Associated Papers
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Schmitz-Abe K et al.
Scientific Reports, 2020
32820185 (PubMed )
Supplement: 41598_2020_70656_MOESM1_ESM.pdf
Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.
Jiang YH et al.
Critical Reviews in Clinical Laboratory Sciences, 2014
Rare inherited variation in autism: beginning to see the forest and a few trees.
Stein JL et al.
Neuron, 2013
Using whole-exome sequencing to identify inherited causes of autism.
Yu TW et al.
Neuron, 2013
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