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Jason E. Hill

Essen BioScience (United States) · US
Area of research
Hematology · Genetics
Research interest
Research interests include Acute Myeloid Leukemia Research, Chronic Lymphocytic Leukemia Research, Chronic Myeloid Leukemia Treatments, and Protein Degradation and Inhibitors.
h-index
29
citations
5,291
works
101
NIH funding
primary concept
Medicine
email

Recent publications

Measurable residual disease and posttransplantation gilteritinib maintenance for patients with <i>FLT3-ITD</i>–mutated AML
Blood 2025cited by 30position: middledoi
Effect of FLT3 maintenance in older FLT3-ITD+ adults undergoing allogeneic HCT. a post hoc analysis of BMT CTN 1506
Blood 2025cited by 1position: middledoi
Gilteritinib as Post-Transplant Maintenance for AML With Internal Tandem Duplication Mutation of <i>FLT3</i>
Journal of Clinical Oncology 2024cited by 177position: middledoi
Gilteritinib in Combination With Induction and Consolidation Chemotherapy and as Maintenance Therapy: A Phase IB Study in Patients With Newly Diagnosed AML
Journal of Clinical Oncology 2023cited by 43position: middledoi
Phase 3 trial of gilteritinib plus azacitidine vs azacitidine for newly diagnosed <i>FLT3</i>mut+ AML ineligible for intensive chemotherapy
Blood 2022cited by 123position: middledoi
Molecular profile of <i>FLT3</i>-mutated relapsed/refractory patients with AML in the phase 3 ADMIRAL study of gilteritinib
Blood Advances 2022cited by 83position: middledoi
Gilteritinib is a clinically active FLT3 inhibitor with broad activity against FLT3 kinase domain mutations
Blood Advances 2020cited by 76position: middledoi
A Somatostatin Receptor Subtype-3 (SST3) Peptide Agonist Shows Antitumor Effects in Experimental Models of Nonfunctioning Pituitary Tumors
Clinical Cancer Research 2019cited by 52position: middledoi
Emerging Mutations at Relapse in Patients with FLT3-Mutated Relapsed/Refractory Acute Myeloid Leukemia Who Received Gilteritinib Therapy in the Phase 3 Admiral Trial
Blood 2019cited by 25position: middledoi
A next-generation sequencing–based assay for minimal residual disease assessment in AML patients with FLT3-ITD mutations
Blood Advances 2018cited by 144position: middledoi
Abstract LB-1: Discovery and optimization of orally bioavailable, selective and potent ATP-independent Akt inhibitors
Cancer Research 2012cited by 0position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Alexander E. Perl · Hospital of the University of Pennsylvania5 papers (2018–2023)Erkut Bahceci · National Center for Tumor Diseases4 papers (2018–2022)Mark J. Levis · University of Turin4 papers (2018–2023)Catherine C. Smith · University of San Francisco3 papers (2019–2022)Jessica K. Altman · Northwestern University3 papers (2018–2023)Stanley C. Gill · Astellas Pharma (United States)2 papers (2022–2023)Matt Rosales · Astellas Pharma (United States)2 papers (2019–2022)Pau Montesinos · Hospital Universitari i Politècnic La Fe2 papers (2019–2022)Wen‐Chien Chou · National Taiwan University2 papers (2019–2022)Elizabeth Rich · Astellas Pharma (United States)2 papers (2022–2023)Ruishan Wu · National Health and Family Planning Commission2 papers (2022–2023) · 1 papers (2019–2019) · 1 papers (2023–2023)Violaine Havelange · de Duve Institute1 papers (2022–2022)Leena Rahmat · Yale Cancer Center1 papers (2020–2020)Chaofeng Liu · Fujian Normal University1 papers (2018–2018)Hisayuki Yokoyama · Yamagata University1 papers (2019–2019) · 1 papers (2019–2019)Shufang Liu · Brainlab (Germany)1 papers (2022–2022)Sung‐Soo Yoon · Seoul National University Hospital and Seoul National University College of Medicine1 papers (2019–2019)