Nenad Sestan, Matthew W State. Neuron 2018
Times Cited: 53
Times Cited: 53
Times Cited
Times Co-cited
Similarity
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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Identification of common genetic risk variants for autism spectrum disorder.
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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
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The contribution of de novo coding mutations to autism spectrum disorder.
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Spatio-temporal transcriptome of the human brain.
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Single-cell genomics identifies cell type-specific molecular changes in autism.
Dmitry Velmeshev, Lucas Schirmer, Diane Jung, Maximilian Haeussler, Yonatan Perez, Simone Mayer, Aparna Bhaduri, Nitasha Goyal, David H Rowitch, Arnold R Kriegstein. Science 2019
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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
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Strong association of de novo copy number mutations with autism.
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Spatiotemporal gene expression trajectories reveal developmental hierarchies of the human cortex.
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
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Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup. Neuron 2011
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
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A Single-Cell Transcriptomic Atlas of Human Neocortical Development during Mid-gestation.
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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.
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Elizabeth K Ruzzo, Laura Pérez-Cano, Jae-Yoon Jung, Lee-Kai Wang, Dorna Kashef-Haghighi, Chris Hartl, Chanpreet Singh, Jin Xu, Jackson N Hoekstra, Olivia Leventhal,[...]. Cell 2019
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.