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Glessner, Joseph

TitleYearPMID
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. 2012 22169095
Integrative genomics identifies LMO1 as a neuroblastoma oncogene. 2011 21124317
Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. 2008 18784189
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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