From the genetic architecture to synaptic plasticity in autism spectrum disorder

By Thomas Bourgeron. Nature Reviews Neuroscience, 2015

892 citations recorded by the source corpus.

Subfields: Cell Biology, Cognitive Neuroscience, Genetics

View Paper: https://www.semanticscholar.org/paper/2472f0533eff7558a915eb23b50d31ed055dc804

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In Cell Biology

1. M. Sheng
2. R. Nicoll
3. R. Jahn
4. Richard L. Huganir
5. R. Malenka
6. C. Hoogenraad
7. T. Sūdhof

In Cognitive Neuroscience

1. Jean-Pierre Changeux
2. Stanislas Dehaene
3. Pieter R. Roelfsema
4. George A. Mashour
5. R. Malenka
6. Richard L. Huganir
7. M. Sheng
8. Tilmann Achsel

In Genetics

1. Huaiyu Mi
2. Christine Ladd-Acosta
3. G. Feng
4. Danielle Posthuma
5. Tilmann Achsel
6. R. Malenka
7. C. Bagni
8. Haiming Tang

Citations in the corpus

• Conscious Processing and the Global Neuronal Workspace Hypothesis (2020, background): “Social relationships, which appear altered in autism and autism spectrum disorder, are thought to affect the GNW architectures for conscious processing (Bourgeron, 2015; Graziano and Kastner, 2011).”
• Phase 2 of CATALISE: a multinational and multidisciplinary Delphi consensus study of problems with language development: Terminology (2017, neutral): “…genetic or neurological causes (Fitzgerald et al., 2015; Shevell, Majnemer, Rosenbaum, & Abrahamowicz, 2001), with the numbers of known aetiology increasing with advances in genetic methods (Bourgeron, 2015; Fitzgerald et al., 2015; Shevell et al., 2001).”
• SynGO: an evidence-based, expert-curated knowledgebase for the synapse (2019, background): “, 2010; Bourgeron, 2015; Grant, 2012; Monday and Castillo, 2017), such as autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), schizophrenia, Alzheimer’s disease, and Parkinson’s disease (Arnsten et al., 2012; Bourgeron, 2015; De Rubeis et al., 2014; Fromer et al., 2014; ”
• The Changing Epidemiology of Autism Spectrum Disorders (2016, background): “Over the past decade, genetic studies have been quite successful at identifying rare genetic variation, including inherited and de novo mutations and copy number variations (CNVs), related to autism or autistic features (18).”
• Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder (2017, neutral): “putative de novo SNVs from the Illumina WGS data of two probands (2-1266-003 and 3-0141-000) in the trio families and from Complete Genomics WGS data of one proband (2-1292-003) in a quartet family for Sanger sequencing ( Supplementary Table 3 ).”