☰

Rui Luo

Affiliations: 
2014 Human Genetics 0994 University of California, Los Angeles, Los Angeles, CA 
Google:
"Rui Luo"
Mean distance: 16.66 (cluster 6)
 		SNBCP
Tree Publications Grants Similar researchers PubMed Report error

Parents

Sign in to add mentor
Daniel Geschwind grad student 2014 UCLA
 (Informing genetic models of autism via transcriptional network analysis in brain and blood.)

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Bakken TE, Miller JA, Luo R, et al. (2015) Spatiotemporal dynamics of the postnatal developing primate brain transcriptome. Human Molecular Genetics. 24: 4327-39
Werling DM, Lowe JK, Luo R, et al. (2014) Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder. Molecular Autism. 5: 13
Chen H, Luo R, Gong S, et al. (2014) Protection genes in nucleus accumbens shell affect vulnerability to nicotine self-administration across isogenic strains of adolescent rat. Plos One. 9: e86214
Parikshak NN, Luo R, Zhang A, et al. (2013) Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell. 155: 1008-21
Konopka G, Friedrich T, Davis-Turak J, et al. (2012) Human-specific transcriptional networks in the brain. Neuron. 75: 601-17
Luo R, Sanders SJ, Tian Y, et al. (2012) Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. American Journal of Human Genetics. 91: 38-55
Celestino-Soper PB, Violante S, Crawford EL, et al. (2012) A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Proceedings of the National Academy of Sciences of the United States of America. 109: 7974-81
Bernard A, Lubbers LS, Tanis KQ, et al. (2012) Transcriptional architecture of the primate neocortex. Neuron. 73: 1083-99
Sanders SJ, Ercan-Sencicek AG, Hus V, et al. (2011) Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85
Langfelder P, Luo R, Oldham MC, et al. (2011) Is my network module preserved and reproducible? Plos Computational Biology. 7: e1001057
See more...