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    Tan I.B. et al., High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer., [Epub ahead of print]., Genome Biology, Feb 12, 2015

    Seiwert T. et al., Integrative and Comparative Genomic Analysis of HPV-Positive and HPV-Negative Head and Neck Squamous Cell Carcinomas., [Epub ahead of print]., Clin. Cancer Res., Feb 01, 2015

    Ananda G. et al., Development and validation of the JAX Cancer Treatment Profileâ„¢ for detection of clinically actionable mutations in solid tumors., [Epub ahead of print]., Experimental and Molecular Pathology, Jan 03, 2015

    Adamo A. et al., 7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages., [Epub ahead of print]., Nature Genetics, Dec 15, 2014

    Asnaghi L. et al., Identification of Multiple DNA Copy Number Alterations Including Frequent 8p11.22 Amplification in Conjunctival Squamous Cell Carcinoma., , IOVS, Dec 09, 2014

    Kim H.S. et al., Phase II Clinical and Exploratory Biomarker Study of Dacomitinib in Patients with Recurrent and/or Metastatic Squamous Cell Carcinoma of Head and Neck., [Epub ahead of print]., Clin. Cancer Res., Nov 24, 2014

    Kim S. et al., High-Throughput Sequencing and Copy Number Variation Detection Using Formalin Fixed Embedded Tissue in Metastatic Gastric Cancer., [Epub ahead of print]., PLoS ONE, Nov 05, 2014

    Ku B.M. et al., High-throughput profiling identifies clinically actionable mutations in salivary duct carcinoma ., [Epub ahead of print]., J. Translational Med., Oct 25, 2014

    Seiwert T.Y. et al., Integrative and Comparative Genomic Analysis of HPV-Positive and HPV-Negative Head and Neck Squamous Cell Carcinomas., , Clin. Cancer Res., Jul 23, 2014

    Brahmachary M. et al., Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with Copy Number Variation of large tandem repeats., [Epub ahead of print]., PLoS Genetics, Jun 19, 2014

    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