Rui Luo

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Yuan Tian, Matthew E Hurles, Irina Voineagu, 2012, American journal of human genetics.

Transcriptional Architecture of the Primate Neocortex

Allan R. Jones, Ed S. Lein, Daniel H. Geschwind, 2012, Neuron.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Is human blood a good surrogate for brain tissue in transcriptional studies?

Peter Langfelder, Steve Horvath, Chaochao Cai, 2010, BMC Genomics.

Spatiotemporal dynamics of the postnatal developing primate brain transcriptome

Ed S. Lein, Daniel H. Geschwind, Trygve E Bakken, 2015, Human molecular genetics.

A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

Bekim Sadikovic, Roger E. Stevenson, Daniel H. Geschwind, 2012, Proceedings of the National Academy of Sciences.