Literature DB >> 18984148

Autism and brain development.

Christopher A Walsh1, Eric M Morrow, John L R Rubenstein.   

Abstract

Genetic studies are refining our understanding of neurodevelopmental mechanisms in autism. Some autism-related mutations appear to disrupt genes regulated by neuronal activity, which are especially important in development of the postnatal nervous system. Gene replacement studies in mice indicate that the developmental window to ameliorate symptoms may be wider than previously anticipated.

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Year:  2008        PMID: 18984148      PMCID: PMC2701104          DOI: 10.1016/j.cell.2008.10.015

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  42 in total

1.  Patterning of frontal cortex subdivisions by Fgf17.

Authors:  Jeremy A Cholfin; John L R Rubenstein
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-18       Impact factor: 11.205

2.  Activity-dependent validation of excitatory versus inhibitory synapses by neuroligin-1 versus neuroligin-2.

Authors:  Alexander A Chubykin; Deniz Atasoy; Mark R Etherton; Nils Brose; Ege T Kavalali; Jay R Gibson; Thomas C Südhof
Journal:  Neuron       Date:  2007-06-21       Impact factor: 17.173

Review 3.  Genomic rearrangements and sporadic disease.

Authors:  James R Lupski
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

4.  MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number.

Authors:  Hsiao-Tuan Chao; Huda Y Zoghbi; Christian Rosenmund
Journal:  Neuron       Date:  2007-10-04       Impact factor: 17.173

5.  Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

Authors:  Emanuela Giacometti; Sandra Luikenhuis; Caroline Beard; Rudolf Jaenisch
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-31       Impact factor: 11.205

6.  Contribution of SHANK3 mutations to autism spectrum disorder.

Authors:  Rainald Moessner; Christian R Marshall; James S Sutcliffe; Jennifer Skaug; Dalila Pinto; John Vincent; Lonnie Zwaigenbaum; Bridget Fernandez; Wendy Roberts; Peter Szatmari; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2007-10-16       Impact factor: 11.025

7.  Reversal of neurological defects in a mouse model of Rett syndrome.

Authors:  Jacky Guy; Jian Gan; Jim Selfridge; Stuart Cobb; Adrian Bird
Journal:  Science       Date:  2007-02-08       Impact factor: 47.728

8.  Disruption of cerebral cortex MET signaling in autism spectrum disorder.

Authors:  Daniel B Campbell; Rosanna D'Oronzio; Krassi Garbett; Philip J Ebert; Karoly Mirnics; Pat Levitt; Antonio M Persico
Journal:  Ann Neurol       Date:  2007-09       Impact factor: 10.422

9.  A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice.

Authors:  Katsuhiko Tabuchi; Jacqueline Blundell; Mark R Etherton; Robert E Hammer; Xinran Liu; Craig M Powell; Thomas C Südhof
Journal:  Science       Date:  2007-09-06       Impact factor: 47.728

10.  Localizing recent adaptive evolution in the human genome.

Authors:  Scott H Williamson; Melissa J Hubisz; Andrew G Clark; Bret A Payseur; Carlos D Bustamante; Rasmus Nielsen
Journal:  PLoS Genet       Date:  2007-04-20       Impact factor: 5.917

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  93 in total

1.  Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Authors:  Rui Luo; Stephan J Sanders; Yuan Tian; Irina Voineagu; Ni Huang; Su H Chu; Lambertus Klei; Chaochao Cai; Jing Ou; Jennifer K Lowe; Matthew E Hurles; Bernie Devlin; Matthew W State; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2012-06-21       Impact factor: 11.025

Review 2.  Annual Research Review: Development of the cerebral cortex: implications for neurodevelopmental disorders.

Authors:  John L R Rubenstein
Journal:  J Child Psychol Psychiatry       Date:  2010-08-24       Impact factor: 8.982

3.  Rapid developmental maturation of neocortical FS cell intrinsic excitability.

Authors:  Ethan M Goldberg; Hyo-Young Jeong; Ilya Kruglikov; Robin Tremblay; Roman M Lazarenko; Bernardo Rudy
Journal:  Cereb Cortex       Date:  2010-08-12       Impact factor: 5.357

Review 4.  Genomic copy number variation in disorders of cognitive development.

Authors:  Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2010-11       Impact factor: 8.829

5.  Pharmacological reversal of synaptic plasticity deficits in the mouse model of fragile X syndrome by group II mGluR antagonist or lithium treatment.

Authors:  Catherine H Choi; Brian P Schoenfeld; Aaron J Bell; Paul Hinchey; Maria Kollaros; Michael J Gertner; Newton H Woo; Michael R Tranfaglia; Mark F Bear; R Suzanne Zukin; Thomas V McDonald; Thomas A Jongens; Sean M J McBride
Journal:  Brain Res       Date:  2010-11-12       Impact factor: 3.252

6.  AMPD1 functional variants associated with autism in Han Chinese population.

Authors:  Lusi Zhang; Jianjun Ou; Xiaojuan Xu; Yu Peng; Hui Guo; Yongcheng Pan; Jingjing Chen; Tianyun Wang; Hao Peng; Qiong Liu; Di Tian; Qian Pan; Xiaobin Zou; Jingping Zhao; Zhengmao Hu; Kun Xia
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2014-08-26       Impact factor: 5.270

7.  Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.

Authors:  Jian Zhou; Christopher Y Park; Chandra L Theesfeld; Aaron K Wong; Yuan Yuan; Claudia Scheckel; John J Fak; Julien Funk; Kevin Yao; Yoko Tajima; Alan Packer; Robert B Darnell; Olga G Troyanskaya
Journal:  Nat Genet       Date:  2019-05-27       Impact factor: 38.330

8.  Phosphorylation keeps PTEN phosphatase closed for business.

Authors:  Alonzo H Ross; Arne Gericke
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-27       Impact factor: 11.205

9.  Changes in prefrontal axons may disrupt the network in autism.

Authors:  Basilis Zikopoulos; Helen Barbas
Journal:  J Neurosci       Date:  2010-11-03       Impact factor: 6.167

10.  Pathogenesis of autism: a patchwork of genetic causes.

Authors:  Elena L Grigorenko
Journal:  Future Neurol       Date:  2009
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