L. J. Medeiros

P53 protein overexpression in de novo acute myeloid leukemia patients with normal diploid karyotype correlates with FLT3 internal tandem duplication and worse relapse‐free survival

M. Konopleva, H. Kantarjian, M. Routbort, 2018, American journal of hematology.

Mutually exclusive recurrent KRAS and MAP2K1 mutations in Rosai–Dorfman disease

Joseph D Khoury, K. Patel, L. Medeiros, 2017, Modern Pathology.

High-resolution structural variant profiling of myelodysplastic syndromes by optical genome mapping uncovers cryptic aberrations of prognostic and therapeutic significance

G. Garcia-Manero, T. Kadia, R. Kanagal-Shamanna, 2022, Leukemia.

Only SF3B1 mutation involving K700E independently predicts overall survival in myelodysplastic syndromes

H. Kantarjian, G. Garcia-Manero, M. Routbort, 2021, Cancer.

Only SF3B1 Mutation involving K700E (And Not Other Codons), Independently Predicts Overall Survival in Myelodysplastic Syndromes

H. Kantarjian, G. Garcia-Manero, M. Routbort, 2020, bioRxiv.

Chromosome 20q deletion: a recurrent cytogenetic abnormality in patients with chronic myelogenous leukemia in remission.

L. Medeiros, C. Yin, Su S. Chen, 2011, American journal of clinical pathology.