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Journal of Neurosurgery|April 6, 2019
Travels to the tropics: Deutschtum and Fedor Krause's visits to BrazilEberval Gadelha Figueiredo, Saul Almeida da Silva, Manoel Jacobsen Teixeira, et al.
World Neurosurgery|May 21, 2026
Lateral thinking: a historical analysis of the evolution of the far lateral approach and associated bony resection strategiesKivanc Yangi, Kashif Qureshi, Egemen Gok, et al.
Leukemia Research|May 14, 2023
Outcomes with high dose cytarabine and mitoxantrone induction for adults with mixed phenotype acute leukemiaEvan Atchley, Taylor M Weis, Andriy Derkach, et al.
The Journal of Clinical Investigation|July 21, 2026
Efferocytosis activates a DNMT3A-mediated oxidized DNA repair pathway to enable tissue resolutionKleopatra Avrampou, Santosh R Sukka, David Ngai, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 12, 2026
Second Primary Malignancy Risk in Patients with Multiple Myeloma Receiving CAR T-Cell Therapy or Other Systemic Anticancer Treatments: A Real-World Comparative StudyAttaya Suvannasankha, Mengying Li, Omonefe Omofuma, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
TET2 and TP53 Mutations Cooperatively Modulate the Response to Inflammation to Promote Leukemic TransformationPablo Sánchez Vela, Brianna Kelly, Claudia Brady, et al.
Blood|January 27, 2009
Genome-wide epigenetic analysis delineates a biologically distinct immature acute leukemia with myeloid/T-lymphoid featuresMaria E Figueroa, Bas J Wouters, Lucy Skrabanek, et al.
PLOS Digital Health|February 22, 2023
Wearable sensor-based performance status assessment in cancer: A pilot multicenter study from the Alliance for Clinical Trials in Oncology (A19_Pilot2)William A Wood, Deepika Dilip, Andriy Derkach, et al.
Blood|August 2, 2018
Genetic and epigenetic evolution as a contributor to WT1-mutant leukemogenesisElodie Pronier, Robert L Bowman, Jihae Ahn, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
Acute myeloid leukemia with mixed phenotype is characterized by RUNX1 mutations, stemness features and limited lineage plasticityPallavi Galera, Deepika Dilip, Andriy Derkach, et al.
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