フォロー
Rui Luo
Rui Luo
確認したメール アドレス: ucla.edu
タイトル
引用先
引用先
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...
Neuron 70 (5), 863-885, 2011
14722011
Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism
NN Parikshak, R Luo, A Zhang, H Won, JK Lowe, V Chandran, S Horvath, ...
Cell 155 (5), 1008-1021, 2013
10582013
Is my network module preserved and reproducible?
P Langfelder, R Luo, MC Oldham, S Horvath
PLoS computational biology 7 (1), e1001057, 2011
9002011
Human-specific transcriptional networks in the brain
G Konopka, T Friedrich, J Davis-Turak, K Winden, MC Oldham, F Gao, ...
Neuron 75 (4), 601-617, 2012
2762012
Transcriptional architecture of the primate neocortex
A Bernard, LS Lubbers, KQ Tanis, R Luo, AA Podtelezhnikov, EM Finney, ...
Neuron 73 (6), 1083-1099, 2012
2462012
Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders
R Luo, SJ Sanders, Y Tian, I Voineagu, N Huang, SH Chu, L Klei, C Cai, ...
The American Journal of Human Genetics, 2012
1932012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
PBS Celestino-Soper, S Violante, EL Crawford, R Luo, AC Lionel, ...
Proceedings of the National Academy of Sciences 109 (21), 7974-7981, 2012
1532012
Is human blood a good surrogate for brain tissue in transcriptional studies?
C Cai, P Langfelder, TF Fuller, MC Oldham, R Luo, LH van den Berg, ...
BMC genomics 11, 1-15, 2010
1252010
Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder
DM Werling, JK Lowe, R Luo, RM Cantor, DH Geschwind
Molecular autism 5, 1-16, 2014
422014
Protection genes in nucleus accumbens shell affect vulnerability to nicotine self-administration across isogenic strains of adolescent rat
H Chen, R Luo, S Gong, SG Matta, BM Sharp
PLoS One 9 (1), e86214, 2014
122014
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