam,et al. whole-genome molecular-interaction network Genetic-linkage mapping of complex hereditary disorders to a data , 2008 .
[12] Peter Szatmari,et al. Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes , 2008, Biological Psychiatry.
[13] Thomas Bourgeron,et al. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders , 2007, Nature Genetics.
[14] P. Bolton,et al. Autism spectrum disorders in Prader–Willi and Angelman syndromes: a systematic review , 2005, Psychiatric genetics.
[15] Robert T. Schultz,et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders , 2009, Nature.
[16] C Eng,et al. Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations , 2005, Journal of Medical Genetics.
[17] Eric M. Morrow,et al. Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry , 2008, Science.
[18] M. Lauritsen,et al. The incidence and prevalence of pervasive developmental disorders: a Danish population-based study , 2004, Psychological Medicine.
[19] S. Spence,et al. The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions. , 2001, American journal of human genetics.
[20] J. Stockman. Association between Microdeletion and Microduplication at 16p11.2 and Autism , 2009 .
[21] Stephen J. Guter,et al. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. , 2001, American journal of human genetics.
[22] E. Hatchwell,et al. Autism and environmental genomics. , 2006, Neurotoxicology.
[23] D. Geschwind,et al. Advances in autism genetics: on the threshold of a new neurobiology , 2008, Nature Reviews Genetics.
[24] J. Lupski,et al. Genomic rearrangements and sporadic disease , 2007, Nature Genetics.
[25] E. Fombonne,et al. The epidemiology of autism: a review , 1999, Psychological Medicine.
[26] Sufen Chiu,et al. Early Acceleration of Head Circumference in Children with Fragile X Syndrome and Autism , 2007, Journal of developmental and behavioral pediatrics : JDBP.
[27] D. Geschwind. Autism: Many Genes, Common Pathways? , 2008, Cell.
[28] P. Bolton,et al. Genetic heterogeneity between the three components of the autism spectrum: a twin study. , 2006, Journal of the American Academy of Child and Adolescent Psychiatry.
[29] A. Lu,et al. A quantitative trait locus analysis of social responsiveness in multiplex autism families. , 2007, The American journal of psychiatry.
[30] D. Geschwind,et al. Autism spectrum disorders: developmental disconnection syndromes , 2007, Current Opinion in Neurobiology.
[31] D. Geschwind,et al. Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs , 2005, Molecular Psychiatry.
[32] D. Geschwind,et al. Evidence for sex-specific risk alleles in autism spectrum disorder. , 2004, American journal of human genetics.
[33] D. Geschwind,et al. A functional genetic link between distinct developmental language disorders. , 2008, The New England journal of medicine.
[34] T. Südhof. Neuroligins and neurexins link synaptic function to cognitive disease , 2008, Nature.
[35] K. Mirnics,et al. Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression , 2009, Molecular Psychiatry.
[36] Bruce Fireman,et al. Maternal and paternal age and risk of autism spectrum disorders. , 2007, Archives of pediatrics & adolescent medicine.
[37] Stephen T Warren,et al. Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. , 2007, Human molecular genetics.
[38] D. Geschwind,et al. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. , 2002, American journal of human genetics.
[39] J. Sebat,et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.
[40] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[41] Pat Levitt,et al. A genetic variant that disrupts MET transcription is associated with autism , 2006, Proceedings of the National Academy of Sciences.
[42] Chun Li,et al. Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder , 2008, Autism research : official journal of the International Society for Autism Research.
[43] J. Soul,et al. Positive Screening for Autism in Ex-preterm Infants: Prevalence and Risk Factors , 2008, Pediatrics.
[44] S. Spence,et al. A genomewide screen of 345 families for autism-susceptibility loci. , 2003, American journal of human genetics.
[45] D. Pinto,et al. Structural variation of chromosomes in autism spectrum disorder. , 2008, American journal of human genetics.
[46] Rebecca C. Knickmeyer,et al. Topical Review: Fetal Testosterone and Sex Differences in Typical Social Development and in Autism , 2006, Journal of child neurology.