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Times Cited: 447
Times Cited: 447
Times Cited
Times Co-cited
Similarity
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
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Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
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The contribution of de novo coding mutations to autism spectrum disorder.
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Identification of common genetic risk variants for autism spectrum disorder.
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Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
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Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
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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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Shank3 mutant mice display autistic-like behaviours and striatal dysfunction.
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Autism spectrum disorder.
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SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs).
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Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism.
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From the genetic architecture to synaptic plasticity in autism spectrum disorder.
Thomas Bourgeron. Nat Rev Neurosci 2015
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Heritability of autism spectrum disorders: a meta-analysis of twin studies.
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Excess of rare, inherited truncating mutations in autism.
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10
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
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Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.
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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
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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
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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Autism spectrum disorder: neuropathology and animal models.
Merina Varghese, Neha Keshav, Sarah Jacot-Descombes, Tahia Warda, Bridget Wicinski, Dara L Dickstein, Hala Harony-Nicolas, Silvia De Rubeis, Elodie Drapeau, Joseph D Buxbaum,[...]. Acta Neuropathol 2017
Merina Varghese, Neha Keshav, Sarah Jacot-Descombes, Tahia Warda, Bridget Wicinski, Dara L Dickstein, Hala Harony-Nicolas, Silvia De Rubeis, Elodie Drapeau, Joseph D Buxbaum,[...]. Acta Neuropathol 2017
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Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Michael J Gandal, Pan Zhang, Evi Hadjimichael, Rebecca L Walker, Chao Chen, Shuang Liu, Hyejung Won, Harm van Bakel, Merina Varghese, Yongjun Wang,[...]. Science 2018
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Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.
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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.
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
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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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
Peter T Tsai, Court Hull, YunXiang Chu, Emily Greene-Colozzi, Abbey R Sadowski, Jarrett M Leech, Jason Steinberg, Jacqueline N Crawley, Wade G Regehr, Mustafa Sahin. Nature 2012
8
The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.
Gloria B Choi, Yeong S Yim, Helen Wong, Sangdoo Kim, Hyunju Kim, Sangwon V Kim, Charles A Hoeffer, Dan R Littman, Jun R Huh. Science 2016
Gloria B Choi, Yeong S Yim, Helen Wong, Sangdoo Kim, Hyunju Kim, Sangwon V Kim, Charles A Hoeffer, Dan R Littman, Jun R Huh. Science 2016
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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The ASD Living Biology: from cell proliferation to clinical phenotype.
Eric Courchesne, Tiziano Pramparo, Vahid H Gazestani, Michael V Lombardo, Karen Pierce, Nathan E Lewis. Mol Psychiatry 2019
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Neuroglial activation and neuroinflammation in the brain of patients with autism.
Diana L Vargas, Caterina Nascimbene, Chitra Krishnan, Andrew W Zimmerman, Carlos A Pardo. Ann Neurol 2005
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Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism.
Simone Gupta, Shannon E Ellis, Foram N Ashar, Anna Moes, Joel S Bader, Jianan Zhan, Andrew B West, Dan E Arking. Nat Commun 2014
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Adult restoration of Shank3 expression rescues selective autistic-like phenotypes.
Yuan Mei, Patricia Monteiro, Yang Zhou, Jin-Ah Kim, Xian Gao, Zhanyan Fu, Guoping Feng. Nature 2016
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8
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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Environmental risk factors for autism: an evidence-based review of systematic reviews and meta-analyses.
Amirhossein Modabbernia, Eva Velthorst, Abraham Reichenberg. Mol Autism 2017
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Behavioural phenotyping assays for mouse models of autism.
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SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
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Elevated immune response in the brain of autistic patients.
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The familial risk of autism.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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Spatio-temporal transcriptome of the human brain.
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The Role of the Immune System in Autism Spectrum Disorder.
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Maternal immune activation: Implications for neuropsychiatric disorders.
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Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition.
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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Autism spectrum disorder: insights into convergent mechanisms from transcriptomics.
Mathieu Quesnel-Vallières, Robert J Weatheritt, Sabine P Cordes, Benjamin J Blencowe. Nat Rev Genet 2019
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Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome.
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Model of autism: increased ratio of excitation/inhibition in key neural systems.
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Autism spectrum disorder.
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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.