Publications by authors named "Matthew Webley"

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Phase Determination and Demonstration of Parental Mosaicism of Intragenic Deletions Initially Identified by Chromosomal Microarray Analysis.
Lauren A Choate, Francis Hoffman, Jessica H Newman, Cassandra Runke, Matthew Webley

Genes (Basel)· May 2025

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Detection of a Cryptic EP300/ZNF384 Gene Fusion by Chromosomal Microarray and Next-Generation Sequencing Studies in a Pediatric Patient with B-Lymphoblastic Leukemia.
Holly E Berg, Patrick R Blackburn, James B Smadbeck, Kirsten E Swanson, Christopher S Rice, Matthew R Webley

Lab Med· May 2021

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Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
Patrick R Blackburn, James B Smadbeck, Iya Znoyko, Matthew R Webley, Beth A Pitel

Genes Chromosomes Cancer· July 2020

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Characterizing false-positive fluorescence in situ hybridization results by mate-pair sequencing in a patient with chronic myeloid leukemia and progression to myeloid blast crisis.
Jaime L Lopes, Matthew Webley, Beth A Pitel, Kathryn E Pearce, James B Smadbeck

Cancer Genet· May 2020

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Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis.
Mary A Gudipati, Elizabeth Waters, Carol Greene, Nidhi Goel, Nicole L Hoppman, Matthew R Webley

Mol Cytogenet· October 2019

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Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation.
Jess F Peterson, Reid G Meyer, Stephanie A Smoley, Matthew Webley, James B Smadbeck

Clin Lymphoma Myeloma Leuk· September 2019

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Identification of a Novel ZBTB20-JAK2 Fusion by Mate-Pair Sequencing in a Young Adult With B-Lymphoblastic Leukemia/Lymphoma.
Jess F Peterson, Patrick R Blackburn, Matthew R Webley, Kathryn E Pearce, Cynthia M Williamson

Mayo Clin Proc· July 2019

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Cryptic ETV6-PDGFRB fusion in a highly complex rearrangement of chromosomes 1, 5, and 12 due to a chromothripsis-like event in a myelodysplastic syndrome/myeloproliferative neoplasm.
Zeba N Singh, Stephanie Richards, Firas El Chaer, Vu H Duong, Mary A Gudipati, Matthew Webley

Leuk Lymphoma· May 2019

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Detection of a cryptic gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemia.
Jess F Peterson, Beth A Pitel, Stephanie A Smoley, James B Smadbeck, Sarah H Johnson, Matthew R Webley

Cold Spring Harb Mol Case Stud· April 2019

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RNA-Seq detects a SAMD12-EXT1 fusion transcript and leads to the discovery of an EXT1 deletion in a child with multiple osteochondromas.
Gavin R Oliver, Patrick R Blackburn, Marissa S Ellingson, Erin Conboy, Filippo Pinto E Vairo, Matthew Webley

Mol Genet Genomic Med· March 2019

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