Author

Harrison Kwei Tsai

Boston Children's HospitalORCID 0000-0003-1134-9331Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Research Focus:differential expression· 3 Organism:human· 3 Approach:statistical model· 3 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Annette S. KimiD· 3 shared Marian H. HarrisiD· 3 shared Valentina NardiiD· 3 shared Leslie Grimmett· 2 shared Adam S. FischiD· 1 shared Andrew E. PlaceiD· 1 shared Arnaldo ArbiniiD· 1 shared Barbara A. DegariD· 1 shared

Activity by Year

2022-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Annette S. KimORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 29, 2024

Acute promyelocytic leukemia with torque teno mini virus (TTMV)::RARA fusion: an approach to screening and diagnosis

Harrison Kwei Tsai, Mark F Sabbagh, Meagan Montesion…·Jacob R. Bledsoe

The paper describes a clinicopathologic approach and tools for diagnosing APL with TTMV::RARA fusion using NGS assays, identifying four cases with poor treatment outcomes.

DOI 10.1101/2024.03.29.24304729

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintJul 29, 2022

Outlier expression of isoforms by targeted RNA sequencing as clinical markers of genomic variants in B lymphoblastic leukemia and other tumor types

Harrison Kwei Tsai, Tasos Gogakos, Va Lip…·Marian H. Harris

The paper identifies outlier RNA isoform expression as a method to detect clinically relevant genomic variants in B-ALL and other cancers with high sensitivity and specificity.

2 citations

humanbulk RNA-seq

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Genetic & Genomic MedicineBlood AdvancesPeer-reviewedMay 18, 2022

Allelic Complexity of KMT2A Partial Tandem Duplications in Acute Myeloid Leukemia and Myelodysplastic Syndromes

Harrison Kwei Tsai, Christopher James Gibson, H. Moses Murdock…·Robert Coleman Lindsley

This study identifies secondary genetic events in KMT2A-PTD patients, showing their association with disease progression and higher RNA expression.

20 citations

humanwhole-exome sequencing

𝕏 PostBluesky