Publications by authors named "Shelly Gunn"

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Analytical performance evaluation of a commercial next generation sequencing liquid biopsy platform using plasma ctDNA, reference standards, and synthetic serial dilution samples derived from normal plasma.
Suman Verma, Mathew W Moore, Rebecca Ringler, Abhisek Ghosal, Kyle Horvath, Shelly Gunn

BMC Cancer· October 2020

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Multiparametric liquid biopsy analysis in metastatic prostate cancer.
Emmanuelle Hodara, Gareth Morrison, Alexander Cunha, Daniel Zainfeld, Tong Xu, Shelly Gunn

JCI Insight· March 2019

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Reference Size Matching, Whole-Genome Amplification, and Fluorescent Labeling as a Method for Chromosomal Microarray Analysis of Clinically Actionable Copy Number Alterations in Formalin-Fixed, Paraffin-Embedded Tumor Tissue.
Shelly R Gunn, Shailin Govender, Cynthe L Sims, Aditi Khurana, Samuel Koo

J Mol Diagn· May 2018

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Reversal of Refractory Ulcerative Colitis and Severe Chronic Fatigue Syndrome Symptoms Arising from Immune Disturbance in an HLA-DR/DQ Genetically Susceptible Individual with Multiple Biotoxin Exposures.
Shelly R Gunn, G Gibson Gunn, Francis W Mueller

Am J Case Rep· May 2016

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The genetics of interdigitating dendritic cell sarcoma share some changes with Langerhans cell histiocytosis in select cases.
Dennis P O'Malley, Lawrence Zuckerberg, Lauren B Smith, Todd S Barry, Shelly Gunn

Ann Diagn Pathol· February 2014

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Molecular cytogenetics as a clinical test for prognostic and predictive biomarkers in newly diagnosed ovarian cancer.
Shelly Gunn, Xavier Reveles, Korrie Weldon, Andres Barrera, Mariam Ishaque

J Ovarian Res· January 2013

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Array-based karyotyping in plasma cell neoplasia after plasma cell enrichment increases detection of genomic aberrations.
Barbara K Zehentner, Luise Hartmann, Krystal R Johnson, Christine F Stephenson, Douglas B Chapman, Shelly R Gunn

Am J Clin Pathol· October 2012

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The clinical effect of the dual-targeting strategy involving PI3K/AKT/mTOR and RAS/MEK/ERK pathways in patients with advanced cancer.
Toshio Shimizu, Anthony W Tolcher, Kyriakos P Papadopoulos, Muralidhar Beeram, Drew W Rasco, Shelly Gunn

Clin Cancer Res· April 2012

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A novel familial 11p15.4 microduplication associated with intellectual disability, dysmorphic features, and obesity with involvement of the ZNF214 gene.
Elvera Sofos, Matthew F Pescosolido, Jose B Quintos, Dianne Abuelo, Shelly Gunn

Am J Med Genet A· January 2012

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Microdeletion of chromosome 15q24.3-25.2 and orofacial clefting.
Bindya Sing, Dongli Song, Glenn DeSandre, Balaji Govindaswami, Scott Rosenthal, Shelly Gunn

Cleft Palate Craniofac J· September 2011

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Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML.
Angelika J Dawson, Shibani Bal, Barry McTavish, Michelle Tomiuk, Ingo Schroedter, Shelly R Gunn

Cancer Genet· June 2011

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The role of new genetic technology in investigating autism and developmental delay.
Natasha Shur, Shelly Gunn, Lloyd Feit, Albert K Oh, Yvette Yatchmink

Med Health R I· May 2011

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Clinical array-based karyotyping of breast cancer with equivocal HER2 status resolves gene copy number and reveals chromosome 17 complexity.
Shelly Gunn, I-Tien Yeh, Irina Lytvak, Budi Tirtorahardjo, Natasha Dzidic

BMC Cancer· July 2010

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The vanguard has arrived in the clinical laboratory: array-based karyotyping for prognostic markers in chronic lymphocytic leukemia.
Shelly R Gunn

J Mol Diagn· March 2010

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Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.
Shelly R Gunn, Aswani R Bolla, Lynn L Barron, Mercedes E Gorre, Mansoor S Mohammed

Leuk Res· September 2009

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Clinical validation of an array CGH test for HER2 status in breast cancer reveals that polysomy 17 is a rare event.
I-Tien Yeh, Mathew A Martin, Ryan S Robetorye, Aswani R Bolla, Chris McCaskill, Shelly R Gunn

Mod Pathol· September 2009

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Clinical application of array-based comparative genomic hybridization for the identification of prognostically important genetic alterations in chronic lymphocytic leukemia.
Russell A Higgins, Shelly R Gunn, Ryan S Robetorye

Mol Diagn Ther· November 2008

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Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
Craig Horbinski, Erika M Carter, Patricia L Heard, Malini Sathanoori, Jie Hu, Shelly Gunn

Am J Med Genet A· November 2008

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Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia.
Shelly R Gunn, Mansoor S Mohammed, Mercedes E Gorre, Philip D Cotter, Jaeweon Kim

J Mol Diagn· September 2008

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The HemeScan test for genomic prognostic marker assessment in chronic lymphocytic leukemia.
Shelly R Gunn, Mansoor S Mohammed, Clemens Hm Mellink, Lynne V Abruzzo, Ryan S Robetorye

Expert Opin Med Diagn· June 2008

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Comparative genomic hybridization arrays in clinical pathology: progress and challenges.
Shelly R Gunn, Ryan S Robetorye, Mansoor S Mohammed

Mol Diagn Ther· June 2007

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Use of DNA sequencing analysis to confirm fungemia due to Trichosporon dermatis in a pediatric patient.
Shelly R Gunn, Xavier T Reveles, Jeanette D Hamlington, Lee C Sadkowski, Teresa L Johnson-Pais

J Clin Microbiol· March 2006

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Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
Shelly R Gunn, Mansoor Mohammed, Xavier T Reveles, David H Viskochil, Janice C Palumbos

Am J Med Genet A· July 2003

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