Gokul Ramaswami, Daniel H Geschwind. Handb Clin Neurol 2018
Times Cited: 84
Times Cited: 84
Times Cited
Times Co-cited
Similarity
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Synaptic, transcriptional and chromatin genes disrupted in autism.
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The contribution of de novo coding mutations to autism spectrum disorder.
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Jon Baio, Lisa Wiggins, Deborah L Christensen, Matthew J Maenner, Julie Daniels, Zachary Warren, Margaret Kurzius-Spencer, Walter Zahorodny, Cordelia Robinson Rosenberg, Tiffany White,[...]. MMWR Surveill Summ 2018
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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
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Identification of common genetic risk variants for autism spectrum disorder.
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De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
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Genomic Patterns of De Novo Mutation in Simplex Autism.
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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
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From the genetic architecture to synaptic plasticity in autism spectrum disorder.
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Matthew J Maenner, Kelly A Shaw, Jon Baio, Anita Washington, Mary Patrick, Monica DiRienzo, Deborah L Christensen, Lisa D Wiggins, Sydney Pettygrove, Jennifer G Andrews,[...]. MMWR Surveill Summ 2020
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Daniel J Weiner, Emilie M Wigdor, Stephan Ripke, Raymond K Walters, Jack A Kosmicki, Jakob Grove, Kaitlin E Samocha, Jacqueline I Goldstein, Aysu Okbay, Jonas Bybjerg-Grauholm,[...]. Nat Genet 2017
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Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
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The Heritability of Autism Spectrum Disorder.
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Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.
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SHANK proteins: roles at the synapse and in autism spectrum disorder.
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Disruptive CHD8 mutations define a subtype of autism early in development.
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Common genetic variants, acting additively, are a major source of risk for autism.
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.
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Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism.
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5
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.