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[HTML][HTML] 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… - The American Journal of …, 2012 - cell.com
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …
被引用次数：194 相关文章

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… - … journal of human …, 2012 - pubmed.ncbi.nlm.nih.gov
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

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… - American Journal of …, 2012 - europepmc.org
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

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… - American Journal of …, 2012 - escholarship.org
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

[引用][C] Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

RUI LUO, SJ SANDERS, ME HURLES… - American journal of …, 2012 - pascal-francis.inist.fr
Author RUI LUO 1 2; SANDERS, Stephan J 3 4 5 6; HURLES, Matthew E 9; DEVLIN, Bernie
12; STATE, Matthew W 3 4 5 6; GESCHWIND, Daniel H 1 2 8; YUAN TIAN 2 7; VOINEAGU …
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[HTML][HTML] 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… - The American Journal of …, 2012 - Elsevier
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

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… - The American Journal of …, 2012 - infona.pl
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

[引用][C] 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… - The American Journal …, 2012 - cir.nii.ac.jp
Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and
Recurrent CNVs in Autism Spectrum Disorders | CiNii Research CiNii 国立情報学研究所 …
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[HTML][HTML] 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… - American Journal of …, 2012 - ncbi.nlm.nih.gov
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …

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… - American Journal of …, 2012 - europepmc.org
Copy-number variants (CNVs) are a major contributor to the pathophysiology of autism
spectrum disorders (ASDs), but the functional impact of CNVs remains largely unexplored …