Troy J. Gliem

发表

Erratum: Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia (The American Journal of Human Genetics (2010) 87 (618-630))

Stephan J Sanders, D. Ledbetter, U. Surti, 2011 .

B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis.

V. Torres, P. Harris, K. Hopp, 2011, Human molecular genetics.

Pediatric Myxopapillary Ependymomas: A Clinicopathologic Evaluation

A. Raghunathan, D. Warad, L. Eckel, 2020, Journal of pediatric hematology/oncology.

Mucinous cystadenoma of ovary in a patient with juvenile polyposis due to 10q23 microdeletion: Expansion of phenotype

B. Scheithauer, E. Thorland, D. Babovic‐Vuksanovic, 2010, American journal of medical genetics. Part A.

Single Nucleotide Polymorphism (SNP) Array for Histologically Ambiguous Melanocytic Tumors: Knowns and Unknowns.

T. Flotte, L. Erickson, R. Guo, 2022, The Journal of molecular diagnostics : JMD.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Edwin Cuppen, Claire Redin, Ryan L. Collins, 2016, Nature Genetics.

Extensive Genomic Copy Number Alterations are common in Squamous Cell Carcinoma Arising in Hidradenitis Suppurativa with Moderate Histological Differentiation.

Katelyn A. Reed, R. Guo, M. Davis, 2022, Human pathology.

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Urvashi Surti, Swaroop Aradhya, Margaret P Adam, 2010, American journal of human genetics.

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities

Swaroop Aradhya, Michael R Rossi, Vineith Kaul, 2011, Genetics in Medicine.

An evidence-based approach to establish the functional and clinical significance of CNVs in intellectual and developmental disabilities

Gabriele, D. Church, W. Sanger, 2022 .

Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?

E. Thorland, R. Ketterling, A. Wiktor, 2007, Genetics in Medicine.

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

U. Aypar, Troy J. Gliem, 2017, The Journal of molecular diagnostics : JMD.

Clinicopathological and genomic copy number variation analysis in nodular hidradenoma and hidradenocarcinoma with focus on prognostically important features.

Katelyn A. Reed, Hong Jiang, R. Guo, 2022, Human pathology.

Anaplastic Kaposi Sarcoma: A Clinicopathologic and Molecular Genetic Analysis.

A. Folpe, J. Hornick, A. Rosenberg, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

MDM2 Amplification Status in a Cohort of Well-Characterized Myxofibrosarcoma: A Clinicopathologic Analysis of 22 Tumors.

K. Fritchie, P. Greipp, A. Bakhshwin, 2023, International journal of surgical pathology.

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Stephan J Sanders, D. Ledbetter, U. Surti, 2010, American journal of human genetics.