Author

Leonard Jeffrey Medeiros

The University of Texas MD Anderson Cancer CenterORCID 0000-0001-6577-8006Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrea LagansoniD· 1 shared Andrew J. CarrolliD· 1 shared Andrew R. StiffiD· 1 shared Ann‐Kathrin EisfeldiD· 1 shared Bayard L. Powell· 1 shared Brynn LevyiD· 1 shared Christopher James WalkeriD· 1 shared Courtney Denton DinardoiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperCancer Biology

Andrea LagansonORCID

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2 papers

Recent·Most cited

Cancer BiologyLeukemiaPeer-reviewedJun 15, 2026

Prognostic and Therapeutic Implications of BRAF Mutations in Acute Myeloid Leukemia

Darren Lee, Yazan Abu-Shihab, Kate Plas…·Linde A. Miles

This study identifies BRAF mutations in AML, showing poor outcomes and unique co-mutation patterns, suggesting potential targeted therapies.

DOI 10.1038/s41375-026-02996-1

humanbulk RNA-seq

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Genetic & Genomic MedicinemedRxivPreprintJan 13, 2021

Application of Optical Genome Mapping For Comprehensive Assessment of Chromosomal Structural Variants for Clinical Evaluation of Myelodysplastic Syndromes

Hui Yang, Guillermo Garcia‐Manero, Diana Marcela Rush…·Rashmi Kanagal‐Shamanna

This study evaluates optical genome mapping's ability to detect chromosomal variants in MDS patients, showing high concordance with standard methods and identifying additional clinically relevant aberrations.

13 citations

humanwhole-genome sequencing

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