Damaging de novo mutations diminish motor skills in children on the autism spectrum

Cerebellar granule cells encode the expectation of reward

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Measuring shared variants in cohorts of discordant siblings with applications to autism

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Current knowledge on motor disorders in children with autism spectrum disorder (ASD)

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Excess of rare, inherited truncating mutations in autism

(2015) Niklas Krumm et al.   NATURE GENETICS

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

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Low load for disruptive mutations in autism genes and their biased transmission

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Sensorimotor dysfunctions as primary features of autism spectrum disorders

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The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

(2015) Justin Cotney et al.   Nature Communications

Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development

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De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

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Synaptic, transcriptional and chromatin genes disrupted in autism

(2014) Silvia De Rubeis et al.   NATURE

The contribution of de novo coding mutations to autism spectrum disorder

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Most genetic risk for autism resides with common variation

(2014) Trent Gaugler et al.   NATURE GENETICS

The Cerebellum, Sensitive Periods, and Autism

(2014) Samuel S.-H. Wang et al.   NEURON

Injury to the Premature Cerebellum: Outcome is Related to Remote Cortical Development

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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De Novo Gene Disruptions in Children on the Autistic Spectrum

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Common genetic variants, acting additively, are a major source of risk for autism

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FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

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Regional Cerebellar Volumes Predict Functional Outcome in Children with Cerebellar Malformations

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Telescoping of caregiver report on the Autism Diagnostic Interview - Revised

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(2011) Hyo Jung Kang et al.   NATURE

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

(2011) Irina Voineagu et al.   NATURE

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

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The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

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Impairment in movement skills of children with autistic spectrum disorders

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Psychometric Properties of the Revised Developmental Coordination Disorder Questionnaire

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Disrupted cerebellar development in preterm infants is associated with impaired neurodevelopmental outcome

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