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    Szatkiewicz J.P. et al., Copy number variation in schizophrenia in Sweden., [Epub ahead of print]., Mol. Psychiatry, Apr 29, 2014

    Cui W. et al., Frequent copy number variations of PI3K/AKT pathway and aberrant protein expressions of PI3K subunits are associated with inferior survival in diffuse large B cell lymphoma., [Epub ahead of print]., J. Trans. Med., Jan 13, 2014

    Tothill R.W. et al., Massively-parallel sequencing assists the diagnosis and guided treatment of cancers of unknown primary., [Epub ahead of print]., Journal of Pathology, Nov 12, 2013

    Tyson C. et al., Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2., [Epub ahead of print]., European Journal of Human Genetics, Sep 18, 2013

    Sailani M.R. et al., The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down Syndrome., [Epub ahead of print]., Genome Res., Jun 19, 2013

    Ruderfer D.F. et al., Mosaic copy number variation in schizophrenia., [Epub ahead of print]., Eur J Hum Genet., Jan 16, 2013

    O'Huallachain M. et al., Extensive genetic variation in somatic human tissues., [Epub ahead of print]., PNAS, Oct 30, 2012

    Northcott P.A. et al., Subgroup-specific structural variation across 1,000 medulloblastoma genomes., [Epub ahead of print]., Nature., Jul 25, 2012

    Iskow R.C. et al., Regulatory element copy number differences shape primate expression profiles., [Epub ahead of print]., PNAS, Jul 13, 2012