Autism: Many Genes, Common Pathways?
暂无分享,去创建一个
[1] Eric M. Morrow,et al. Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry , 2008, Science.
[2] D. Geschwind,et al. Advances in autism genetics: on the threshold of a new neurobiology , 2008, Nature Reviews Genetics.
[3] Joshua M. Korn,et al. Association between microdeletion and microduplication at 16p11.2 and autism. , 2008, The New England journal of medicine.
[4] D. Pinto,et al. Structural variation of chromosomes in autism spectrum disorder. , 2008, American journal of human genetics.
[5] Katarzyna Chawarska,et al. Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders. , 2008, American journal of human genetics.
[6] J. Sebat,et al. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. , 2008, American journal of human genetics.
[7] Tanya M. Teslovich,et al. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. , 2008, American journal of human genetics.
[8] Kenny Q. Ye,et al. A unified genetic theory for sporadic and inherited autism , 2007, Proceedings of the National Academy of Sciences.
[9] J. Lupski,et al. Genomic rearrangements and sporadic disease , 2007, Nature Genetics.
[10] C. Lajonchere,et al. Paternal age and autism are associated in a family-based sample , 2007, Molecular Psychiatry.
[11] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[12] Thomas Bourgeron,et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements , 2007, Nature Genetics.
[13] D. Geschwind,et al. Autism spectrum disorders: developmental disconnection syndromes , 2007, Current Opinion in Neurobiology.
[14] Pat Levitt,et al. A genetic variant that disrupts MET transcription is associated with autism , 2006, Proceedings of the National Academy of Sciences.
[15] Mark Weiser,et al. Advancing paternal age and autism. , 2006, Archives of general psychiatry.
[16] R Redon,et al. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders , 2006, Journal of Medical Genetics.
[17] D. Stephan,et al. Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2. , 2006, The New England journal of medicine.
[18] U. Frith,et al. The Weak Coherence Account: Detail-focused Cognitive Style in Autism Spectrum Disorders , 2006, Journal of autism and developmental disorders.
[19] Emanuel Dicicco-Bloom,et al. Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus. , 2005, American journal of human genetics.
[20] D. Geschwind,et al. Replication of autism linkage: fine-mapping peak at 17q21. , 2005, American journal of human genetics.
[21] J. Bressler,et al. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A , 2004, American journal of medical genetics. Part A.
[22] Edwin H Cook,et al. Autism as a paradigmatic complex genetic disorder. , 2004, Annual review of genomics and human genetics.
[23] Kenny Q. Ye,et al. Large-Scale Copy Number Polymorphism in the Human Genome , 2004, Science.
[24] 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.
[25] E. Gershon,et al. Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7 , 2002, Molecular Psychiatry.