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Wang, Kai

Zilkha Neurogenetic Institute, Los Angeles.

TitleYearPMID
Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. 2014 25062598
CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. 2013 23533600
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. 2011 22138692
Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 2011 21124317
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. 2011 21194676
A genome-wide scan for common alleles affecting risk for autism. 2010 20663923
A genome-wide study reveals copy number variants exclusive to childhood obesity cases. 2010 20950786
Analysing biological pathways in genome-wide association studies. 2010 21085203
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. 2010 20601685
Functional impact of global rare copy number variation in autism spectrum disorders. 2010 20531469
Large copy-number variations are enriched in cases with moderate to extreme obesity. 2010 20622171
Rare variants create synthetic genome-wide associations. 2010 20126254
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. 2009 19404257
Common genetic variants on 5p14.1 associate with autism spectrum disorders. 2009 19404256
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. 2008 18784189
Pathway-based approaches for analysis of genomewide association studies. 2007 17966091
PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. 2007 17921354
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