Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
暂无分享,去创建一个
Fikret Erdogan | Reinhard Ullmann | Wei Chen | Michael J Owen | Nadine Norton | George Kirov | G. Kirov | M. Owen | Wei Chen | N. Norton | H. Ropers | M. O’Donovan | R. Ullmann | F. Erdogan | L. Georgieva | Lyudmila Georgieva | Michael C O'Donovan | Dilihan Gumus | Murat Sari | Hans-Hilger Ropers | D. Gumus | Murat Sari
[1] T. Brugha,et al. SCAN. Schedules for Clinical Assessment in Neuropsychiatry. , 1990, Archives of general psychiatry.
[2] K. Irie,et al. Nectin‐dependent localization of ZO‐1 at puncta adhaerentia junctions between the mossy fiber terminals and the dendrites of the pyramidal cells in the CA3 area of adult mouse hippocampus , 2003, The Journal of comparative neurology.
[3] M. Merzenich,et al. Model of autism: increased ratio of excitation/inhibition in key neural systems , 2003, Genes, brain, and behavior.
[4] Thomas Bourgeron,et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements , 2007, Nature Genetics.
[5] Wei Chen,et al. CGHPRO – A comprehensive data analysis tool for array CGH , 2005, BMC Bioinformatics.
[6] S. Cooper,et al. Mental ill-health in adults with intellectual disabilities: prevalence and associated factors , 2007, British Journal of Psychiatry.
[7] D J Porteous,et al. Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family. , 2001, American journal of human genetics.
[8] T. Südhof,et al. Genetic Analysis of Mint/X11 Proteins: Essential Presynaptic Functions of a Neuronal Adaptor Protein Family , 2006, The Journal of Neuroscience.
[9] Sarah Barber,et al. A set of BAC clones spanning the human genome. , 2004, Nucleic acids research.
[10] D. Conrad,et al. A high-resolution survey of deletion polymorphism in the human genome , 2006, Nature Genetics.
[11] Sarah Barber,et al. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation. , 2006, American journal of human genetics.
[12] R. Weksberg,et al. Chromosomal abnormalities and schizophrenia. , 2000, American journal of medical genetics.
[13] T. Südhof,et al. α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis , 2003, Nature.
[14] I. Gottesman,et al. Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics. , 2000, American journal of medical genetics.
[15] Evan E Eichler,et al. Widening the spectrum of human genetic variation , 2006, Nature Genetics.
[16] Thomas Bourgeron,et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism , 2003, Nature Genetics.
[17] J. Schiffman,et al. Minor physical anomalies and schizophrenia spectrum disorders: a prospective investigation. , 2002, The American journal of psychiatry.
[18] C. Garner,et al. MAGUKs in synapse assembly and function: an emerging view , 2004, Cellular and Molecular Life Sciences CMLS.
[19] A. Rzhetsky,et al. Probing genetic overlap among complex human phenotypes , 2007, Proceedings of the National Academy of Sciences.
[20] Carolyn J. Brown,et al. A comprehensive analysis of common copy-number variations in the human genome. , 2007, American journal of human genetics.
[21] N. C. Schanen,et al. High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage. , 2004, American journal of human genetics.
[22] V. Kalscheuer,et al. Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation , 2006, Cytogenetic and Genome Research.
[23] Paul J. Harrison. The neuropathology of schizophrenia , 2008 .
[24] Jocelyn M. Bischof,et al. A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues , 2001, BMC Genetics.
[25] M. Owen,et al. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS) , 1999, Schizophrenia Research.
[26] Woon Kyu Lee,et al. Identification of DNA copy-number aberrations by array-comparative genomic hybridization in patients with schizophrenia. , 2006, Biochemical and biophysical research communications.
[27] Andrew J Sharp,et al. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome , 2006, Nature Genetics.
[28] Jonathan Sebat,et al. Major changes in our DNA lead to major changes in our thinking , 2007, Nature Genetics.
[29] T. Südhof,et al. Cartography of neurexins: More than 1000 isoforms generated by alternative splicing and expressed in distinct subsets of neurons , 1995, Neuron.
[30] Kenny Q. Ye,et al. Strong Association of De Novo Copy Number Mutations with Autism , 2007, Science.
[31] J. Sutcliffe,et al. Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures , 2003, BMC Genomics.
[32] S. Jóźwiak,et al. Positive and negative regulation of TSC2 activity and its effects on downstream effectors of the mTOR pathway , 2007, NeuroMolecular Medicine.
[33] Charles E. Schwartz,et al. High frequency of neurexin 1β signal peptide structural variants in patients with autism , 2006, Neuroscience Letters.
[34] Jacqueline Blundell,et al. A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice , 2007, Science.
[35] Albert David,et al. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. , 2004, American journal of human genetics.
[36] Edwin H Cook,et al. Autism as a paradigmatic complex genetic disorder. , 2004, Annual review of genomics and human genetics.
[37] D. Conrad,et al. Global variation in copy number in the human genome , 2006, Nature.
[38] T. Südhof,et al. Mints as Adaptors , 2000, The Journal of Biological Chemistry.
[39] Paul J. Harrison,et al. Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence , 2005, Molecular Psychiatry.
[40] L. Petrangeli,et al. Schedules for Clinical Assessment in Neuropsychiatry , 1997, Epidemiologia e Psichiatria Sociale.
[41] J. Posner,et al. Cloning of a leucine-zipper protein recognized by the sera of patients with antibody-associated paraneoplastic cerebellar degeneration. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[42] T. Südhof,et al. Activity-Dependent Validation of Excitatory versus Inhibitory Synapses by Neuroligin-1 versus Neuroligin-2 , 2007, Neuron.
[43] Ann Marie Craig,et al. Neurexin–neuroligin signaling in synapse development , 2007, Current Opinion in Neurobiology.
[44] K. Coleman,et al. A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: Implications for clinical evaluation and treatment , 2007, Current psychiatry reports.
[45] I. Gottesman. Schizophrenia Genesis: The Origins of Madness , 1990 .
[46] T. Südhof,et al. Munc18-1 binds directly to the neuronal SNARE complex , 2007, Proceedings of the National Academy of Sciences.
[47] N. Williams,et al. Gene copy number variation in schizophrenia , 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[48] N. Carter,et al. DNA microarrays for comparative genomic hybridization based on DOP‐PCR amplification of BAC and PAC clones , 2003, Genes, chromosomes & cancer.
[49] Ivan Nikolov,et al. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria , 2004, Biological Psychiatry.
[50] D. Blackwood,et al. Chromosomal abnormalities and mental illness , 2003, Molecular Psychiatry.
[51] Ton Feuth,et al. Diagnostic genome profiling in mental retardation. , 2005, American journal of human genetics.
[52] T. Südhof,et al. Extracellular domains of alpha-neurexins participate in regulating synaptic transmission by selectively affecting N- and P/Q-type Ca2+ channels. , 2005, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[53] T. Südhof,et al. Extracellular Domains of α-Neurexins Participate in Regulating Synaptic Transmission by Selectively Affecting N- and P/Q-Type Ca2+ Channels , 2005, The Journal of Neuroscience.
[54] W. Honer,et al. DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling. , 2006, Human molecular genetics.
[55] M. Dalva,et al. Cell adhesion molecules: signalling functions at the synapse , 2007, Nature Reviews Neuroscience.
[56] V. Liebscher,et al. Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation. , 2007, American journal of human genetics.
[57] Bradley P. Coe,et al. A tiling resolution DNA microarray with complete coverage of the human genome , 2004, Nature Genetics.
[58] Robin M. Murray,et al. The Epidemiology of Schizophrenia , 2004 .