Publications by authors named "Troy Gliem"

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Pediatric-type Myoid Neoplasms of Somatic Soft Tissue: A Clinicopathological and Molecular Genetic Study of 78 Tumors, Highlighting Indolent Clinical Behavior and Frequent SRF Gene Rearrangements.
Erin L J Alston, Judith Jebastin Thangaiah, Ross Rowsey, Christopher D Hofich, Troy Gliem

Mod Pathol· May 2025

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Amplification Status in a Cohort of Well-Characterized Myxofibrosarcoma: A Clinicopathologic Analysis of 22 Tumors.
Nooshin K Dashti, Judith Jebastin Thangaiah, Troy Gliem, Darlene Knutson, Sara Kloft-Nelson

Int J Surg Pathol· May 2024

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TET2 somatic copy number alterations and allelic imbalances in chronic myelomonocytic leukemia.
Mark Gurney, Patricia T Greipp, Troy Gliem, Ryan Knudson, Aref Al-Kali

Leuk Res· November 2023

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Anaplastic Kaposi Sarcoma: A Clinicopathologic and Molecular Genetic Analysis.
Grant M Fischer, Troy J Gliem, Patricia T Greipp, Andrew E Rosenberg, Andrew L Folpe

Mod Pathol· August 2023

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Clinicopathological and genomic copy number variation analysis in nodular hidradenoma and hidradenocarcinoma with focus on prognostically important features.
Hong Jiang, Kabeer Shah, Katelyn A Reed, Troy J Gliem, Ruifeng Guo

Hum Pathol· November 2022

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Single-Nucleotide Polymorphism Array for Histologically Ambiguous Melanocytic Tumors.
Katherine B Geiersbach, Troy J Gliem, Sarah M Jenkins, Athanasios G Gaitatzes, Pamela R Brodersen

J Mol Diagn· November 2022

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Extensive genomic copy number alterations are common in squamous cell carcinoma arising in hidradenitis suppurativa with moderate histological differentiation.
Casey Gleue, Kabeer Shah, Troy Gliem, Katelyn Reed, Mark D P Davis

Hum Pathol· August 2022

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Pediatric Myxopapillary Ependymomas: A Clinicopathologic Evaluation.
Kathryn L Eschbacher, Amulya Nageswara Rao, Patricia T Greipp, Troy J Gliem, David J Daniels

J Pediatr Hematol Oncol· November 2021

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Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed, Paraffin-Embedded Products of Conception Specimens.
Troy J Gliem, Umut Aypar

J Mol Diagn· November 2017

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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Troy Gliem

Nat Genet· January 2017

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Troy J Gliem

Genet Med· September 2011

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B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.
Katharina Hopp, Christina M Heyer, Cynthia J Hommerding, Susan A Henke, Jamie L Sundsbak, Troy J Gliem

Hum Mol Genet· July 2011

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Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Daniel Moreno-De-Luca, , Jennifer G Mulle, , Erin B Kaminsky, Troy J Gliem

Am J Hum Genet· November 2010

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Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: expansion of phenotype.
Nikola Babovic, Patricia S Simmons, Christopher Moir, Erik C Thorland, Bernd Scheithauer, Troy J Gliem

Am J Med Genet A· October 2010

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Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?
Erik C Thorland, Patrick R Gonzales, Troy J Gliem, Anne E Wiktor, Rhett P Ketterling

Genet Med· September 2007

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